[1] The evidence is given at length in R.H. Charles' _Ethiopic Text
of Enoch_, pp. xxvii-xxxiii.
ENOMOTO, BUYO, VISCOUNT (1839-1909), Japanese vice-admiral, was born in
Tokyo. He was the first officer sent by the Tokugawa government to study
naval science in Europe, and after going through a course of instruction
in Holland he returned in command of the frigate "Kaiyo Maru," built at
Amsterdam to order of the Yedo administration. The salient episode of
his career was an attempt to establish a republic at Hakodate. Finding
himself in command of a squadron which represented practically the whole
of Japan's naval forces, he refused to acquiesce in the deposition of
the Shogun, his liege lord, and, steaming off to Yezo (1867), proclaimed
a republic and fortified Hakodate. But he was soon compelled to
surrender. The newly organized government of the empire, however,
instead of inflicting the death penalty on him and his principal
followers, as would have been the inevitable sequel of such a drama in
previous times, punished them with imprisonment only, and four years
after the Hakodate episode, Enomoto received an important post in
Hokkaido, the very scene of his wild attempt. Subsequently (1874), as
his country's representative in St Petersburg, he concluded the treaty
by which Japan exchanged the southern half of Saghalien for the Kuriles.
He received the title of viscount in 1885, and afterwards held the
portfolios of communications, education and foreign affairs. He died at
Tokyo in 1909.
ENOS (anc. _Aenos_), a town of European Turkey, in the vilayet of
Adrianople; on the southern shore of the river Maritza, where its
estuary broadens to meet the Aegean Sea in the Gulf of Enos. Pop. (1905)
about 8000. Enos occupies a ridge of rock surrounded by broad marshes.
It is the seat of a Greek bishop, and the population is mainly Greek. It
long possessed a valuable export trade, owing to its position at the
mouth of the Maritza, the great natural waterway from Adrianople to the
sea. But its commerce has declined, owing to the unhealthiness of its
climate, to the accumulation of sandbanks in its harbour, which now only
admits small coasters and fishing-vessels, and to the rivalry of
Dedeagatch, a neighbouring seaport connected with Adrianople by rail.
ENRIQUEZ GOMEZ, ANTONIO (c. 1601-c. 1661), Spanish dramatist, poet and
novelist of Portuguese-Jewish origin, was known in the early part of his
career as Enrique Enriquez de Paz. Born at Segovia, he entered the army,
obtained a captaincy, was suspected of heresy, fled to France about
1636, assumed the name of Antonio Enriquez Gomez, and became majordomo
to Louis XIII., to whom he dedicated _Luis dado de Dios a Anna_ (Paris,
1645). Some twelve years later he removed to Amsterdam, avowed his
conversion to Judaism, and was burned in effigy at Seville on the 14th
of April 1660. He is supposed to have returned to France, and to have
died there in the following year. Three of his plays, _El Gran Cardenal
de Espana_, _don Gil de Albornoz_, and the two parts of _Fernan Mendez
Pinto_ were received with great applause at Madrid about 1629; in 1635
he contributed a sonnet to Montalban's collection of posthumous
panegyrics on Lope de Vega, to whose dramatic school Enriquez Gomez
belonged. The _Academias morales de las Musas_, consisting of four plays
(including _A lo que obliga el honor_, which recalls Calderon's _Medico
de su honra_), was published at Bordeaux in 1642; _La Torre de
Babilonia_, containing the two parts of _Fernan Mendez Pinto_, appeared
at Rouen in 1647; and in the preface to his poem, _El Samson Nazareno_
(Rouen, 1656), Enriquez Gomez gives the titles of sixteen other plays
issued, as he alleges, at Seville. There is no foundation for the theory
that he wrote the plays ascribed to Fernando de Zarate. His dramatic
works, though effective on the stage, are disfigured by extravagant
incidents and preciosity of diction. The latter defect is likewise
observable in the mingled prose and verse of _La Culpa del primer
peregrino_ (Rouen, 1644) and the dialogues entitled _Politica Angelica_
(Rouen, 1647). Enriquez Gomez is best represented by _El Siglo
Pitagorico y Vida de don Gregorio Guadana_ (Rouen, 1644), a striking
picaresque novel in prose and verse which is still reprinted.
ENSCHEDE, a town in the province of Overysel, Holland, near the
Prussian frontier, and a junction station 5 m. by rail S.E. of Hengelo.
Pop. (1900) 23,141. It is important as the centre of the flourishing
cotton-spinning and weaving industries of the Twente district; while by
the railway via Gronau and Koesfeld to Dortmund it is in direct
communication with the Westphalian coalfields. Enschede possesses
several churches, an industrial trade school, and a large park intended
for the benefit of the working classes. About two-thirds of the town was
burnt down in 1862.
ENSENADA, CENON DE SOMODEVILLA, MARQUES DE LA (1702-1781), Spanish
statesman, was born at Alesanco near Logrono on the 2nd of June 1702.
When he had risen to high office it was said that his pedigree was
distinguished, but nothing is known of his parents--Francisco de
Somodevilla and his wife Francisca de Bengoechea,--nor is anything known
of his own life before he entered the civil administration of the
Spanish navy as a clerk in 1720. He served in administrative capacities
at the relief of Ceuta in that year and in the reoccupation of Oran in
1731. His ability was recognized by Don Jose Patinos, the chief minister
of King Philip V. Somodevilla was much employed during the various
expeditions undertaken by the Spanish government to put the king's sons
by his second marriage with Elizabeth Farnese, Charles and Philip, on
the thrones of Naples and Parma. In 1736 Charles, afterwards King
Charles III. of Spain, conferred on him the Neapolitan title of Marques
de la Ensenada. The name can be resolved into the three Spanish words
"en se nada," meaning "in himself nothing." The courtly flattery of the
time, and the envy of the nobles who disliked the rise of men of
Ensenada's class, seized upon this poor play on words; an _Ensenada_ is,
however, a roadstead or small bay. In 1742 he became secretary of state
and war to Philip, duke of Parma. In the following year (11th of April
1743), on the death of Patinos's successor Campillo, he was chosen by
Philip V. as minister of finance, war, the navy and the Indies (i.e. the
Colonies). Ensenada met the nomination with a becoming _nolo
episcopari_, professing that he was incapable of filling the four posts
at once. His reluctance was overborne by the king, and he became in fact
prime minister at the age of forty-one. During the remainder of the
king's reign, which lasted till the 11th of July 1746, and under his
successor Ferdinand VI. until 1754, Ensenada was the effective prime
minister. His administration is notable in Spanish history for the
vigour of his policy of internal reform. The reports on the finances and
general condition of the country, which he drew up for the new king on
his accession, and again after peace was made with England at
Aix-la-Chapelle on the 18th of October 1748, are very able and
clear-sighted. Under his direction the despotism of the Bourbon kings
became paternal. Public works were undertaken, shipping was encouraged,
trade was fostered, numbers of young Spaniards were sent abroad for
education. Many of them abused their opportunity, but on the whole the
prosperity of the country revived, and the way was cleared for the more
sweeping innovations of the following reign. Ensenada was a strong
partizan of a French alliance and of a policy hostile to England. Sir B.
Keene, the English minister, supported the Spanish court party opposed
to him, and succeeded in preventing him from adding the foreign office
to others which he held. Ensenada would probably have fallen sooner but
for the support he received from the Portuguese queen, Barbara. In 1754
he offended her by opposing an exchange of Spanish and Portuguese
colonial possessions in America which she favoured. On the 20th of July
of that year he was arrested by the king's order, and sent into mild
confinement at Granada, which he was afterwards allowed to exchange for
Puerto de Santa Maria. On the accession of Charles III. in 1759, he was
released from arrest and allowed to return to Madrid. The new king named
him as member of a commission appointed to reform the system of
taxation. Ensenada could not renounce the hope of again becoming
minister, and entered into intrigues which offended the king. On the
18th of April 1766 he was again exiled from court, and ordered to go to
Medina del Campo. He had no further share in public life, and died on
the 2nd of December 1781. Ensenada acquired wealth in office, but he was
never accused of corruption. Though, like most of his countrymen, he
suffered from the mania for grandeur, and was too fond of imposing
schemes out of all proportion with the resources of the state, he was
undoubtedly an able and patriotic man, whose administration was
beneficial to Spain.
For his administration see W. Coxe, _Memoirs of the Kings of Spain of
the House of Bourbon_ (London, 1815), but the only complete account of
Ensenada is by Don Antonio Rodriguez Villa, _Don Cenon de Somodevilla,
Marques de la Ensenada_ (Madrid, 1878). (D. H.)
ENSIGN (through the Fr. _enseigne_ from the Latin plural _insignia_), a
distinguishing token, emblem or badge such as symbols of office, or in
heraldry, the ornament or sign, such as the crown, coronet or mitre
borne above the charge or arms. The word is more particularly used of a
military or naval standard or banner. In the British navy, ensign has a
specific meaning, and is the name of a flag having a red, white or blue
ground, with the Union Jack in the upper corner next the staff. The
white ensign (which is sometimes further distinguished by having the St
George's Cross quartered upon it) is only used in the royal navy and the
royal yacht squadron, while the blue and red ensigns are the badges of
the naval reserve, some privileged companies, and the merchant service
respectively (see FLAG). Until 1871 the lowest grade of commissioned
officers in infantry regiments of the British army had the title of
ensign (now replaced by that of second lieutenant). It is the duty of
the officers of this rank to carry the colours of the regiment (see
COLOURS, MILITARY). In the 16th century ensign was corrupted into
"ancient," and was used in the two senses of a banner and the bearer of
the banner. In the United States navy, the title ensign superseded in
1862 that of _passed midshipman_. It designates an officer ranking with
second lieutenant in the army.
ENSILAGE, the process of preserving green food for cattle in an undried
condition in a silo (from Gr. [Greek: siros], Lat. _sirus_, a pit for
holding grain), i.e. a pit, an erection above ground, or stack, from
which air has been as far as possible excluded. The fodder which is the
result of the process is called silage. In various parts of Germany a
method of preserving green fodder precisely similar to that used in the
case of _Sauerkraut_ has prevailed for upwards of a century. Special
attention was first directed to the practice of ensilage by a French
agriculturist, Auguste Goffart of the district of Sologne, near Orleans,
who in 1877 published a work (_Manuel de la culture et de l'ensilage des
mais et autres fourrages verts_) detailing the experiences of many years
in preserving green crops in silos. An English translation of Goffart's
book by J.B. Brown was published in New York in 1879, and, as various
experiments had been previously made in the United States in the way of
preserving green crops in pits, Goffart's experience attracted
considerable attention. The conditions of American dairy farming proved
eminently suitable for the ensiling of green maize fodder; and the
success of the method was soon indisputably demonstrated among the New
England farmers. The favourable results obtained in America led to much
discussion and to the introduction of the system in the United Kingdom,
where, with different conditions, success has been more qualified.
It has been abundantly proved that ensilage forms a wholesome and
nutritious food for cattle. It can be substituted for root crops with
advantage, because it is succulent and digestible; milk resulting from
it is good in quality and taste; it can be secured largely irrespective
of weather; it carries over grass from the period of great abundance and
waste to times when none would otherwise be available; and a larger
number of cattle can be supported on a given area by the use of ensilage
than is possible by the use of green crops.
Early silos were made of stone or concrete either above or below
ground, but it is recognized that air may be sufficiently excluded in a
tightly pressed stack, though in this case a few inches of the fodder
round the sides is generally useless owing to mildew. In America round
erections made of wood and 35 or 40 ft. in depth are most commonly used.
The crops suitable for ensilage are the ordinary grasses, clovers,
lucerne, vetches, oats, rye and maize, the latter being the most
important silage crop in America; various weeds may also be stored in
silos with good results, notably spurrey (_Spergula arvensis_), a most
troublesome plant in poor light soils. As a rule the crop should be mown
when in full flower, and deposited in the silo on the day of its
cutting. Maize is cut a few days before it is ripe and is shredded
before being elevated into the silo. Fair, dry weather is not essential;
but it is found that when moisture, natural and extraneous, exceeds 75%
of the whole, good results are not obtained. The material is spread in
uniform layers over the floor of the silo, and closely packed and
trodden down. If possible, not more than a foot or two should be added
daily, so as to allow the mass to settle down closely, and to heat
uniformly throughout. When the silo is filled or the stack built, a
layer of straw or some other dry porous substance may be spread over the
surface. In the silo the pressure of the material, when chaffed,
excludes air from all but the top layer; in the case of the stack extra
pressure is applied by means of planks or other weighty objects in order
to prevent excessive heating.
The closeness with which the fodder is packed determines the nature of
the resulting silage by regulating the chemical changes which occur in
the stack. When closely packed, the supply of oxygen is limited; and the
attendant acid fermentation brings about the decomposition of the
carbohydrates present into acetic, butyric and lactic acids. This
product is named "sour silage." If, on the other hand, the fodder be
unchaffed and loosely packed, or the silo be built gradually, oxidation
proceeds more rapidly and the temperature rises; if the mass be
compressed when the temperature is 140 deg.-160 deg. F., the action
ceases and "sweet silage" results. The nitrogenous ingredients of the
fodder also suffer change: in making sour silage as much as one-third of
the albuminoids may be converted into amino and ammonium compounds;
while in making "sweet silage" a less proportion is changed, but they
become less digestible. In extreme cases, sour silage acquires a most
disagreeable odour. On the other hand it keeps better than sweet silage
when removed from the silo.
ENSTATITE, a rock-forming mineral belonging to the group of orthorhombic
pyroxenes. It is a magnesium metasilicate, MgSiO3, often with a little
iron replacing the magnesium: as the iron increases in amount there is a
transition to bronzite (q.v.), and with still more iron to hypersthene
(q.v.). Bronzite and hypersthene were known long before enstatite, which
was first described by G.A. Kenngott in 1855, and named from [Greek:
enstates], "an opponent," because the mineral is almost infusible before
the blowpipe: the material he described consisted of imperfect prismatic
crystals, previously thought to be scapolite, from the serpentine of
Mount Zdjar near Schonberg in Moravia. Crystals suitable for goniometric
measurement were later found in the meteorite which fell at Breitenbach
in the Erzgebirge, Bohemia. Large crystals, a foot in length and mostly
altered to steatite, were found in 1874 in the apatite veins traversing
mica-schist and hornblende-schist at the apatite mine of Kjorrestad,
near Brevig in southern Norway. Isolated crystals are of rare
occurrence, the mineral being usually found as an essential constituent
of igneous rocks; either as irregular masses in plutonic rocks (norite,
peridotite, pyroxenite, &c.) and the serpentines which have resulted by
their alteration, or as small idiormorphic crystals in volcanic rocks
(trachyte, andesite). It is also a common constituent of meteoric
stones, forming with olivine the bulk of the material: here it often
forms small spherical masses, or chondrules, with an internal radiated
structure.
Enstatite and the other orthorhombic pyroxenes are distinguished from
those of the monoclinic series by their optical characters, viz.
straight extinction, much weaker double refraction and stronger
pleochroism: they have prismatic cleavages (with an angle of 88 deg.
16') as well as planes of parting parallel to the planes of symmetry in
the prism-zone. Enstatite is white, greenish or brown in colour; its
hardness is 5-1/2, and sp. gr. 3.2-3.3. (L. J. S.)
ENTABLATURE (Lat. _in_, and _tabula_, a tablet), the architectural term
for the superstructure carried by the columns in the classic orders
(q.v.). It usually consists of three members, the architrave (the
supporting member carried from column to column, pier or wall); the
frieze (the decorative member); and the cornice (the projecting and
protective member). Sometimes the frieze is omitted, as in the
entablature of the portico of the caryatides of the Erechtheum. There is
every reason to believe that the frieze did not exist in the archaic
temple of Diana at Ephesus; and it is not found in the Lycian tombs,
which are reproductions in the rock of timber structures based on early
Ionian work.
ENTADA, in botany, a woody climber belonging to the family _Leguminosae_
and common throughout the tropics. The best-known species is _Entada
scandens_, the sword-bean, so called from its large woody pod, 2 to 4
ft. in length and 3 to 4 in. broad, which contains large flat hard
polished chestnut-coloured seeds or "beans." The seeds are often made
into snuff-boxes or match-boxes, and a preparation from the kernel is
used as a drug by the natives in India. The seeds will float for a long
time in water, and are often thrown up on the north-western coasts of
Europe, having been carried by the Gulf-stream from the West Indies;
they retain their vitality, and under favourable conditions will
germinate. Linnaeus records the germination of a seed on the coast of
Norway.
ENTAIL (from Fr. _tailler_, to cut; the old derivation from _tales
haeredes_ is now abandoned), in law, a limited form of succession
(q.v.). In architecture, the term "entail" denotes an ornamental device
sunk in the ground of stone or brass, and subsequently filled in with
marble, mosaic or enamel.
ENTASIS (from Gr. [Greek: enteinein], to stretch a line or bend a bow),
in architecture, the increment given to the column (q.v.), to correct
the optical illusion which produces an apparent hollowness in an
extended straight line. It was referred to by Vitruvius (iii. 3), and
was first noticed in the columns of the Doric orders in Greek temples by
Allason in 1814, and afterwards measured and verified by Penrose. It
varies in different temples, and is not found in some: it is most
pronounced in the temple of Jupiter Olympius, most delicate in the
Erechtheum. The entasis is almost invariably introduced in the spires of
English churches.
ENTERITIS (Gr. [Greek: enteron], intestine), a general medical term for
inflammation of the bowels. According to the anatomical part specially
attacked, it is subdivided into duodenitis, jejunitis, ileitis,
typhlitis, appendicitis, colitis, proctitis. The chief symptom is
diarrhoea. The term "enteric fever" has recently come into use instead
of "typhoid" for the latter disease; but see TYPHOID FEVER.
ENTHUSIASM, a word originally meaning inspiration by a divine afflatus
or by the presence of a god. The Gr. [Greek: enthousiasmos], from which
the word is adapted, is formed from the verb [Greek: enthousiazein], to
be [Greek: entheos], possessed by a god [Greek: theos]. Applied by the
Greeks to manifestations of divine "possession," by Apollo, as in the
case of the Pythia, or by Dionysus, as in the case of the Bacchantes and
Maenads, it was also used in a transferred or figurative sense; thus
Socrates speaks of the inspiration of poets as a form of enthusiasm
(Plato, _Apol. Soc._ 22 C). Its uses, in a religious sense, are confined
to an exaggerated or wrongful belief in religious inspiration, or to
intense religious fervour or emotion. Thus a Syrian sect of the 4th
century was known as "the Enthusiasts"; they believed that by perpetual
prayer, ascetic practices and contemplation, man could become inspired
by the Holy Spirit, in spite of the ruling evil spirit, which the fall
had given to him. From their belief in the efficacy of prayer [Greek:
euche], they were also known as Euchites. In ordinary usage,
"enthusiasm" has lost its peculiar religious significance, and means a
whole-hearted devotion to an ideal, cause, study or pursuit; sometimes,
in a depreciatory sense, it implies a devotion which is partisan and is
blind to difficulties and objections. (See further INSPIRATION, for a
comparison of the religious meanings of "enthusiasm," "ecstasy" and
"fanaticism.")
ENTHYMEME (Gr. [Greek: en, thymos]), in formal logic, the technical
name of a syllogistic argument which is incompletely stated. Any one of
the premises may be omitted, but in general it is that one which is most
obvious or most naturally present to the mind. In point of fact the full
formal statement of a syllogism is rare, especially in rhetorical
language, when the deliberate omission of one of the premises has a
dramatic effect. Thus the suppression of the conclusion may have the
effect of emphasizing the idea which necessarily follows from the
premises. Far commoner is the omission of one of the premises which is
either too clear to need statement or of a character which makes its
omission desirable. A famous instance quoted in the _Port Royal Logic_,
pt. iii. ch. xiv., is Medea's remark to Jason in Ovid's _Medea_,
"Servare potui, perdere an possim rogas?" where the major premise "Qui
servare, perdere possunt" is understood. This use of the word enthymeme
differs from Aristotle's original application of it to a syllogism based
on probabilities or signs ([Greek: ex eikoton e semeion]), i.e. on
propositions which are generally valid ([Greek: eikota]) or on
particular facts which may be held to justify a general principle or
another particular fact (_Anal. prior._ [beta] xxvii. 70 a 10).
See beside text-books on logic, Sir W. Hamilton's _Discussions_
(1547); Mansel's ed. of Aldrich, Appendix F; H.W.B. Joseph, _Introd.
to Logic_, chap. xvi.
ENTOMOLOGY (Gr. [Greek: entoma,] insects, and [Greek: logos], a
discourse), the science that treats of insects, i.e. of the animals
included in the class Hexapoda of the great phylum (or sub-phylum)
Arthropoda. The term, however, is somewhat elastic in its current use,
and students of centipedes and spiders are often reckoned among the
entomologists. As the number of species of insects is believed to exceed
that of all other animals taken together, it is no wonder that their
study should form a special division of zoology with a distinctive name.
Beetles (Scarabaei) are the subjects of some of the oldest sculptured
works of the Egyptians, and references to locusts, bees and ants are
familiar to all readers of the Hebrew scriptures. The interest of
insects to the eastern races was, however, economic, religious or moral.
The science of insects began with Aristotle, who included in a class
"Entoma" the true insects, the arachnids and the myriapods, the
Crustacea forming another class ("Malacostraca") of the "Anaema" or
"bloodless animals." For nearly 2000 years the few writers who dealt
with zoological subjects followed Aristotle's leading.
In the history of the science, various lines of progress have to be
traced. While some observers have studied in detail the structure and
life-history of a few selected types (insect anatomy and development),
others have made a more superficial examination of large series of
insects to classify them and determine their relationships (systematic
entomology), while others again have investigated the habits and
life-relations of insects (insect bionomics). During recent years the
study of fossil insects (palaeoentomology) has attracted much attention.
The foundations of modern entomology were laid by a series of wonderful
memoirs on anatomy and development published in the 17th and 18th
centuries. Of these the most famous are M. Malpighi's treatise on the
silkworm (1669) and J. Swammerdam's _Biblia naturae_, issued in 1737,
fifty years after its author's death, and containing observations on the
structure and life-history of a series of insect types. Aristotle and
Harvey (_De generatione animalium_, 1651) had considered the insect larva
as a prematurely hatched embryo and the pupa as a second egg. Swammerdam,
however, showed the presence under the larval cuticle of the pupal
structures. His only unfortunate contribution to entomology--indeed to
zoology generally--was his theory of pre-formation, which taught the
presence within the egg of a perfectly formed but miniature adult. A year
before Malpighi's great work appeared, another Italian naturalist, F.
Redi, had disproved by experiment the spontaneous generation of maggots
from putrid flesh, and had shown that they can only develop from the eggs
of flies.
Meanwhile the English naturalist, John Ray, was studying the
classification of animals; he published, in 1705, his _Methodus
insectorum_, in which the nature of the metamorphosis received due
weight. Ray's "Insects" comprised the Arachnids, Crustacea, Myriapoda
and Annelida, in addition to the Hexapods. Ray was the first to
formulate that definite conception of the species which was adopted by
Linnaeus and emphasized by his binominal nomenclature. In 1735 appeared
the first edition of the _Systema naturae_ of Linnaeus, in which the
"Insecta" form a group equivalent to the Arthropoda of modern
zoologists, and are divided into seven orders, whose names--Coleoptera,
Diptera, Lepidoptera, &c., founded on the nature of the wings--have
become firmly established. The fascinating subjects of insect bionomics
and life-history were dealt with in the classical memoirs (1734-1742) of
the Frenchman R.A.F. de Reaumur, and (1752-1778) of the Swede C. de
Geer. The freshness, the air of leisure, the enthusiasm of discovery
that mark the work of these old writers have lessons for the modern
professional zoologist, who at times feels burdened with the accumulated
knowledge of a century and a half. From the end of the 18th century
until the present day, it is only possible to enumerate the outstanding
features in the progress of entomology. In the realm of classification,
the work of Linnaeus was continued in Denmark by J.C. Fabricius
(_Systema entomologica_, 1775), and extended in France by G.P.B. Lamarck
(_Animaux sans vertebres_, 1801) and G. Cuvier (_Lecons d'anatomie
comparee_, 1800-1805), and in England by W.E. Leach (_Trans. Linn. Soc._
xi., 1815). These three authors definitely separated the Arachnida,
Crustacea and Myriapoda as classes distinct from the Insecta (see
HEXAPODA). The work of J.O. Westwood (_Modern Classification of
Insects_, 1839-1840) connects these older writers with their successors
of to-day.
In the anatomical field the work of Malpighi and Swammerdam was at first
continued most energetically by French students. P. Lyonnet had
published in 1760 his elaborate monograph on the goat-moth caterpillar,
and H.E. Strauss-Durckheim in 1828 issued his great treatise on the
cockchafer. But the name of J.C.L. de Savigny, who (_Mem. sur les
animaux sans vertebres_, 1816) established the homology of the jaws of
all insects whether biting or sucking, deserves especial honour. Many
anatomical and developmental details were carefully worked out by L.
Dufour (in a long series of memoirs from 1811 to 1860) in France, by G.
Newport ("Insecta" in _Encyc. Anat. and Physiol._, 1839) in England, and
by H. Burmeister (_Handbuch der Entomologie_, 1832) in Germany. Through
the 19th century, as knowledge increased, the work of investigation
became necessarily more and more specialized. Anatomists like F. Leydig,
F. Muller, B.T. Lowne and V. Graber turned their attention to the
detailed investigation of some one species or to special points in the
structure of some particular organs, using for the elucidation of their
subject the ever-improving microscopical methods of research.
Societies for the discussion and publication of papers on entomology
were naturally established as the number of students increased. The
Societe Entomologique de France was founded in 1832, the Entomological
Society of London in 1834. Few branches of zoology have been more
valuable as a meeting-ground for professional and amateur naturalists
than entomology, and not seldom has the amateur--as in the case of
Westwood--developed into a professor. During the pre-Linnaean period,
the beauty of insects--especially the Lepidoptera--had attracted a
number of collectors; and these "Aurelians"--regarded as harmless
lunatics by most of their friends--were the forerunners of the
systematic students of later times. While the insect fauna of European
countries was investigated by local naturalists, the spread of
geographical exploration brought ever-increasing stores of exotic
material to the great museums, and specialization--either in the fauna
of a small district or in the world-wide study of an order or a group of
families--became constantly more marked in systematic work. As examples
may be instanced the studies of A.H. Haliday and H. Loew on the European
Diptera, of John Curtis on British insects, of H.T. Stainton and O.
Staudinger on the European Lepidoptera, of R. M'Lachlan on the European
and of H.A. Hagen on the North American Neuroptera, of D. Sharp on the
_Dyticidae_ and other families of Coleoptera of the whole world.
The embryology of insects is entirely a study of the last century. C.
Bonnet indeed observed in 1745 the virgin-reproduction of Aphids, but it
was not until 1842 that R.A. von Kolliker described the formation of the
blastoderm in the egg of the midge _Chironomus_. Later A. Weismann
(1863-1864) traced details of the growth of embryo and of pupa among the
Diptera, and A. Kovalevsky in 1871 first described the formation of the
germinal layers in insects. Most of the recent work on the embryology of
insects has been done in Germany or the United States, and among
numerous students V. Graber, K. Heider, W.M. Wheeler and R. Heymons may
be especially mentioned.
The work of de Reaumur and de Geer on the bionomics and life-history of
insects has been continued by numerous observers, among whom may be
especially mentioned in France J.H. Fabre and C. Janet, in England W.
Kirby and W. Spence, J. Lubbock (Lord Avebury) and L.C. Miall, and in
the United States C.V. Riley. The last-named may be considered the
founder of the strong company of entomological workers now labouring in
America. Though Riley was especially interested in the bearings of
insect life on agriculture and industry--economic entomology (q.v.)--he
and his followers have laid the science generally under a deep
obligation by their researches.
After the publication of C. Darwin's _Origin of Species_ (1859) a fresh
impetus was given to entomology as to all branches of zoology, and it
became generally recognized that insects form a group convenient and
hopeful for the elucidation of certain problems of animal evolution. The
writings of Darwin himself and of A.R. Wallace (both at one time active
entomological collectors) contain much evidence drawn from insects in
favour of descent with modification. The phylogeny of insects has since
been discussed by F. Brauer, A.S. Packard and many others; mimicry and
allied problems by H.W. Bates, F. Muller, E.B. Poulton and M.C. Piepers;
the bearing of insect habits on theories of selection and
use-inheritance by A. Weismann, G.W. and E. Peckham, G.H.T. Eimer and
Herbert Spencer; variation by W. Bateson and M. Standfuss.
BIBLIOGRAPHY.--References to the works of the above authors, and to
many others, will be found under HEXAPODA and the special articles on
various insect orders. Valuable summaries of the labours of Malpighi,
Swammerdam and other early entomologists are given in L.C. Miall and
A. Denny's _Cockroach_ (London, 1886), and L. Henneguy's _Les
Insectes_ (Paris, 1904). (G. H. C.)
ENTOMOSTRACA. This zoological term, as now restricted, includes the
Branchiopoda, Ostracoda and Copepoda. The Ostracoda have the body
enclosed in a bivalve shell-covering, and normally unsegmented. The
Branchiopoda have a very variable number of body-segments, with or
without a shield, simple or bivalved, and some of the postoral
appendages normally branchial. The Copepoda have normally a segmented
body, not enclosed in a bivalved shell-covering, the segments not
exceeding eleven, the limbs not branchial.
Under the heading CRUSTACEA the Entomostraca have already been
distinguished not only from the Thyrostraca or Cirripedes, but also from
the Malacostraca, and an intermediate group of which the true position
is still disputed. The choice is open to maintain the last as an
independent subclass, and to follow Claus in calling it the Leptostraca,
or to introduce it among the Malacostraca as the Nebaliacea, or with
Packard and Sars to make it an entomostracan subdivision under the title
Phyllocarida. At present it comprises the single family _Nebaliidae_.
The bivalved carapace has a jointed rostrum, and covers only the front
part of the body, to which it is only attached quite in front, the
valve-like sides being under control of an adductor muscle. The eyes are
stalked and movable. The first antennae have a lamellar appendage at the
end of the peduncle, a decidedly non-entomostracan feature. The second
antennae, mandibles and two pairs of maxillae may also be claimed as of
malacostracan type. To these succeed eight pairs of foliaceous branchial
appendages on the front division of the body, followed on the hind
division by four pairs of powerful bifurcate swimming feet and two
rudimentary pairs, the number, though not the nature, of these
appendages being malacostracan. On the other hand, the two limbless
segments that precede the caudal furca are decidedly non-malacostracan.
The family was long limited to the single genus _Nebalia_ (Leach), and
the single species _N. bipes_ (O. Fabricius). Recently Sars has added a
Norwegian species, _N. typhlops_, not blind but weak-eyed. There are
also now two more genera, _Paranebalia_ (Claus, 1880), in which the
branchial feet are much longer than in _Nebalia_, and _Nebaliopsis_
(Sars, 1887), in which they are much shorter. All the species are
marine.
BRANCHIOPODA.--In this order, exclusion of the Phyllocarida will leave
three suborders of very unequal extent, the Phyllopoda, Cladocera,
Branchiura. The constituents of the last have often been classed as
Copepoda, and among the Branchiopods must be regarded as aberrant, since
the "branchial tail" implied in the name has no feet, and the actual
feet are by no means obviously branchial.
_Phyllopoda._--This "leaf-footed" suborder has the appendages which
follow the second maxillae variable in number, but all foliaceous and
branchial. The development begins with a free nauplius stage. In the
outward appearance of the adults there is great want of uniformity, one
set having their limbs sheltered by no carapace, another having a broad
shield over most of them, and a third having a bivalved shell-cover
within which the whole body can be enclosed. In accord with these
differences the sections may be named Gymnophylla, Notophylla,
Conchophylla. The equivalent terms applied by Sars are Anostraca,
Notostraca, Conchostraca, involving a termination already appropriated
to higher divisions of the Crustacean class, for which it ought to be
reserved.
1. Gymnophylla.--These singular crustaceans have long soft flexible
bodies, the eyes stalked and movable, the first antennae small and
filiform, the second lamellar in the female, in the male prehensile;
this last character gives rise to some very fanciful developments.
There are three families, two of which form companies rather severely
limited. Thus the _Polyartemiidae_, which compensate themselves for
their stumpy little tails by having nineteen instead of the normal
eleven pairs of branchial feet, consist exclusively of _Polyartemia
forcipata_ (Fischer, 1851). This species from the high north of Europe
and Asia carries green eggs, and above them a bright pattern in
ultramarine (Sars, 1896, 1897). The _Thamnocephalidae_ have likewise
but a single species, _Thamnocephalus platyurus_ (Packard, 1877),
which justifies its title "bushy-head of the broad tail" by a
singularity at each end. Forward from the head extends a long ramified
appendage described as the "frontal shrub," backward from the fourth
abdominal segment of the male spreads a fin-like expansion which is
unique. In the ravines of Kansas, pools supplied by torrential rains
give birth to these and many other phyllopods, and in turn "millions
of them perish by the drying up of the pools in July" (Packard). The
remaining family, the _Branchipodidae_, includes eight genera. In the
long familiar _Branchipus_, _Chirocephalus_ and _Streptocephalus_ the
males have frontal appendages, but these are wanting in the
"brine-shrimp" _Artemia_, and the same want helps to distinguish
_Branchinecta_ (Verrill, 1869) from the old genus _Branchipus_. Of
_Branchiopsyllus_ (Sars, 1897) the male is not yet known, but in his
genera of the same date, the Siberian _Artemiopsis_ and the South
African _Branchipodopsis_ (1898), there is no such appendage. Of the
last genus the type species _B. hodgsoni_ belongs to Cape Colony, but
the specimens described were born and bred and observed in Norway. For
the study of fresh-water Entomostraca large possibilities are now
opened to the naturalist. A parcel of dried mud, coming for example
from Palestine or Queensland, and after an indefinite interval of time
put into water in England or elsewhere, may yield him living forms,
both new and old, in the most agreeable variety. Some caution should
be used against confounding accidentally introduced indigenous species
with those reared from the imported eggs. Those, too, who send or
bring the foreign soil should exercise a little thought in the choice
of it, since dry earth that has never had any Entomostraca near it at
home will not become fertile in them by the mere fact of exportation.
2. Notophylla.--In this division the body is partly covered by a broad
shield, united in front with the head; the eyes are sessile, the first
antennae are small, the second rudimentary or wanting; of the numerous
feet, sometimes sixty-three pairs, exceeding the number of segments to
which they are attached, the first pair are more or less unlike the
rest, and in the female the eleventh have the epipod and exopod
(flabellum and sub-apical lobe of Lankester) modified to form an
ovisac. Development begins with a nauplius stage. Males are very rare.
The single family _Apodidae_ contains only two genera, _Apus_ and its
very near neighbour _Lepidurus_. _Apus australiensis_ (Spencer and
Hall, 1896) may rank as the largest of the Entomostraca, reaching in
the male, from front of shield to end of telson, a length of 70 mm.,
in the female of 64 mm. In a few days, or at most a fortnight, after a
rainfall numberless specimens of these sizes were found swimming
about, "and as not a single one was to be found in the water-pools
prior to the rain, these must have been developed from the egg."
Similarly, in Northern India _Apus himalayanus_ was "collected from a
stagnant pool in a jungle four days after a shower of rain had
fallen," following a drought of four months (Packard).
3. Conchophylla.--Though concealed within the bivalved shell-cover,
the mouth-parts are nearly as in the Gymnophylla, but the flexing of
the caudal part is in contrast, and the biramous second antennae
correspond with what is only a larval character in the other
phyllopods. In the male the first one or two pairs of feet are
modified into grasping organs. The small ova are crowded beneath the
dorsal part of the valves. The development usually begins with a
nauplius stage (Sars, 1896, 1900). There are four families: (a) The
_Limnadiidae_, with feet from 18 to 32 pairs, comprise four (or five)
genera. Of these _Limnadella_ (Girard, 1855) has a single eye. It
remains rather obscure, though the type species originally "was
discovered in great abundance in a roadside puddle subject to
desiccation." _Limnadia_ (Brongniart, 1820) is supposed to consist of
species exclusively parthenogenetic. But when asked to believe that
males never occur among these amazons, one cannot but remember how
hard it is to prove a negative. (b) The _Lynceidae_, with not more
than twelve pairs of feet. This family is limited to the species,
widely distributed, of the single genus _Lynceus_, established by O.F.
Muller in 1776 and 1781, and first restricted by Leach in 1816 in the
_Encyclopaedia Britannica_ (art. "Annulosa," of that edition). Leach
there assigns to it the single species _L. brachyurus_ (Muller), and
as this is included in the genus _Limnetis_ (Loven, 1846), that genus
must be a synonym of _Lynceus_ as restricted. (c) _Leptestheriidae_.
_Estheria_ (Ruppell, 1837) was instituted for the species
_dahalacensis_, which Sars includes in his genus _Leptestheria_
(1898); but _Estheria_ was already appropriated, and of its synonyms
_Cyzicus_ (Audouin, 1837) is lost for vagueness, while _Isaura_ (Joly,
1842) is also appropriated, so that _Leptestheria_ becomes the name of
the typical genus, and determines the name of the family. (d)
_Cyclestheriidae_. This family consists of the single species
_Cyclestheria hislopi_ (Baird), reported from India, Ceylon, Celebes,
Australia, East Africa and Brazil. Sars (1887) having had the
opportunity of raising it from dried Australian mud, found that,
unlike other phyllopods, but like the Cladocera, the parent keeps its
brood within the shell until their full development.
_Cladocera._--In this suborder the head is more or less distinct, the
rest of the body being in general laterally compressed and covered by a
bivalved test. The title "branching horns" alludes to the second
antennae, which are two-branched except in the females of _Holopedium_,
with each branch setiferous, composed of only two to four joints. The
mandibles are without palp. The pairs of feet are four to six. The eye
is single, and in addition to the eye there is often an "eye-spot,"
_Monospilus_ being unique in having the eye-spot alone and no eye, while
_Leydigiopsis_ (Sars, 1901) has an eye with an eye-spot equal to it or
larger. The heart has a pair of venous ostia, often blending into one,
and an anterior arterial aorta. Respiration is conducted by the general
surface, by the branchial lamina (external branch) of the feet, and the
vesicular appendage (when present) at the base of this branch. The
"abdomen," behind the limbs, is usually very short, occasionally very
long. The "postabdomen," marked off by the two postabdominal setae,
usually has teeth or spines, and ends in two denticulate or ciliate
claws, or it may be rudimentary, as in _Polyphemus_. Many species have a
special glandular organ at the back of the head, which _Sida
crystallina_ uses for attaching itself to various objects. The Leydigian
or nuchal organ is supposed to be auditory and to contain an otolith.
The female lays two kinds of eggs--"summer-eggs," which develop without
fertilization, and "winter-eggs" or resting eggs, which require to be
fertilized. The latter in the _Daphniidae_ are enclosed in a modified
part of the mother's shell, called the ephippium from its resemblance to
a saddle in shape and position. In other families a less elaborate case
has been observed, for which Scourfield has proposed the term
protoephippium. In _Leydigia_ he has recently found a structure almost
as complex as that of the _Daphniidae_. In some families the resting
eggs escape into the water without special covering. Only the embryos of
_Leptodora_ are known to hatch out in the nauplius stage. _Penilia_
(Dana, 1849) is perhaps the only exclusively marine genus. The great
majority of the Cladocera belong to fresh water, but their adaptability
is large, since _Moina rectirostris_ (O.F. Muller) can equally enjoy a
pond at Blackheath, and near Odessa live in water twice as salt as that
of the ocean. In point of size a Cladoceran of 5 mm. is spoken of as
colossal.
Dr Jules Richard in his revision (1895) retains the sections proposed
by Sars in 1865, Calyptomera and Gymnomera. The former, with the feet
for the most part concealed by the carapace, is subdivided into two
tribes, the Ctenopoda, or "comb-feet," in which the six pairs of
similar feet, all branchial and nonprehensile, are furnished with
setae arranged like the teeth of a comb, and the Anomopoda, or
"variety-feet," in which the front feet differ from the rest by being
more or less prehensile, without branchial laminae.
The Ctenopoda comprise two families: (a) the _Holopediidae_, with a
solitary species, _Holopedium gibberum_ (Zaddach), queerly clothed in
a large gelatinous involucre, and found in mountain tarns all over
Europe, in large lakes of N. America, and also in shallow ponds and
waters at sea-level; (b) the _Sididae_, with no such involucre, but
with seven genera, and rather more than twice as many species. Of
_Diaphanosoma modiglianii_ Richard says that at different points of
Lake Toba in Sumatra millions of specimens were obtained, among which
he had not met with a single male.
The Anomopoda are arranged in four families, all but one very
extensive. (a) _Daphniidae_. Of the seven genera, the cosmopolitan
_Daphnia_ contains about 100 species and varieties, of which Thomas
Scott (1899) observes that "scarcely any of the several characters
that have at one time or another been selected as affording a means
for discriminating between the different forms can be relied on as
satisfactory." Though this may dishearten the systematist, Scourfield
(1900) reminds us that "It was in a water-flea that Metschnikoff first
saw the leucocytes (or phagocytes) trying to get rid of disease germs
by swallowing them, and was so led to his epoch-making discovery of
the part played by these minute amoeboid corpuscles in the animal
body." For _Scapholeberis mucronata_ (O.F. Muller), Scourfield has
shown how it is adapted for movement back downwards in the water along
the underside of the surface film, which to many small crustaceans is
a dangerously disabling trap. (b) _Bosminidae_. To _Bosmina_ (Baird,
1845) Richard added _Bosminopsis_ in 1895. (c) _Macrotrichidae._ In
this family _Macrothrix_ (Baird, 1843) is the earliest genus, among
the latest being _Grimaldina_ (Richard, 1892) and _Jheringula_ (Sars,
1900). Dried mud and vegetable debris from S. Paulo in Brazil supplied
Sars with representatives of all the three in his Norwegian aquaria,
in some of which the little _Macrothrix elegans_ "multiplied to such
an extraordinary extent as at last to fill up the water with immense
shoals of individuals." "The appearance of male specimens was always
contemporary with the first ephippial formation in the females." For
_Streblocerus pygmaeus_, grown under the same conditions, Sars
observes: "This is perhaps the smallest of the Cladocera known, and is
hardly more than visible to the naked eye," the adult female scarcely
exceeding 0.25 mm. Yet in the next family _Alonella nana_ (Baird)
disputes the palm and claims to be the smallest of all known
Arthropoda. (d) _Chydoridae._ This family, so commonly called
_Lynceidae_, contains a large number of genera, among which one may
usually search in vain, and rightly so, for the genus _Lynceus_. The
key to the riddle is to be found in the _Encyclopaedia Britannica_ for
1816. There, as above explained, Leach began the subdivision of
Muller's too comprehensive genus, the result being that _Lynceus_
belongs to the Phyllopoda, and _Chydorus_ (Leach, 1816) properly gives
its name to the present family, in which the doubly convoluted
intestine is so remarkable. Of its many genera, _Leydigia_,
_Leydigiopsis_, _Monospilus_ have been already mentioned. _Dadaya
macrops_ (Sars, 1901), from South America and Ceylon, has a very large
eye and an eye-spot fully as large, but it is a very small creature,
odd in its behaviour, moving by jumps at the very surface of the
water. "To the naked eye it looked like a little black atom darting
about in a most wonderful manner."
[Illustration: FIG. 1.--_Dolops ranarum_ (Stuhlmann).]
The Gymnomera, with a carapace too small to cover the feet, which are
all prehensile, are divided also into two tribes, the Onychopoda, in
which the four pairs of feet have a toothed maxillary process at the
base, and the Haplopoda, in which there are six pairs of feet, without
such a process. To the _Polyphemidae_, the well-known family of the
former tribe, Sars in 1897 added two remarkable genera, _Cercopagis_,
meaning "tail with a sling," and _Apagis_, "without a sling," for
seven species from the Sea of Azov. The Haplopoda likewise have but a
single family, the _Leptodoridae_, and this has but the single genus
_Leptodora_ (Lilljeborg, 1861). Dr Richard (1895, 1896) gives a
Cladoceran bibliography of 601 references.
_Branchiura._--This term was introduced by Thorell in 1864 for the
_Argulidae_, a family which had been transferred to the Branchiopoda by
Zenker in 1854, though sometimes before and since united with the
parasitic Copepoda. Though the animals have an oral siphon, they do not
carry ovisacs like the siphonostomous copepods, but glue their eggs in
rows to extraneous objects. Their lateral, compound, feebly movable eyes
agree with those of the Phyllopoda. The family are described by Claus as
"intermittent parasites," because when gorged they leave their hosts,
fishes or frogs, and swim about in freedom for a considerable period.
The long-known _Argulus_ (O.F. Muller) has the second maxillae
transformed into suckers, but in _Dolops_ (Audouin, 1837) (fig. 1), the
name of which supersedes the more familiar _Gyropeltis_ (Heller, 1857),
these effect attachment by ending in strong hooks (Bouvier, 1897). A
third genus, _Chonopeltis_ (Thiele, 1900), has suckers, but has lost its
first antennae, at least in the female.
OSTRACODA.--The body, seldom in any way segmented, is wholly encased in
a bivalved shell, the caudal part strongly inflexed, and almost always
ending in a furca. The limbs, including antennae and mouth organs, never
exceed seven definite pairs. The first antennae never have more than
eight joints. The young usually pass through several stages of
development after leaving the egg, and this commonly after, even long
after, the egg has left the maternal shell. Parthenogenesis is frequent.
The four tribes instituted by Sars in 1865 were reduced to two by G.W.
Muller in 1894, the Myodocopa, which almost always have a heart, and the
Podocopa, which have none.
_Myodocopa._--These have the furcal branches broad, lamellar, with at
least three pairs of strong spines or ungues. Almost always the shell
has a rostral sinus. Muller divides the tribe into three families,
_Cypridinidae, Halocypridae_, and the heartless _Polycopidae_, which
constituted the tribe Cladocopa of Sars. From the first of these Brady
and Norman distinguish the Asteropidae (fig. 3), remarkable for seven
pairs of long branchial leaves which fold over the hinder extremity of
the animal, and the _Sarsiellidae_, still somewhat obscure, besides
adding the _Rutidermatidae_, knowledge of which is based on skilful
maceration of minute and long-dried specimens. The _Halocypridae_ are
destitute of compound lateral eyes, and have the sexual orifice
unsymmetrically placed.
_Podocopa._--In these the furcal branches are linear or rudimentary,
the shell is without rostral sinus, and, besides distinguishing
characters of the second antennae, they have always a branchial plate
well developed on the first maxillae, which is inconstant in the other
tribe. There are five families: (a) _Cyprididae_ (? including
_Cypridopsidae_ of Brady and Norman). In some of the genera
parthenogenetic propagation is carried to such an extent that of the
familiar _Cypris_ it is said, "until quite lately males in this genus
were unknown; and up to the present time no male has been found in the
British Islands" (Brady and Norman, 1896). On the other hand, the
ejaculatory duct with its verticillate sac in the male of _Cypris_ and
other genera is a feature scarcely less remarkable. (b) _Bairdiidae_,
which have the valves smooth, with the hinge untoothed. (c)
_Cytheridae_ (? including _Paradoxostomatidae_ of Brady and Norman),
in which the valves are usually sculptured, with toothed hinge. Of
this family the members are almost exclusively marine, but
_Limnicythere_ is found in fresh water, and _Xestoleberis bromeliarum_
(Fritz Muller) lives in the water that collects among the leaves of
Bromelias, plants allied to the pine-apples. (d) _Darwinulidae_,
including the single species _Darwinula stevensoni_, Brady and
Robertson, described as "perhaps the most characteristic Entomostracan
of the East Anglian Fen District." (e) _Cytherellidae_, which, unlike
the Ostracoda in general, have the hinder part of the body segmented,
at least ten segments being distinguishable in the female. They have
the valves broad at both ends, and were placed by Sars in a separate
tribe, called Platycopa.
The range in time of the Ostracoda is so extended that, in G.W.
Muller's opinion, their separation into the families now living may have
already taken place in the Cambrian period. Their range in space,
including carriage by birds, may be coextensive with the distribution of
water, but it is not known what height of temperature or how much
chemical adulteration of the water they can sustain, how far they can
penetrate underground, nor what are the limits of their activity between
the floor and the surface of aquatic expanses, fresh or saline. In
individual size they have never been important, and of living forms the
largest is one of recent discovery, _Crossophorus africanus_, a
Cypridinid about three-fifths of an inch (15.5 mm.) long; but a length
of one or two millimetres is more common, and it may descend to the
seventy-fifth of an inch. By multitude they have been, and still are,
extremely important.
Though the exterior is more uniform than in most groups of Crustacea,
the bivalved shell or carapace may be strongly calcified and diversely
sculptured (fig. 2), or membranaceous and polished, hairy or smooth,
oval or round or bean-shaped, or of some less simple pattern; the
valves may fit neatly, or one overlap the other, their hinge may have
teeth or be edentulous, and their front part may be excavated for the
protrusion of the antennae or have no such "rostral sinus." By various
modifications of their valves and appendages the creatures have become
adapted for swimming, creeping, burrowing, or climbing, some of them
combining two or more of these activities, for which their structure
seems at the first glance little adapted. Considering the imprisonment
of the ostracod body within the valves, it is more surprising that the
_Asteropidae_ and _Cypridinidae_ should have a pair of compound and
sometimes large eyes, in addition to the median organ at the base of
the "frontal tentacle," than that other members of the group should be
limited to that median organ of sight, or have no eyes at all. The
median eye when present may have or not have a lens, and its three
pigment-cups may be close together or wide apart and the middle one
rudimentary. As might be expected, in thickened and highly embossed
valves thin spaces occur over the visual organ. The frontal organ
varies in form and apparently in function, and is sometimes absent.
The first antennae, according to the family, may assist in walking,
swimming, burrowing, climbing, grasping, and besides they carry
sensory setae, and sometimes they have suckers on their setae (see
Brady and Norman on _Cypridina norvegica_). The second antennae are
usually the chief motor-organs for swimming, walking and climbing. The
mandibles are normally five-jointed, with remnants of an outer branch
on the second joint, the biting edge varying from strong development
to evanescence, the terminal joints or "palp" giving the organ a
leg-like appearance and function, which disappears in suctorial genera
such as _Paracytherois_. The variable first maxillae are seldom
pediform, their function being concerned chiefly with nutrition,
sensation and respiration. The variability in form and function of the
second maxillae is sufficiently shown by the fact that G.W. Muller,
our leading authority, adopts the confusing plan of calling them
second maxillae in the _Cypridinidae_ (including _Asteropidae_),
maxillipeds in the _Halocypridae_ and _Cyprididae_, and first legs in
the _Bairdiidae_, _Cytheridae_, _Polycopidae_ and _Cytherellidae_, so
that in his fine monograph he uses the term first leg in two quite
different senses. The first legs, meaning thereby the sixth pair of
appendages, are generally pediform and locomotive, but sometimes
unjointed, acting as a kind of brushes to cleanse the furca, while in
the _Polycopidae_ they are entirely wanting. The second legs are
sometimes wanting, sometimes pediform and locomotive, sometimes
strangely metamorphosed into the "vermiform organ," generally long,
many-jointed, and distally armed with retroverted spines, its function
being that of an extremely mobile cleansing foot, which can insert
itself among the eggs in the brood-space, between the branchial leaves
of _Asterope_ (fig. 3), and even range over the external surface of
the valves. The "brush-formed" organs of the Podocopa are medially
placed, and, in spite of their sometimes forward situation, Muller
believes among other possibilities that they and the penis in the
_Cypridinidae_ may be alike remnants of a third pair of legs, not
homologous with the penis of other Ostracoda (Podocopa included). The
furca is, as a rule, a powerful motor-organ, and has its laminae edged
with strong teeth (ungues) or setae or both. The young, though born
with valves, have at first a nauplian body, and pass through various
stages to maturity.
[Illustration: FIG. 2.--_Cythereis ornata_ (G.W. Muller). One
eye-space is shown above on the left.]
[Illustration: FIG. 3.--_Asterope arthuri_. Left valve removed.
M, End of adductor muscle.
OC, Eye.
AI, Second antenna.
MX. 1, First maxilla.
MX. 2, Second maxilla.
P. 1, First foot.
V. O, Vermiform organ.
BR, Seven branchial leaves.
F, Projecting ungues of the furca.]
Brady and Norman, in their _Monograph of the Ostracoda of the North
Atlantic and North-Western Europe_ (1889), give a bibliography of 125
titles, and in the second part (1896) they give 55 more. The lists are
not meant to be exhaustive, any more than G.W. Muller's literature
list of 125 titles in 1894. They do not refer to Latreille, 1802, with
whom the term Ostracoda originates.
COPEPODA.--The body is not encased in a bivalved shell; its articulated
segments are at most eleven, those behind the genital segment being
without trace of limbs, but the last almost always carrying a furca.
Sexes separate, fertilization by spermatophores. Ova in single or double
or rarely several packets, attached as ovisacs or egg-strings to the
genital openings, or enclosed in a dorsal marsupium, or deposited singly
or occasionally in bundles. The youngest larvae are typical nauplii. The
next, the copepodid or cyclopid, stage is characterized by a cylindrical
segmented body, with fore- and hind-body distinct, and by having at most
six cephalic limbs and two pairs of swimming feet.
The order thus defined (see Giesbrecht and Schmeil, _Das Tierreich_,
1898), with far over a thousand species (Hansen, 1900), embraces forms
of extreme diversity, although, when species are known in all their
phases and both sexes, they constantly tend to prove that there are no
sharply dividing lines between the free-living, the semi-parasitic, and
those which in adult life are wholly parasitic and then sometimes
grotesquely unlike the normal standard. Giesbrecht and Hansen have shown
that the mouth-organs consist of mandibles, first and second maxillae
and maxillipeds; and Claus himself relinquished his long-maintained
hypothesis that the last two pairs were the separated exopods and
endopods of a single pair of appendages. Thorell's classification (1859)
of Gnathostoma, Poecilostoma, Siphonostoma, based on the mouth-organs,
was long followed, though almost at the outset shown by Claus to depend
on the erroneous supposition that the Poecilostoma were devoid of
mandibles. Brady added a new section, Choniostomata, in 1894, and
another, Leptostomata, in 1900, each for a single species. Canu in 1892
proposed two groups, Monoporodelphya and Diporodelphya, the copulatory
openings of the female being paired in the latter, unpaired in the
former. It may be questioned whether this distinction, however important
in itself, would lead to a satisfactory grouping of families. In the
same year Giesbrecht proposed his division of the order into Gymnoplea
and Podoplea.
In appearance an ordinary Copepod is divided into fore- and hind-body,
of its eleven segments the composite first being the head, the next five
constituting the thorax, and the last five the abdomen. The coalescence
of segments, though frequent, does not after a little experience
materially confuse the counting. But there is this peculiarity, that the
middle segment is sometimes continuous with the broader fore-body,
sometimes with the narrower hind-body. In the former case the hind-body,
consisting only of the abdomen, forms a pleon or tail-part devoid of
feet, and the species so constructed are Gymnoplea, those of the naked
or footless pleon. In the latter case the middle segment almost always
carries with it to the hind-body a pair of rudimentary limbs, whence the
term Podoplea, meaning species that have a pleon with feet. It may be
objected that hereby the term pleon is used in two different senses,
first applying to the abdomen alone and then to the abdomen plus the
last thoracic segment. Even this verbal flaw would be obviated if
Giesbrecht could prove his tentative hypothesis, that the Gymnoplea may
have lost a pre-genital segment of the abdomen, and the Podoplea may
have lost the last segment of the thorax. The classification is worked
out as follows:--
1. _Gymnoplea._--First segment of hind-body footless, bearing the
orifices of the genital organs (in the male unsymmetrically placed);
last foot of the fore-body in the male a copulatory organ; neither, or
only one, of the first pair of antennae in the male geniculating;
cephalic limbs abundantly articulated and provided with many plumose
setae; heart generally present. Animals usually free-living, pelagic
(Giesbrecht and Schmeil).
This group, with 65 genera and four or five hundred species, is
divided by Giesbrecht into tribes: (a) Amphaskandria. In this tribe
the males have both antennae of the first pair as sensory organs.
There is but one family, the _Calanidae_, but this is a very large
one, with 26 genera and more than 100 species. Among them is the
cosmopolitan _Calanus finmarchicus_, the earliest described (by Bishop
Gunner in 1770) of all the marine free-swimming Copepoda. Among them
also is the peacock Calanid, _Calocalanus pavo_ (Dana), with its
highly ornamented antennae and gorgeous tail, the most beautiful
species of the whole order (fig. 4). (b) Heterarthrandria. Here the
males have one or the other of the first pair of antennae modified
into a grasping organ for holding the female. There are four families,
the _Diaptomidae_ with 27 genera, the _Pontellidae_ with 10, the
_Pseudocyclopidae_ and _Candaciidae_ each with one genus. The first of
these families is often called _Centropagidae_, but, as Sars has
pointed out, _Diaptomus_ (Westwood, 1836) is the oldest genus in it.
Of 177 species valid in the family Giesbrecht and Schmeil assign 67 to
_Diaptomus_. In regard to one of its species Dr Brady says: "In one
instance, at least (Talkin Tarn, Cumberland) I have seen the net come
up from a depth of 6 or 8 ft. below the surface with a dense mass
consisting almost entirely of _D. gracilis_." The length of this
net-filling species is about a twentieth of an inch.
[Illustration: FIG. 4.--_Calocalanus pavo_ (Dana).]
2. _Podoplea._--The first segment of the hind-body almost always with
rudimentary pair of feet; orifices of the genital organs
(symmetrically placed in both sexes) in the following segment; neither
the last foot of the fore-body nor the rudimentary feet just mentioned
acting as a copulatory organ in the male; both or neither of the first
pair of antennae in the male geniculating; cephalic limbs less
abundantly articulated and with fewer plumose setae or none, but with
hooks and clasping setae. Heart almost always wanting. Free-living
(rarely pelagic) or parasitic (Giesbrecht and Schmeil).
This group is also divided by Giesbrecht into two tribes,
Ampharthrandria and Isokerandria. In 1892 he distinguished the former
as those in which the first antennae of the male have both members
modified for holding the female, and the genital openings of the
female have a ventral position, sometimes in close proximity,
sometimes strongly lateral; the latter as those in which the first
antennae of the male are similar to those of the female, the function
of holding her being transferred to the male maxillipeds, while the
genital openings of the female are dorsal, though at times strongly
lateral. In 1899, with a view to the many modifications exhibited by
parasitic and semi-parasitic species, the definitions, stripped of a
too hampering precision, took a different form: (a) Ampharthrandria.
"Swimming Podoplea with geniculating first antennae in the male sex,
and descendants of such; first antennae in female and male almost
always differently articulated." The families occupy fresh water as
well as the sea. Naturally "descendants" which have lost the
characteristic feature of the definition cannot be recognized without
some further assistance than the definition supplies. Of the families
comprised, the _Mormonillidae_ consist only of _Mormonilla_
(Giesbrecht), and are not mentioned by Giesbrecht in 1899 in the
grouping of this section. The _Thaumatoessidae_ include _Thaumatoessa_
(Kroyer), established earlier than its synonym _Thaumaleus_ (Kroyer),
or than _Monstrilla_ (Dana, 1849). The species are imperfectly known.
The defect of mouth-organs probably does not apply to the period of
youth, which some of them spend parasitically in the body-cavity of
worms (Giard, 1896). To the _Cyclopidae_ six genera are allotted by
Giesbrecht in 1900. _Cyclops_ (O.F. Muller, 1776), though greatly
restricted since Muller's time, still has several scores of species
abundantly peopling inland waters of every kind and situation, without
one that can be relied on as exclusively marine like the species of
_Oithona_ (Baird). The _Misophriidae_ are now limited to _Misophria_
(Boeck). The presence of a heart in this genus helps to make it a link
between the Podoplea and Gymnoplea, though in various other respects
it approaches the next family. The _Harpacticidae_ owe their name to
the genus _Arpacticus_ (Milne-Edwards, 1840). Brady in 1880 assigns to
this family 33 genera and 81 species. Canu (1892) distinguishes eight
sub-families, _Longipediinae_, _Peltidiinae_, _Tachidiinae_,
_Amymoninae_, _Harpacticinae_, _Idyinae_, _Canthocamptinae_ (for which
_Canthocampinae_ should be read), and _Nannopinae_, adding
_Stenheliinae_ (Brady) without distinctive characters for it. The
_Ascidicolidae_ have variable characters, showing a gradual adaptation
to parasitic life in Tunicates. Giesbrecht (1900) considers Canu quite
right in grouping together in this single family those parasites of
ascidians, simple and compound, which had been previously distributed
among families with the more or less significant names
_Notodelphyidae_, _Doropygidae_, _Buproridae_, _Schizoproctidae_,
_Kossmechtridae_, _Enterocolidae_, _Enteropsidae_. Further, he
includes in it his own _Enterognathus comatulae_, not from an
ascidian, but from the intestine of the beautiful starfish _Antedon
rosaceus_. The _Asterocheridae_, which have a good swimming capacity,
except in the case of _Cancerilla tubulata_ (Dalyell), lead a
semi-parasitic life on echinoderms, sponges, &c., imbibing their food.
Giesbrecht, displacing the older name _Ascomyzontidae_, assigns to
this family 21 genera in five subfamilies, and suggests that the
long-known but still puzzling _Nicothoe_ from the gills of the lobster
might be placed in an additional subfamily, or be made the
representative of a closely related family. The _Dichelestiidae_, on
account of their sometimes many-jointed first antennae, are referred
also to this tribe by Giesbrecht. (b) Isokerandria. "Swimming Podoplea
without genicullating first antennae in the male sex, and descendants
of such. First antennae of male and female almost always articulated
alike." To this tribe Giesbrecht assigns the families _Clausidiidae_,
_Corycaeidae_, _Oncaeidae_, _Lichomolgidae_, _Ergasilidae_,
_Bomolochidae_, _Clausiidae_, _Nereicolidae_. Here also must for the
time be placed the _Caligidae_, _Philichthyidae_ (_Philichthydae_ of
Vogt, Carus, Claus), _Lernaeidae_, _Chondracanthidae_,
_Sphaeronellidae_ (better known as _Choniostomatidae_, from H.J.
Hansen's remarkable study of the group), _Lernaeopodidae_,
_Herpyllobiidae_, _Entomolepidae_. For the distinguishing marks of all
these, the number of their genera and species, their habits and
transformations and dwellings, the reader must be referred to the
writings of specialists. Sars (1901) proposed seven
suborders--Calanoida, Harpacticoida, Cyclopoida, Notodelphoida,
Monstrilloida, Caligoida, Lernaeoida.
AUTHORITIES.--(The earlier memoirs of importance are cited in
Giesbrecht's _Monograph of Naples_, 1892); Canu, "Hersiliidae," _Bull.
Sci. France belgique_, ser. 3, vol. i. p. 402 (1888); and _Les
Copepodes du Boulonnais_ (1892); Cuenot, _Rev. biol. Nord France_,
vol. v. (1892); Giesbrecht, "Pelag. Copepoden." _F. u. fl. des Golfes
von Neapel_ (Mon. 19, 1892); Hansen, _Entomol. Med._ vol. iii. pt. 5
(1892); I.C. Thompson, "Copepoda of Liverpool Bay," _Trans. Liv. Biol.
Soc._ vol. vii. (1893); Schmeil, "Deutschlands Copepoden,"
_Bibliotheca zoologica_ (1892-1897); Brady, _Journ. R. Micr. Soc._ p.
168 (1894); T. Scott, "Entomostraca from the Gulf of Guinea," _Trans.
Linn. Soc. London_, vol. vi. pt. 1 (1894); Giesbrecht, _Mitteil. Zool.
Stat. Neapel_, vol. xi. p. 631; vol. xii. p. 217 (1895); T. and A.
Scott, _Trans. Linn. Soc. London_, ser. 2, vol. vi. p. 419 (1896);
Hansen "Choniostomatidae" (1897); Sars, _Proc. Mus. Zool. St
Petersburg_, "Caspian Entomostraca" (1897); Giesbrecht and Schmeil,
"Copepoda gymnoplea," _Das Tierreich_ (1898); Giesbrecht,
"Asterocheriden," _F. u. fl. Neapel_ (Mon. 25, 1899); Bassett-Smith,
"Copepoda on Fishes," _Proc. Zool. Soc. London_, p. 438 (1899); Brady,
_Trans. Zool. Soc. London_, vol. xv. pt. 2, p. 31 (1899); Sars, _Arch.
Naturv._ vol. xxi. No. 2 (1899); Giesbrecht, _Mitteil. Zool. Stat.
Neapel_, vol. xiv. p. 39 (1900); Scott, "Fish Parasites," _Scottish
Fishery Board_, 18th Ann. Rep. p. 144 (1900); Stebbing, _Willey's
Zool. Results_, pt. 5, p. 664 (1900); Embleton, _Journ. Linn. Soc.
London_, vol. xxviii. p. 211 (1901); Sars, _Crustacea of Norway_, vol.
iv. (1901). (T. R. R. S.)
ENTRAGUES, CATHERINE HENRIETTE DE BALZAC D' (1579-1633), marquise de
Verneuil, mistress of Henry IV., king of France, was the daughter of
Charles Balzac d'Entragues and of Marie Touchet, mistress of Charles IX.
Ambitious and intriguing, she succeeded in inducing Henry IV. to promise
to marry her after the death of Gabrielle d'Estrees, a promise which led
to bitter scenes at court when shortly afterwards Henry married Marie
de' Medici. She carried her spite so far as to be deeply compromised in
the conspiracy of Marshal Biron against the king in 1606, but escaped
with a slight punishment, and in 1608 Henry actually took her back into
favour again. She seems then to have been involved in the Spanish
intrigues which preceded the death of the king in 1610.
See H. de la Ferriere, _Henri IV. le roi, l'amoureux_ (Paris, 1890).
ENTRECASTEAUX, JOSEPH-ANTOINE BRUNI D' (1739-1793), French navigator,
was born at Aix in 1739. At the age of fifteen he entered the navy. In
the war of 1778 he commanded a frigate of thirty-two guns, and by his
clever seamanship was successful in convoying a fleet of merchant
vessels from Marseilles to the Levant, although they were attacked by
two pirate vessels, each of which was larger than his own ship. In 1785
he was appointed to the command of the French fleet in the East Indies,
and two years later he was named governor of the Mauritius and the Isle
of Bourbon. While in command of the East India fleet he made a voyage to
China, an achievement which, in 1791, led the French government to
select him to command an expedition which it was sending out to seek
some tidings of the unfortunate La Perouse, of whom nothing had been
heard since February 1788. Rear-admiral d'Entrecasteaux's expedition
comprised the "Recherche" and "L'Esperance," with Captain Huon de
Kermadec as second in command. No tidings were obtained of the missing
navigator, but in the course of his search Entrecasteaux made important
geographical discoveries. He traced the outlines of the eastern coast of
New Caledonia, made extensive surveys round the Tasmanian coast, and
touched at several places on the south coast of New Holland. The two
ships entered Storm Bay, Tasmania, on the 21st of April 1792, and
remained there until the 16th of May, surveying and naming the
d'Entrecasteaux Channel, the entrances to the Huon and Derwent rivers,
Bruni Island, Recherche Bay, Port Esperance and various other
localities. Excepting the name of the river Derwent (originally called
Riviere du Nord by its French discoverers), these foregoing appellations
have been retained. Leaving Tasmania the expedition sailed northward for
the East Indies, and while coasting near the island of Java,
Entrecasteaux was attacked by scurvy and died on the 20th of July 1793.
ENTRE MINHO E DOURO (popularly called _Minho_), a former province of
Northern Portugal; bounded on the N. by Galicia in Spain, E. by
Traz-os-Montes, S. by Beira and W. by the Atlantic Ocean. Pop. (1900)
1,170,361; area 2790 sq. m. Though no longer officially recognized, the
old provincial name remains in common use. The coast-line of Entre Minho
e Douro is level and unbroken except by the estuaries of the main
rivers; inland, the elevation gradually increases towards the north and
east, where several mountain ranges mark the frontier. Of these, the
most important are the Serra da Peneda (4728 ft.), between the rivers
Minho and Limia; the Serra do Gerez (4357 ft.), on the Galician border;
the Serra da Cabreira (4021 ft.), immediately to the south; and the
Serra de Marao (4642 ft.), in the extreme south-east. As its name
implies, the province is bounded by two great rivers, the Douro (q.v.)
on the south, and the Minho (Spanish _Mino_) on the north; but a small
tract of land south of the Douro estuary is included also within the
provincial boundary. There are three other large rivers which, like the
Minho, flow west-south-west into the Atlantic. The Limia or Antela
(Spanish _Linia_) rises in Galicia, and reaches the sea at Vianna do
Castello; the Cavado springs from the southern foot hills of La Raya
Seca, on the northern frontier of Traz-os-Montes, and forms, at its
mouth, the small harbour of Espozende; and the Ave descends from its
sources in the Serra da Cabreira to Villa do Conde, where it enters the
Atlantic. A large right-hand tributary of the Douro, the Tamega, rises
in Galicia, and skirts the western slopes of the Serra de Marao.
The climate is mild, except among the mountains, and such plants as
heliotrope, fuchsias, palms, and aloes thrive in the open throughout the
year. Wheat and maize are grown on the plains, and other important
products are wine, fruit, olives and chestnuts. Fish abound along the
coast and in the main rivers; timber is obtained from the mountain
forests, and dairy-farming and the breeding of pigs and cattle are
carried on in all parts. As the province is occupied by a hardy and
industrious peasantry, and the density of population (419.5 per sq. m.)
is more than twice that of any other province on the Portuguese
mainland, the soil is very closely cultivated. The methods and
implements of the farmers are, however, most primitive, and at the
beginning of the 20th century it was not unusual to see a mule, or even
a woman, harnessed with the team of oxen to an old-fashioned wooden
plough. Small quantities of coal, iron, antimony, lead and gold are
mined; granite and slate are quarried; and there are mineral springs at
Moncao (pop. 2283) on the Minho. The Oporto-Corunna railway traverses
the western districts and crosses the Spanish frontier at Tuy; its
branch lines give access to Braga, Guimaraes and Povoa de Varzim; and
the Oporto-Salamanca railway passes up the Douro valley. The greater
part of the north and west can only be reached by road, and even the
chief highways are ill-kept. In these regions the principal means of
transport is the springless wooden cart, drawn by one or more of the
tawny and under-sized but powerful oxen, with immense horns and
elaborately carved yoke, which are characteristic of northern Portugal.
For administrative purposes the province is divided into three
districts: Vianna do Castello in the north, Braga in the centre, Oporto
in the south. The chief towns are separately described; they include
Oporto (167,955), one of the greatest wine-producing cities in the
world; Braga (24,202), the seat of an archbishop who is primate of
Portugal; the seaports of Povoa de Varzim (12,623) and Vianna do
Castello (9990); and Guimaraes (9104), a place of considerable
historical interest.
ENTREPOT (a French word, from the Lat. _interpositum_, that which is
placed between), a storehouse or magazine for the temporary storage of
goods, provisions, &c.; also a place where goods, which are not allowed
to pass into a country duty free, are stored under the superintendence
of the custom house authorities till they are re-exported. In a looser
sense, any town which has a considerable distributive trade is called an
_entrepot_. The word is also used attributively to indicate the kind of
trade carried on in such towns.
ENTRE RIOS (Span. "between rivers"), a province of the eastern Argentine
Republic, forming the southern part of a region sometimes described as
the Argentine Mesopotamia, bounded N. by Corrientes, E. by Uruguay with
the Uruguay river as the boundary line, S. by Buenos Aires and W. by
Santa Fe, the Parana river forming the boundary line with these two
provinces. Pop. (1895) 292,019; (1905, est.) 376,600. The province has
an area of 28,784 sq. m., consisting for the most part of an undulating,
well-watered and partly-wooded plain, terminating in a low, swampy
district of limited extent in the angle between the two great rivers.
The great forest of Monteil occupies an extensive region in the N.,
estimated at nearly one-fifth the area of the province. Its soil is
exceptionally fertile and its climate is mild and healthy. The province
is sometimes called the "garden of Argentina," which would probably be
sufficiently correct had its population devoted as much energy to
agriculture as they have to political conflict and civil war. Its
principal industry is that of stock-raising, exporting live cattle,
horses, hides, jerked beef, tinned and salted meats, beef extract,
mutton and wool. Its agricultural products are also important, including
wheat, Indian corn, barley and fruits. Lime, gypsum and firewood are
also profitable items in its export trade. The Parana and Uruguay rivers
provide exceptional facilities for the shipment of produce and the Entre
Rios railways, consisting of a trunk line running E. and W. across the
province from Parana to Concepcion del Uruguay and several tributary
branches, afford ample transportation facilities to the ports. Another
railway line follows the Uruguay from Concordia northward into
Corrientes. Entre Rios has been one of the most turbulent of the
Argentine provinces, and has suffered severely from political disorder
and civil war. Comparative quiet reigned from 1842 to 1870 under the
autocratic rule of Gen. J.J. Urquiza. After his assassination in 1870
these partizan conflicts were renewed for two or three years, and then
the province settled down to a life of comparative peace, followed by an
extraordinary development in her pastoral and agricultural industries.
Among these is the slaughtering and packing of beef, the exportation of
which has reached large proportions. The capital is Parana, though the
seat of government was originally located at Concepcion del Uruguay, and
was again transferred to that town during Urquiza's domination.
Concepcion del Uruguay, or Concepcion (founded 1778), is a flourishing
town and port on the Uruguay, connected by railway with an extensive
producing region which gives it an important export trade, and is the
seat of a national college and normal school. Its population was
estimated at 9000 in 1905. Other large towns are Gualeguay and
Gualeguaychu.
ENVOY (Fr. _envoye_, "sent"), a diplomatic agent of the second rank. The
word _envoye_ comes first into general use in this connexion in the 17th
century, as a translation of the Lat. _ablegatus_ or _missus_ (see
DIPLOMACY). Hence the word envoy is commonly used of any one sent on a
mission of any sort.
ENZIO (c. 1220-1272), king of Sardinia, was a natural son of the
emperor Frederick II. His mother was probably a German, and his name,
Enzio, is a diminutive form of the German _Heinrich_. His father had a
great affection for him, and he was probably present at the battle of
Cortenuova in 1237. In 1238 he was married, in defiance of the wishes of
Pope Gregory IX., to Adelasia, widow of Ubaldo Visconti and heiress of
Torres and Gallura in Sardinia. Enzio took at once the title of king of
Torres and Gallura, and in 1243 that of king of Sardinia, but he only
spent a few months in the island, and his sovereignty existed in name
alone. In July 1239 he was appointed imperial vicegerent in Italy, and
sharing in his father's excommunication in the same year, took a
prominent part in the war which broke out between the emperor and the
pope. He commenced his campaign by subduing the march of Ancona, and in
May 1241 was in command of the forces which defeated the Genoese fleet
at Meloria, where he seized a large amount of booty and captured a
number of ecclesiastics who were proceeding to a council summoned by
Gregory to Rome. Later he fought in Lombardy. In 1248 he assisted
Frederick in his vain attempt to take Parma, but was wounded and taken
prisoner by the Bolognese at Fossalta on the 26th of May 1249. His
captivity was a severe blow to the Hohenstaufen cause in Italy, and was
soon followed by the death of the emperor. He seems to have been well
treated by the people of Bologna, where he remained a captive until his
death on the 14th of March 1272. He was apparently granted a magnificent
funeral, and was buried in the church of St Dominic at Bologna. During
his imprisonment Enzio is said to have been loved by Lucia da Viadagola,
a well-born lady of Bologna, who shared his captivity and attempted to
procure his release. Some doubt has, however, been cast upon this story,
and the same remark applies to another which tells how two friends had
almost succeeded in freeing him from prison concealed in a wine-cask,
when he was recognized by a lock of his golden hair. His marriage with
Adelasia had been declared void by the pope in 1243, and he left one
legitimate, and probably two illegitimate daughters. Enzio forms the
subject of a drama by E.B.S. Raupach and of an opera by A.F.B. Dulk.
See F.W. Grossman, _Konig Enzio_ (Gottingen, 1883); and H. Blasius,
_Konig Enzio_ (Breslau, 1884).
ENZYME (Gr. [Greek: enzymos], leavened, from [Greek: en], in, and
[Greek: zyme], leaven), a term, first suggested by Kuhne, for an
unorganized ferment (see FERMENTATION), a group of substances, in the
constitution of plants and animals, which decompose certain carbon
compounds occurring in association with them. See also PLANTS:
_Physiology_; NUTRITION, &c.
EOCENE (Gr. [Greek: eos], dawn, [Greek: kainos], recent), in geology,
the name suggested by Sir C. Lyell in 1833 for the lower subdivision of
the rocks of the Tertiary Era. The term was intended to convey the idea
that this was the period which saw the dawn of the recent or existing
forms of life, because it was estimated that among the fossils of this
period only 3-1/2% of the species are still living. Since Lyell's time
much has been learned about the fauna and flora of the period, and many
palaeontologists doubt if any of the Eocene _species_ are still extant,
unless it be some of the lowest forms of life. Nevertheless the name is
a convenient one and is in general use. The Eocene as originally defined
was not long left intact, for E. Beyrich in 1854 proposed the term
"Oligocene" for the upper portion, and later, in 1874, K. Schimper
suggested "Paleocene" as a separate appellation for the lower portion.
The Oligocene division has been generally accepted as a distinct period,
but "Paleocene" is not so widely used.
In north-western Europe the close of the Cretaceous period was marked
by an extensive emergence of the land, accompanied, in many places, by
considerable erosion of the Mesozoic rocks; a prolonged interval elapsed
before a relative depression of the land set in and the first Eocene
deposits were formed. The early Eocene formations of the
London-Paris-Belgian basin were of fresh-water and brackish origin;
towards the middle of the period they had become marine, while later
they reverted to the original type. In southern and eastern Europe
changes of sea-level were less pronounced in character; here the late
Cretaceous seas were followed without much modification by those of the
Eocene period, so rich in foraminiferal life. In many other regions, the
great gap which separates the Tertiary from the Mesozoic rocks in the
neighbourhood of London and Paris does not exist, and the boundary line
is difficult to draw. Eocene strata succeed Cretaceous rocks without
serious unconformity in the Libyan area, parts of Denmark, S.E. Alps,
India, New Zealand and central N. America. The unconformity is marked in
England, parts of Egypt, on the Atlantic coastal plain and in the
eastern gulf region of N. America, as well as in the marine Eocene of
western Oregon. The clastic Flysch formation of the Carpathians and
northern Alps appears to be of Eocene age in the upper and Cretaceous in
the lower part. The Eocene sea covered at various times a strip of the
Atlantic coast from New Jersey southward and sent a great tongue or bay
up the Mississippi valley; similar epicontinental seas spread over parts
of the Pacific border, but the plains of the interior with the mountains
on the west were meanwhile being filled with terrestrial and lacustrine
deposits which attained an enormous development. This great extension of
non-marine formations in the Eocene of different countries has
introduced difficulties in the way of exact correlation; it is safer,
therefore, in the present state of knowledge, to make no attempt to find
in the Eocene strata of America and India, &c., the precise equivalent
of subdivisions that have been determined with more or less exactitude
in the London-Paris-Belgian area.
[Illustration: Distribution of Eocene Rocks.]
It is possible that in Eocene times there existed a greater continuity
of the northern land masses than obtains to-day. Europe at that time was
probably united with N. America through Iceland and Greenland; while on
the other side, America may have joined Asia by the way of Alaska. On
the other hand, the great central, mediterranean sea which stretched
across the Eurasian continents sent an arm northward somewhere just east
of the Ural mountains, and thus divided the northern land mass in that
region. S. America, Australia and perhaps Africa _may_ have been
connected more or less directly with the Antarctic continent.
Associated, no doubt, with the crustal movements which closed the
Cretaceous and inaugurated the Eocene period, there were local and
intermittent manifestations of volcanic activity throughout the period.
Diabases, gabbros, serpentines, soda-potash granites, &c., are found in
the Eocene of the central and northern Apennines. Tuffs occur in the
Veronese and Vicentin Alps--Ronca and Spelecco schists. Tuffs, basalts
and other igneous rocks appear also in Montana, Wyoming, California,
Oregon, Washington, Idaho, Colorado; also in Central America, the
Antillean region and S. America.
It has been very generally assumed by geologists, mainly upon the
evidence of plant remains, that the Eocene period opened with a
temperate climate in northern latitudes; later, as indicated by the
London Clay, Alum Bay and Bournemouth beds, &c., the temperature appears
to have been at least subtropical. But it should be observed that the
frequent admixture of temperate forms with what are now tropical species
makes it difficult to speak with certainty as to the degree of warmth
experienced. The occurrence of lignites in the Eocene of the Paris
basin, Tirol and N. America is worthy of consideration in this
connexion. On the other hand, the coarse boulder beds in the lower
Flysch have been regarded as evidence of local glaciation; this would
not be inconsistent with a period of widespread geniality of climate, as
is indicated by the large size of the nummulites and the dispersion of
the marine Mollusca, but the evidence for glaciation is not yet
conclusive.
_Eocene Stratigraphy._--In Britain, with the exception of the Bovey
beds (q.v.) and the leaf-bearing beds of Antrim and Mull, Eocene rocks
are confined to the south-eastern portion of England. They lie in the
two well-marked synclinal basins of London and Hampshire which are
conterminous in the western area (Hampshire, Berkshire), but are
separated towards the east by the denuded anticline of the Weald. The
strata in these two basins have been grouped in the following manner:--
_London Basin._ _Hampshire Basin._
Upper Upper Bagshot Sands. Headon Hill and Barton Sands.
/ Middle Bagshot Beds and Bracklesham Beds and leaf
Middle < part of Lower Bagshot beds of Bournemouth and
\ Beds. Alum Bay.
/ Part of Lower Bagshot
| Beds, London Clay,
| Blackheath and Oldhaven London Clay and the equivalent
Lower < Beds, Woolwich and Bognor Beds, Woolwich
| Reading Beds, Thanet and Reading Beds.
\ Sands.
The Thanet sands have not been recognized in the Hampshire basin; they
are usually pale yellow and greenish sands with streaks of clay and at
the base; resting on an evenly denuded surface of chalk is a very
constant layer of green-coated, well-rounded chalk flint pebbles. It
is a marine formation, but fossils are scarce except in E. Kent, where
it attains its most complete development. The Woolwich and Reading
beds (see READING BEDS) contain both marine and estuarine fossils. In
western Kent, between the Woolwich beds and the London Clay are the
Oldhaven beds or Blackheath pebbles, 20 to 40 ft., made up almost
entirely of well-rounded flint pebbles set in sand; the fossils are
marine and estuarine. The London Clay, 500 ft. thick, is a marine
deposit consisting of blue or brown clay with sandy layers and
septarian nodules; its equivalent in the Hampshire area is sometimes
called the Bognor Clay, well exposed on the coast of Sussex. The
Bagshot, Bracklesham and Barton beds will be found briefly described
under those heads.
Crossing the English Channel, we find in northern France and Belgium a
series of deposits identified in their general characters with those
of England. The anticlinal ridge of the English Weald is prolonged
south-eastwards on to the continent, and separates the Belgian from
the French Eocene areas much as it separates the areas of London and
Hampshire; and it is clear that at the time of deposition all four
regions were intimately related and subject to similar variations of
marine and estuarine conditions. With a series of strata so variable
from point to point it is natural that many purely local phases should
have received distinctive names; in the Upper Eocene of the Paris
basin the more important formations are the highly fossiliferous
marine sands known as the "Sands of Beauchamp" and the local
fresh-water limestone, the "Calcaire de St Ouen." The Middle Eocene is
represented by the well-known "Calcaire grossier," about 90 ft. thick.
The beds in this series vary a good deal lithologically, some being
sandy, others marly or glauconitic; fossils are abundant. The Upper
Calcaire grossier or "Caillasses" is a fresh-water formation; the
middle division is marine; while the lower one is partly marine,
partly of fresh-water origin. The numerous quarries and mines for
building stone in the neighbourhood of Paris have made it possible to
acquire a very precise knowledge of this division, and many of the
beds have received trade names, such as "Rochette," "Roche," "Banc
franc," "Banc vert," "Cliquart," "Saint Nom;" the two last named are
dolomitic. Below these limestones are the nummulitic sands of Cuise
and Soissons. The Lower Eocene contains the lignitic plastic clay
(_argile plastique_) of Soissons and elsewhere; the limestones of
Rilly and Sezanne and the greenish glauconitic sands of Bracheux. The
relative position of the above formations with respect to those of
Belgium and England will be seen from the table of Eocene strata. The
Eocene deposits of southern Europe differ in a marked manner from
those of the Anglo-Parisian basin. The most important feature is the
great development of nummulitic limestone with thin marls and
nummulitic sandstones. The sea in which the nummulitic limestones were
formed occupied the site of an enlarged Mediterranean communicating
with similar waters right round the world, for these rocks are found
not only in southern Europe, including all the Alpine tracts, Greece
and Turkey and southern Russia, but they are well developed in
northern Africa, Asia Minor, Palestine, and they may be followed
through Persia, Baluchistan, India, into China, Tibet, Japan, Sumatra,
Borneo and the Philippines. The nummulitic limestones are frequently
hard and crystalline, especially where they have been subjected to
elevation and compression as in the Alpine region, 10,000 ft. above
the sea, or from 16,000, to 20,000 ft., in the central Asian plateau.
Besides being a widespread formation the nummulitic limestone is
locally several thousand feet thick.
While the foraminiferal limestones were being formed over most of
southern Europe, a series of clastic beds were in course of formation
in the Carpathians and the northern Alpine region, viz. the Flysch and
the Vienna sandstone. Some portions of this Alpine Eocene are coarsely
conglomeratic, and in places there are boulders of non-local rocks of
enormous dimensions included in the argillaceous or sandy matrix. The
occurrence of these large boulders together with the scarceness of
fossils has suggested a glacial origin for the formation; but the
evidence hitherto collected is not conclusive. C.W. von Gumbel has
classified the Eocene of the northern Alps (Bavaria, &c.) as follows:--
Upper Eocene, Flysch and Vienna sandstone, with younger nummulitic
beds and Haring group.
Middle " Kressenberg Beds, with older nummulitic beds.
Lower " Burberg Beds, Greensands with small nummulites.
The Haring group of northern Tirol contains lignite beds of some
importance. In the southern and S.E. Alps the following divisions are
recognized.
Upper Eocene, Macigno or Tassello--Vienna Sandstone, conglomerates,
marls and shales.
Middle " Nummulitic limestones, three subdivisions.
Lower " Liburnian stage (or Proteocene), foraminiferal
limestones with fresh-water intercalations at the top
and bottom, the _Cosina_ beds, fresh-water in the
middle of the series.
In the central and northern Apennines the Eocene strata have been
subdivided by Prof. F. Sacco into an upper Bartonian, a middle
Parisian and a lower Suessonian series. In the middle member are the
representatives of the Flysch and the Macigno. These Eocene strata are
upwards of 5500 ft. thick. In northern Africa the nummulitic
limestones and sandstones are widely spread; the lower portions
comprise the Libyan group and the shales of Esneh on the Nile
(Flandrien), the _Alveolina_ beds of Sokotra and others; the Mokattam
stage of Egypt is a representative of the later Eocene. Much of the N.
African Eocene contains phosphatic beds. In India strata of Eocene age
are extensively developed; in Sind the marine Ranikot beds, 1500 to
2000 ft., consisting of clays with gypsum and lignite, shales and
sandstones; these beds have, side by side with Eocene nummulites, a
few fossils of Cretaceous affinities. Above the Ranikot beds are the
massive nummulitic limestones and sandstones of the Kirthar group;
these are succeeded by the nummulitic limestones and shales at the
base of the Nari group. In the southern Himalayan region the
nummulitic phase of Eocene deposit is well developed, but there are
difficulties in fixing the line of demarcation between this and the
younger formations. The lower part of the Sirmur series of the Simla
district may belong to this period; it is subdivided into the Kasauli
group and the Dagshai group with the Subathu group at the base.
Beneath the thick nummulitic Eocene limestone of the Salt Range are
shales and marls with a few coal seams. The marine Eocene rocks of N.
America are most extensively developed round the coast of the Gulf of
Mexico, whence they spread into the valley of the Mississippi and, as
a comparatively narrow strip, along the Atlantic coastal plain to New
Jersey.
The series in Alabama, which may be taken as typical of the Gulf coast
Eocene, is as follows:--
Upper Jacksonian, White limestone of Alabama (and Vicksburg?).
Middle Claibornian, Claiborne series.
Buhrstone series.
Lower, Chickasawan Sands and lignites.
Midwayan or Clayton formation, limestones.
The above succession is not fully represented in the Atlantic coast
states.
On the Pacific coast marine formations are found in California and
Oregon; such are the Tejon series with lignite and oil; the Escondido
series of S. California (7000 ft.), part of the Pascadero series of
the Santa Cruz Mountains; the Pulaski, Tyee, Arago and Coaledo
beds--with coals--in Oregon. In the Puget formation of Washington we
have a great series of sediments, largely of brackish water origin,
and in parts coal-bearing. The total thickness of this formation has
been estimated at 20,000 ft. (it may prove to be less than this), but
it is probable that only the lower portion is of Eocene age. The most
interesting of the N. American Eocene deposits are those of the Rocky
Mountains and the adjacent western plains, in Wyoming, Nevada,
Nebraska, Colorado, &c.; they are of terrestrial, lacustrine or
aeolian origin, and on this account and because they were not strictly
synchronous, there is considerable difficulty in placing them in their
true position in the time-scale. The main divisions or groups are
generally recognized as follows:--
Mammalian
Zonal Forms.
Upper [1] Uinta Group, 800 ft. (? = Jacksonian) _Diplacodon._
_Telmatotherium._