Posts Tagged ‘Shelled Egg’

The Hazards of Hatching

Sunday, April 15th, 2012


The protection which the shelled egg gives to the developing embryo is its most obvious contribution to the survival of the species – but scarcely less important is the fact that when it hatches, it lets out into the world a tiny a tiny miniature of an adult, equipped from the beginning to make its own way in its environment. But to reach this perfected state the embryo needs a long period of development in the egg. Turtles like the snappers at left need two to three months; the primitive but specialized New Zealand tuatara needs more than a year. During these long incubations the eggs must be protected from predators and other dangers.

 

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Cutting Out to Meet the World

Tuesday, April 3rd, 2012


How tentative and experimental the reptiles still are in their efforts to abandon the egg and bear their young alive is dramatically demonstrated by a special little tool which all of them, even the live-born, still have. This is the egg tooth, a sharp protrusion on the snout with which a baby reptile can cut its way out of its tough, membrane-lined shell. To be sure, in live-bearing species which have no need for it the egg tooth is degenerating (even the egg-layers drop it soon after birth). But it still stands as a reminder of the difficult escape problem the shelled egg has always presented for the beak-less reptiles.

 

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By Their Hips We Shall Know Them

Thursday, March 22nd, 2012


There’s predatory pressure in the sea, so some of the shallow-water vertebrates, seeking food and refuge ashore, gradually acquired legs, lungs, scales and the shelled egg, and thus developed as last into land reptiles which were able to forage for insects in the forest.

The process, of course, was not quite that flowing and easily traced. There is a good deal of controversy among experts about the order in which the separate innovations appeared and what immediate selective advantage was gained in each case. One fact is clear, however. Of all the adaptations that fitted the vertebrates into their increasingly refined roles on land, none was more fundamental than the reptilian egg.

Most people, thinking of an egg, think of a bird; but they are being led astray by seeing eggs mainly at breakfast. The birds did not invent the shelled egg, they inherited it, and it has undergone no important evolution in their possession. The first shelled land eggs were reptilian, and the reptiles were reptiles only when they had evolved such an egg. The old riddle, “which came first, the hen or the egg,” is just whimsey when the hen is a bird. But applied to reptiles the question is valid, and paleontologists are still getting testy with each other trying to answer it.

The reptiles came from amphibian ancestors. The egg of the usual amphibian is almost naked, enclosed only by a jelly envelope. The jelly supports each egg separately in the mass, keeps out small invaders and discourages predation by larger animals, but it gives almost no protection against drying up. A typical frog egg on land on a clear day will quickly wither. Thus, no matter how far the adult frog may be able to move from water in the course of its own daily activities, when it comes time to provide new frogs most species have to go home to the water. The sons of male frogs all over the world calling the females to the ponds show how strong the obligation is.

The egg as the reptiles developed it – which was essentially as we know it today – had no such limitation. Its smooth shell tightly shut in white and yolk. Like any egg, as it incubated it got more complex inside, and the complexity was not just in the forming body of the new animal but also in the structures required to keep the embryo alive in its shell – to keep it supported, fed, unpoisoned and unasphyxiated.

The structures that did this are known as the embryonic membranes. They were evolved by the reptiles and kept by the birds; and, with modifications, they also serve as embryonic structures of the mammals. Because they occur both in the shelled egg and in the uterine development of the mammal, all three higher vertebrate classes – mammals, reptiles and birds – are collectively called amniotes. The name refers to one of the embryonic membranes, the amnion, which shuts in a fluid in which the embryo is able to go on leading an essentially aquatic existence as it develops. A yolk sac is stalked from the belly region of the embryo, and just behind its attachment is that of the allantois, another sac which partly fills the space between the amnion and a third membrane, the chorion, which lies just beneath the shell. The allantois receives and stores embryonic waste, serving as a sort of bladder. It also has blood vessels that pick up oxygen that passes through the shell and conduct it to the embryo. The shell cuts down evaporation, but it is porous and does not wall the embryo off completely. It shuts out prying small animals, for example, but not the oxygen the embryo requires to live. For the embryo to thrive, such an egg must be kept warm and not too dry.

 

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Reptiles During Permian Period

Sunday, March 18th, 2012


No student of the history life on earth will deny that the coming of the reptiles was one of the great events. As the first truly terrestrial vertebrates, the early reptiles not only filled out the faunal picture for their own time in arresting ways, but they also set the stage for later dramatic happenings like the rise of the dinosaurs, the beginnings of birds and the age-long evolution of the mammal line.

The reptiles went ashore during the Permian, more than 250 million years ago. There was growing opportunity in the Permian land, and by a surprising twist of history, the reptile ancestors had already evolved equipment to take advantage of the opportunity and become the first terrestrial pioneers. During the time of the coal forests, land vegetation had become well developed. Ferns, seed ferns and their kin covered the low-lying land, the energy of the sun was being caught by chlorophyll, insects had made their appearance and food was wasting on the shore. It was almost certainly the insects as a source of animal food that attracted the reptile ancestors living harassed lives at the rim of the land. If one had to work out this bit of paleontology by logic, one would probably do it this way: the insects were there, vertebrate life was under competitive and predatory pressure in the sea, so some of the shallow-water vertebrates, seeking food and refuge ashore, gradually acquired legs, lungs, scales and the shelled egg, and thus developed at last into land reptiles which were able to forage for insects in the forest.

 

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The Miraculous Shelled Egg 2

Friday, August 13th, 2010


All the live-bearing reptiles of modern times are lizards and snakes. Turtles and crocodilians produce only eggs, and so does the tuatara. It is significant that of the three reptiles which venture farthest north, even across the Arctic Circle, two – the European viper and the lizard Lacerta vivipara – bear their young alive. So does the slowworm (Anguis), another venturer into northern regions. The cold ground of those areas, no doubt, is not well suited to incubating eggs. Neither is water, so far as shelled eggs are concerned, which explains why most  reptiles with strongly aquatic habits also bear their young alive.

Many of the live-bearing reptiles, however, belong to groups that have egg-laying members too. The skinks, the lacertas, the boids and the vipers are examples. There are even species that lay eggs in some parts of their ranges but bear live young in other parts. This suggests that their viviparity – as the ability to produce live young is called – is not so formal an undertaking as it is in mammals, and this is true. Some reptiles merely keep the eggs inside the body, for varying periods up to and after hatching time. In others there are extensive, placentalike connections with the tissues of the maternal oviduct. In one type the yolk sac is merely plastered against the wall of the oviduct, and is used primarily for respiration. In a more advanced type the embryonic membranes,the chorion and allantois, interfold with maternal tissues and the embryo not only gets water and nourishment as well as oxygen, but conveniently has its excretory wastes taken away too. None of the live-bearing reptiles has dispensed with a big store of yolk as the main source nourishment for the growing embryo.

All reptiles practice internal fertilization. In all modern forms except the tuatara the male has an organ kept turned outside in, in the base of the tail, and everted through the opening of the cloaca during erection. In the tuatara the transfer of sperm is accomplished by bringing the genital openings into contact, as in birds. This was probably the method used by the ancestral reptiles – it is clear, in any case, that the penis had separate origin in turtles, crocodilians and mammals on the one hand, and in lizards and snakes on the other.

Thus, male lizards and snakes have not just one, but a pair of hollow structures called hemipenes, which make up their copulatory organs. located as they are in the tail just behind the opening of the cloaca, the hemipenes often give the tail of the male a thicker, more gradually tapering contour than that of the female, and in many species the sexes can be distinguished by this difference. A groove that serves as a channel for the sperm extends from the opening of the sperm ducts along the inner wall (which is the outer wall during erection) of each hemipenis, and the surface may be pleated or set with spines that keep it in place in the oviduct of the female during mating. Either one of the hemipenis may be used, but only one, the one nearest to the female, is everted and protruded from the cloaca during erection, which is brought about by a combination of muscular action and distension of the walls with blood.

Among different reptiles fertilization is scheduled differently with respect to the time of nesting. In most species it seems to occur, as might be expected, just before the eggs are laid; but in some the sperm may live on in the reproductive tract of the female and continue to fertilize eggs months or even years after copulation has taken place. The longest known periods of such deferment of fertilization are four years for the diamond back terrapin of the southern United States, and five years in the case of the tropical American cat-eye snake. The green turtle, which evidently mates only in the sea off the nesting beach, often does so after the female has gone ashore and laid her eggs. Since a given female makes her migration to the nesting ground only once in three, or more turtles.

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The Miraculous Shelled Egg

Monday, August 9th, 2010


Reptiles are sexual animals and are the group that introduced internal fertilization to the vertebrate line. Thus, in a manner of speaking, they laid the foundation for the family unit in higher vertebrates, and from this came human society itself, with all its excitement and troubles. The ancestral amphibians deposited their eggs virtually naked in the water, and fertilized them by simply releasing sperm in the general vicinity. The hazards of such an informal operation to both sperm and egg are obvious. The reptilian egg, however, enters the world already fertilized, and packaged against a certain amount of environmental adversity. One need only compare the dozen or so eggs laid by the average lizard with the thousands laid by toads to see the great economy the new method has brought.

But even an egg with a shell is delicate. It can incubate successfully only within a narrow range of conditions of temperature, humidity and concealment. It is thus not surprising to find that a few reptiles have independently hit upon the recourse that we think of as one of the main attributes of the mammals – that of producing living young.

A fertile sea turtle lays round in a hole it has dug in warm, incubating sand of Australia’s Great barrier Reef. When about 100 eggs are laid, it will cover the hole and depart. During one breeding season a mature female will deposit from two to five clutches.

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