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3. One important evolutionary change is from fish to amphibians, the first air breathing, four-legged animals. A. What is one
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A)

first air breathing 4 leg ambhibian

Ichthyostega was one of the first primitive amphibians, with nostrils and more efficient lungs. It had four sturdy limbs, a neck, a tail with fins and a skull very similar to that of the lobe-finned fish, Eusthenopteron. Amphibians evolved adaptations that allowed them to stay out of the water for longer periods.

The First Amphibians

As is often the case in evolutionary history, it's impossible to pinpoint the exact moment when the first tetrapods, the four-legged fish that crawled out of the shallow seas 400 million years ago and swallowed gulps of air with primitive lungs, turned into the first true amphibians. In fact, until recently, it was fashionable to describe these tetrapods as amphibians, until it occurred to experts that most tetrapods didn't share the full spectrum of amphibian characteristics. For example, three important genera of the early Carboniferous period—Eucritta, Crassigyrinus, and Greererpeton—can be variously described as either tetrapods or amphibians, depending on which features are being considered.

It's only in the late Carboniferous period, from about 310 to 300 million years ago, that we can comfortably refer to the first true amphibians. By this time, some genera had attained relatively monstrous sizes—a good example being Eogyrinus ("dawn tadpole"), a slender, crocodile-like creature that measured 15 feet from head to tail. Interestingly, the skin of Eogyrinus was scaly rather than moist, evidence that the earliest amphibians needed to protect themselves from dehydration. Another late Carboniferous/early Permian genus, Eryops, was much shorter than Eogyrinus but more sturdily built, with massive, tooth-studded jaws and strong legs.

At this point, it's worth noting a rather frustrating fact about amphibian evolution: Modern amphibians, which are technically known as "lissamphibians," are only remotely related to these early monsters. Lissamphibians, which include frogs, toads, salamanders, newts, and rare earthworm-like amphibians called "caecilians," are believed to have radiated from a common ancestor that lived in the middle Permian or early Triassic periods, and it's unclear what relationship this common ancestor may have had to late Carboniferous amphibians like Eryops and Eogyrinus. It's possible that modern lissamphibians branched off from the late Carboniferous Amphibamus, but not everyone subscribes to this theory.

B)

Structure and Function in Amphibians

Amphibians are vertebrates that exist in two worlds: they divide their time between freshwater and terrestrial habitats. They share a number of features with air-breathing lungfish, but they also differ from lungfish in many ways. One way they differ is their appendages. Modern amphibians include frogs, salamanders, and caecilian.

Amphibians are the first true tetrapods, or vertebrates with four limbs. Amphibians have less variation in size than fish, ranging in length from 1 centimeter (2.5 inches) to 1.5 meters (about 5 feet). They generally have moist skin without scales. Their skin contains keratin, a tough, fibrous protein found in the skin, scales, feathers, hair, and nails of tetrapod vertebrates, from amphibians to humans. Some forms of keratin are tougher than others. The form in amphibian skin is not very tough, and it allows gases and water to pass through their skin.

Amphibian Ectothermy

Amphibians are ectothermic, so their internal body temperature is generally about the same as the temperature of their environment. When it’s cold outside, their body temperature drops, and they become very sluggish. When the outside temperature rises, so does their body temperature, and they are much more active. What do you think might be some of the pros and cons of ectothermy in amphibians?

Amphibian Organ Systems

All amphibians have digestive, excretory, and reproductive systems. All three systems share a body cavity called the cloaca. Wastes enter the cloaca from the digestive and excretory systems, and gametes enter the cloaca from the reproductive system. An opening in the cloaca allows the wastes and gametes to leave the body.

Amphibians have a relatively complex circulatory system with a three-chambered heart. Their nervous system is also rather complex, allowing them to interact with each other and their environment. Amphibians have sense organs to smell and taste chemicals. Other sense organs include eyes and ears. Of all amphibians, frogs generally have the best vision and hearing. Frogs also have a larynx, or voice box, to make sounds.

Most amphibians breathe with gills as larvae and with lungs as adults. Additional oxygen is absorbed through the skin in most species. The skin is kept moist by mucus, which is secreted by mucous glands. In some species, mucous glands also produce toxins, which help protect the amphibians from predators.

Summary

  • Amphibians are ectothermic vertebrates that divide their time between freshwater and terrestrial habitats.
  • Amphibians are the first true tetrapods, or vertebrates with four limbs.
  • Amphibians breathe with gills as larvae and with lungs as adults. They have a three-chambered heart and relatively complex nervous system.

Characteristics of Amphibians

As tetrapods, most amphibians are characterized by four well-developed limbs. Some species of salamanders and all caecilians are functionally limbless; their limbs are vestigial. An important characteristic of extant amphibians is a moist, permeable skin that is achieved via mucus glands that keep the skin moist; thus, exchange of oxygen and carbon dioxide with the environment can take place through it (cutaneous respiration). Additional characteristics of amphibians include pedicellate teeth—teeth in which the root and crown are calcified, separated by a zone of noncalcified tissue—and a papilla amphibiorum and papilla basilaris, structures of the inner ear that are sensitive to frequencies below and above 10,00 hertz, respectively. Amphibians also have an auricular operculum, which is an extra bone in the ear that transmits sounds to the inner ear.

The fossil record provides evidence of amphibian species, now extinct, that arose over 400 million years ago as the first tetrapods. Amphibia can be divided into three clades: salamanders (Urodela), frogs (Anura), and caecilians (Apoda). The life cycle of frogs, like the majority of amphibians, consists of two distinct stages: the larval stage and metamorphosis to an adult stage. Some species in all orders bypass a free-living larval stage. All extant adult amphibians are carnivorous, and some terrestrial amphibians have a sticky tongue that is used to capture prey.

C) changes during dovelopment fish to ambhibia

Territorial behaviour

Little is known of the territorial behaviour of caecilians, but some frogs and salamanders defend home ranges. These are usually feeding, breeding or sheltering sites. Males normally exhibit such behaviour though in some species, females and even juveniles are also involved. Although in many frog species, females are larger than males, this is not the case in most species where males are actively involved in territorial defence. Some of these have specific adaptations such as enlarged teeth for biting or spines on the chest, arms or thumb.

In salamanders, defence of a territory involves adopting an aggressive posture and if necessary attacking the intruder. This may involve snapping, chasing and sometimes biting, occasionally causing the loss of a tail. The behaviour of red back salamanders (Plethodon cinereus) has been much studied. 91% of marked individuals that were later recaptured were within a metre (yard) of their original daytime retreat under a log or rock. A similar proportion, when moved experimentally a distance of 30 metres (98 ft), found their way back to their home base. The salamanders left odour marks around their territories which averaged 0.16 to 0.33 square metres (1.7 to 3.6 sq ft) in size and were sometimes inhabited by a male and female pair. These deterred the intrusion of others and delineated the boundaries between neighbouring areas. Much of their behaviour seemed stereotyped and did not involve any actual contact between individuals. An aggressive posture involved raising the body off the ground and glaring at the opponent who often turned away submissively. If the intruder persisted, a biting lunge was usually launched at either the tail region or the naso-labial grooves. Damage to either of these areas can reduce the fitness of the rival, either because of the need to regenerate tissue or because it impairs its ability to detect food.

In frogs, male territorial behaviour is often observed at breeding locations; calling is both an announcement of ownership of part of this resource and an advertisement call to potential mates. In general, a deeper voice represents a heavier and more powerful individual, and this may be sufficient to prevent intrusion by smaller males. Much energy is used in the vocalization and it takes a toll on the territory holder who may be displaced by a fitter rival if he tires. There is a tendency for males to tolerate the holders of neighbouring territories while vigorously attacking unknown intruders. Holders of territories have a "home advantage" and usually come off better in an encounter between two similar-sized frogs. If threats are insufficient, chest to chest tussles may take place. Fighting methods include pushing and shoving, deflating the opponent's vocal sac, seizing him by the head, jumping on his back, biting, chasing, splashing, and ducking him under the water.

The origins and evolutionary relationships between the three main groups of amphibians is a matter of debate. A 2005 molecular phylogeny, based on rDNA analysis, suggests that salamanders and caecilians are more closely related to each other than they are to frogs. It also appears that the divergence of the three groups took place in the Paleozoic or early Mesozoic (around 250 million years ago), before the breakup of the supercontinent Pangaea and soon after their divergence from the lobe-finned fish. The briefness of this period, and the swiftness with which radiation took place, would help account for the relative scarcity of primitive amphibian fossils. There are large gaps in the fossil record, but the discovery of a Gerobatrachus hottoni from the Early Permian in Texas in 2008 provided a missing link with many of the characteristics of modern frogs. Molecular analysis suggests that the frog–salamander divergence took place considerably earlier than the palaeontological evidence indicates. Newer research indicates that the common ancestor of all Lissamphibians lived about 315 million years ago, and that stereospondyls are the closest relatives to the caecilians.

As they evolved from lunged fish, amphibians had to make certain adaptations for living on land, including the need to develop new means of locomotion. In the water, the sideways thrusts of their tails had propelled them forward, but on land, quite different mechanisms were required. Their vertebral columns, limbs, limb girdles and musculature needed to be strong enough to raise them off the ground for locomotion and feeding. Terrestrial adults discarded their lateral line systems and adapted their sensory systems to receive stimuli via the medium of the air. They needed to develop new methods to regulate their body heat to cope with fluctuations in ambient temperature. They developed behaviours suitable for reproduction in a terrestrial environment. Their skins were exposed to harmful ultraviolet rays that had previously been absorbed by the water. The skin changed to become more protective and prevent excessive water loss

The first major groups of amphibians developed in the Devonian period, around 370 million years ago, from lobe-finned fish which were similar to the modern coelacanth and lungfish. These ancient lobe-finned fish had evolved multi-jointed leg-like fins with digits that enabled them to crawl along the sea bottom. Some fish had developed primitive lungs that help them breathe air when the stagnant pools of the Devonian swamps were low in oxygen. They could also use their strong fins to hoist themselves out of the water and onto dry land if circumstances so required. Eventually, their bony fins would evolve into limbs and they would become the ancestors to all tetrapods, including modern amphibians, reptiles, birds, and mammals. Despite being able to crawl on land, many of these prehistoric tetrapodomorph fish still spent most of their time in the water. They had started to develop lungs, but still breathed predominantly with gills.

Many examples of species showing transitional features have been discovered. Ichthyostega was one of the first primitive amphibians, with nostrils and more efficient lungs. It had four sturdy limbs, a neck, a tail with fins and a skull very similar to that of the lobe-finned fish, Eusthenopteron. Amphibians evolved adaptations that allowed them to stay out of the water for longer periods. Their lungs improved and their skeletons became heavier and stronger, better able to support the weight of their bodies on land. They developed "hands" and "feet" with five or more digits; the skin became more capable of retaining body fluids and resisting desiccation. The fish's hyomandibula bone in the hyoid region behind the gills diminished in size and became the stapes of the amphibian ear, an adaptation necessary for hearing on dry land. An affinity between the amphibians and the teleost fish is the multi-folded structure of the teeth and the paired supra-occipital bones at the back of the head, neither of these features being found elsewhere in the animal kingdom.

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