A. Pupils contracted to a horizontal slit. Typically arciferous.

a. Australian. Tympanum invisible. Fingers and toes not dilated.

1. With vomerine teeth. Both the omo- and meta-sternum are rudimentary. East Australia: .......... Notaden bennetti.

2. Without vomerine teeth. Omosternum absent. Metasternum cartilaginous: .......... Pseudophryne, p. 168.

b. Not Australian.

1. Omosternum narrow and cartilaginous. Metasternum with a bony style ending in a cartilaginous disc. Fingers and toes slightly swollen. Neotropical: .......... Engystomops, p. 168.

2. Omosternum absent. Metasternum cartilaginous.

α. Fingers and toes webbed; terminal phalanges T-shaped and with adhesive broadened tips. Africa and India: .......... Nectophryne, p. 169.

β. Fingers free, toes webbed; terminal phalanges simple, not dilated. Tympanum distinct. Java: .......... Nectes, p. 169.

3. Metasternum cartilaginous, sometimes ossified along the middle. Fingers free; toes more or less webbed; tips simple or dilated into very small discs: .......... Bufo, p. 169.

B. Pupil a vertical slit. The epicoracoid cartilages are narrow and scarcely overlap. Omosternum absent except in Cophophryne. Vomerine teeth absent. Sacral diapophyses strongly dilated. The terminal phalanges are simple and the tips are pointed.

a. Australian. Tympanum distinct. The metasternum is calcified along the middle: .......... Myobatrachus, p. 184.

b. Mexican. Tympanum absent. Metasternum rudimentary: .......... Rhinophrynus, p. 185.

c. Himalayan. Tympanum absent. Metasternum with a slender bony style: .......... Cophophryne sikkimensis.

Engystomops is interesting because it closely resembles the Cystignathoid genus Paludicola, and thereby seems to connect these two families. It differs from Paludicola chiefly by the absence of teeth, by the moderately dilated sacral diapophyses and by the slightly swollen tips of the fingers and toes, the end-phalanges of which are, in one species, E. petersi, T- or anchor-shaped The tympanic disc is either distinct or hidden. The males have a large subgular vocal sac. The generic name refers to the small head with a prominent snout. Three species are known from Central America and Ecuador.

Pseudophryne appears to be another link with the Cystignathidae by its resemblance to the Australian genus Crinia, from which it differs by the absence of teeth and by the absence of an omosternum. The sacral diapophyses are but moderately dilated. The males have a flat oval gland on the hinder side of the thighs, and they are provided with a subgular vocal sac. The 3 or 4 species of this genus which live in Australia, both East and West, are not unlike Bombinator in their general shape, short limbs and coloration. The skin of P. australis and P. bibroni is covered with small smooth warts and is blackish brown, while the under parts are blackish with large yellow patches. Total length little more than one inch. Concerning the breeding habits, see p. 223.

Nectophryne.–The sacral diapophyses are strongly dilated. N. afra, without a tympanum, but with fully-webbed digits and several broad, cushion-like or lamellar pads on the fingers and toes, inhabits the Cameroons, N. tuberculosa of Malabar, and N. guentheri and N. hosei of Borneo, have a visible tympanum and the fingers are webbed at the base only. These slender and long-legged species are most probably arboreal, as indicated by the broadened, but truncated, tips of their fingers and toes. N. hosei is about 4 inches long, N. misera is a little creature of only ¾ inch in length. Nectes, hitherto known by one species, N. subasper of Java, is a swimmer and exceeds 6 inches in length. The tympanum is very distinct; the small nostrils look upwards. The toes are long and webbed to the tips; the hind-limbs are very long. The sacral diapophyses are strongly dilated. The skin of the upper parts is very rugose, covered with round warts, and dark brown; the under parts are granular and uniformly light brown.

Bufo.–The great number of species, more than 100, renders a strict definition of this genus difficult. The tongue is pear-shaped, thicker in front, entire, not cut out, but free behind, so that it can be projected. The fingers are free, the toes more or less webbed although never completely so. The terminal phalanges are obtuse and sometimes carry tiny discs. The omosternum is absent or merely vestigial. The metasternum is a rather large cartilaginous plate with a waist, which is sometimes incompletely calcified. The sacral diapophyses are moderately dilated. The tympanum is distinct or hidden. The skin of the upper parts is always rich in specific poison-glands, a concentration of which forms in many species very conspicuous, thickened parotoid glands. The surface of the skin may be smooth, moist and slimy, or rough and warty, sometimes covered with tiny, sharp, horny spikes and quite dry.

The genus is cosmopolitan, with the exception of the whole Australian region and Madagascar, from which we may perhaps conclude that its original centre was not in Notogaea, in spite of the diversity of species in the Neotropical region, which now contains about half of all the species known. Next to Central America the Indian region is richest in species of Bufo.

B. vulgaris.–The Common Toad of the Palaearctic region. The skin of the upper parts is much wrinkled and beset with numerous round warts or poison-glands, the openings of which can be seen with the naked eye, especially on the large parotoid complexes. The outermost layer of the epiderm, in fact all that portion which is periodically shed, is elevated into numerous little cornified spines. The extent of their development varies much; southern specimens, especially those from Portugal, being perhaps the roughest. Others appear quite smooth to the touch, and this is the case with many English specimens. The skin of the under parts is more granular and devoid of specific glands. The general colour of the upper parts is olive grey to dark brown, more or less mottled; the under parts are whitish, often with a brown, yellow or reddish tinge.

The coloration of this species varies considerably and is moreover very changeable. These changes depend chiefly upon the surroundings and the locality, in which certain styles of coloration seem to be the fashion, not necessarily to the absolute exclusion of others. Some specimens are of a rich brown colour, with or without dark brown spots and patches, and these are sometimes confluent, forming irregular, longitudinal bands. The ground-colour of other individuals is olive grey, with or without darker patches, and these paler tones prevail in toads which live on light-coloured soil, for instance on chalk. I recently found one between two dark-coloured slates, and this creature was so black that it gave the impression of having soiled itself with coal-dust. One and the same specimen will appear paler or darker according to its mood and the leading tones of its immediate surroundings, but it cannot change its dominant ground-colour. A third colour-variety occurs more frequently in the mountainous districts of Southern Europe. I have obtained the most handsome specimens in the Serra Gerez, in North Portugal. Their ground-colour is pale brownish-yellow, with many large and small, rich brown patches, or if the latter colour predominates, these patches and spots are separated from each other by creamy seams, with the occasional effect of dark brown, yellow-ringed eyes. Eastern Asiatic specimens often have a fine yellow vertebral line and the under parts are inclined to be marked with dark spots.

The iris is red or coppery, mottled with black. The male has no vocal sacs, and, besides being smaller than the female, is distinguished by slight nuptial excrescences in the shape of little horny brushes on the inside of the inner palmar tubercle and the three inner fingers. The full size of this toad varies extremely. Taking the standard of everyday experience in England and Central Europe, one would call any female beyond 3½ inches in length, and any male of more than 2½ inches, unusually large. But occasionally they grow to a much larger size, especially in the mountains of Southern Europe, provided there is a rich vegetation of meadows and deciduous trees so as to insure a variety of plentiful food. Although Fatio[79] mentions a toad 153 mm. = 6 inches long, and Boulenger succeeded in getting a toad from Paris which measured 132 mm., i.e. almost 5¼ inches, one of my specimens from the Serra Gerez seems to hold the record with a total length from snout to vent of 135 mm. or more than 5¼ inches. Jersey is also famous for its large toads, possibly on account of the many large greenhouses. These large specimens do not constitute a special race. The monsters among them are without exception females, often but not always sterile, as I have often found large masses of eggs in them. Food is the chief cause. At least I have observed that the more voracious of some Spanish and Portuguese specimens, which were already 3½ inches long, and therefore entitled to respect, continued to grow rather rapidly, adding about half an inch within a year. Again, if the growth of a promising toad is arrested for a season–not necessarily by starvation, but by uncongenial surroundings, sameness, and unvaried nature of food–they consolidate so to say, or settle down, and no amount of future good feeding will turn them into exceptionally big specimens. There are no data to tell how old such monsters really are. At least ten years are required by the Southerners to reach four inches. The usual length of life attained by a toad is likewise unknown. Boulenger kept one in a box provided with a sod, a pan of water and plenty of varied food, but twelve years of close captivity did not make any appreciable difference in its appearance.

fig35

Fig. 35.Bufo vulgaris. Portuguese specimen. × ⅔.

A number of large Spanish and Portuguese specimens in my greenhouse were at first very shy, and tried every possible means of escape or sullen hiding, but gradually they condescended to take food when lifted on to the slate-covered stage upon which their food was spread. After a few weeks they had learned this so thoroughly that, towards the usual hour of feeding, they climbed most laboriously on to the slates, lying in wait between the flower-pots, and coming forward when we entered the house. The rest of the day and night they spent on the ground, under stones or plants, each in its individual lair. The biggest of all, and several others, became so tame that they took food whilst sitting on the hand, and then they looked up for more. The food must be alive and show movement. Mealworms, snails, beetles and other small creatures are first carefully inspected with bent-down head, and are sometimes followed for a few inches; then comes an audible snap, a flash of the rosy tongue and the prey has disappeared. Large earthworms are nipped up with the jaws and laboriously poked in with the hands, the fingers being so placed as to clean the worm of adherent soil and other impurities. Very large worms are shaken, twisted, pressed against the ground and gulped down with convulsive movements, but not unfrequently the tip-end remains for some minutes sticking out of the tightly shut mouth. Several are taken at one sitting, until the toad is gorged. One of the biggest took full-grown mice, which were not "fascinated by the fiery eyes" but were stalked into a corner and then pounced upon immediately when they moved. The shells of snails can for half a day be felt through the body; they then dissolve or are disgorged. The dung, which is passed in large, long masses, is often full of fine earthy matter, the contents of the earthworm's intestines, and sometimes it contains the chitinous remains of certain beetles which are supposed to be excessively rare. I know of no instance of slugs being eaten.

The regular hunting-time begins with the evening and is continued throughout bright nights, the toads crawling and hopping about. They are expert climbers of rocks, and succeed in reaching apparently inaccessible places by shoving themselves up between vertical walls, and taking advantage of any roughnesses for foothold. Every few weeks they shed their skins. Without any preliminary symptoms or loss of appetite or liveliness, the body makes a few twisting motions, the back is now and then curved, and the skin splits down the middle line. Owing to the more forcible contortions of the body it slides down to the right and left of the back, whereupon the toad gets hold of the peeling-off skin with fingers and toes, scraping the head and sides, and conveys the thin, transparent, slightly tinged skin into the mouth, slips out of it backwards and swallows it. The new surface is then quite wet and shiny, but it soon dries and hardens.

Many toads, for instance the Common Toad and the Pantherine Toad, assume a peculiar attitude when surprised. Instead of blowing themselves up by filling their lungs with air, they raise themselves upon their four limbs as high as possible, but turning the back towards the enemy in a slanting position, either to the right or to the left side, apparently in order to present as much surface as possible, in other words to look their biggest.

Some of my specimens hibernated regularly for a few months, burying themselves completely in loose, dry soil, under leaves, or,–a favourite place,–in a heap of cocoa-nut fibre. Others, and this applies also to English specimens transferred from the garden into the greenhouse, are lively all the year round, but even they withdraw for an occasional sleep of a few weeks at any time of the year.

The whole family of large toads came to a sad end after four years, when they were put into new temporary quarters, a slate-bottomed terrarium. Being kept during my absence in wringing wet moss, which became fouled by their own excretions, they contracted a mysterious disease from which they never recovered. They are rather averse to wet surroundings, and except during the short pairing season they live in cool, shady places, preferably with just a little dampness. Occasionally they take a soaking bath. One specimen, living in the garden, repaired during the hot and dry summer nights to a standpipe in the garden, enjoying the occasional drips of water.

Considering the amount of snails and other noxious creatures destroyed by them during their regular nocturnal hunts, toads are eminently useful creatures. Nevertheless, they suffer much through the stupid superstition of people who ought to know better. It is difficult to find a gentle, absolutely harmless and useful creature that is more maligned than the European toad. It brings ill-luck to the house, the "slimy toad" spits venom, sucks the cows' udders and after that destroys their power of giving milk; it poisons the milk in the cellar, and a certain builder's horse, which was grazing in the grounds of the Cambridge Museums, and died there from a large concrement obstructing its bowels, was solemnly declared to have swallowed one of my toads. Silly superstitions, owing to faulty, or rather entire want of, observation! The toad is not slimy, but dry; it is often found in buildings, where it keeps down the woodlice; it cannot suck, nor does it drink at all; it does not spit venom, but becomes covered with milky white and very strong poison when in acute agony, for instance when trodden upon; and unless the big skin-glands be forcibly squeezed, there will be no squirting. Therefore, leave it alone, or put down food on its evening beat, and it will soon come to know and to recognise its friends.

The Common Toad can exist without food for a long time, provided the locality is cool and damp, but it wastes away almost to skin and bones. In order to disprove the persistently cropping up fable and sensational newspaper-accounts of toads having been discovered immured in buildings, where they were supposed to have lived for many years, Frank Buckland put a dozen specimens into separate holes bored in a block of porous limestone, covered them up tightly with a glass plate and buried the block a yard deep in the soil. A second dozen were treated similarly, but were put into a block of dense sandstone. After a year and two weeks all the toads enclosed in the latter block were of course found dead and decomposed, but most of those in the porous block were still alive, with their eyes open, and did not succumb to starvation until eighteen months of confinement. These poor creatures could of course not move about, and were practically undergoing enforced continuous hibernation. Otherwise they would soon have wasted away and have died within six months. Those which tumble into deep and dry wells remain rather small, but generally manage to keep alive for years on the spiders, woodlice, earwigs and other insects which likewise tumble in.

Toads hibernate far from the water in dry holes or clefts, retiring in the middle of October in Central Europe, and they do not reappear before March. Soon after, and this depends naturally upon the season, they congregate in ponds or pools, and the males, which far outnumber the females, for whom they fight, make a peculiar little noise, something like the whining bleat of a lamb, uttering this sound day and night. The male having, after much wrestling with competitors, secured a female, which is often several times bigger than himself, clasps her tightly, by pressing his fists into the armpits, and the pair swim or crawl about in this position sometimes for a week before the spawning takes place. The number of eggs laid at one sitting is enormous, varying from 2000 to 7000. They are very small, only 1.5-2.0 mm. in diameter, and are expelled in two double rows or strings, one coming out of each oviduct. These strings consist of a soft gelatinous mass, in which the double rows of entirely black eggs are imbedded, and they measure in the swollen condition about 6 mm. or ¼ inch in diameter, and from 10 to 15 feet in length. The strings are wound round and between water-plants by the parents, which move about during the laying and fertilising process. According to the coldness or warmth of the season the larvae are hatched in about a fortnight, and for the next few days they hang on to the dissolving gelatinous mass of the egg-strings. They then leave the slime and fasten themselves by means of their suckers to the under side of grasses and water-plants or sticks, with their tails hanging downwards, still in a rudimentary condition, but henceforth progressing rapidly.

Fischer-Sigwart[80] found the time of development as follows:–The eggs were laid on the 6th of March; the larvae left the jelly on the 16th, being 4 mm. long. On the 2nd of April they measured 13 mm.; on the 25th, 20 mm. On the 7th of May the hind-limbs appeared. On the 18th of May the tadpoles had reached their greatest length, namely 24 mm., and this is a rather small size for so large a species. The fore-limbs broke through on the 28th, and the metamorphosis was completed eighty-five days after the eggs were laid, the creatures leaving the water on the 30th of May. The tadpoles showed a preference for rotten pieces of Agaricus, which were floating in the water. The little baby-toads are surprisingly small, scarcely 15 mm. long, and live in the grass, under stones, in cracks of the ground, and hop about in much better style than their heavier and more clumsy-looking parents. Where many broods have been hatched they can be met with in myriads, the ground literally swarming with them, and as they are naturally stirred up by a sudden warm rain, perhaps after a drought, people will occasionally state it as an observed and well-ascertained fact that "it has rained toads."

What becomes of all these hopeful little creatures? Although it takes them fully five years to reach maturity, one would expect that the whole country would be swarming with toads; but since this is not the case, there being not more toads now than there were before, it follows that their enormous fecundity is only just sufficient to keep the race going. Adult toads seem to have scarcely any enemies except the Grass Snake, which takes them in default of anything better. But how about the reduction where there are no snakes? We know nothing about epidemics which might carry them off, but elderly toads are liable to a horrible disease produced by various kinds of flies, notably by Lucilia bufonivora and Calliphora silvatica, the maggots of which somehow or other eat their way from the nostrils into the brain and into the eyes. Those which reach the brain at first produce effects similar to those of Coenurus cerebralis, the hydatid or bladder-worm of sheep. The toad inclines its head towards one side, and cannot crawl straight, but walks in a circle. By eating away the brain they gradually destroy the host's life. But if none enter the brain, and a few only find their way into the eye, they only impair or destroy its sight. Such toads show signs of pain, poking at or stroking the affected eye, which becomes inflamed, and ultimately remains enlarged, with the iris partially or entirely destroyed by the maggot, which does not develop further, but dies in the eye-chamber, this being really an unsuitable place for it. The eyesight is of course affected, and is mostly, but not in all cases, lost. Such half-blind individuals–the disease affecting sometimes one eye only–recover their health, and except for a little awkwardness, behave like normal specimens. This applies to Bufo vulgaris as well as to B. calamita. Australian Anura are cursed with a fly of their own, called Batrachomyia.[81]

B. vulgaris inhabits almost the whole of the Palaearctic region;–the whole of Europe, with the exception of Ireland, the Balearic Islands, Sardinia and Corsica. Northwards it extends to Trondhjem, and thence along a line drawn across Russia and Siberia to the Amoor. Its southern limit in Asia is indicated by a line drawn from the Caucasus through the Himalayas into China. In Asia Minor and in Persia it is absent. South of the Mediterranean it occurs only in Morocco and Algeria.

B. melanostictus is the common toad of the whole Indian region and of the Malay Archipelago. The epidermis of the fingers and toes is thicker and more cornified than usual, and is stained black brown, hence its specific name. The male has a subgular vocal sac. In other respects the Indian species much resembles the more spinous or rough-skinned and brown varieties of the European species. According to S. S. Flower this toad is very common in the Straits Settlements, hiding by day under stones or logs, or in holes, coming out shortly before sunset, and remaining abroad till dawn; it may be met with on the roads and in the grass, hopping or crawling about in search of ants, bees, and similar food. It utters a rather feeble, plaintive cry when handled for the first time. It can change its colour from light yellowish to dark brown. The spawn, which resembles that of B. vulgaris, may be seen in March and April in ponds, in long strings twined about the water-weeds. The tadpoles are very like those of the common English toad in form, size, colour, and structure of mouth. The largest adult found in Penang measured 115 mm. (about 4 inches) from snout to vent.

B. lentiginosus s. americanus is the common toad of North America, from Mexico to the Great Bear Lake. It is worth noting that this species resembles in its coloration the Eastern races of B. vulgaris, in so far as they generally have a light vertebral line, and frequently dark spots on the under surface. The upper parts are brown and olive, with darker spots, two of which form a chevron behind the eyes. But the tympanum is large, and the male has a subgular vocal sac; the inner metatarsal tubercle is very large, and is used as a kind of digging spur. During the pairing time they take to the pools in great numbers, uttering their music, which consists of a prolonged trill, continued by different individuals, both day and night. Holbrook knew an individual which was kept for a long time, and became perfectly tame. During the summer months it retired to a corner of the room into a habitation which it had prepared for itself in a small quantity of earth placed there for its convenience. Towards the evening it wandered about in search of food. Some water having been squeezed from a sponge upon its head one hot day in July, it returned the next day to the spot, and seemed well pleased with the repetition, nor did it fail during the extreme heat of the summer to repair to it frequently in search of its shower-bath.

Several varieties of this widely distributed species, whose average length is 2½ inches, have been described. The prettiest was called B. quercinus by Holbrook–according to whom it is mostly found in sandy places covered with a small species of oak–which springs up abundantly where pine-forests have been destroyed. It is called the "oak-frog," as it spends most of its time in concealment under fallen oak-leaves, or partially buried in the sand.

B. marinus s. agua is the giant among toads, and is one of the commonest species of the Neotropical region, ranging from the Antilles and Mexico to Argentina. It frequently reaches a length of 6 inches, with a width of 4 inches when squatting down in its favourite attitude. The upper parts are rough, owing to the prominent warty glands, of which the parotoid complex is enormous. The general colour above is dark brown, with sooty dark patches; below whitish, often with blackish patches. This creature appears at dusk, often in large numbers, especially during the rainy season, hopping about, not crawling, with surprising activity. The voice of the male, strengthened by a subgular sac, is said to be a kind of loud snoring bark. The pairing time begins, according to Hensel,[82] with the winter rainy season, especially June, and lasts several months, until October, but it is interrupted by the cold, which in the hills of South-Eastern Brazil covers the ponds with ice. Then the tremulous bass voice of the males is heard no longer; they have all withdrawn beneath stones and trees in the neighbourhood of the water. The eggs are laid in strings. The larvae are at first quite black and very small, and the young baby-toads are only 1 cm. in length. They differ considerably from the adult until they are more than 1 inch long; the upper parts are yellowish brown, with darker ocellated patches, each with a light seam, most conspicuous along the sides of the head and back. The under parts are grey, finely stippled with yellow.

Budgett[83] remarks that B. marinus feeds on all kinds of insects. "One half-grown specimen sitting by a man's foot picked off fifty-two mosquitoes in the space of one minute, picking them up with the tongue as they settled. The call of this very common toad consists of three bell-like notes; the middle one being the highest. The enormous parotoid glands are discharged like squirts when the creature is roughly handled. When wet weather comes on it hops out from its hiding-place to sit in a puddle, with its head out."

In many species of Bufo the crown of the head forms more or less prominent ridges, especially strong in the region between the eyes; for instance, in B. melanostictus and B. lentiginosus. The skin overlying these ridges is liable to be involved in the cranial ossification, and this reaches its greatest extent in the two Cuban species B. empusus and B. peltocephalus. It is a curious coincidence, to say the least, that such dermal ossifications should be best developed in Neotropical species, in those very countries which amongst the Cystignathidae have produced the abnormal genera Triprion, Calyptocephalus, and Pternohyla. The most peculiar and odd-looking species is Bufo ceratophrys, a native of Ecuador, which has the upper eyelid produced into a horn-like appendage, the two sharply-pointed cones standing out transversely, reminding us of several species of the Cystignathoid genus Ceratophrys; there is also a series of four small pointed appendages on each side of the body. Protective concealment is possibly the reason of these queer outgrowths.

B. viridis s. variabilis, the Green or Variable Toad, reaches a length of about 3 inches, and is the prettiest toad of Europe. The skin is distinctly smooth, the numerous porous, large and small warts being flattened. Parotoid glands are well developed, and a similar pair of glands sometimes occurs on the inner side of the calf, especially in Central Asiatic and in Algerian specimens. The coloration is very variable and changeable. The ground-colour of the upper parts is creamy, with large and small, partly confluent and irregularly shaped spots and patches of green, here and there interspersed with vermilion-red specks, especially along the sides of the back. The under parts are whitish, sometimes spotted with black. The iris is brass-coloured, greenish-yellow, with fine dark dots. The male does not differ from the female in size, but has an internal subgular vocal sac, a conspicuous callosity on the inner side of the first finger, and nuptial brushes on the first three fingers and on the inner palmar tubercle.

The changing of colour affects mainly the intensity of the green; the same individual which now looks almost uniformly dull, almost grey, with dusky olive patches, will, if put into grass and sprinkled with water, within a few minutes appear in a tastefully combined garb of grass-green on a creamy ground. Some Southern and Eastern specimens have a creamy stripe along the vertebral line, thereby closely resembling B. calamita, from which, however, they can always be distinguished by the little pads below the joints of the toes; these pads being single in B. viridis, and double in B. calamita and in B. vulgaris.

The Green Toad spends most of the day in holes, although it is not averse to daylight, and it roams about chiefly in the evening. It can jump well, much better and oftener than the Brown Toad. The food consists strictly of insects of all kinds, and most individuals prefer slow starvation to eating an earthworm. Although continuing to live four or five years in captivity, they do not readily become tame; they are indeed no longer wild, and when handled they no longer emit their peculiar insipid smell, but on being approached they still crouch deeply into the grass, or withdraw into their holes, just as they did when recently caught. The voice is heard during the pairing season, and sounds like the slow creaking of a door, or a combination of a spinning top and rattle. In Germany, during the months of April and May, they take to the ponds, or, improvident like the common frog, to a roadside ditch. The male sits upon the female and grasps her below the arms, his hands on her breast, and in this position they remain for days. The eggs are laid in two strings, twisted around water-plants, and are very numerous. Héron-Royer has calculated them at 10,000 or more in one set. The embryos are hatched, like those of the Common Toad, before the appearance of the external gills and of the tail. In this imperfect condition they remain in the jelly of the egg-strings for a few days, while their external gills sprout out like unbranched little stumps, only to disappear again. In about eight weeks the tadpoles, which reach a length little more than 1½ inch or 40 mm., have metamorphosed and leave the water as baby-toads scarcely half an inch in length.

This species has a very wide range, namely, the whole of Middle Europe excepting the British Isles, France and the Iberian Peninsula; the region between the Elbe and Rhine being its western limit; southwards it extends over all the Mediterranean islands and the north coast of Africa, eastwards through the whole of Russia, Western and Central Asia, not entering India, but spreading along the Himalayas into China. Stoliczka mentions its having been found in the Himalayas at an altitude of 15,000 feet, the highest record of any Amphibian, at least in such latitudes.

B. calamita.–The Natterjack is practically the representative of the Green Toad in Western Europe, but both species occur together in Denmark, Southern Sweden, and nearly the whole of Germany. Its southern limit is Gibraltar. In the British Isles it occurs in South-Western Ireland, in Co. Kerry, and in England and Wales, being however local, and preferring sandy localities, where it is found in considerable numbers. This predilection is shown by its frequency on the sandy dunes of most of the islands off the German and Dutch coast, where it may be seen running about in glaring sunshine.

Besides in the coloration, it differs from B. viridis in the following points. The little subarticular pads of the toe-joints are paired, not single, and the hind-limbs are decidedly shorter, so much so that this species cannot hop. But it runs well, like a mouse, generally in jerks, stopping every few seconds, and owing to this habit it is called the "running toad" by the field-labourers of Cambridgeshire. The skin is smooth, but less so than in B. viridis, owing to the slightly more prominent warts; the parotoids are small; a similar pair of glands lies on the upper surface of the fore-arm and another on the calf. The tympanum is rather indistinct. The ground-colour of the upper parts is light brownish yellow, with a green tinge and scattered green spots; most specimens have a narrow yellow stripe along the vertebral line and over the head. The under parts are white, more or less speckled with black. The iris is greenish yellow and speckled. The male, which is of the same size as the female,–very large specimens reaching 3 inches in length,–has a large subgular vocal sac, and develops nuptial brushes on the first three fingers, but the first lacks the thickened pad of B. viridis.

The yellow vertebral line is sometimes absent in specimens from the south of France and the Iberian Peninsula; and since these southerners are as a rule more handsomely marked, the green being more pronounced and arranged in larger patches, interspersed with red spots, they much resemble B. viridis. Boulenger, who has paid especial attention to this vertebral streak, which is a not uncommon design in various species of different families, has made the interesting observation that the streak has never been found in Danish and German specimens of B. viridis, where B. calamita occurs also, while it is not uncommon in B. viridis of Italy, South-Eastern Europe, Asia, and North Africa, where B. calamita is not found. Lastly, he remarks that in Eastern Asia, where neither B. viridis nor B. calamita with such a line occurs, the same character is assumed by some specimens of B. vulgaris. The only conclusion we can draw from these facts is, that for some unknown reason the streak is a desirable, but not necessary, possession, but that it is not kept by two species in the same country, B. viridis dropping it entirely where the typically streaked species, B. calamita, also occurs. The breeding season does not begin in England and Middle Europe until the end of April, in cold springs not before May, but it lasts for several months. The males, congregating in pools in great numbers, make a loud noise, each individual uttering a rattling note which lasts a few seconds, the repetition distending its bluish throat into the shape of a globe as large as its head. As the note is taken up by all the other males, a continuous chorus is established, which on warm and still nights can be heard nearly a mile off. Single croaks are uttered at any time of the day. The embrace, the male digging its fists into the armpits of the female, often takes place on land, near the edge of the water, to which they resort in the night for spawning. The egg-strings are slung around water-plants, unless the water is a mere puddle, and are much shorter than those of B. viridis, measuring only 5 to 6 feet, and containing altogether 3000 to 4000 eggs. The larvae, when hatched, are very small, imperfect, and blackish; the external gills last a very short time. The young tadpoles live on mud, subsisting on diatoms and low Algae; they are the smallest tadpoles of all the European kinds, scarcely reaching more than one inch in length, and they metamorphose quickly, the baby-toads leaving the water and running about in less than six weeks, when they are only 10 mm., scarcely three-eighths of an inch, in length. By the end of their second summer they are still only three-quarters of an inch long, and they do not reach maturity until the fourth or fifth year, with a size of 1½ to 2 inches; still smaller young males become mature several years before they are full grown.

Natterjacks stand captivity well and become very tame. When discovered, they first do their best to run away, instead of hiding or squatting down, and when caught they become covered with a slightly foamy lather, the exudation of their glands, which has a peculiar smell, reminding some people of gunpowder, others of india-rubber. They are not very particular as to food, all sorts of insects and earthworms being taken. Natterjacks are great climbers and diggers. Many of mine have established themselves in the peat with which the walls of the greenhouse are covered, where they have dug out, or enlarged, holes in which they pass the daytime, just peeping out with their bright eyes; others sit high up, always in dry places, and bask. In the evening they descend, hunting about on the ground, and occasionally they go into the water, whereupon they become quite flaccid and soft. When taken up and held between two fingers, being slightly pressed under the armpits, both sexes utter little jerky notes, as–by the way–most toads and frogs do under similar conditions.

In Cambridgeshire they frequent certain clay-pits surrounded by high and steep walls of sand, the breeding places of large colonies of sand-martins. During the months of May and June they are found in the shallow water, running about on the mud, sometimes swimming, in which they are not very proficient, and rarely diving. But they spend most of the time on land. Early in October they climb up and enter the holes of the sand-martins, or they dig large, deep burrows for hibernation, and the old males are the first to disappear.

B. mauritanica s. pantherina.–The "Pantherine Toad" is one of the few African species, and is one of the prettiest of all toads. The skin is almost smooth, although provided with porous glands. The parotoids are large, but flat; large glandular complexes on the legs or arms are absent. The tympanum is very distinct. The upper parts are adorned with a delicate pattern of dark-edged, rich brown or olive patches upon a light, buff-coloured ground; the under parts are uniform white; the male has a subgular vocal sac. The total length is 3 to 4 inches. This beautiful species is one of the gentlest, and it becomes tame enough to lap up food whilst sitting on one's hand. It lives entirely upon insects, prefers shade and dusky light, and utters a sound like "kooh-rr." It is a native of North-Western Africa, Algiers, and Morocco. In the rest of Africa, from Egypt to the Cape, Senegambia to Abyssinia, it is represented by B. regularis. This species has often little spiny tubercles upon the warts, and occasionally a light vertebral line; the colour of the upper parts either closely resembles that of the previous species, or it is uniform light brown, while the under parts are whitish, or variegated with brownish patches. West African specimens are the smallest, only 2 inches long; those of the Cape are the largest, reaching 5 to 6 inches.

The next two genera approach the Engystomatinae, and thereby lead from the arciferous towards the firmisternal type. The epicoracoid cartilages are narrow, and they scarcely overlap, so that by a further step in this direction they could easily fuse into the firmisternal condition. Another bond between these two genera and the Engystomatinae is their habits, they being ant-eaters of an extremely stout appearance, with exclusively short limbs and very small heads.

Myobatrachus gouldi, living in Australia, has a smooth skin, brown above, lighter beneath, and is about 2 inches long.

Rhinophrynus dorsalis of Mexico is remarkable for its tongue, which is elongated, subtriangular and free in front, so that it can be protruded directly–not by reversion as in other toads–and can be used for licking up the termites which seem to be its principal food. The body of this ugly creature is almost egg-shaped, and the head is merged into this mass, only the narrow truncated snout protruding. The limbs are very short and stout. The toes are more than half webbed, and there is a large oval, shovel-like metatarsal tubercle, covered with horn and used for digging. The general colour is brown, with a yellow stripe along the spine and with irregular spots and patches on the flanks and limbs. Total length 2 to 2½ inches.

fig36

Fig. 36.–Map showing distribution of Hylidae. The vertically shaded countries are inhabited by Hyla and by other genera of Hylidae; the horizontally shaded countries only by Hyla.

Fam. 4. Hylidae (Tree-frogs).–The upper jaw–in Amphignathodon the lower jaw also–and the vomers carry teeth; Triprion and Diaglena alone have teeth on the parasphenoid also, and the latter genus is further distinguished by possessing palatine teeth. The vertebrae are procoelous and have no ribs; the sacral diapophyses are dilated. The omo- and meta-sternum are cartilaginous, the latter forming a plate with scarcely any basal or style-shaped constriction. The terminal phalanges are invariably claw-shaped and swollen at the base, and carry a flattened, roundish, adhesive cushion. The tympanic disc is variable in appearance, being either free, or more or less hidden by the skin. The tongue is also variable in its shape and in the extent to which it can be protruded.

Most, if not all, Hylidae are climbers, and many lead an arboreal life, but it does not follow that all the "Tree-frogs" are green.

Their distribution is very remarkable. To say that this family is cosmopolitan with the exception of the African region, is literally true, but very misleading. There are in all about 150 species, and of these 100 are Notogaean; one-half of the whole number, or 75, being Neotropical; 23 are Central American, 7 Antillean, and about 18 are found in North America. One species, Hyla arborea, extends over nearly the whole Palaearctic sub-region, and two closely allied forms occur in Northern India and Southern China. Consequently, with this exception of three closely allied species, the Hylidae are either American or Australian. We conclude that their original home was Notogaea, and that they have spread northwards through Central and into North America. The enormous moist and steamy forests of South America naturally suggest themselves as a paradise for tree-frogs, and it is in this country, especially in the Andesian and the adjoining Central American sub-regions, that the greatest diversity of generic and specific forms has been produced. It is all the more remarkable that similar forest-regions, like those of Borneo and other Malay islands, are absolutely devoid of Hylidae (while there are about a dozen species in Papuasia), whose place has however been taken for all practical purposes by correspondingly modified Ranidae, notably the genus Rhacophorus. Lastly, the fact that tropical evergreen forests of Africa and Madagascar possess no Hylidae, but are inhabited by several kinds of tree-climbing Rhacophorus, points with certainty to the conclusion that the origin of this large and flourishing family of Hylidae was not in Arctogaea.

The versatility and the wide distribution of the Hylidae has naturally produced cases of convergent analogy, and the various species of one "genus" may be in reality a heterogeneous assembly. Such an instance is probably the genus Hylella, of which four species live in the Andesian and Central American provinces, while the two others occur in New Guinea and Australia.

The two North American genera Chorophilus and Acris, and the Brazilian Thoropa, connect the Hylidae with the Cystignathidae, in so far as their finger-discs are very small, or even absent, and their sacral diapophyses are only slightly dilated. On the other hand, it has to be emphasised that the possession of adhesive discs on the fingers and toes does not necessarily constitute a member of the Hylidae. That requires the further combination of an arciferous sternum, with dilated sacral diapophyses and teeth in the upper jaw. Finger-discs are easily developed, and still more easily lost. Those of the typical Hylidae are constructed as follows. The terminal phalanx is elongated, claw-shaped, swollen at its base. Between it and the penultimate phalanx lies an interphalangeal cartilaginous disc which projects ventrally below the end-phalanx, thus assisting the formation of the ventral pad, and the turning upwards of the whole disc-like phalanx like the claw of a cat. This peculiar motion can be well observed in Tree-frogs which are at rest upon a horizontal leaf, or, better still, upon a rough stone, when the creatures take good care to adjust their discs into a safe and easy position. The pad or disc itself is furnished with unstriped, smooth muscular fibres, the contraction of which produces one or more longitudinal furrows on the under side. When the disc is in action or adhering, being flattened to a smooth surface, the end-phalanx sinks into the cushion; when not in action, the cushion swells and the phalanx appears as a slight dorsal ridge. The disc is rich in lymph-spaces, and its surface contains mucilaginous glands.

Various suggestions have been made to explain the function of these discs. Suction, adhesion, and glueing-on have been resorted to. Suction, through production of a vacuum, is quite imaginary and does not exist. The question has been thoroughly studied by Schuberg.[84] Adhesion is due to the molecular attraction of two closely appressed bodies. The less air remains between them the stronger it is. Consequently it can be increased by the interference of a thin layer of fluid, which as everyday observation shows, possesses both adhesion and cohesion. The more sticky the fluid, the more effective it is, as shown experimentally by Schuberg, who moistened the under surface of a glass plate, and pressed it against a little disc of glass from which was suspended a weight. A disc of 16 square millimetres, approximately equal to the aggregate surface of the 18 discs of a European tree-frog of 4 grammes in weight, carried with water-adhesion no less than 14 grammes, with glycerine-solution 20 grammes,–more than sufficient to suspend the frog. The sticky secretion of its glands greatly enhances the adhesive power. Tree-frogs, when hopping on to a vertical plane of clean glass, slide down a little, probably until the secretion stiffens, or dries into greater consistency. After a few days I find the glass-walls of their recently cleaned cage quite dirty, covered everywhere with their finger-marks. On the other hand, wet leaves or moist glass-walls afford no hold. The adhesion of these frogs is assisted in most cases by their soft and moist bellies, just as a dead frog will stick to a pane of glass.

All Hylidae have a voice, often very loud, and enhanced by vocal sacs, which are either internal, swelling out the throat, or external, paired or unpaired.

The various Hylidae resort to all kinds of modes of rearing their broods. Most of them lay many eggs, up to one thousand, in the water, not coherent in strings but in clumps; others lay only a few, attach them to various parts of the body, or, as in the genus Nototrema, the female receives them in a dorsal pouch. These modifications will be described in connexion with the different species.

Sub-Fam. 1. Amphignathodontinae.Both upper and lower jaw with teeth.

Amphignathodon, of which only one species is known, A. guentheri of Ecuador, agrees with Nototrema in all important characters except that it possesses teeth in the lower jaw in addition to those in the upper. There are further differences, but they are of degree only. The sacral diapophyses are more strongly dilated and the omosternum is absent. The tympanum is distinct. The pupil is horizontal; the roundish tongue is slightly free behind. The terminal phalanges are claw-shaped and carry large discs. The female has a dorsal pouch opening backwards. The skin of the head is involved in the ossification of the cranial bones. The skin of the back is smooth, slightly tubercular, non-granular below. The middle of the upper eyelid carries a small, pointed, cutaneous appendage, and even this little character occurs also in some species of Nototrema, e.g. in N. longipes and in N. cornutum. The heel carries a triangular little flap. The upper parts are olive in spirit-specimens, probably green in life; the borders of the dorsal pouch are black. The sides of the body are adorned with a black, white-edged streak, the limbs are whitish, with black cross-bars. The total length of the female type-specimen is 3 inches.

Sub-Fam. 2. Hylinae.Lower jaw toothless.

The Hylinae are divided by Boulenger into 13 genera, which can be recognised by the following key, without reference to their natural affinities:–