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THE NEW
TREE OF LIFE

The continuation of the dinosaur lineage over the last 65 million years has meant that these magnificent creatures have flourished, expanded and diversified with the same vigour as in the previous 150 million years. More so, in fact, since the last 65 million years have witnessed sweeping changes on the Earth’s surface.
Most of the dinosaur lineages had actually died out long before the end of the Cretaceous period, and the dinosaurs that are alive today are descended from the most vigorous of the late Cretaceous groups.
The lightly built meat-eating saurischians, or ‘coelurosaurs’, that evolved from the coelophysids have thrived, being very versatile and capable of a great deal of evolutionary change.
The heavy meat-eaters, or ‘carnosaurs’, evolved from the teratosaurs, have not fared so well. By the end of the Cretaceous period only the huge tyrannosaurs were expanding. The megalosaurs, are maintaining their numbers but the carnosaur line is not increasing significantly.
The prosauropods died out at the end of the Triassic, but their descendants – the heavy long-necked plant-eating saurischians, or ‘sauropods’, became abundant in the Jurassic period, but only existed in the late Cretaceous period in places where they were not ousted by the ornithopods. Those that survive today are mainly descendants of the titanosaurs and generally live on the southern continents.
The small bipedal ornithischians – the ‘ornithopods’ – that evolved from the heterodontosaurs (pages 14-15), like the small meat-eating saurischians, have adapted and flourished, adjusting to the great changes in environment with ease. Most of the plant-eaters today have evolved from this stock.
Ceratopsians – the horned ornithischians – were very successful at the end of the Cretaceous and are still found in one form or another today.
The stegosaurs – plated ornithischians – had almost all gone by Cretaceous times except for an isolated group in India. The group did not survive the Ice Age.
Ankylosaurs – heavily armoured ornithischians – were a successful Cretaceous group and have survived.
Then there are the flying pterosaurs. Despite competition from the birds, the pterosaurs have survived.
Of the spectacular swimming reptiles, the long and short-necked plesiosaurs, and the mosasaurs have survived, but the fish-like ichthyosaurs have become extinct.
And the mammals? They began in the Triassic period as small insectivorous creatures. By the end of the Cretaceous they were still small insectivorous creatures. They have had no opportunity to expand and diversify, and are small insectivorous creatures to this day.

Coelophysis skeleton
The coelophysids were the basic Triassic stock of lightly built meat-eating saurischian dinosaurs. From them evolved the very similar and successful coelurids and the birds, the bird-like omithomimids and egg-eating oviraptorids.

Deinonychus skeleton
The dromaeosaurs and saurornithoids were two more specialized offshoots from the coelophysids. Both fierce hunters, they each had a killing claw on the hind foot. The saurornithoids were particularly successful.

Megalosaur skeleton
The megalosaurs were among the earliest, but most successful, of the heavy meat-eaters. They were similar in build to the shorter-lived meat-eaters, like the huge allosaurs, the sail-backed spinosaurs and the horn-faced ceratosaurs.

Tyrannosaurus skeleton
The tyrannosaurs were among the last of the heavy meat-eaters to evolve, not appearing until Cretaceous times. They developed from the megalosaur line and became the biggest and heaviest meat-eating animals to have existed.

Apatosaurus skeleton
There were several families of long-necked plant-eating saurischian dinosaurs. The earliest were the cetiosaurs, brachiosaurs and diplodocids. The camarosaurs ranged for longer but it was the more lightly built titanosaurs that were ultimately the most successful.

 

Heterodontosaurus skeleton
The heterodontosaurs were the basic group of the two-footed plant-eating ornithischian dinosaurs, appearing in the Triassic. From them evolved several groups that were successful and long-lasting.

Hypsilophodon skeleton
The hypsilophodonts were perhaps the most successful of the smaller two-footed plant-eaters. They evolved in the Jurassic as lightly built running animals, fleet of foot and able to escape their enemies quickly.

Parasaurolophus skeleton
Appearing in late Cretaceous times, hadrosaurs became the most abundant heavy two-footed plant-eaters. They divided early into the crested lambeosaurines and the crestless hadrosaurines.

Stegoceras skeleton
Pachycephalosaurs evolved and expanded in the late Cretaceous period. They were the boneheads, and resembled the other two-footed plant-eaters but for the heavy bony structures on their heads.

Triceratops skeleton
Ceratopsians were horned dinosaurs – a successful group that evolved in the Cretaceous. They developed from the psittacosaurs – a family of bipedal herbivores like hypsilophodonts.

Stegosaurus skeleton
Armoured dinosaurs fell into two main groups – the plated stegosaurs that were most successful in the Jurassic period, and the spiked nodosaurs, and ankylosaurs that expanded in the Cretaceous period.

Pteranodon skeleton
Pterosaurs, like dinosaurs, evolved from the thecodonts. They started flying during the Triassic period. The early long-tailed rhamphorhynchids died out in the Jurassic and were replaced by the short-tailed pterodactyls.

Plesiosaurus skeleton
The paddle-limbed plesiosaurs were the most successful of the sea reptiles, longer-ranging than the fish-like ichthyosaurs. There were two main lines of plesiosaur evolution – the long-necked elasmosaurs, and the short-necked pliosaurs.

The KRAKEN (page 107) and the COCONUT GRAB (page 99) are invertebrates descended from the cephalopods, therefore do not appear on this chart.

PALAEOGEOGRAPHY

THE EVER-CHANCING LANDSCAPE

Throughout the main part of the Age of Reptiles, the continents had been moving apart. During the Triassic period all the continents of the Earth were fused together into one great supercontinent called Pangaea, consisting of a northern section, Laurasia, and a southern section, Gondwana. During the Jurassic period this supercontinent began to split up, and in the Cretaceous period the separating continents were well on their way to their present-day positions.
Over the last 65 million years, since the end of the Cretaceous period, the greatest movement of continents took place in the southern hemisphere. At the very end of the Cretaceous, the continent of Australia was still attached to that of Antarctica. It subsequently split away and moved northwards until the continent reached its present position, in the southern tropical climatic belt. The continental block that now comprises India travelled northwards across the Indian Ocean, and it finally collided with the huge northern continent. As it split away from the original position as part of the east African landmass, it sheared away other continental fragments as well, and these have been left as the islands, known as Madagascar and the Seychelles, and a number of scattered submerged fragments. A seaway, called the Tethys, still separated the continents we now call Europe and Asia from that of Africa, but this seaway slowly closed and narrowed. At the other side of the globe the two continents of the Americas were quite separate, only connected by a string of islands during the earliest Tertiary times and with a permanent land bridge developing quite recently. North America, however, was almost permanently united with Asia across the Bering land bridge – a land bridge that has only recently become submerged.
The continental movement had an effect on the climate. With a continuous seaway around the world, made up of the Tethys and the gap between the Americas, there was a constant westward flowing equatorial current driven by the prevailing winds. This brought warm, moist climates to the edges of most of the continents. The water warmed in this current was swirled about to reach up along the coastlines in the north of the northern hemisphere and far down towards Antarctica in the south. Climates were warm and equable and humid forests grew on most of the continents.
As the continents moved, the Tethys Sea closed up. At the same time Australasia drifted away from the Antarctica and a circumpolar seaway opened up, allowing a continuous eastward-flowing current to sweep around the cold Antarctic continent. The equatorial current was therefore lost, and consequently the warm climates. There was now less mixing of warm tropical water and cool polar water, and climates increasingly differed over wide areas. The drier, cooler conditions that resulted meant that the lush tropical forests began to give way to grasslands – a new habitat.

Pangaea
The Triassic period was the time when the supercontinent of Pangea was at its most complete. It was divided into two huge sections, each section far bigger than the greatest of today’s continents. The northernmost part, consisting of modern North America, Europe and Asia, has been given the name Laurasia. The southern section, consisting of South America, Africa, India, Antarctica and Australia, is called Gondwana. An arm of the sea, called the Tethys, reached in from the east and almost separated the two sections. The rest of the sea area was united into a world ocean called Panthalassa.

Early Tertiary
As the elements of Pangaea separated, there was a clear seaway around the world near the equator, with a westward flowing equatorial current that modified the world’s climate.

Late Tertiary
Continued movements closed the equatorial seaway and opened up a circumpolar seaway around the Antarctic continent. Now the ocean circulation had no unifying effect on the global climate.

The progressively cooler climates produced caps of ice at the poles of the globe. The Arctic ocean was nearly land-locked and the constant inflow from rivers diluted the salty water. As there was little mixing with warmer water from the south, this northern ocean froze over permanently. In the southern hemisphere the continent of Antarctica lay over the pole. This continent was far away from the warm ocean currents and effectively insulated from them by the circumpolar current. As a result Antarctica also froze over.
The climates continued to cool until the Ice Age, about 1.7 million years ago. Glaciers swept south from the polar ocean and down from the mountains, and the climatic zones were compressed upon one another towards the equator.
The topography of the world today is a direct consequence of this continental movement. When a continent moves, it tends to accrete mountain ranges along its leading edge. The greatest mountain chains of the Earth are the Himalayas along the join between India and Asia, where the two continents converged and collided 50 million years ago, and the Coast Mountains and the Andes along the west coasts of North and South America, where the westward movement is still taking place. The movement of the African continent against the European has created some contorted mountain chains in that area, producing the Atlas, the Appennines, the Alps and the other mountains that surround the Mediterranean. The string of East Indian islands between Asia and Australasia can be thought of as submarine mountain ranges, produced by the movement of submerged continental masses and ocean floors. Most of the other great mountain ranges of the world are old and worn away – relics of the continental movements of former times. The old mountains of the Appalachians along the east coast of North America were once continuous with the Scottish Highlands and the Norwegian Mountains along the edge of northern Europe, before these continents split apart. The Urals, the old mountain range between Europe and Asia, demonstrates where these two continents collided 300 million years ago. The movements that tore Pangaea apart are still at work. When a continent splits, it rises into a ridge, and cracks along the crest. The east African highlands represent such a rise, and the cracks are present as the Great Rift Valley that runs up the length of the continent to the opening fissure of the Red Sea.

Modern plate movements
The Earth’s crust is still in motion, and the plates are still continually shifting the continents. Along the active zones, where plates converge, mountains and volcanoes can be forced upwards.

Continental movements have a great effect on the wildlife. A continent may move from one climatic area to another, and consequently the animal and plant life has to evolve to adjust to the changing conditions. In another situation, the continent may move up against a neighbouring landmass and the two populations mix. All these effects are taken into account in the concept of zoogeography, that determines what assemblages of animals live in which areas of the world.

ZOOGEOGRAPHY

THE WORLD DISTRIBUTION OF ANIMALS

Animals are not the same the world over. There are a number of rules that define the kinds of animals that can live in one particular place and not in another.
The most obvious factor that determines the animal life of a particular area is the environment of that area – the climate, the terrain, the plants that grow there, other animals that exist there, in fact everything that contributes to the surroundings and habitat. We can see straight away that an animal that lives in a mountain environment, and is particularly well suited to live in a mountain environment, will not survive long if introduced into a swamp region – and vice versa. A mountain animal's tolerance of high altitudes would be useless in an area of low-lying wetland, and a swamp animal’s stream-lined shape would be quite out of place on craggy mountain peaks. Yet, despite this profound influence of environment, a mountain animal may be quite closely related to a swamp region animal that lives on the same continent. They may both have evolved from the same ancestor just a few million years ago. On another continent on the other side of the world there may be mountain animals and swamp region animals that are likewise closely related to each other, but these will be quite unrelated to those on the first continent. The two mountain animals may look quite like one another, and the two swamp animals will share the same adaptations, but they will all have evolved quite independently.
Grouping the animals of the world according to their evolutionary relationships, rather than according to the environments in which they live, can divide the world into convenient regions known as ZOOGEOGRAPHIC REALMS. Each zoogeographic realm will contain a collection of animals that is peculiar to itself and that has evolved relatively independently from the animal assemblage of another realm. The boundaries between the realms may be well marked, as by oceans, or may be quite hazy, with several types of animals able to cross over from one to another. The existence of the realms is effected by the natural barriers to migration that arise because of the physical geography. A mountain range or a desert may divide one assemblage of animals from the next.
The ETHIOPIAN REALM consists of the majority of what we call the continent of Africa. The northern boundary effectively runs through the Sahara and Arabian deserts. Few animals can cross such a barrier, and the animals to the south have tended to develop in isolation from those to the north. The island of Madagascar is part of the Ethiopian Realm, although it is isolated from the continent and could be regarded as a little zoogeographic realm in itself.
The PALAEARCTIC REALM consists of the continents of Europe and Asia north of the Himalayas. It also includes the north coast of Africa. The Sahara desert represents a more powerful barrier to migration than does the Mediterranean Sea.

Environmental influence
During the Cretaceous the hypsilophodonts were very successful. A subgroup – the thescelosaurs – evolved in North America. The balaclav and watergulp are two thescelosaur descendants from the western realms. One lives in mountains, the other in swamps, and so physically, they differ greatly from one another. In the Oriental realm, the taddey and the glub are descendants of the main hypsilophodont group. The mountain form reveals the same adaptations as the balaclav, and the swamp form resembles the watergulp, but they are not closely related.

The zoogeographic realms
The landmasses of the modern world can be divided into six faunal zones, or zoogeographic realms, each realm with a completely different animal population. The boundaries between each realm are marked by barriers to migration and usually consist of deserts, mountains or seaways. The boundaries can be well-marked or indistinct. One great landmass on the globe – the continent of Antarctica – is so devoid of life that it is not contained in any of the zoogeographic realms.

The NEARCTIC REALM is the continent of North America, north of the Mexican desert. This desert isolates the realm from the continent to the south. The Bering strait isolates it from the Palaearctic realm to the north and west, but this is a very temporary barrier and the two realms share similar features.
The NEOTROPICAL REALM consists of the continent of South America and the island bridge of Central America. For most of the last 65 million years this has been a separate island, but quite recently it connected with the Nearctic realm and the creation of a land bridge has meant that the two realms are not as distinct as they once were.
The ORIENTAL REALM consists of what we call South-East Asia. The area of Asia south and east of the Himalayas, including most of the islands of the East Indies, comprises the Oriental realm. The mountains in the north and the desert in the west provide the barriers between this realm and the rest of the continent.
The AUSTRALASIAN REALM is perhaps the most truly isolated of all the realms. It has been an island continent ever since it was broken away from the continent of Antarctica and both plant and animal life there has developed in its own way.
To this list of six zoogeographic realms we have added a seventh, that of the OCEANS. Unlike the continents, the oceans
are continuous and there are no physical barriers between one ocean and another. Animal life found in the oceans tends to be widely distributed and based upon temperatures and water conditions - in other words the environment – rather than the evolutionary development of particular areas. On the continents, the collections of animals found in each realm reflect the history of that realm. They depend upon when and how animal life migrated to that particular area and upon the subsequent development of environmental conditions such as geographic and climatic factors, that influence the animals living in that area.
In a world in which the dinosaurs and the other Mesozoic creatures survive, the animal life is still subject to the constraints of modern zoogeography. This book is divided accordingly. With no extinction of reptiles there has been no development of mammal life, and no evolution of human beings, and therefore no training of geographers. Hence the places of the world have not been given the names that they are known by today. Therefore, for the purposes of this book, we have dispensed with the common geographical names that are based on cultural and political divisions and reflect human exploration and history, and throughout we shall only refer to places in the context of their zoogeographic realms.


CONTENTS

FOREWORD
THE GREAT EXTINCTION 6
WHAT IS A DINOSAUR? 10
THE NEW TREE OF LIFE 12
PALAEOGEOGRAPHY 16
ZOOGEOGRAPHY 18

THE HABITATS 20

THE NEW DINOSAURS 29
THE ETHIOPIAN REALM 30
THE PALAEARCTIC REALM 42
THE NEARCTIC REALM 54
THE NEOTROPICAL REALM 66
THE ORIENTAL REALM 78
THE AUSTRALASIAN REALM 88
THE OCEANS 100
CONCLUSION 108

AFTERWORD 109
GLOSSARY 113
FURTHER READING 115
INDEX 116
ACKNOWLEDGEMENTS 120