Lower [3] Wind River Group, 800 ft. _Bathyopsis._
[4] Wasatch Group, 2000 ft. (? = Chickasawan) _Coryphodon._
Basal [5] Torrejon Group, 300 ft. _Pantolambda._
[6] Puerco Group, 500 to 1000 ft. _Polymastodon._
[1] South of the Uinta Mts. in Utah.
[2] Fort Bridger Basin.
[3] Wind river in Wyoming.
[4] Wasatch Mts. in Utah.
[5] Torrejon in New Mexico.
[6] Puerco river, New Mexico.
The Fort Union beds of Canada and parts of Montana and N. Dakota are
probably the oldest Eocene strata of the Western Interior; they are
some 2000 ft. thick and possibly are equivalent to the Midwayan group.
But in these beds, as in those known as Arapahoe, Livingston, Denver,
Ohio and Ruby, which are now often classed as belonging to the upper
Laramie formation, it is safer to regard them as a transitional series
between the Mesozoic and Tertiary systems. There is, however, a marked
unconformity between the Eocene Telluride or San Miguel and Poison
Canyon formations of Colorado and the underlying Laramie rocks.
Many local aspects of Eocene rocks have received special names, but
too little is known about them to enable them to be correctly placed
in the Eocene series. Such are the Clarno formation (late Eocene) of
the John Day basin, Oregon, the Pinyon conglomerate of Yellowstone
Park, the Sphinx conglomerate of Montana, the Whitetail conglomerate
of Arizona, the Manti shales of Utah, the Mojave formation of S.
California and the Amyzon formation of Nevada.
Of the Eocene of other countries little is known in detail. Strata of
this age occur in Central and S. America (Patagonia-Megellanian
series--Brazil, Chile, Argentina), in S. Australia (and in the Great
Australian Bight), New Zealand, in Seymour Island near Graham Land in
the Antarctic Regions, Japan, Java, Borneo, New Guinea, Moluccas,
Philippines, New Caledonia, also in Greenland, Bear Island,
Spitzbergen and Siberia.
_Organic Life of the Eocene Period._--As it has been observed above, the
name Eocene was given to this period on the ground that in its fauna
only a small percentage of _living_ species were present; this estimation
was founded upon the assemblage of invertebrate remains in which, from
the commencement of this period until the present day, there has been
comparatively little change. The real biological interest of the period
centres around the higher vertebrate types. In the marine mollusca the
most noteworthy change is the entire absence of ammonoids, the group
which throughout the Mesozoic era had taken so prominent a place, but
disappeared completely with the close of the Cretaceous. Nautiloids were
more abundant than they are at present, but as a whole the Cephalopods
took a more subordinate part than they had done in previous periods. On
the other hand, Gasteropods and Pelecypods found in the numerous shallow
seas a very suitable environment and flourished exceedingly, and their
shells are often preserved in a state of great perfection and in
enormous numbers. Of the Gasteropod genera _Cerithium_ with its
estuarine and lagoonal forms _Potamides_, _Potamidopsis_, &c., is very
characteristic; _Rostellaria_, _Voluta_, _Fusus_, _Pleurotoma_, _Conus_,
_Typhis_, may also be cited. _Cardium_, _Venericardia_, _Crassatella_,
_Corbulomya_, _Cytherea_, _Lucina_, _Anomia_, _Ostrea_ are a few of the
many Pelecypod genera. Echinoderms were represented by abundant
sea-urchins, _Echinolampas_, _Linthia_, _Conoclypeus_, &c. Corals
flourished on the numerous reefs and approximated to modern forms
(_Trochosmilia_, _Dendrophyllia_). But by far the most abundant marine
organisms were the foraminifera which flourished in the warm seas in
countless myriads. Foremost among these are the _Nummulites_, which by
their extraordinary numerical development and great size, as well as by
their wide distribution, demand special recognition. Many other genera
of almost equal importance as rock builders, lived at the same time:
_Orthophragma_, _Operculina_, _Assilina_, _Orbitolites_, _Miliola_,
_Alveolina_. Crustacea were fairly abundant (_Xanthopsis_, _Portunus_),
and most of the orders and many families of modern insects were
represented.
When we turn to the higher forms of life, the reptiles and mammals,
we find a remarkable contrast between the fauna of the Eocene and those
periods which preceded and succeeded it. The great group of Saurian
reptiles, whose members had held dominion on land and sea during most of
the Mesozoic time, had completely disappeared by the beginning of the
Eocene; in their place placental mammals made their appearance and
rapidly became the dominant group. Among the early Eocene mammals no
trace can be found of the numerous and clearly-marked orders with which
we are familiar to-day; instead we find obscurely differentiated forms,
which cannot be fitted without violence into any of the modern orders.
The early placental mammals were generalized types (with certain
non-placental characters) with potentialities for rapid divergence and
development in the direction of the more specialized modern orders.
Thus, the Creodonta foreshadowed the Carnivora, the Condylarthra
presaged the herbivorous groups; but before the close of this period, so
favourable were the conditions of life to a rapid evolution of types,
that most of the great _orders_ had been clearly defined, though none of
the Eocene _genera_ are still extant. Among the early carnivores were
_Arctocyon_, _Palaeonictis_, _Amblyctonus_, _Hyaenodon_, _Cynodon_,
_Provivera_, _Patriofelis_. The primitive dog-like forms did not appear
until late in the period, in Europe; and true cats did not arrive until
later, though they were represented by _Eusmilus_ in the Upper Eocene of
France. The primitive ungulates (Condylarths) were generalized forms
with five effective toes, exemplified in _Phenacodus_. The gross
Amblypoda, with five-toed stumpy feet (_Coryphodon_), were prominent in
the early Eocene; particularly striking forms were the _Dinoceratidae_,
_Dinoceras_, with three pairs of horns or protuberances on its massive
skull and a pair of huge canine teeth projecting downwards; _Tinoceras_,
_Uintatherium_, _Loxophodon_, &c.; these elephantine creatures, whose
remains are so abundant in the Eocene deposits of western America, died
out before the close of the period. The divergence of the hoofed mammals
into the two prominent divisions, the odd-toed and even-toed, began in
this period, but the former did not get beyond the three-toed stage. The
least differentiated of the odd-toed group were the Lophiodonts: tapirs
were foreshadowed by _Systemodon_ and similar forms (_Palaeotherium_,
_Paloplotherium_); the peccary-like _Hyracotherium_ was a forerunner of
the horse, _Hyrochinus_ was a primitive rhinoceros. The evolution of the
horse through such forms as _Hyracotherium_, _Pachynolophus_,
_Eohippus_, &c., appears to have proceeded along parallel lines in
Eurasia and America, but the true horse did not arrive until later.
Ancestral deer were represented by _Dichobune_, _Amphitragulus_ and
others, while many small hog-like forms existed (_Diplopus_, _Eohyus_,
_Hyopotamus_, _Homacodon_). The primitive stock of the camel group
developed in N. America in late Eocene time and sent branches into S.
America and Eurasia. The edentates were very generalized forms at this
period (Ganodonta); the rodents (Tillodontia) attained a large size for
members of this group, e.g. _Tillotherium_. The Insectivores had Eocene
forerunners, and the Lemuroids--probable ancestors of the apes--were
forms of great interest, _Anaptomorphus_, _Microsyops_, _Heterohyus_,
_Microchaerus_, _Coenopithecus_; even the Cetaceans were well
represented by _Zeuglodon_ and others.
+--------------+-------------------------+----------------------+-------------------+---------------+------------------+------------------+
| | | | | Mediterranean | | |
| | | | | regions and | Flysch | |
| Stages. | Paris Basin. | England. | Belgian Basin. | Great Central | Phase. | North America. |
| | | | | sea. | | |
+--------------+-------------------------+----------------------+-------------------+---------------+------------------+------------------+
| Bartonien.[1]| Limestone of Saint-Ouen.| Barton beds. | | | | Unita Group and |
| | Sands of Mortefontaine. | | Sands of Lede. | | | Jacksonian. |
| | Sands of Beauchamp. | Upper Bagshot sands. | | | | |
| | Sands of Auvers. | | | | | |
+--------------+-------------------------+----------------------+-------------------+ | | |
| | | Bracklesham and | Laekenien. | | | Bridger Group |
| Lutetien. | Calcaire grossier. | Bournemouth beds. | Bruxellien. | | | and |
| | | Lower Bagshot sands. | Paniselien. | | Upper part of the| Claibornian. |
+--------------+-------------------------+----------------------+-------------------+ | Alpine Flysch | |
| Ypresien. | Nummulitic sands of | Alum Bay leaf beds. | Sands of Mons en | | and Vienna and | Wind River Group.|
| | Soissons and Sands of | | Pevele. | Nummulitic | Carpathian | Wasatch Group |
| | Cuise and Aizy. | | Flanders Clay. | limestones, | sandstones. | and |
| | | | | sandstones | | |
+---+----------+ | +-------------------+ and shales. | | |
| | | | London Clay. | | | Macigno of the | |
| L | | | Oldhaven beds. | Upper Landenien | | Apennines and | |
| a | Sparna- | | | sands. | | Maritime Alps. | Chickasawan. |
| n | cien. | Plastic Clay and lignite| Woolwich and Reading | | | | |
| d | | beds. | beds. | Sands of | | | |
| e |----------+-------------------------+----------------------+ Ostricourt. | | | Torrejon Group |
| n | | Limestones of Rilly and | | | | | and |
| i | | Sezanne. | Thanet sands. | Landenien tuffeau.| | | Midwayan. |
| e |Thanetien.| Sands of Rilly and | | | | | |
| n | | Bracheux. | | Marls of Gelinden.| | | Puerco Group. |
| | | | | | | | |
+---+----------+-------------------------+----------------------+-------------------+---------------+------------------+------------------+
The non-placental mammals although abundant were taking a secondary
place; _Didelphys_, the primitive opossum, is noteworthy on account of
its wide geographical range.
Among the birds, the large flightless forms, _Eupterornis_, _Gastornis_,
were prominent, and many others were present, such as the ancestral
forms of our modern gulls, albatrosses, herons, buzzards, eagles, owls,
quails, plovers. Reptiles were poorly represented, with the exception of
crocodilians, tortoises, turtles and some large snakes.
The flora of the Eocene period, although full of interest, does not
convey the impression of newness that is afforded by the fauna of the
period. The reason for this difference is this: the newer flora had been
introduced and had developed to a considerable extent in the Cretaceous
period, and there is no sharp break between the flora of the earlier and
that of the later period; in both we find a mixed assemblage--what we
should now regard as tropical palms, growing side by side with
mild-temperate trees. Early Eocene plants in N. Europe, oaks, willows,
chestnuts (Castanea), laurels, indicate a more temperate climate than
existed in Middle Eocene when in the Isle of Wight, Hampshire and the
adjacent portions of the continent, palms, figs, cinnamon flourished
along with the cactus, magnolia, sequoia, cypress and ferns. The late
Eocene flora of Europe was very similar to its descendant in modern
Australasia.
See A. de Lapparent, _Traite de geologie_, vol. iii. (5th ed., 1906),
which contains a good general account of the period, with numerous
references to original papers. Also R.B. Newton, _Systematic List of
the Frederick E. Edwards Collection of British Oligocene and Eocene
Mollusca in the British Museum_ (_Natural History_) (1891), pp.
299-325; G.D. Harris, "A Revision of our Lower Eocenes," _Proc.
Geologists' Assoc._ x., 1887-1888; W.B. Clark, "Correlation Papers:
Eocene" (1891), _U.S. Geol. Survey Bull. No. 83._ For more recent
literature consult _Geological Literature added to the Geological
Society's Library_, published annually by the society. (J. A. H.)