CHAPTER II

THE PHYSICAL CONDITIONS OF THE ABYSS

It is not surprising that the naturalists of the early part of the

present century could not believe in the existence of a fauna at the

bottom of the deep seas.

The extraordinary conditions of such a region—the enormous pressure, the

absolute darkness, the probable absence of any vegetable life from want

of direct sunlight—might very well have been considered sufficient to

form an impassable barrier to the animals migrating from the shallow

waters and to prevent the development of a fauna peculiarly its own.

The fragmentary accounts of animals brought up by sounding lines from

great depths might, it is true, have thrown doubts on the current views;

but they were not of sufficient importance in themselves, nor were the

observations made with such regard to the possibility of error, as to

withstand the critical remarks that were made to explain them away.

The absence of any evidence obtained by accurate systematic research,

together with the consideration of the physical character of the ocean

bed, were quite sufficient to lead scientific men of that period to

doubt the existence of any animal life in water deeper than a few

hundred fathoms.

We now know, however, that there is a very considerable fauna at

enormous depths in all the great oceans, and we have acquired, moreover,

considerable information concerning some of those peculiar physical

conditions of the abyss that fifty years ago were merely matters of

speculation among scientific men.

The relation between animals and their environment is now a question of

such great interest and importance that it is necessary in any

description of the fauna of a particular region to consider its physical

conditions and the influence that it may be supposed to have had in

producing the characteristics of the fauna.

The peculiar physical conditions of the deep seas may be briefly stated

to be these: It is absolutely dark so far as actual sunlight is

concerned, the temperature is only a few degrees above freezing point,

the pressure is enormous, there is little or no movement of the water,

the bottom is composed of a uniform fine soft mud, and there is no plant

life.

All of these physical conditions we can appreciate except the enormous

pressure. Absolute darkness we know, the temperature of the deep seas is

not an extraordinary one, the absence of movement in the water and the

fine soft mud are conditions that we can readily appreciate; but the

pressure is far greater than anything we can realise.

At a depth of 2,500 fathoms the pressure is, roughly speaking, two and a

half tons per square inch—that is to say, several times greater than the

pressure exerted by the steam upon the piston of our most powerful

engines. Or, to put the matter in other words, the pressure per square

inch upon the body of every animal that lives at the bottom of the

Atlantic Ocean is about twenty-five times greater than the pressure that

will drive a railway train.

A most beautiful experiment to illustrate the enormous force of this

pressure was made during the voyage of H.M.S. ‘Challenger.’ I give the

description of it in the words of the late Professor Moseley.

‘Mr. Buchanan hermetically sealed up at both ends a thick glass tube

full of air, several inches in length. He wrapped this sealed tube in

flannel, and placed it, so wrapped up, in a wide copper tube, which was

one of those used to protect the deep-sea thermometers when sent down

with the sounding apparatus.

‘This copper tube was closed by a lid fitting loosely, and with holes in

it, and the copper bottom of the tube similarly had holes bored through

it. The water thus had free access to the interior of the tube when it

was lowered into the sea, and the tube was necessarily constructed with

that object in view, in order that in its ordinary use the water should

freely reach the contained thermometer.

‘The copper case containing the sealed glass tube was sent down to a

depth of 2,000 fathoms and drawn up again. It was then found that the

copper wall of the case was bulged and bent inwards opposite the place

where the glass tube lay, just as if it had been crumpled inward by

being violently squeezed.

‘The glass tube itself, within its flannel wrapper, was found when

withdrawn, reduced to a fine powder, like snow almost. What had happened

was that the sealed glass tube, when sinking to gradually increasing

depths, had held out long against the pressure, but this at last had

become too great for the glass to sustain, and the tube had suddenly

given way and been crushed by the violence of the action to a fine

powder. So violent and rapid had been the collapse that the water had

not had time to rush in by means of the holes at both ends of the copper

cylinder and thus fill the empty space left behind by the collapse of

the glass tube, but had instead crushed in the copper wall and brought

equilibrium in that manner. The process is exactly the reverse of an

explosion, and is termed by Sir Wyville Thomson an “implosion.”’

It is but reasonable to suppose that the ability to sustain this

enormous pressure can only be acquired by animals after generations of

gradual migrations from shallow waters. Those forms that are brought up

by the dredge from the depths of the ocean are usually killed and

distorted by the enormous and rapid diminution of pressure in their

journey to the surface, and it is extremely probable that shallow-water

forms would be similarly killed and crushed out of shape were they

suddenly plunged into very deep water. The fish that live at these

enormous depths are in consequence of the enormous pressure liable to a

curious form of accident. If, in chasing their prey or for any other

reason, they rise to a considerable distance above the floor of the

ocean, the gases of their swimming bladder become considerably expanded

and their specific gravity very greatly reduced. Up to a certain limit

the muscles of their bodies can counteract the tendency to float upwards

and enable the fish to regain its proper sphere of life at the bottom;

but beyond that limit the muscles are not strong enough to drive the

body downwards, and the fish, becoming more and more distended as it

goes, is gradually killed on its long and involuntary journey to the

surface of the sea. The deep-sea fish, then, are exposed to a danger

that no other animals in this world are subject to, namely that of

tumbling upwards.

That such accidents do occasionally occur is evidenced by the fact that

some fish, which are now known to be true deep-sea forms, were

discovered dead and floating on the surface of the ocean long before our

modern investigations were commenced.

Until quite recently, every one agreed that no rays of sunlight could

possibly penetrate the sea to a greater depth than a few hundred

fathoms.

Moseley says that ‘probably all is dark below 200 fathoms excepting in

so far as light is given out by phosphorescent animals,’ and Wyville

Thomson speaks of the ‘utter darkness of the deep-sea bottom.’

Within the last few years a few authors have maintained that it is quite

possible that a few rays of sunlight do penetrate even to the greatest

depths of the ocean—a view mainly based on the fact that so many

deep-sea animals possess extremely perfect and complicated eyes and very

brilliant colours. Verrill says: ‘It seems to me probable that more or

less sunlight does actually penetrate to the greatest depths of the

ocean, in the form of a soft sea-green light, perhaps at 2,000 or 3,000

fathoms equal in intensity to our partially moonlight nights and

possibly at the greatest depths equal only to starlight. It must be

remembered that in the deep sea far away from land the water is far more

transparent than near the coast.’ Packard is of a similar opinion.

There seem to me to be very slight grounds for this view. The fact that,

comparatively speaking, shallow-water fish avoid nets that are rendered

phosphorescent by entangled jelly-fish does not justify us in assuming

that deep-sea fish avoid regions where there are phosphorescent

Gorgonians or Pennatulids. It is not by any means certain that fish

avoid sunken nets on account of their phosphorescence. Most fish

possess, as is well known, a very acute sense of smell, and it is very

probable that they avoid such nets on account of the putrid odours of

the dead animals that remain attached to them.

Nor is there much strength in the further argument that it can hardly be

possible that there can be an amount of phosphorescent light regularly

evolved by the few deep-sea animals, having this power, sufficient to

cause any general illumination, or powerful enough to have influenced,

over the whole ocean, the evolution of complex eyes, brilliant and

complex protective colours, and complex commensal adaptations.

We have no sound information to go upon to be able to judge of the

amount of light given off by phosphorescent animals at the bottom of the

deep sea. The faint light they show on deck after their long journey

from the depths in which they live to the surface may be extremely small

compared with the light they give in their natural home under a pressure

of 2½ tons to the square inch. The complex eyes that many deep-sea

animals exhibit were almost certainly not evolved as such, but are

simple modifications of eyes possessed by a shallow-water ancestry.

The more recent experiments that have been made, tend to show that no

sunlight whatever penetrates to a greater depth, to take an extreme

limit, than 500 fathoms.

Fol and Sarasin, experimenting with very sensitive bromo-gelatine

plates, found that there was no reaction after ten minutes’ exposure at

a depth of 400 metres on a sunny day in March.

But although it is highly probable that not a glimmer of sunlight ever

penetrates to the depths of the ocean, there is in some places,

undoubtedly, a very considerable illumination due to the phosphorescence

of the inhabitants of the deep waters.

All the Alcyonarians are, according to Moseley, brilliantly

phosphorescent when brought to the surface. Many deep-sea fish possess

phosphorescent organs, and it is quite possible that many of the

deep-sea Protozoa, Tunicates, Jelly-fish, and Crustacea are in their

native haunts capable of giving out a very considerable amount of

phosphorescent light.

If we may be allowed to compare the light of abysmal animals with that

of surface forms, we can readily imagine that some regions of the sea

may be as brightly illuminated as a European street is at night—an

illumination with many very bright centres and many dark shadows, but

quite sufficient for a vertebrate eye to distinguish readily and at a

considerable distance both form and colour.

To give an example of the extent to which the illumination due to

phosphorescent organisms may reach, I may quote a passage from the

writings of the late Sir Wyville Thomson.

‘After leaving the Cape Verde Islands the sea was a perfect blaze of

phosphorescence. There was no moon, and although the night was perfectly

clear and the stars shone brightly, the lustre of the heavens was fairly

eclipsed by that of the sea. It was easy to read the smallest print,

sitting at the after-port in my cabin, and the bows shed on either side

rapidly widening wedges of radiance so vivid as to throw the sails and

rigging into distinct lights and shadows.’

A very similar sight may frequently be seen in the Banda seas, where on

calm nights the whole surface of the ocean seems to be a sheet of milky

fire. The light is not only to be seen where the crests of waves are

breaking, or the surface disturbed by the bows of the boat, but the

phosphorescence extends as far as the eye can reach in all directions.

It is impossible, of course, to say with any degree of certainty whether

phosphorescence such as this exists at the bottom of the deep sea, but

it is quite probable that it does in some places, and hence the

well-developed eyes and brilliant colours of some of the deep-sea

animals.

On the other hand the entire absence or rudimentary condition of the

eyes of a very considerable proportion of deep-sea animals seems to

prove that the phosphorescent illumination is not universally

distributed, and that there must be some regions in which the darkness

is so absolute that it can only be compared with the darkness of the

great caves.

It is difficult to believe that the eyes of such animals as crabs and

prawns for example would undergo degeneration if there were a glimmer of

light in their habitat, a light even so faint as that of a starlight

night in shallow water. With the faintest light the eyes would be of use

to them in seeking their prey, avoiding their enemies, and finding their

mates, and any diminution in the keenness of this sense would probably

be of considerable disadvantage to them and tend to their ultimate

extinction.

It might be argued that the animals of the abysses of the ocean probably

feed chiefly upon the carcases of pelagic animals that have fallen from

the upper regions of the sea, and that the sense of smell is probably

the most important for them in searching for their food. That is quite

probable; but many shallow-water animals invariably seek their food by

their sense of smell without showing any traces of a weakness in their

sense of sight. It may be taken as an axiom of biology that unless a

particular sense is absolutely useless to an animal or a positive

disadvantage to it, that sense will be retained.

It may be stated then with some confidence that in the abysmal depths of

the ocean there is no trace of sunlight. It is highly improbable, on the

face of it, that any ray of light could penetrate through a stratum of

water four miles in thickness, even if the water were perfectly pure and

clear, but when we remember that the upper regions, at least, are

crowded with pelagic organisms provided with skeletons of lime and

silica, we may justly consider that it is impossible.

The temperature of the water in the abyss is by no means constant for a

constant depth nor does it vary with the latitude. It is true that, as a

rule, the water is colder at greater depths than in shallower ones, and

that the deeper the thermometer is lowered into the sea, the lower the

mercury sinks. This is consistent with physical laws. If there is any

difference at all in the temperature of a column of water that has had

time to settle, the thermometer will always reach its highest point at

the top of the column and its lowest at the bottom, for the colder

particles being of greater specific gravity than the warmer ones will

sink, and the warmer ones will rise.

The truth of this will be clear if we imagine a locality at the bottom

of a deep ocean with a source of great heat such as an active volcano.

Such a source of heat would, it is true, raise the temperature of the

water in its immediate vicinity, but the particles of water thus heated

would immediately commence to rise through the superjacent layers of

colder water, and colder particles would fall to take their places. Thus

the effect of an active volcano at the bottom of the deep sea would not

be apparent at any very great distance in the same plane. In fact,

unless the bottom of the ocean was closely studded with volcanoes we

should expect to find, as indeed we do find, that the temperature of the

sea rises as the water shallows.

If then we were to consider a great ocean as simply a huge basin of

water, we should expect to find the water at the surface warmer than the

water at the bottom. The temperature of the surface would vary

constantly with the temperature of the air above it. That is to say, it

would be warmer at the equator than in the temperate regions. The

temperature at the bottom would be the same as the lowest temperature of

the basin, that is, of the earth that supports it.

The great oceans however cannot be regarded as simple basins of water

such as this. The temperature of the surface water varies only

approximately with the latitude. It is generally speaking hottest at the

equator and coldest at the poles, but surface currents in the

intermediate regions produce many irregularities in the surface

temperature.

Again, although we have no means of knowing what the temperature of the

earth is at 1,000 fathoms below the surface of the ocean, it is very

probable that in the great oceans the temperature of the deepest stratum

of water is considerably lower than the true earth temperature. This is

due to currents of cold water constantly flowing from the poles towards

the equator. If these polar currents were at any time to cease, the

temperature of the lowest strata of water would rise.

Although the polar currents cannot be actually demonstrated nor their

exact rapidity be accurately determined, the deduction from the known

facts of physical geography that they do actually exist is perfectly

sound and beyond dispute. A few considerations will, I think, make this

clear.

If the ocean were a simple basin somewhat deeper at the equator than at

the poles, the cold water at the poles would gradually sink down the

slopes of the basin towards the latitude of the equator, and the bottom

temperature of the water would be constant all the world over.

A few hills here and there would not affect the general statement that

for a constant depth the temperature of the lowest stratum of water

would be constant.

But in some places ridges occur stretching across the oceans from

continent to continent, and these ridges shut off the cold water at the

bottom of the sea on the polar side from reaching the bottom of the sea

on the equator side.

If A (fig. 1) represents a ridge stretching from continent to continent

across an ocean, and the arrow represents the direction of the current,

then the water that flows across the ridge from the polar side to the

equator side will be drawn from the layers of water lying above the

level of the ridge, and consequently none of the coldest water will ever

get across it, and from the level of the ridge to the bottom of the sea

on the equatorial side the water will have the same temperature as the

water at the level of the ridge on the polar side.

It follows from this that in places where there are deep holes in the

bed of the ocean surrounded on all sides by considerable elevations, the

temperature of the water at the bottom will be the same as the

temperature of the water on the summit of the lowest ridges that

surround them.

[Illustration: FIG. 1.—Diagram illustrating the passage of an ocean

current across a barrier (A).]

This explains why it is that we find that the bottom temperature for a

given depth is frequently less in one place than it is in another, even

in places of the same parallel of latitude. One or two examples may be

taken to illustrate these points. The temperature off Rio Janeiro in

lat. 20° S. was found by the ‘Challenger’ to be 0·6° C. at a depth of

2,150 fathoms. In a similar latitude north of the equator at a depth of

2,900 fathoms the temperature was found to be 2·2° C., and at a point

near Porto Rico there is a deep hole of 4,561 fathoms with a bottom

temperature of 2·2° C.

Again it has been shown by the American expedition that the temperature

of the water at the deepest point in the Gulf of Mexico, 2,119 fathoms,

is the same as that of the bottom of the Straits of Yucatan, 1,127

fathoms, namely 4·1° C. And, passing to another part of the world

altogether, we find in the small but deep sea that lies between the

Philippines and Borneo that, at a depth of 2,550 fathoms, the

temperature is 10·2° C.

These facts then show that, although at the bottom of the deep seas the

water is always very cold, the degree of coldness is by no means

constant in the same latitude for the same depth.

We must now return to the polar currents. We have assumed above that

these currents do exist, and it is probable that by this time the reader

must have seen why they are assumed to exist.

The water at the bottom of the ocean is exceedingly cold. Where does

this coldness come from? It is obvious that in temperate and tropical

climes it does not come from the surface. Nor is it at all probable that

it comes from the earth upon which the water rests; for, if it were so,

the temperature for water of a given depth would always be the same. We

should not find the bottom temperature of 0·4° C. at 2,900 fathoms off

Rio de la Plata and a temperature of 2·2° F. in 4,561 fathoms off Porto

Rico.

In fact the only hypothesis that can with any show of reason be put

forward to account for the temperature of the bottom of the ocean is

that which derives its coldness from the Polar ice.

We have at present very little evidence to enable us to judge of the

force and direction of the polar currents in the two hemispheres, but

the researches of the ‘Challenger’ prove almost conclusively that in the

Atlantic Ocean there is a very strong predominance of the Antarctic

polar current. In fact it seems very probable that the Arctic polar

current, if it exist at all, is very small and confined to the eastern

and western shores of the North Atlantic.

It is very probable, however, that these currents at the bottom of the

ocean are extremely slow, and, as the water is never affected by tides

or storms, the general character of the deep sea is probably one of calm

repose. This is a matter of no little importance; for, in the

consideration of the characters presented by the fauna of any particular

region, it is always necessary to take into account the physical

difficulties the animals have to contend against and the modifications

of structure they present to combat these difficulties.

Thus in a region such as that presented by the deep sea, where there are

no rapid tides, we should not expect to find such a powerful set of body

muscles in the free-swimming forms nor such a firm vertebral column as

in the animals that live in more lively water.

Perhaps it is of the nature of an assumption to say that there are no

rapid currents and tides in the abysmal depths of the ocean, for we have

no means of demonstrating or even of calculating the rate of flow of

these waters. But it is a reasonable hypothesis and one that we may well

use until the contrary is proved.

A fact of some importance that supports this hypothesis, as regards some

parts of the ocean at least, is presented by the sea-anemones.

Many of the shallow-water Actinians are known to possess minute slits in

the tentacles and disc, affording a free communication between the

general body cavity or cœlenteron and the exterior.

In many deep-sea forms the tentacles are considerably shorter and the

apertures larger than they are in shallow-water forms. It is difficult

to believe that such forms, perforated by, comparatively speaking, large

holes, could manage to live in rapidly flowing water, for if they did so

they would soon be smothered by the fine mud that composes the floor of

all the deep seas. In fact anemones of the type presented by such forms

as _Sicyonis crassa_ are only fitted for existence in sluggish or still

water.

[Illustration: FIG. 2.—_Sicyonis crassa._ M, mouth; S, ciliated groove;

T, tentacles. Each tentacle is perforated by a single large aperture.

(After Hertwig.)]

Another character that must be taken into consideration is that

presented by the floor of the great oceans. The floor of the ocean, if

it were laid bare, would probably present a vast undulating plain of

fine mud. Not a rock, not even a stone would be visible for miles.

The mud varies in different parts of the globe according to the depth,

the proximity to land, the presence of neighbouring volcanoes or the

mouths of great rivers.

The Globigerina ooze is perhaps the best known of all the different

deep-sea deposits. It was discovered and first described by the officers

of the American Coast Survey in 1853. It is found in great abundance in

the Atlantic Ocean in regions shallower than 2,200 fathoms. Deeper than

this, it gradually merges into the ‘Red mud.’ It is mainly composed of

the shells of Foraminifera, and of these the different species of

Globigerina are the most abundant. It is probably formed partly by the

shells of the dead Foraminifera that actually live on the bottom of the

ocean and partly by the shells of those that live near the surface or in

intermediate depths and fall to the bottom when their lives are done.

So abundant are the shells of these Protozoa that nearly 95 per cent. of

the Globigerina ooze is composed of carbonate of lime. The remaining

five per cent. is composed of sulphate and phosphate of lime, carbonate

of ammonia, the oxides of iron and manganese, and argillaceous matters.

The oxides of iron and manganese are probably of meteoric origin; the

argillaceous matter may be due to the trituration of lumps of pumice

stone and to the deposits caused by dust storms.

[Illustration: FIG. 3.—Globigerina ooze. (After Agassiz.)]

Globigerina ooze may be found on the floor of the ocean at depths

ranging from 500 to 2,800 fathoms of water in equatorial and temperate

latitudes. The reason that it is not found in Arctic seas may be that

the cold surface waters of these regions do not bear such an abundant

fauna of Foraminifera. This is supported by the fact that it extends ten

degrees further north than south in the Atlantic, the warm water of the

Gulf Stream bearing a richer fauna than the waters of a corresponding

degree of latitude in the Southern Sea.

The Pteropod ooze has only twenty-five per cent. of carbonate of lime.

It contains numerous shells of various Pteropods, Heteropods, and

Foraminifera, but nearly fifty per cent. of its substance is composed of

the siliceous skeletons of Radiolaria and the frustules of diatoms.

According to Murray it is found in tropical and subtropical seas at

depths of less than 1,500 fathoms.

The Radiolarian ooze is found only in the deepest waters of the Central

and Western Pacific Ocean. In some of the typical examples, not a trace

of carbonate of lime was to be found, but in somewhat shallower waters a

few small fragments occurred.

A Diatom ooze, mainly composed of the skeletons of diatoms, has also

been found in deep water near the Antarctic Circle, but it has not

apparently a very wide range.

Of all the deep-sea deposits, however, the so-called ‘Red mud’ has by

far the widest distribution. It is supposed to extend over one-third of

the earth’s surface. It is essentially a deep-sea deposit, and one that

is found in its typical condition at some considerable distance from

continental land. Like the Globigerina ooze it is never found in

enclosed seas. To the touch it is plastic and greasy when fresh, but it

soon hardens into solid masses. When examined with the microscope it is

seen to be composed of extremely minute fragments rarely exceeding 0·05

mm. in diameter. It contains a large amount of free silica that is

probably formed by the destruction of numerous siliceous skeletons, and

a small proportion of silicate of alumina. It usually contains the

remains of diatoms, radiolaria, and sponge spicules, and occasionally

lumps of pumice stone, meteoric nodules, and, in colder regions, stones

and other materials dropped by passing icebergs.

In the great oceans, then, we find in the deepest places red mud, or,

where there is an abundant Radiolarian surface fauna, Radiolarian ooze;

in water that is not deeper than about 2,000 fathoms, we find the

Globigerina ooze; in shallower waters and in some localities only

Pteropod ooze.

It must not be supposed that sharp limits can anywhere be drawn between

these different kinds of deposits, for they pass gradually into one

another and present many intermediate forms.

It is probable that the sea water by virtue of the free carbonic acid it

contains in solution is able to exert a solvent action upon the calcium

carbonate shells of animals as they sink to the bottom, and during the

long and very slow journey from the surface to the bottom of the deepest

seas these shells are completely dissolved.

The first to be dissolved would be the thin delicate shells of the

Pteropods and Heteropods, for besides the fact that they present a wider

surface to the solvent action of the water they are probably influenced

more by tide and currents, sink more slowly and erratically, and thus

have a longer journey to perform.

Then the smaller but more solid and compact shells of the Foraminifera

are dissolved, and lastly, in the deepest water only the siliceous

skeletons of the radiolaria and diatoms are able to reach their last

resting place at the bottom of the ocean.

These four oozes then are characteristic of the floor of the deep

oceans. In the proximity of land and in inland seas where deep water

occurs, other muds are found differing from one another in accordance

with the character of the coasts in their vicinity. It is not necessary

to give a detailed account of them, but a few remarks on some of the

more pronounced forms may not be without interest.

The blue mud contains eighty per cent. of a mixture of quartz, mica,

felspar, hornblende, and other minerals, mixed with a considerable

quantity of decomposing animal and vegetable substance, the calcareous

remains of foraminifera, mollusca, worms, echinoderms, alcyonaria and

corals, and the siliceous skeletons of radiolaria and diatoms.

The green mud is characterised by a large percentage of glauconite.

The red muds characteristic of the Brazilian coast contain a large

amount of ochreous matter brought into the sea by the great rivers.

In the neighbourhood of active volcanoes there is a characteristic

volcanic mud, and in the coral seas the deep-sea deposits contain a

large percentage of the calcareous remains of dead corals.

One more character of the deep-sea region must be referred to before we

pass on, and that is the absence of vegetable life. It has not been

determined yet with any degree of accuracy where we are to place the

limit of vegetable life, but it seems probable that below a hundred

fathoms no organisms, excepting a few parasitic fungi, are to be found

that can be included in the vegetable kingdom. While then the researches

of recent times have proved beyond a doubt that there is no depth of the

ocean that can be called azoic, they have but confirmed the perfectly

just beliefs of the older naturalists that there is a limit where

vegetable life becomes extinct. It is not difficult to see the reason

for this. All plants, except a few parasites and saprophytes, are

dependent upon the influence of direct sunlight, and as it has been

shown above that the sunlight cannot penetrate more than a few hundred

fathoms of sea water, it is impossible for plants to live below that

depth.

The absence of vegetable life is an important point in the consideration

of the abysmal fauna, for it is in consequence necessary to bear in mind

that the food of deep-sea animals must be derived from the surface. It

is possible that deep-sea fish, in some cases, feed upon one another and

upon deep-sea crustacea, that deep-sea crustacea feed upon deep-sea

worms, that deep-sea echinoderms feed upon deep-sea foraminifera, and so

on through all the different combinations; but the fauna would soon

become exhausted if it had no other source of food supply. This other

source of food supply is derived from the bodies of pelagic organisms

that fall from the upper waters of the ocean, and is composed of

protozoa, floating tunicates, crustacea, fish, and other animals,

together with diatoms and fragments of sea-weed.

The fauna of the deep sea · 第 2 / 8 章