Vertebrates generally have a ventral aorta and dorsal aorta, with six pairs of aortic arches that branch off and pass through gill arches. In fishes, the six pairs of arches each pass blood through the gills. Over time, some arches reduce or disappear, with sharks having five pairs and most fish having four functional pairs. In land vertebrates like reptiles, amphibians, birds and mammals, the number of arches reduces further to three pairs or less as lungs replace gills and the circulatory system evolves to separate oxygenated and deoxygenated blood.
The basic fundamental plan of the aortic arches is similar in different vertebrates during embryonic stages.
But in adult the condition of the arrangement is changed either being lost or modified considerably.
The number of aortic arches is gradually reduced as the scale of evolution of vertebrates is ascended.
The embryonic aortic arches were basically six pairs.
But with progressive evolution , there has been consequent reduction in numbers of aortic arches.
In the basic pattern the major arterial channels consists of
A ventral aorta emerging from the heart and passing forward beneath the pharynx
A dorsal aorta paired above the pharynx and passing caudal above the digestive tract.
Six pairs of aortic arches connecting ventral aorta to with the dorsal aorta.
1st aortic arch= Mandibular aortic arch
2nd Aortic arch= hyoid aortic arch
3rd ,4th ,5th and 6th aortic arches in case of aquatic animal , known as branchial aortic arches.
The document discusses the development and modifications of aortic arches across vertebrates. In early embryos, most vertebrates develop 6 pairs of aortic arches that connect the dorsal aorta to the ventral aorta and carry blood to the gills. Over evolution, there is a reduction in arches as respiration moves from gills to lungs. By adulthood, mammals and birds typically have 3 pairs of arches - the third becomes the carotid artery, fourth becomes systemic arteries, and sixth becomes pulmonary arteries.
The document summarizes the evolution of kidneys and urino-genital ducts in vertebrates. It describes how the pronephros, mesonephros and metanephros kidney systems develop and how their associated ducts give rise to the male and female reproductive tracts. It explains that in females, the Müllerian ducts form the oviducts, while in males the mesonephric ducts form parts of the reproductive system or are reduced. The kidneys and ducts show adaptations for waste excretion, sperm transport, and supporting embryo development across vertebrate groups.
Evolutionary change in heart of vertebrates
Heart is situated ventral to the oseophagus in the pericardial section of the coelom.
Heart is a highly muscular pumping organ that pumps blood into arteries and sucks it back through the veins.
In vertebrates it has undergone transformation by twisting from a straight tube to a complex multi-chambered organ.
. There has been an increase in the number of chambers in heart during evolution of vertebrates.
The heart is covered by a transparent protective covering, called pericardium. It is a single layer in fish.
Within pericardium there is a pericardial fluid, protects the heart from the external injury.
The evolution of the heart is based on the separation of oxygenated blood from deoxygenated blood for efficient oxygen transport.
Vertebrates generally have a ventral aorta and dorsal aorta, with six pairs of aortic arches that branch off and pass through gill arches. In fishes, the six pairs of arches each pass blood through the gills. Over time, some arches reduce or disappear, with sharks having five pairs and most fish having four functional pairs. In land vertebrates like reptiles, amphibians, birds and mammals, the number of arches reduces further to three pairs or less as lungs replace gills and the circulatory system evolves to separate oxygenated and deoxygenated blood.
The circulatory system transports nutrients, oxygen, carbon dioxide and waste through blood vessels. Vertebrates have a closed circulatory system with blood contained within vessels. The human circulatory system, also called the cardiovascular system, consists of the heart, arteries, capillaries and veins. The heart pumps oxygenated blood received from the lungs through the arteries and returns deoxygenated blood to the lungs through veins. Birds and mammals have further developed separate pulmonary and systemic circulatory circuits to oxygenate blood in the lungs before distributing it to the body.
Comparative Anatomy of Digestive System of VertebratesRameshPandi4
This document provides an overview of the comparative anatomy of the digestive system across different vertebrates. It describes the basic components and functions of the digestive tract, including the mouth, esophagus, stomach, intestines, and associated glands like the liver and pancreas. The key differences in digestive anatomy are often correlated with differences in diet, such as whether the food is readily absorbed or requires extensive breakdown, and whether the food supply is constant or scattered. Examples of digestive systems from various vertebrates like fish, frogs, reptiles, birds, and mammals are then described in more detail.
Vertebrates generally have a ventral aorta and dorsal aorta, with six pairs of aortic arches that branch off and pass through gill arches. In fishes, the six pairs of arches each pass blood through the gills. Over time, some arches reduce or disappear, with sharks having five pairs and most fish having four functional pairs. In land vertebrates like reptiles, amphibians, birds and mammals, the number of arches reduces further to three pairs or less as lungs replace gills and the circulatory system evolves to separate oxygenated and deoxygenated blood.
The basic fundamental plan of the aortic arches is similar in different vertebrates during embryonic stages.
But in adult the condition of the arrangement is changed either being lost or modified considerably.
The number of aortic arches is gradually reduced as the scale of evolution of vertebrates is ascended.
The embryonic aortic arches were basically six pairs.
But with progressive evolution , there has been consequent reduction in numbers of aortic arches.
In the basic pattern the major arterial channels consists of
A ventral aorta emerging from the heart and passing forward beneath the pharynx
A dorsal aorta paired above the pharynx and passing caudal above the digestive tract.
Six pairs of aortic arches connecting ventral aorta to with the dorsal aorta.
1st aortic arch= Mandibular aortic arch
2nd Aortic arch= hyoid aortic arch
3rd ,4th ,5th and 6th aortic arches in case of aquatic animal , known as branchial aortic arches.
The document discusses the development and modifications of aortic arches across vertebrates. In early embryos, most vertebrates develop 6 pairs of aortic arches that connect the dorsal aorta to the ventral aorta and carry blood to the gills. Over evolution, there is a reduction in arches as respiration moves from gills to lungs. By adulthood, mammals and birds typically have 3 pairs of arches - the third becomes the carotid artery, fourth becomes systemic arteries, and sixth becomes pulmonary arteries.
The document summarizes the evolution of kidneys and urino-genital ducts in vertebrates. It describes how the pronephros, mesonephros and metanephros kidney systems develop and how their associated ducts give rise to the male and female reproductive tracts. It explains that in females, the Müllerian ducts form the oviducts, while in males the mesonephric ducts form parts of the reproductive system or are reduced. The kidneys and ducts show adaptations for waste excretion, sperm transport, and supporting embryo development across vertebrate groups.
Evolutionary change in heart of vertebrates
Heart is situated ventral to the oseophagus in the pericardial section of the coelom.
Heart is a highly muscular pumping organ that pumps blood into arteries and sucks it back through the veins.
In vertebrates it has undergone transformation by twisting from a straight tube to a complex multi-chambered organ.
. There has been an increase in the number of chambers in heart during evolution of vertebrates.
The heart is covered by a transparent protective covering, called pericardium. It is a single layer in fish.
Within pericardium there is a pericardial fluid, protects the heart from the external injury.
The evolution of the heart is based on the separation of oxygenated blood from deoxygenated blood for efficient oxygen transport.
Vertebrates generally have a ventral aorta and dorsal aorta, with six pairs of aortic arches that branch off and pass through gill arches. In fishes, the six pairs of arches each pass blood through the gills. Over time, some arches reduce or disappear, with sharks having five pairs and most fish having four functional pairs. In land vertebrates like reptiles, amphibians, birds and mammals, the number of arches reduces further to three pairs or less as lungs replace gills and the circulatory system evolves to separate oxygenated and deoxygenated blood.
The circulatory system transports nutrients, oxygen, carbon dioxide and waste through blood vessels. Vertebrates have a closed circulatory system with blood contained within vessels. The human circulatory system, also called the cardiovascular system, consists of the heart, arteries, capillaries and veins. The heart pumps oxygenated blood received from the lungs through the arteries and returns deoxygenated blood to the lungs through veins. Birds and mammals have further developed separate pulmonary and systemic circulatory circuits to oxygenate blood in the lungs before distributing it to the body.
Comparative Anatomy of Digestive System of VertebratesRameshPandi4
This document provides an overview of the comparative anatomy of the digestive system across different vertebrates. It describes the basic components and functions of the digestive tract, including the mouth, esophagus, stomach, intestines, and associated glands like the liver and pancreas. The key differences in digestive anatomy are often correlated with differences in diet, such as whether the food is readily absorbed or requires extensive breakdown, and whether the food supply is constant or scattered. Examples of digestive systems from various vertebrates like fish, frogs, reptiles, birds, and mammals are then described in more detail.
The primitive blueprint for the heart and circulatory system emerged with the arrival of the third mesodermal germ layer in bilaterians. Since then, hearts in animals have evolved from a single layered tube to a multiple chambered heart in due course of time.
1. All chordates have a circulatory system with blood and lymph traveling through separate yet interconnected vessels.
2. In vertebrates the blood vascular system is closed, with a contractile heart and continuous vessels. The heart pumps oxygenated blood from the veins into the arteries.
3. Over the course of evolution, the structure of the heart has become more complex and compartmentalized. In early vertebrates like sharks the heart had two chambers, while in advanced mammals it is a four-chambered heart that fully separates pulmonary and systemic circulation.
Fertilization involves the fusion of male and female gametes. It can occur externally or internally. In external fertilization, gametes fuse outside the female body, while in internal fertilization fusion occurs inside. The key stages of fertilization are the approach and fusion of sperm and egg, capacitation of sperm, the acrosomal reaction which allows sperm penetration, activation of the egg, and fusion of the male and female pronuclei through amphimixis. Fertilization ensures the restoration of diploidy and genetic variation in offspring.
comparative anatomy of respiratory system of Reptiles, Birds and Mammals.UttamaTungkhang
This document compares and contrasts the respiratory systems of reptiles, birds, and mammals. It notes that all three use aerial respiration through lungs, but that some reptiles and birds undergo specialized adaptations related to their habitats. For example, crocodilians have a bony secondary palate for breathing underwater, while some lizards can increase stamina through buccal pumping. The document outlines key parts of the respiratory tract and how gas exchange occurs differently depending on the type of animal.
The vertebrate brain
The vertebrate brain is the main part of the central nervous system. The brain and the spinal cord make up the central nervous system,
In most of the vertebrates the brain is at the front, in the head. It is protected by the skull and close to the main sense organs.
Brains are extremely complex and the part of human and animal body. The brain controls the other organs of the body, either by activating muscles or by causing secretion of chemicals such as hormones and neurotransmitters.
Muscular action allows rapid and coordinated responses to changes in the environment.
The brain of an adult human weights about 1300–1400 grams .
In vertebrates, the spinal cord by itself can cause reflex responses as well as simple movement such as swimming or walking. However, sophisticated control of behaviour requires a centralized brain.
The structure of all vertebrate brains is basically the same.
At the same time, during the course of evolution, the vertebrate brain has undergone changes, and become more effective.
In so-called 'lower' animals, most or all of the brain structure is inherited, and therefore their behaviour is mostly instinctive.
In mammals, and especially in man, the brain is developed further during life by learning. This has the benefit of helping them fit better into their environment. The capacity to learn is seen best in the cerebral cortex.
Three principles
The brain and nervous system is essentially a system which makes connections. It has input from sense organs and output to muscles. It is connected in several ways with the endocrine system, which makes hormones, and the digestive system and sex system. Hormones work slowly, so those changes are gradual.
The brain is a kind of department store. It has, all inter-connected, departments which do different things. They all help each other gather senses.
Much of what the body does is not conscious. Basically, much of the body runs on automatic (breathing, heart beat, hungry, hair growth) adjusted by the autonomic nervous system. The brain, too, does much of its work without a person noticing it. The unconscious mind refers to the brain activities which are hardly ever noticed.
In primitive vertebrates, such as the lancelet (petromyzon), the circulating fluid moves without a heart as the central organ of circulation.
In fishes’ single-circuit system, the gills and the heart are placed in series. The two-chambered heart supplies the blood to gills with pressures that exceed those in the arteries. Largely devoid of gravity, fish depend on water for respiration, fluid balance, thermoregulation, reproduction, and fin development.
The amphibians are adapted to life in water only during early stages of their development. Transition to land is marked by loss of fins and gills, and the emergence of tail and limbs.
Adaptation to air respiration introduces a fundamental change in the structure of the cardiovascular system. The heart and the lung are joined by a newly formed pulmonary circulation placed in parallel with the systemic circulation. In contrast to fish, the circulatory loops cross and assume the shape of a lemniscate (figure-eight or ∞-shaped curves).
The heart acquires a new chamber, the left atrium, while a common ventricle is shared between the pulmonary and systemic loops. Amphibians continue to depend for temperature, reproduction, and part of their respiratory needs on water (skin respiration).
Through the development of complicated organ systems such as thermoregulation, respiration, excretion, inner reproduction, and locomotion, mammals have attained a high degree of environmental liberation.
The cardiovascular system consists of two anatomically separate, but functionally unified, parts—the systemic and pulmonary circulations—placed in series.
In addition to an independent inner watery environment, mammals have developed an “inner atmosphere,” reflected primarily in the partial pressure of oxygen and nitrogen in the blood that parallels the atmospheric pressure.
The essential new feature of the mammalian circulation is a pressurized arterial compartment. The similarity of arterial pressure across the mammalian species suggests that the pressure as such does not serve the blood propulsion.
Vertebrate Circulatory Systems:
transport gases, nutrients, waste products, hormones, heat, & various other materials
consist of heart, arteries, capillaries, & veins:
Arteries
carry blood away from the heart
have muscular, elastic walls
terminate in capillary beds
Capillaries
have very thin walls (endothelium only)
are the site of exchange between the blood and body cells
Veins
carry blood back to the heart
have less muscle in their walls than arteries but the walls are very elastic
begin at the end of capillary beds
Heart
a muscular pump (cardiac muscle)
contains a pacemaker to regulate rate but rate can also be influenced by the Autonomic Nervous System
The nervous system is divided into the central nervous system (CNS) and peripheral nervous system (PNS). The CNS includes the brain and spinal cord, while the PNS includes nerves that connect the CNS to sensory receptors and effectors throughout the body. Neurons are the basic functional units that transmit nerve impulses and include dendrites, a cell body, and an axon. Neuroglia provide support to neurons. The PNS includes spinal and cranial nerves, with different types serving sensory, motor, or integrative functions.
The document summarizes the development and comparative anatomy of the vertebrate brain. It describes how the embryonic brain divides into three primary vesicles - the prosencephalon, mesencephalon, and rhombencephalon. It then discusses the specific structures that develop from each of these regions across different vertebrate groups, including differences in brain structure between cyclostomes, fish, amphibians, reptiles, birds, and mammals. Key differences include the size of regions like the cerebrum, cerebellum, and olfactory bulbs across the groups.
DENTITION IN MAMMALS
The study of arrangement structure and number of types of teeth collectively is called as dentition. Teeth are present in the foetal as well as in adults of mammals, based on the presence of teeth Mammals are two types.
Edentata : In some animals teeth are absent hence called as edentate. e.g., Echidna or spiny ant-eater (Tachyglossus) the teeth are absent in all stages of life.
Dentata : Teeth are present in all mammals though a secon¬dary toothless condition is found in some mammals. Modern turtles and birds lack teeth. The adult platypus (Ornithorhynchus) bears epidermal teeth but no true teeth are present. In platypus embryonic teeth are replaced by horny epidermal teeth in adult.
Classification According to the Shape and Size of the Teeth:
Homodont:
Homodont or Isodont type of teeth is a condition where the teeth are all alike in their shape and size in the toothed whales e.g., Pinnipedians. Fishes, amphibians, reptiles and in the extinct toothed birds.
Heterodont
Heterodont condition is the usual feature in mammals, i.e. the teeth are distinguished according to their shape, size and function. The function is also different at different parts of the tooth row.
According to the Mode of Attachment of Teeth:
Thecodont : The teeth are lodged in bony sockets or alveoli of the jaw bone and capillaries and nerves enter the pulp cavity through the open tips of the hollow roots e.g., mammals, crocodiles and in some fishes.
Acrodont: The teeth are fused to the surface of the underlying jawbone. They have no roots and are attached to the edge of the jawbone by fibrous membrane e.g., fishes, amphibians and some reptiles.
Pleurodont:
The teeth are attached to the inner-side of the jawbone. The tooth touches the bone only with the outer surface of its root. In acrodont and pleurodont types of dentition, there are no roots, and nerves and blood vessels do not enter the pulp cavity at the base, e.g., Necturus (Amphibia) and some reptiles.
According to the Succession or Replace¬ment of Teeth:
Comparative account of vertebrate heartSUTAPA DATTA
The document compares the heart structures of various vertebrate groups. It notes that hearts evolve from two longitudinal tubes fusing in the mesoderm. The simplest hearts are found in cephalochordates like Branchiostoma, consisting of a sinus venosus, auricle and ventricle. Lampreys and harks have slightly more complex hearts with these chambers plus a conus arteriosus. Elasmobranch fish hearts are S-shaped tubes with these chambers. Teleost fish hearts are two-chambered with a sinus venosus, auricle, ventricle and bulbus arteriosus. Lungfish have transitional three-chambered hearts. Higher vertebrates evolve four-chamber
succession of kidneys in a vertebrate seriesNaman Sharma
1. Kidneys evolve from the primitive archinephros to the pronephros, mesonephros, and finally the metanephros, which is the definitive kidney of amniotes.
2. The pronephros is the first to develop and is functional only in embryonic or larval stages. The mesonephros follows and is functional in embryos and adults of some species.
3. The metanephros is the adult kidney of amniotes and shows greater complexity with millions of nephrons and additional structures like loops of Henle in mammals.
This document provides information about the cardiovascular systems of humans, ruminants, birds, and fish. It describes the key components of the cardiovascular system including the heart, blood vessels, and blood. For each species, it highlights some distinguishing features of their circulatory system, such as birds having a more efficient 4-chambered heart than other vertebrates and fish having the simplest heart with only two chambers. The document also provides typical heart rate ranges for different species.
osmoregulation in invertebrates- it is a processes by which any organisms maintains the fluid and salt balance of its body, which is important for proper functioning of organs .
INTRODUCTION
The jaw (Upper and lower) is any opposable articulated structure at the entrance of the mouth.
It is typically used for grasping and manipulating food.
Jaw suspension means the fusion of upper jaw and lower jaw or skull for efficient biting.
There are different ways in which these attachments are attained depending upon the modifications in visceral arches in vertebrates.
In most vertebrates, the jaws are bony or cartilaginous and oppose vertically.
The vertebrate jaw is derived from the most anterior two pharyngeal arches supporting the gills, and usually bears numerous teeth.
The vertebrate jaw probably originally evolved in the Silurian period and appeared in the Placoderm fish which further diversified in the Devonian.
It is believed that the hyoid system suspends the jaw from the brain case of the skull, permitting great mobility of the jaws.
The original selective advantage offered by the jaw may not be related to feeding, but rather to increased respiration efficiency.
The jaws were used in the buccal pump (observable in modern fish and amphibians) that pumps water across the gills of fish or air into the lungs in the case of amphibians.
Over evolutionary time the more familiar use of jaws (to humans), in feeding, was selected for and became a very important function in vertebrates. Many teleost fish have substantially modified jaws for suction feeding and jaw protrusion, resulting in highly complex jaws with dozens of bones involved.
Jaw Suspension or Suspensoria:
The method by which the upper and lower jaws are suspended or attached from the chondrocranium is known as jaw suspension or suspensorium.
Amongst the visceral arches, the first (mandibular) arch consists of
= a dorsal palato pterygoquadrate bar forming the upper jaw,
= and ventral Meckel’s cartilage forms the lower jaw.
The second (hyoid) arch consists of = a dorsal hyomandibular supporting and suspending the jaws with the cranium, and a ventral hyoid.
The remaining visceral arches support the gills and are, hence, called branchial arches. Thus, splanchnocranium forms the jaws and suspends them with the chondrocranium.
The document summarizes the development of the kidney in vertebrates. It discusses the three main stages of kidney development: (1) the pronephros, which is an initial kidney that forms but then degenerates; (2) the mesonephros, which briefly functions as a kidney in some species; and (3) the metanephros, which develops from the intermediate mesoderm and ureteric buds and forms the permanent kidney through reciprocal interactions between epithelial and mesenchymal tissues. The ureteric buds branch and induce surrounding mesenchyme to form nephrons, while the mesenchyme causes further branching of the ureteric ducts, resulting in the
The document discusses the integumentary system across different chordate groups. It describes the key features of skin in protochordates, cyclostomes, fish, amphibians, reptiles, birds, and mammals. The integumentary system generally consists of an outer epidermis layer and inner dermis layer, with variations in features like keratinization, glands, scales/feathers/hair, and pigment cells across groups. The skin serves protective, sensory, and excretory functions for chordates.
This document discusses various forms of parental care exhibited by amphibians to increase offspring survival. It outlines nine types of parental care observed in amphibians: 1) selection of safe egg-laying sites, 2) frothing of water around eggs, 3) defending egg territories, 4) building nests from mud, leaves, or plant shoots, 5) direct development from egg to juvenile, 6) carrying eggs attached to the body, 7) carrying larvae between water bodies, 8) brooding eggs in vocal sacs or pouches on the back, and 9) retaining eggs internally in a uterus for viviparous development.
Visceral arches are pieces of cartilage or bone that support the pharyngeal region in vertebrates and help attach the jaws to the skull. There are typically 7 pairs of visceral arches that are modified differently in vertebrate groups depending on the presence of gills and jaw suspension type. Cyclostomes lack identifiable typical cartilage patterns and have a fused branchial basket to support gills. Elasmobranchs have a full set of visceral arches and 3 unpaired branchial cartilages. Bony fishes have modifications for jaw movement and suspension with a reduced last arch. Amphibians have 6 arches as larvae with the last 3 bearing gills, and modifications form their air breathing
Comparative Anatomy of Respiratory System of VertebratesRameshPandi4
The document discusses the comparative anatomy of the respiratory systems of various vertebrates. It describes how respiration occurs through the skin, gills, lungs, and gas bladders in different organisms. It explains key differences in respiratory structures between cartilaginous fishes, bony fishes, and jawless fishes. Mechanisms of gas exchange are covered for fishes, as well as respiratory organs and processes for amphibians, reptiles, birds, and mammals.
Blood vessel development occurs through vasculogenesis and angiogenesis. The major vessels form through vasculogenesis while the rest develop via angiogenesis. During development, the aortic arches form pairs that connect the aortic sac to the dorsal aortae and pharyngeal arches. Most of the arches regress except for parts that form portions of the carotid, pulmonary and subclavian arteries. Other changes accompany arch regression like dorsal aorta obliteration and heart descent into the thorax. The vitelline and umbilical arteries supply the gut and placenta, respectively, and remodel after birth. Coronary arteries arise from angioblasts and the epicardium, connecting to the aorta
Vertebrates generally have a ventral aorta and dorsal aorta, with six pairs of aortic arches that branch off and pass through gill arches. In fishes, the six pairs of arches each pass blood through the gills. Over time, some arches reduce or disappear, with sharks having five pairs and most fish having four functional pairs. In land vertebrates like reptiles, amphibians, birds and mammals, the number of arches reduces further to three pairs or less as lungs replace gills and the circulatory system evolves to separate oxygenated and deoxygenated blood.
The primitive blueprint for the heart and circulatory system emerged with the arrival of the third mesodermal germ layer in bilaterians. Since then, hearts in animals have evolved from a single layered tube to a multiple chambered heart in due course of time.
1. All chordates have a circulatory system with blood and lymph traveling through separate yet interconnected vessels.
2. In vertebrates the blood vascular system is closed, with a contractile heart and continuous vessels. The heart pumps oxygenated blood from the veins into the arteries.
3. Over the course of evolution, the structure of the heart has become more complex and compartmentalized. In early vertebrates like sharks the heart had two chambers, while in advanced mammals it is a four-chambered heart that fully separates pulmonary and systemic circulation.
Fertilization involves the fusion of male and female gametes. It can occur externally or internally. In external fertilization, gametes fuse outside the female body, while in internal fertilization fusion occurs inside. The key stages of fertilization are the approach and fusion of sperm and egg, capacitation of sperm, the acrosomal reaction which allows sperm penetration, activation of the egg, and fusion of the male and female pronuclei through amphimixis. Fertilization ensures the restoration of diploidy and genetic variation in offspring.
comparative anatomy of respiratory system of Reptiles, Birds and Mammals.UttamaTungkhang
This document compares and contrasts the respiratory systems of reptiles, birds, and mammals. It notes that all three use aerial respiration through lungs, but that some reptiles and birds undergo specialized adaptations related to their habitats. For example, crocodilians have a bony secondary palate for breathing underwater, while some lizards can increase stamina through buccal pumping. The document outlines key parts of the respiratory tract and how gas exchange occurs differently depending on the type of animal.
The vertebrate brain
The vertebrate brain is the main part of the central nervous system. The brain and the spinal cord make up the central nervous system,
In most of the vertebrates the brain is at the front, in the head. It is protected by the skull and close to the main sense organs.
Brains are extremely complex and the part of human and animal body. The brain controls the other organs of the body, either by activating muscles or by causing secretion of chemicals such as hormones and neurotransmitters.
Muscular action allows rapid and coordinated responses to changes in the environment.
The brain of an adult human weights about 1300–1400 grams .
In vertebrates, the spinal cord by itself can cause reflex responses as well as simple movement such as swimming or walking. However, sophisticated control of behaviour requires a centralized brain.
The structure of all vertebrate brains is basically the same.
At the same time, during the course of evolution, the vertebrate brain has undergone changes, and become more effective.
In so-called 'lower' animals, most or all of the brain structure is inherited, and therefore their behaviour is mostly instinctive.
In mammals, and especially in man, the brain is developed further during life by learning. This has the benefit of helping them fit better into their environment. The capacity to learn is seen best in the cerebral cortex.
Three principles
The brain and nervous system is essentially a system which makes connections. It has input from sense organs and output to muscles. It is connected in several ways with the endocrine system, which makes hormones, and the digestive system and sex system. Hormones work slowly, so those changes are gradual.
The brain is a kind of department store. It has, all inter-connected, departments which do different things. They all help each other gather senses.
Much of what the body does is not conscious. Basically, much of the body runs on automatic (breathing, heart beat, hungry, hair growth) adjusted by the autonomic nervous system. The brain, too, does much of its work without a person noticing it. The unconscious mind refers to the brain activities which are hardly ever noticed.
In primitive vertebrates, such as the lancelet (petromyzon), the circulating fluid moves without a heart as the central organ of circulation.
In fishes’ single-circuit system, the gills and the heart are placed in series. The two-chambered heart supplies the blood to gills with pressures that exceed those in the arteries. Largely devoid of gravity, fish depend on water for respiration, fluid balance, thermoregulation, reproduction, and fin development.
The amphibians are adapted to life in water only during early stages of their development. Transition to land is marked by loss of fins and gills, and the emergence of tail and limbs.
Adaptation to air respiration introduces a fundamental change in the structure of the cardiovascular system. The heart and the lung are joined by a newly formed pulmonary circulation placed in parallel with the systemic circulation. In contrast to fish, the circulatory loops cross and assume the shape of a lemniscate (figure-eight or ∞-shaped curves).
The heart acquires a new chamber, the left atrium, while a common ventricle is shared between the pulmonary and systemic loops. Amphibians continue to depend for temperature, reproduction, and part of their respiratory needs on water (skin respiration).
Through the development of complicated organ systems such as thermoregulation, respiration, excretion, inner reproduction, and locomotion, mammals have attained a high degree of environmental liberation.
The cardiovascular system consists of two anatomically separate, but functionally unified, parts—the systemic and pulmonary circulations—placed in series.
In addition to an independent inner watery environment, mammals have developed an “inner atmosphere,” reflected primarily in the partial pressure of oxygen and nitrogen in the blood that parallels the atmospheric pressure.
The essential new feature of the mammalian circulation is a pressurized arterial compartment. The similarity of arterial pressure across the mammalian species suggests that the pressure as such does not serve the blood propulsion.
Vertebrate Circulatory Systems:
transport gases, nutrients, waste products, hormones, heat, & various other materials
consist of heart, arteries, capillaries, & veins:
Arteries
carry blood away from the heart
have muscular, elastic walls
terminate in capillary beds
Capillaries
have very thin walls (endothelium only)
are the site of exchange between the blood and body cells
Veins
carry blood back to the heart
have less muscle in their walls than arteries but the walls are very elastic
begin at the end of capillary beds
Heart
a muscular pump (cardiac muscle)
contains a pacemaker to regulate rate but rate can also be influenced by the Autonomic Nervous System
The nervous system is divided into the central nervous system (CNS) and peripheral nervous system (PNS). The CNS includes the brain and spinal cord, while the PNS includes nerves that connect the CNS to sensory receptors and effectors throughout the body. Neurons are the basic functional units that transmit nerve impulses and include dendrites, a cell body, and an axon. Neuroglia provide support to neurons. The PNS includes spinal and cranial nerves, with different types serving sensory, motor, or integrative functions.
The document summarizes the development and comparative anatomy of the vertebrate brain. It describes how the embryonic brain divides into three primary vesicles - the prosencephalon, mesencephalon, and rhombencephalon. It then discusses the specific structures that develop from each of these regions across different vertebrate groups, including differences in brain structure between cyclostomes, fish, amphibians, reptiles, birds, and mammals. Key differences include the size of regions like the cerebrum, cerebellum, and olfactory bulbs across the groups.
DENTITION IN MAMMALS
The study of arrangement structure and number of types of teeth collectively is called as dentition. Teeth are present in the foetal as well as in adults of mammals, based on the presence of teeth Mammals are two types.
Edentata : In some animals teeth are absent hence called as edentate. e.g., Echidna or spiny ant-eater (Tachyglossus) the teeth are absent in all stages of life.
Dentata : Teeth are present in all mammals though a secon¬dary toothless condition is found in some mammals. Modern turtles and birds lack teeth. The adult platypus (Ornithorhynchus) bears epidermal teeth but no true teeth are present. In platypus embryonic teeth are replaced by horny epidermal teeth in adult.
Classification According to the Shape and Size of the Teeth:
Homodont:
Homodont or Isodont type of teeth is a condition where the teeth are all alike in their shape and size in the toothed whales e.g., Pinnipedians. Fishes, amphibians, reptiles and in the extinct toothed birds.
Heterodont
Heterodont condition is the usual feature in mammals, i.e. the teeth are distinguished according to their shape, size and function. The function is also different at different parts of the tooth row.
According to the Mode of Attachment of Teeth:
Thecodont : The teeth are lodged in bony sockets or alveoli of the jaw bone and capillaries and nerves enter the pulp cavity through the open tips of the hollow roots e.g., mammals, crocodiles and in some fishes.
Acrodont: The teeth are fused to the surface of the underlying jawbone. They have no roots and are attached to the edge of the jawbone by fibrous membrane e.g., fishes, amphibians and some reptiles.
Pleurodont:
The teeth are attached to the inner-side of the jawbone. The tooth touches the bone only with the outer surface of its root. In acrodont and pleurodont types of dentition, there are no roots, and nerves and blood vessels do not enter the pulp cavity at the base, e.g., Necturus (Amphibia) and some reptiles.
According to the Succession or Replace¬ment of Teeth:
Comparative account of vertebrate heartSUTAPA DATTA
The document compares the heart structures of various vertebrate groups. It notes that hearts evolve from two longitudinal tubes fusing in the mesoderm. The simplest hearts are found in cephalochordates like Branchiostoma, consisting of a sinus venosus, auricle and ventricle. Lampreys and harks have slightly more complex hearts with these chambers plus a conus arteriosus. Elasmobranch fish hearts are S-shaped tubes with these chambers. Teleost fish hearts are two-chambered with a sinus venosus, auricle, ventricle and bulbus arteriosus. Lungfish have transitional three-chambered hearts. Higher vertebrates evolve four-chamber
succession of kidneys in a vertebrate seriesNaman Sharma
1. Kidneys evolve from the primitive archinephros to the pronephros, mesonephros, and finally the metanephros, which is the definitive kidney of amniotes.
2. The pronephros is the first to develop and is functional only in embryonic or larval stages. The mesonephros follows and is functional in embryos and adults of some species.
3. The metanephros is the adult kidney of amniotes and shows greater complexity with millions of nephrons and additional structures like loops of Henle in mammals.
This document provides information about the cardiovascular systems of humans, ruminants, birds, and fish. It describes the key components of the cardiovascular system including the heart, blood vessels, and blood. For each species, it highlights some distinguishing features of their circulatory system, such as birds having a more efficient 4-chambered heart than other vertebrates and fish having the simplest heart with only two chambers. The document also provides typical heart rate ranges for different species.
osmoregulation in invertebrates- it is a processes by which any organisms maintains the fluid and salt balance of its body, which is important for proper functioning of organs .
INTRODUCTION
The jaw (Upper and lower) is any opposable articulated structure at the entrance of the mouth.
It is typically used for grasping and manipulating food.
Jaw suspension means the fusion of upper jaw and lower jaw or skull for efficient biting.
There are different ways in which these attachments are attained depending upon the modifications in visceral arches in vertebrates.
In most vertebrates, the jaws are bony or cartilaginous and oppose vertically.
The vertebrate jaw is derived from the most anterior two pharyngeal arches supporting the gills, and usually bears numerous teeth.
The vertebrate jaw probably originally evolved in the Silurian period and appeared in the Placoderm fish which further diversified in the Devonian.
It is believed that the hyoid system suspends the jaw from the brain case of the skull, permitting great mobility of the jaws.
The original selective advantage offered by the jaw may not be related to feeding, but rather to increased respiration efficiency.
The jaws were used in the buccal pump (observable in modern fish and amphibians) that pumps water across the gills of fish or air into the lungs in the case of amphibians.
Over evolutionary time the more familiar use of jaws (to humans), in feeding, was selected for and became a very important function in vertebrates. Many teleost fish have substantially modified jaws for suction feeding and jaw protrusion, resulting in highly complex jaws with dozens of bones involved.
Jaw Suspension or Suspensoria:
The method by which the upper and lower jaws are suspended or attached from the chondrocranium is known as jaw suspension or suspensorium.
Amongst the visceral arches, the first (mandibular) arch consists of
= a dorsal palato pterygoquadrate bar forming the upper jaw,
= and ventral Meckel’s cartilage forms the lower jaw.
The second (hyoid) arch consists of = a dorsal hyomandibular supporting and suspending the jaws with the cranium, and a ventral hyoid.
The remaining visceral arches support the gills and are, hence, called branchial arches. Thus, splanchnocranium forms the jaws and suspends them with the chondrocranium.
The document summarizes the development of the kidney in vertebrates. It discusses the three main stages of kidney development: (1) the pronephros, which is an initial kidney that forms but then degenerates; (2) the mesonephros, which briefly functions as a kidney in some species; and (3) the metanephros, which develops from the intermediate mesoderm and ureteric buds and forms the permanent kidney through reciprocal interactions between epithelial and mesenchymal tissues. The ureteric buds branch and induce surrounding mesenchyme to form nephrons, while the mesenchyme causes further branching of the ureteric ducts, resulting in the
The document discusses the integumentary system across different chordate groups. It describes the key features of skin in protochordates, cyclostomes, fish, amphibians, reptiles, birds, and mammals. The integumentary system generally consists of an outer epidermis layer and inner dermis layer, with variations in features like keratinization, glands, scales/feathers/hair, and pigment cells across groups. The skin serves protective, sensory, and excretory functions for chordates.
This document discusses various forms of parental care exhibited by amphibians to increase offspring survival. It outlines nine types of parental care observed in amphibians: 1) selection of safe egg-laying sites, 2) frothing of water around eggs, 3) defending egg territories, 4) building nests from mud, leaves, or plant shoots, 5) direct development from egg to juvenile, 6) carrying eggs attached to the body, 7) carrying larvae between water bodies, 8) brooding eggs in vocal sacs or pouches on the back, and 9) retaining eggs internally in a uterus for viviparous development.
Visceral arches are pieces of cartilage or bone that support the pharyngeal region in vertebrates and help attach the jaws to the skull. There are typically 7 pairs of visceral arches that are modified differently in vertebrate groups depending on the presence of gills and jaw suspension type. Cyclostomes lack identifiable typical cartilage patterns and have a fused branchial basket to support gills. Elasmobranchs have a full set of visceral arches and 3 unpaired branchial cartilages. Bony fishes have modifications for jaw movement and suspension with a reduced last arch. Amphibians have 6 arches as larvae with the last 3 bearing gills, and modifications form their air breathing
Comparative Anatomy of Respiratory System of VertebratesRameshPandi4
The document discusses the comparative anatomy of the respiratory systems of various vertebrates. It describes how respiration occurs through the skin, gills, lungs, and gas bladders in different organisms. It explains key differences in respiratory structures between cartilaginous fishes, bony fishes, and jawless fishes. Mechanisms of gas exchange are covered for fishes, as well as respiratory organs and processes for amphibians, reptiles, birds, and mammals.
Blood vessel development occurs through vasculogenesis and angiogenesis. The major vessels form through vasculogenesis while the rest develop via angiogenesis. During development, the aortic arches form pairs that connect the aortic sac to the dorsal aortae and pharyngeal arches. Most of the arches regress except for parts that form portions of the carotid, pulmonary and subclavian arteries. Other changes accompany arch regression like dorsal aorta obliteration and heart descent into the thorax. The vitelline and umbilical arteries supply the gut and placenta, respectively, and remodel after birth. Coronary arteries arise from angioblasts and the epicardium, connecting to the aorta
Vertebrates generally have a ventral aorta and dorsal aorta, with six pairs of aortic arches that branch off and pass through gill arches. In fishes, the six pairs of arches each pass blood through the gills. Over time, some arches reduce or disappear, with sharks having five pairs and most fish having four functional pairs. In land vertebrates like reptiles, amphibians, birds and mammals, the number of arches reduces further to three pairs or less as lungs replace gills and the circulatory system evolves to separate oxygenated and deoxygenated blood.
1) In vertebrate embryos, the major arterial channels are the ventral and dorsal aortas, connected by 6 pairs of aortic arches.
2) The aortic arches undergo modifications from lower to higher vertebrates as respiration shifts from gills to lungs. Lower vertebrates like fish retain more pairs of arches, while mammals and birds retain only 3 pairs.
3) In terrestrial vertebrates, the 3 remaining arches are the 3rd, 4th, and 6th arches, connected to the divided ventricle. The 4th arch forms the systemic artery and the 6th forms the pulmonary trunk.
1. The aortic arches develop from the primitive aorta and pharyngeal arch arteries during embryonic development.
2. The right and left 3rd aortic arches normally form the common carotid arteries, while the 4th arches form the subclavian arteries.
3. A number of anomalies can occur if parts of the arches fail to regress as normal or persist that typically regress. This includes double aortic arch, right aortic arch, patent ductus arteriosus, and interrupted aortic arch.
4. Proper development and regression of the aortic arches is required for normal formation of the branches of the aortic arch.
The aortic arches give rise to important adult structures through a process of remodeling. The dorsal aortae initially form as paired vessels but fuse caudally to form the descending aorta. Changes in the aortic arch system result in obliteration of some arches and portions of the dorsal aortae. This remodeling leads to derivatives like the brachiocephalic artery, common carotid arteries, subclavian arteries, and arch of the aorta. The pattern of remodeling differs between the right and left sides, resulting in anomalies such as coarctation of the aorta, double aortic arch, and right aortic arch.
The document summarizes the development of the cardiovascular system from formation of the heart tube through septation and development of arteries and veins. Key events include:
1) Lateral plate mesoderm splits to form the pericardial cavity and heart-forming regions that fuse to form the endocardial heart tube.
2) The heart tube develops five dilations that undergo looping to form heart structures and septa divide the heart into chambers.
3) Arteries develop from aortic arches and dorsal/ventral vessels while veins form from vitelline, umbilical and cardinal veins.
This document summarizes vascular development from the arterial and venous systems. It describes how the arterial system develops from aortic arches which give rise to major arteries. It also describes how the venous system initially develops from vitelline, umbilical and cardinal veins. Defects that can occur in vascular development are also discussed such as patent ductus arteriosus, coarctation of the aorta and interrupted aortic arch.
Fishes have a closed circulatory system with a two-chambered heart that pumps deoxygenated blood to the gills and then oxygenated blood throughout the body in a single loop. The heart consists of four parts - the sinus venosus, atrium, ventricle, and bulbus arteriosus. Prawns have an open circulatory system where blood is pumped into body cavities and tissues are surrounded by blood, with no true blood vessels. Their circulatory system includes a heart, arteries that branch throughout the body, and blood sinuses where arteries end instead of forming capillaries.
The circulatory system of the shark Scoliodon consists of blood, a heart, arteries and veins. The heart has four chambers - sinus venosus, auricle, ventricle, and conus arteriosus. Blood enters the heart through the sinus venosus and is pumped through the arteries to the body and gills before returning to the heart through the veins to complete the circulatory loop. Valves in the heart prevent backflow of blood between chambers during pumping.
The arterial system of Scoliodon consists of afferent and efferent branchial arteries. Afferent branchial arteries carry impure blood from the ventral aorta to the gills. Efferent branchial arteries collect purified blood from the gills and carry it to the dorsal aorta. There are five pairs of afferent branchial arteries that arise from the ventral aorta and supply blood to the gills. Nine efferent branchial vessels on each side collect blood from the gill capillaries and join to form loops and arteries that unite to form the dorsal aorta. The dorsal aorta runs the length of the body and gives rise to various arteries that supply different organs.
The circulatory system transports nutrients, oxygen, carbon dioxide and waste through the body. Components include blood, heart and blood vessels. Vertebrates have a closed circulatory system with blood contained within vessels. The heart pumps blood through arteries, capillaries and veins. Early vertebrates had simpler hearts but over time hearts evolved to have more chambers and septa to separate oxygenated and deoxygenated blood. Birds and mammals have four-chambered hearts with complete septation allowing for dual circulation.
1) The first arteries to develop in the embryo are the primitive aortae, consisting of the ventral aorta, first aortic arch, and dorsal aorta.
2) The aortic arches arise from the aortic sac and terminate in the dorsal aorta. The first two pairs of arches usually disappear, while the third, fourth, and sixth pairs form important adult structures.
3) Derivatives of the third arch include the common and internal carotid arteries. Derivatives of the fourth arch include parts of the aortic arch and subclavian arteries. Derivatives of the sixth arch include the pulmonary arteries.
Circulatory systems transport nutrients, oxygen, waste and more throughout an animal's body. There are two main types - open systems where blood flows freely through tissues, and closed systems where blood remains confined to vessels. The vertebrate heart has chambers and valves that work in a coordinated cycle to pump blood. Contractions are regulated by electrical signals from a pacemaker, moving blood to the lungs and throughout the body in separate oxygenated and deoxygenated loops.
The head and neck region receives most of its blood supply from the carotid and subclavian arteries. The common carotid arteries branch into the internal and external carotid arteries. The internal carotid arteries supply the brain while the external carotid arteries supply the neck and face. Venous drainage from the head and neck flows into the internal and external jugular veins and subclavian veins and returns blood to the heart.
This document provides an overview of heart development and comparative anatomy across vertebrates. It describes how the heart originates from mesodermal tissue and develops into a tubular structure. Across species, the heart evolves from a two-chambered structure in fish to a four-chambered heart with complete separation of oxygenated and deoxygenated blood in mammals. Key developments include the formation of four chambers, completion of the interatrial and interventricular septa, and separation of pulmonary and systemic circulation. Differences in heart structure across fish, amphibians, reptiles, birds, and mammals are also summarized.
This document provides information about the circulatory system of a rat. It includes labeled diagrams showing the major arteries and veins of the rat. The text then provides instructions to trace various branches of arteries and veins, labeling key blood vessels like the aortic arch, abdominal aorta, renal arteries, inferior and superior vena cava, and hepatic vein. Checkboxes are included for the student to check off structures as they are located during the dissection.
The heart begins developing in the third week of gestation from mesodermal cells that form the cardiac tube. This tube undergoes looping and partitioning to form the four chambers. Septa form between the atria and ventricles, dividing them into left and right sides. In fetal circulation, three shunts allow oxygenated blood from the placenta to bypass the lungs and mix with deoxygenated blood before returning to the placenta. After birth, closure of the shunts and changes in hemodynamics establish the postnatal circulation.
The document provides information about the cardiovascular system including:
- The cardiac cycle which describes how blood flows through the heart in two circuits, pulmonary and systemic.
- Key structures of the heart including the four chambers, valves, and major blood vessels.
- The conduction of blood through arteries and veins in the body, including those in the neck, arms, and legs.
- Additional details are given about heart anatomy and circulation to specific regions like the coronary arteries and veins.
The document discusses the structure and function of hearts in humans, reptiles, and fish. It describes that the human heart has four chambers consisting of two atria and two ventricles separated by a septum. Reptiles typically have a three-chambered heart with two atria and one partially divided ventricle, except for crocodiles which have a four-chambered heart like mammals and birds. Fish have the simplest heart consisting of only two chambers, one atrium and one ventricle, without a septum.
The document compares the heart structure of humans, reptiles, and fish. It notes that while the human heart has four chambers, reptile hearts typically have three chambers except for crocodiles which have four chambers like humans. Fish have the simplest heart structure with only two chambers. The document also discusses differences in circulatory systems, the presence of septums between ventricles, and the role of the sinus venosus between the species.
Similar to EVOLUTION OF AORTIC ARCHES IN VERTEBRATES (20)
This presentation includes basic of PCOS their pathology and treatment and also Ayurveda correlation of PCOS and Ayurvedic line of treatment mentioned in classics.
This presentation was provided by Steph Pollock of The American Psychological Association’s Journals Program, and Damita Snow, of The American Society of Civil Engineers (ASCE), for the initial session of NISO's 2024 Training Series "DEIA in the Scholarly Landscape." Session One: 'Setting Expectations: a DEIA Primer,' was held June 6, 2024.
How to Add Chatter in the odoo 17 ERP ModuleCeline George
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How to Build a Module in Odoo 17 Using the Scaffold MethodCeline George
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How to Manage Your Lost Opportunities in Odoo 17 CRMCeline George
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हिंदी वर्णमाला पीपीटी, hindi alphabet PPT presentation, hindi varnamala PPT, Hindi Varnamala pdf, हिंदी स्वर, हिंदी व्यंजन, sikhiye hindi varnmala, dr. mulla adam ali, hindi language and literature, hindi alphabet with drawing, hindi alphabet pdf, hindi varnamala for childrens, hindi language, hindi varnamala practice for kids, https://www.drmullaadamali.com
Walmart Business+ and Spark Good for Nonprofits.pdfTechSoup
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Strategies for Effective Upskilling is a presentation by Chinwendu Peace in a Your Skill Boost Masterclass organisation by the Excellence Foundation for South Sudan on 08th and 09th June 2024 from 1 PM to 3 PM on each day.
ISO/IEC 27001, ISO/IEC 42001, and GDPR: Best Practices for Implementation and...PECB
Denis is a dynamic and results-driven Chief Information Officer (CIO) with a distinguished career spanning information systems analysis and technical project management. With a proven track record of spearheading the design and delivery of cutting-edge Information Management solutions, he has consistently elevated business operations, streamlined reporting functions, and maximized process efficiency.
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Date: May 29, 2024
Tags: Information Security, ISO/IEC 27001, ISO/IEC 42001, Artificial Intelligence, GDPR
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2. ☆SYNOPSIS☆
• 1)Introduction
• 2) Basic plan
• 3) Development of the basic pattern and associated arteries
• 4) Modification of aortic arches
• 5) Scheme of evolution
• PRIMITIVE VERTEBRATES
• FISHES
• TETRAPODS
• AMPHIBIANS
• REPTILES
• BIRDS
• MAMMALS
• 6)Evolutionary Significance of Aortic Arches
• 7)Conclusion
• 8)Reference
3. 1) INTRODUCTION:“Theaorticarchesare the blood vessels
thatsupplythe pharyngeal arches,and theyserveas a
communication betweenthe ventraland dorsalaortae.”
• In typical vertebrate embryo, major arterial channels: Ventral aorta,
Dorsal aorta and 6 pairs of Aortic Arches connecting Ventral & Dorsal
aorta.
• Blood leaves heart through ventral aorta and runs forward-
>midventrally, beneath the pharynx branches -> anteriorly into a pair
of External Carotid Arteries into Head.
• Each aortic arch consists of a Ventral Afferent Branchial Artery
carrying venous blood to capillaries in a gill Dorsal Efferent Branchial
Artery taking arterial blood from the gills. efferent branchial arteries
of the same side join dorsally to form a Lateral Dorsal Aorta/ Radix.
Radix extend into head as Internal Carotid Artery.
4. 2) BASIC PLAN:
• Continuous vessels.
• Typical number 6 pairs (7 in primitive shark, many in
cyclostome).
• Developed in a similar fashion (anterior to posterior).
• First (I): Mandibular arch (proceed upward on either side of
pharynx).
• Second (II): Hyoid arch.
• Rest: III (1st branchial), IV (2nd branchial), V (3rd branchial),
VI (4th branchial) aortic arch.
6. 3)DEVELOPMENTOF BASIC PATTERN AND
ASSOCIATED ARTERIES:
● l. The first pair of aortic arches is formed by the curving of the ventral
aorta into the primitive dorsal aorta. This arch is hidden in the
mandibular arch and participates in formation of the maxillary artery,
and contribute to the external carotid artery.
• II. The second pair of aortic arches make their appearance in the
middle of week 4. They cross the second branchial arches and give rise
to the stapedial and hyoid arteries.
• III. The third pair of aortic arches make their appearance at the end of
week 4. They give rise to the common carotids and proximal portions
of the internal carotid arteries. The latter are the short cephalic
prolongations of the primitive dorsal aortas and are associate with
development and supply of the brain.
7. • (A)THE INTERNAL CAROTID ARTERIES are secondarily attached to the
cranial portions of the dorsal aortas, which form the remainder of the carotid
artery.
• (B) THE ORIGIN OFTHE EXTERNAL CAROTID ARTERIES is controversial, but in
later stages of development, they are found to sprout from aortic arch II
(Arch I, however, has been implicated in its developmental contribution)
IV. The fourth pair of aortic arches make their appearance shortly after the
third arches, at the end of week 4. Their development is different for the
right and left sides.
A.ON THE RIGHT SIDE arch IV forms the proximal portion of the right
subclavian artery and is continuous with the seventh segmental artery
• 1. The caudal portion of the right primitive dorsal aorta disappears
• 2. The distal portion of the subclavian artery forms from the right dorsal
aorta and the right seventh intersegmental artery
8. B. ON THE LEFT SIDE arch IV persists as the arch of the aorta, which grows
significantly and is continuous with the primitive left dorsal aorta.1. The
left subclavian artery (or seventh segmental) arises directly from the
aorta.
C. THE SHORT PORTION of the right primitive ventral aorta, which persists
between arches IV and VI, forms the brachiocephalic arterial trunk and
the first portion of the aortic arch.
V. The fifth pair of aortic arches: in 50% of embryos, these arches are
rudimentary vessels that degenerate with no derivatives. In fact, they
may never even develop.
VI. The sixth pair of aortic arches make their appearance in the middle of
week 5 and give rise to the right and left pulmonary arteries. After
pulmonary vascularization is established, the communication with the
corresponding primitive dorsal aorta regresses.
9. 4)Modification of aortic arches in different
vertebrates during evolution is based on
following:
1) The number of aortic arches is different in different adult
vertebrates but They built on same fundamental plan in
embryonic life .
2) The differences in number of aortic arches in different
vertebrates are due to the complexity of heart circulation In
the mode of living from aquatic to terrestrial respiration.
3) There is progressive reduction of aortic arches in different
vertebrates series during evolution.
10. ●PRIMITIVE VERTEBRATES》
• Branchiostoma (Amphioxus): nearly 60 pairs of aortic arches are
present, connecting the ventral and dorsal aortae.
• Petromyzon: 7 pairs of aortic arches are found.
• Other cyclostomes: varies from 6 (Myxine) to 15 pairs (Eptatretus).
●Cyclostomes: 1. In lampreys (Petromyzon) there are eight pairs of aortic
arches and in hag fishes (Bdellostoma) there are fifteen pairs. The aortic
arch is divided into afferent branchial artery and efferent branchial
artery.2. In lampreys each aortic arch divides and sends branches to the
posterior hemi-branch and anterior hemi-branch of the adjacent gill
pouch. In hagfishes each arch supplies to the hemi—branch of a single gill-
pouches.
11. ●FISHES》
• Primitive fishes, represented by sharks, have six paired gill arches. In
teleosts, the gill arch arteries are reduced to form four pairs in the
caudal branchial arches. First pair (mandibular) and second pair
(hyoidean) are lost. In most fishes, the aortic arches deliver
deoxygenated blood to the respiratory surfaces of the gills and then
distribute oxygenated blood to tissues of the head (via the carotids)
and remainder of the body (via the dorsal aortae).
• Among dipnoans there are four or five aortic arches that develop from
the ventral aorta which supply blood to the gills. In the Protopterus the
aortic arches retain second, third, fourth, fifth and sixth. The arches like
the fish have afferent and efferent divisions. They have two pulmonary
arteries which develop from the efferent division of the sixth arch.
12. •Elasmobranchs (Cartilaginous fishes):
1. Generally there are five pairs of aortic arches in elasmobranchs but in
some cases there is a variation. In Hexanchus there are six pairs of aortic
arches. In Heptranchias there are seven pairs.
2. In elasmobranchs the first pair of aortic arches (mandibular) disappear.
Second to sixth pair of aortic arches (II-VI) persist as branchial arteries. Each
aortic arch is divided into afferent and efferent branchial arteries.
3. Five pairs afferent arteries arise from ventral aorta and supply
deoxygenated blood to the respective gills. The ventral aorta divides into two
branches, called innominate arteries which again bifurcate into the first and
second afferent branchial arteries. From the gills the oxygenated blood is
collected by efferent branchial arteries.
4. In elasmobranchs there are nine pair’s efferent branchial arteries of which
the first eight arteries form a series of four complete loops but ninth efferent
branchial artery collects blood from the demi- branch of the fifth gill pouch.
13. •Teleosts(Bony fishes):
• 1. In teleosts there are four pairs of aortic arches. First pair
(mandibular) and second pair (hyoidean) are lost, only four pairs
(third to sixth) persist as branchial arteries. Four pairs afferent
branchial arteries arise from the ventral aorta.
• 2. They supply deoxygenated blood to the gills for aeration. The
ventral aorta bifurcates anteriorly to form the first pair of
afferent branchial arteries. In sturgeon (Acipenser) and Amia
each afferent branchial arch bifurcates as in elasmobranchs.
14. •Dipnoans(Lung fishes):
1. In lungfishes, as in other bony fishes, the first pharyngeal slit is
reduced to a spiracle that has no respiratory function.
2. Its associated aortic arch (I) is reduced as well as the Iind arch.
3. In the Australian lungfish, Neoceratodus, the remaining five
pharyngeal slits open to fully functional gills supplied by four aortic
arches (III–VI).
4. In the African lungfish, Protopterus, the functional gills are reduced
further. The third and fourth gills are absent entirely, but their aortic
arches (III–IV) persist.
5. In all lungfishes, the efferent vessel of the most posterior aortic arch
(VI) gives rise to the pulmonary artery but maintains its connection to
the dorsal aorta via the short ductus arteriosus.
17. •AMPHIBIANS》
•In amphibians, the first two aortic arches (I, II) disappear early in
development. The pattern of the remaining arches differs between larvae
and metamorphosed adults.
•In adult amphibians, the gill arches are lost and the aortic arch
vasculature remains bilaterally symmetrical.
•Oxygenated and deoxygenated blood enter the ventricle through the
right and left atrium and leaves the heart through a single outflow tract
containing a spiral valve.
•The aortic arches contribute to the pulmonary arch, the arterial circuit to
the lungs, and the systemic arches, the arterial circuits to the rest of the
body. The carotid arteries still bear the primary responsibility for
supplying blood to the head, but now they usually branch from one of the
major systemic arches.
18. (1) URODELES:
• Aortic arches show modification due to loss of gills and
appearance of the lungs.
• In urodeles there are external gills present as respiratory organs
in addition to lungs.
• The III, IV, V and VI aortic arches are present, though the fifth
pair is much reduced in Siren, Amphiuma and Necturus.
• The lateral dorsal aortae between the III and IV aortic arches
persist as a vascular connection, the ductus caroticus.
• The VI aortic arch forms the pulmocutaneous arch or artery on
either side taking blood to the lung and skin.
• It also retains a connection with the lateral dorsal aorta known
as a ductus arteriosus (duct of Botalli).
19. (2) ANURANS:
•In the larva of anuran (frog tadpole), arrangement of aortic arches is like an
adult urodele due to presence of gills. At metamorphosis, with the loss of
gills, I, II, and V aortic arches disappear completely, only the IIIrd, Ivth and
Vlth aortic arches are present.
•The lateral dorsal aorta between the third and fourth aortic arches (ductus
caroticus) also disappears. Thus, the third aortic arch along with a part of the
ventral aorta becomes the carotid arch carrying oxygenated blood to the
head region.
•The fourth aortic arch along its lateral dorsal aorta forms the systemic
arch.The sixth aortic arch becomes the pulmocutaneous arch supplying
venous blood to lungs and skin.The ductus arteriosus disappears during
metamorphosis. Thus, adult anurans have only III,IV &VI aortic arches.These
are also retained by amniotes.
20. •REPTILES》
In reptiles, the gills are fully replaced by lungs. With the partial separation of the
ventricle into two parts, the distal portion of the conus arteriosus and the entire ventral
aorta are split into three vessels, i.e., two aortic or systemic and one pulmonary.
• Only III, IV and VI aortic arches are present.
• Right systemic arch (IV) arise from the left ventricle carrying oxygenated blood to the
carotid arch (III).
• The left systemic (IV) and pulmonary aortae (VI) take their origin from the right
ventricle.
• The left systemic carries deoxygenated or mixed blood to the body through dorsal
aorta. While the pulmonary artery takes deoxygenated blood to the lungs.
• The ductus caroticus disappears, but it persists in snakes and some lizards (Uromastix).
• The ductus arteriosus disappears in most reptiles though it persists in a reduced form
in sphenodon and some turtles.
21. •BIRDS》
1. In birds, the right systemic arch becomes predominant. The bases of the aortic arch, the
right aortic arch (IV), and the adjoining section of the right dorsal aorta form the right
systemic arch during embryonic development.
2. Its opposite member, the left systemic arch, never fully develops.
3. The carotids arise generally from the same components of the aortic arches as in reptiles
(aortic arch III and parts of the ventral and dorsal aortae), and they branch from the right
systemic arch. However, the paired subclavians to the wings arise from the internal carotids
and not from the dorsal aorta.
4. The common carotids and subclavians supply the head and forelimbs, respectively. The
common carotids can branch from the right systemic arch separately, or both can join to form
a single carotid.
5. A short but major vessel, the brachiocephalic artery, is present in a few reptiles, especially
turtles, but serves as the major anterior vessel in many birds. It too branches from the right
systemic arch. Beyond this junction of the brachiocephalic artery, the systemic arch curves
posteriorly to supply the rest of the body. In birds as in reptiles, the pulmonary arch forms
from the bases of the paired sixth arch and their branches to supply both lungs.
22. ●MAMMALS》
1. Up to six aortic arches arise in the mammalian embryo, but only three persist in the
adult as the major anterior arteries: the carotid arteries, the pulmonary arch, and the
systemic arch.
2. The carotid arteries and pulmonary arch are assembled from the same arch
components as those of reptiles. The mammalian carotids arise from the paired aortic
arches (III) and parts of the ventral and dorsal aortae.
3. The pulmonary arch forms from the bases of the paired sixth arch and its branches.
4. The systemic arch arises embryonically from the left aortic arch (IV) and left member of
the paired dorsal aorta, and therefore is a left systemic arch in mammals. The common
carotids may share a brachiocephalic origin or branch independently from different points
on the aortic arch.
5. The other notable difference in mammals is in the formation of the subclavian arteries.
The left subclavian departs from the left systemic arch in mammals. The right subclavian,
however, includes the right aortic arch (IV), part of the adjoining right dorsal aorta, and
the arteries that grow from these into the right limb.
23. 7)Evolutionary Significance of Aortic Arches:
A) In most fishes, the aortic arches deliver deoxygenated blood to the
respiratory surfaces of the gills and then distribute oxygenated blood to
tissues of the head (via the carotids) and remainder of the body (via the
dorsal aortae).
b) In lungfishes and tetrapods, the aortic arches contribute to the pulmonary
arch, the arterial circuit to the lungs, and the systemic arches, the arterial
circuits to the rest of the body. The carotid arteries still bear the primary
responsibility for supplying blood to the head in tetrapods, but now they
usually branch from one of the major systemic arches.
c) The double systemic arches (left and right) present in amphibians and
reptiles become reduced to a single systemic arch— the right in birds, the
left in mammals.
24. D) Although birds and mammals share many similarities, including
endothermy, active lives, and diverse radiation, they arose out of
different reptilian ancestries. Any similarities in their cardiovascular
anatomies represent independent evolutionary innovations.
e) The basic six-arch pattern of aortic arches is a useful concept that
allows us to track aortic arch derivatives and organize the diversity of
anatomical modifications we encounter. Furthermore, the appearance of
six aortic arches during the embryonic development of living
gnathostomes suggests that this is the ancestral pattern.
f) However, as we have seen, the actual adult anatomy can be quite
varied among different species.
26. 8) Conclusion:
The aortic arches or pharyngeal arch arteries or branchial arches
develop from the aortic sac, with a pair of branches (right and left)
traveling within each pharyngeal arch and ending in the dorsal aorta.
Initially, the arches arise in symmetrical pairs, but after remodeling,
the arches become asymmetric, and several of the arches regress.
From above discussion it is becomes evident that there is a slow and
gradually reduction in the number of aortic arches from lower to
higher vertebrates.
27. 9)REFERENCES:
1)Comparative anatomy of vertebrates by R.K Saxena
And Sumitra Saxena.
2)Comparative anatomy of vertebrates by Dr. Jyoti kamal deep
And Manideep Raj.
3)A TextBook of Cordates: Dr.H.S.Bhamrah
And Kavita Juneja.
4)Modern textbook of zoology vertebrates by R.L.Kotpal
5)Unifie Zoology(BSc-Second year)
6)https://www.zoologytalks.com/aortic-arches-in-vertebrates/
7)https://www.britannica.com/science/aortic-arch
8)http://uam-web2.uamont.edu/facultyweb/huntj/Comparative—
Aortic%20Arch%20Modifications.htm
9)Internet.