Class 11 Biology NCERT Solutions
~5 min readThe complete NCERT exercise solutions for Chapter 15, Body Fluids and Circulation — 14 questions from Ex, each worked through step by step in the CBSE marking pattern. The composition and properties of blood and lymph, the human circulatory system, cardiac cycle, cardiac output and disorders.
Chapter 15 carries 1 exercise question, numbered Ex. All of them are solved step by step on this page, along with the chapter's key formulas and exam pointers.
This chapter is the longest of the three human physiology chapters and the fourteen questions below are the complete rationalised NCERT exercise set for Chapter 15, worked in the board pattern. The material is of three quite different kinds, and the questions divide along those lines. The first block is descriptive, on blood, plasma, the formed elements, the blood groups, the clotting mechanism and lymph. The second block is numerical and definitional, on the ABO and Rh groups, the cardiac cycle, the stroke volume and the cardiac output. The third block is functional, on the evolution of the vertebrate heart, the nodal tissue and the conduction system, the regulation of the heart, the heart sounds and the ECG. The single most examined group of questions is the last one, because the pacemaker, the atrio-ventricular bundle, the myogenic heart and the heart sounds all recur from one paper to another, whereas the descriptive blocks are more secure once the terms are known.
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14Exercise questions
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The formed elements of blood are erythrocytes, leucocytes and platelets, and together they constitute nearly 45 per cent of the blood. Erythrocytes, or red blood cells, are the most abundant of all the cells in blood, a healthy adult man having on an average 5 millions to 5.5 millions of RBCs per mm3, and they are formed in the red bone marrow in the adults. They are devoid of nucleus in most of the mammals and are biconcave in shape, and they have a red coloured, iron containing complex protein called haemoglobin, hence the colour and the name of these cells. Their major function is the transport of respiratory gases, these haemoglobin molecules playing a significant role in it, and a healthy individual has 12 to 16 g of haemoglobin in every 100 ml of blood. Their average life span is 120 days, after which they are destroyed in the spleen, which is called the graveyard of RBCs. Leucocytes, or white blood cells, are colourless due to the lack of haemoglobin, and they are nucleated and relatively lesser in number, averaging 6000 to 8000 per mm3 of blood, and are generally short lived. Their major function is defence of the body against infection. They fall into granulocytes, namely neutrophils, eosinophils and basophils, and agranulocytes, namely lymphocytes and monocytes. Neutrophils are the most abundant at 60 to 65 per cent of the total WBCs, and neutrophils and monocytes, the latter at 6 to 8 per cent, are phagocytic cells which destroy foreign organisms entering the body. Basophils are the least numerous at 0.5 to 1 per cent and secrete histamine, serotonin, heparin and similar substances, being involved in inflammatory reactions. Eosinophils, at 2 to 3 per cent, resist infections and are also associated with allergic reactions, while lymphocytes, at 20 to 25 per cent, are of two major types, the B and T forms, and both B and T lymphocytes are responsible for the immune responses of the body. Platelets, also called thrombocytes, are cell fragments produced from megakaryocytes, which are special cells in the bone marrow, and blood normally contains 1,500,00 to 3,500,00 platelets per mm3. Their major function is clotting, since platelets can release a variety of substances most of which are involved in the coagulation or clotting of blood, and a reduction in their number can lead to clotting disorders which will lead to excessive loss of blood from the body. In short, the erythrocytes transport the respiratory gases, the leucocytes defend the body against infection, and the platelets bring about clotting.
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Plasma proteins are important for three distinct reasons, one for each of the major proteins. Plasma is a straw coloured, viscous fluid constituting nearly 55 per cent of the blood, of which 90 to 92 per cent is water and proteins contribute 6 to 8 per cent, and the major proteins are fibrinogen, globulins and albumins. Fibrinogen is needed for the clotting or coagulation of blood, since it is converted into the fibrin threads that form the clot, so without it a wound could not be sealed. Globulins are primarily involved in the defence mechanisms of the body, so they are the plasma's contribution to immunity. Albumins help in osmotic balance, so they maintain the osmotic pressure of the blood and thereby the correct distribution of water between the blood and the tissues. Plasma proteins also matter in two further ways. Plasma contains small amounts of minerals such as Na+, Ca++, Mg++, HCO3- and Cl-, and it carries glucose, amino acids and lipids, since these are always in transit in the body. Most importantly of all, the factors for the coagulation or clotting of blood are already present in the plasma in an inactive form, ready to be activated at the site of an injury, and plasma from which the clotting factors have been removed is called serum. So plasma proteins are indispensable for sealing wounds, for defence and for osmotic balance, and they also carry the entire dormant clotting cascade.
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The correct matching is (a) with (iii), (b) with (v), (c) with (ii), (d) with (i) and (e) with (iv). Eosinophils match Resist Infections, since eosinophils constitute 2 to 3 per cent of the total WBCs and the chapter states that they resist infections and are also associated with allergic reactions. RBC matches Gas transport, because the red coloured, iron containing complex protein in the erythrocytes is haemoglobin and these molecules play a significant role in the transport of respiratory gases, a healthy individual having 12 to 16 g of haemoglobin in every 100 ml of blood. AB Group matches Universal Recipient, because the AB group has both antigens A and B on its RBCs and nil antibodies in its plasma, so persons with AB group can accept blood from persons with AB as well as from the other groups of blood and are therefore called universal recipients. Platelets match Coagulation, since platelets can release a variety of substances most of which are involved in the coagulation or clotting of blood, and a reduction in their number can lead to clotting disorders which lead to excessive loss of blood from the body. Systole matches Contraction of Heart, because systole is the contraction phase of the cardiac cycle, the atrial systole being the simultaneous contraction of both atria and the ventricular systole the contraction of the ventricular muscles, systole and diastole of both the atria and ventricles together constituting the cardiac cycle.
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We consider blood to be a connective tissue because the chapter defines it as one, blood being a special connective tissue consisting of a fluid matrix, plasma, and formed elements. The reason is the structure rather than the label. A connective tissue is characterised by cells scattered in an abundant matrix, and in blood this is exactly what is found: plasma is a straw coloured, viscous fluid constituting nearly 55 per cent of the blood, and the formed elements, namely erythrocytes, leucocytes and platelets, are suspended in it and constitute the remaining nearly 45 per cent. The cells are not packed closely together as they would be in an epithelial tissue, and the erythrocytes are themselves biconcave and devoid of nucleus in most of the mammals, so the tissue is a suspension of free cells in a fluid matrix. The function confirms the classification. Blood performs long-distance transport, carrying oxygen, nutrients, hormones and other essential substances to the cells and carrying carbon dioxide and other waste away for elimination, and transport of this kind is a characteristic connective-tissue function. The origin agrees as well, since the heart that pumps this fluid is described as a mesodermally derived organ, and mesoderm is the germ layer from which connective tissues arise. So blood qualifies as a connective tissue on its matrix, on its suspended and non-adherent cells, on its transport function and on its developmental origin.
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Lymph and blood differ in origin, composition, route and function. In origin, blood is the fluid circulated by the heart through the blood vascular system, the network of closed branching blood vessels, whereas lymph begins as interstitial fluid or tissue fluid. This tissue fluid arises when, as the blood passes through the capillaries in tissues, some water along with many small water soluble substances move out into the spaces between the cells of the tissues, leaving the larger proteins and most of the formed elements in the blood vessels. In composition, the consequence of this filtration is that lymph is poor in proteins and lacks the formed elements, since the erythrocytes, leucocytes and platelets are left behind in the blood vessels, whereas blood is rich in proteins and in formed elements. Lymph does carry its own specialised lymphocytes, which are responsible for the immune responses of the body, and its mineral distribution is the same as that of plasma. In route, the fluid that becomes lymph is collected by an elaborate network of vessels called the lymphatic system, which drains it back to the major veins, so lymph is a one-way overflow that rejoins the blood, whereas blood is continuously circulated through the closed vascular system. In function, blood is the general transport medium, carrying oxygen, nutrients, hormones and other essential substances to the tissues and carrying carbon dioxide and other harmful substances away for elimination, while lymph is concerned with immune defence through its lymphocytes, with returning tissue fluid to the veins, and with transport in general, being an important carrier for nutrients, hormones and similar substances, and with the absorption of fats, which are absorbed through lymph in the lacteals present in the intestinal villi.
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Double circulation is the type of circulation in which the oxygenated and deoxygenated blood received by the left and right atria respectively passes on to the ventricles of the same sides and the ventricles pump it out without any mixing up, so that two separate circulatory pathways are present in the animal. The two pathways are the pulmonary and the systemic circulations. The blood pumped by the right ventricle enters the pulmonary artery and is passed on to the lungs, from where the oxygenated blood is carried by the pulmonary veins into the left atrium, and this constitutes the pulmonary circulation. The oxygenated blood entering the aorta is carried by a network of arteries, arterioles and capillaries to the tissues, from where the deoxygenated blood is collected by a system of venules, veins and vena cava and emptied into the right atrium, and this is the systemic circulation. The structural basis of the arrangement is the four-chambered heart, since crocodiles, birds and mammals possess a 4-chambered heart with two atria and two ventricles, and the separation of the two sides prevents the two bloods from meeting. Its significance is threefold. First, the oxygenated and deoxygenated blood remain completely separate, so the tissues are supplied with blood of fully oxygenated content and the oxygenation of the blood is not compromised by any mixing. Second, the flow to the lungs and the flow to the tissues can be regulated independently, which the chapter links to the general advantage of the closed pattern, namely that the flow of fluid can be more precisely regulated. Third, this supports the high rate of oxygen delivery that birds and mammals require, and it is the reason they are able to sustain the high metabolic demands of warm-blooded life. The contrast makes the point clear: fishes have single circulation, the heart pumping deoxygenated blood that is oxygenated by the gills and supplied to the body parts, whereas in amphibians and reptiles the oxygenated and deoxygenated bloods get mixed up in the single ventricle, which pumps out mixed blood, and that is why this is called incomplete double circulation.
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The four differences are as follows. First, between blood and lymph. Blood is the fluid circulated by the heart through the blood vascular system, the network of closed branching blood vessels, and it is rich in proteins and in the formed elements, namely erythrocytes, leucocytes and platelets, and its functions are to carry oxygen, nutrients, hormones and other essential substances to the tissues and to take carbon dioxide and other harmful substances away. Lymph is the tissue fluid collected by an elaborate network of vessels called the lymphatic system, which drains it back to the major veins; it is poor in proteins and lacks the formed elements, though it does contain specialised lymphocytes responsible for the immune responses of the body, and it also serves as an important carrier for nutrients and hormones and as the route by which fats are absorbed in the lacteals present in the intestinal villi. Second, between open and closed systems of circulation. An open circulatory system is present in arthropods and molluscs, in which the blood pumped by the heart passes through large vessels into open spaces or body cavities called sinuses. A closed circulatory system is present in annelids and chordates, in which the blood pumped by the heart is always circulated through a closed network of blood vessels, and this pattern is considered to be more advantageous as the flow of fluid can be more precisely regulated. Third, between systole and diastole. Systole is the phase of contraction, the atrial systole being the simultaneous contraction of both atria and the ventricular systole the contraction of the ventricular muscles, whereas diastole is the phase of relaxation, the atria undergoing relaxation coinciding with the ventricular systole and the ventricles relaxing during the ventricular diastole. Systole and diastole of both the atria and ventricles together constitute the cardiac cycle. Fourth, between the P-wave and the T-wave. The P-wave represents the electrical excitation, or depolarisation, of the atria, which leads to the contraction of both the atria, so it corresponds to atrial activity and the start of atrial systole, whereas the T-wave represents the return of the ventricles from the excited to the normal state, that is repolarisation, and the end of the T-wave marks the end of systole. In each pair the two terms are the contrasting halves of the same process, whether of the fluid, of the circuit, of the muscular phase or of the electrical event.
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The pattern of the heart changes along the vertebrate series by progressive subdivision, from two chambers in fishes to four in the highest groups, and all vertebrates possess a muscular chambered heart. Fishes have a 2-chambered heart with an atrium and a ventricle. The heart pumps out deoxygenated blood which is oxygenated by the gills and supplied to the body parts, from where the deoxygenated blood is returned to the heart, and since only one circuit is involved this is single circulation. Amphibians and the reptiles, except crocodiles, show the next stage, with a 3-chambered heart having two atria and a single ventricle. This is the first step towards keeping the two bloods apart, because the left atrium receives the oxygenated blood from the gills, lungs or skin while the right atrium gets the deoxygenated blood from other body parts. However, the separation is incomplete: the two bloods get mixed up in the single ventricle, which pumps out mixed blood, so amphibians and reptiles have an incomplete double circulation. Crocodiles, birds and mammals complete the trend, possessing a 4-chambered heart with two atria and two ventricles. Here the oxygenated and deoxygenated blood received by the left and right atria respectively passes on to the ventricles of the same sides, and the ventricles pump it out without any mixing up, so two separate circulatory pathways are present and these animals have double circulation. Structurally the change is a matter of septation, seen clearly in the human heart, which has four chambers, with a thin muscular wall called the inter-atrial septum separating the right and the left atria and a thick-walled inter-ventricular septum separating the left and the right ventricles. The functional meaning of the whole trend is that the increasing subdivision of the heart progressively prevents the mixing of oxygenated and deoxygenated blood, so the tissues receive better oxygenated blood and the flow can be regulated more precisely, which suits the rising metabolic demand of the higher vertebrates, complete separation being reached only in crocodiles, birds and mammals.
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The heart is called myogenic because its normal activities are regulated intrinsically, that is, auto regulated by specialised muscles, the nodal tissue, and hence the heart is called myogenic. A specialised cardiac musculature called the nodal tissue is distributed in the heart, comprising the sino-atrial node, the atrio-ventricular node, the atrio-ventricular bundle with its right and left branches, and the purkinje fibres. The decisive property is that the nodal musculature has the ability to generate action potentials without any external stimuli, that is, it is autoexcitable, so the heart supplies its own stimulus and is able to beat on its own. The stimulation is also rhythmic and ordered, since the number of action potentials that could be generated in a minute varies at different parts of the nodal system, and the sino-atrial node can generate the maximum number, 70 to 75 per minute, and is responsible for initiating and maintaining the rhythmic contractile activity of the heart, which is why it is called the pacemaker, and our heart normally beats 70 to 75 times in a minute, an average of 72 beats per minute. The term myogenic is used in contrast to extrinsic control. A special neural centre in the medulla oblongata can moderate the cardiac function through the autonomic nervous system, with sympathetic signals able to increase the rate of heart beat, the strength of ventricular contraction and thereby the cardiac output, and parasympathetic signals able to decrease the rate of heart beat, the speed of conduction of the action potential and thereby the cardiac output, and adrenal medullary hormones able to increase the cardiac output. So neural and hormonal influences only adjust a beat which the heart has already initiated by itself, and the heart would continue to beat if those extrinsic controls were removed.
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The sino-atrial node is called the pacemaker because it can generate the maximum number of action potentials, that is 70 to 75 per minute, and is responsible for initiating and maintaining the rhythmic contractile activity of the heart. The reason it outranks the other parts of the nodal system is that although the nodal musculature as a whole is autoexcitable, the number of action potentials that could be generated in a minute varies at different parts of the nodal system, and the sino-atrial node is the fastest, so it sets the pace and the slower nodes merely follow it. Its position also suits the role, a patch of this tissue being present in the right upper corner of the right atrium, and the right atrium is the chamber that receives the deoxygenated blood from the body and fills first in each cycle. What the node starts is the whole cardiac sequence: the action potential it generates stimulates both the atria to undergo a simultaneous contraction, the atrial systole, and this increases the flow of blood into the ventricles by about 30 per cent. The single impulse is then transmitted in order to the ventricular side by the atrio-ventricular node and atrio-ventricular bundle, from where the bundle of His transmits it through the entire ventricular musculature, causing the ventricular muscles to contract. The numbers confirm the claim, since our heart normally beats 70 to 75 times in a minute, an average of 72 beats per minute, and that many cardiac cycles are performed per minute, which is precisely the intrinsic firing rate of the sino-atrial node.
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The atrio-ventricular node and the atrio-ventricular bundle are the conducting link between the atria and the ventricles, and both are needed for two reasons, a relay function and a delay function. The atrio-ventricular node is a mass of nodal tissue seen in the lower left corner of the right atrium close to the atrio-ventricular septum, and the atrio-ventricular bundle is a bundle of nodal fibres that continues from it, passes through the atrio-ventricular septa to emerge on the top of the inter-ventricular septum and immediately divides into a right and a left bundle. Their significance as a relay is that the action potential generated by the sino-atrial node is conducted to the ventricular side by the atrio-ventricular node and the atrio-ventricular bundle, and this is the only route, because the atrium and the ventricle of the same side are separated by a thick fibrous tissue called the atrio-ventricular septum, through which the chambers are connected. Their significance as a delay is that the impulse must traverse this node before the ventricles can be excited, and the effect is that the atria complete their contraction and empty their blood into the ventricles before the ventricles begin to contract, the atrial systole having increased the flow of blood into the ventricles by about 30 per cent, so filling is completed before emptying begins. The bundle then serves as a distribution system. Having emerged on the top of the inter-ventricular septum, it divides into a right and a left bundle, and these branches give rise to minute fibres throughout the ventricular musculature of the respective sides, called the purkinje fibres, so the bundle of His transmits the impulse through the entire ventricular musculature. The result is that the ventricular contraction is coordinated and near-simultaneous over both ventricles, which makes the ventricular systole an effective pump rather than a local contraction, and an interruption anywhere along this node-and-bundle pathway would break the link between the atrial and the ventricular phases of the cardiac cycle.
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The cardiac cycle is the sequential event in the heart which is cyclically repeated, and it consists of the systole and the diastole of both the atria and the ventricles. Since the heart beats 72 times per minute, that many cardiac cycles are performed per minute, and the duration of a cardiac cycle is 0.8 seconds. One complete cycle runs as follows. It begins in joint diastole, when all four chambers are relaxed, the tricuspid and bicuspid valves are open so that blood from the vena cava and the pulmonary veins flows into the right and the left ventricle respectively through the right and left atria, and the semilunar valves are closed. The sino-atrial node then generates an action potential which stimulates both the atria to undergo a simultaneous contraction, the atrial systole, increasing the flow of blood into the ventricles by about 30 per cent. The action potential is conducted to the ventricular side by the atrio-ventricular node and atrio-ventricular bundle, from where the bundle of His transmits it through the entire ventricular musculature, causing the ventricular muscles to contract, the ventricular systole, while the atria relax, the atrial diastole, coinciding with it. The rising ventricular pressure closes the tricuspid and bicuspid valves against any attempted backflow into the atria, and as the pressure increases further the semilunar valves guarding the pulmonary artery and the aorta are forced open, allowing the blood to flow out through these vessels. The ventricles then relax, the ventricular diastole, the falling pressure closing the semilunar valves and preventing backflow into the ventricles, and as the pressure declines further the tricuspid and bicuspid valves are pushed open by the pressure of the blood being emptied into the atria by the veins, so the heart returns to joint diastole and the cycle begins again. The cardiac output is the volume of blood pumped out by each ventricle per minute. It is obtained in two steps: during a cardiac cycle each ventricle pumps out approximately 70 mL of blood, which is called the stroke volume, and the stroke volume multiplied by the heart rate gives the cardiac output. The cardiac output averages 5000 mL, or 5 litres, in a healthy individual, which checks arithmetically since 70 mL multiplied by 72 beats per minute is 5040 mL per minute. Finally, the body has the ability to alter the stroke volume as well as the heart rate and thereby the cardiac output, and the cardiac output of an athlete will be much higher than that of an ordinary man.
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During each cardiac cycle two prominent sounds are produced, which can be easily heard through a stethoscope, and they are of clinical diagnostic significance. The first heart sound, lub, is associated with the closure of the tricuspid and bicuspid valves. It occurs at the beginning of the ventricular systole: as the action potential from the sino-atrial node is conducted through the atrio-ventricular node and the bundle of His to the entire ventricular musculature, the ventricular muscles contract, and the resulting increase in ventricular pressure causes the closure of the tricuspid and bicuspid valves due to attempted backflow of blood into the atria. The closure is a safety action, since the atrio-ventricular valves allow the flow of blood only in one direction, from the atria to the ventricles, and prevent any backward flow. The second heart sound, dub, is associated with the closure of the semilunar valves. It occurs at the beginning of the ventricular diastole: the ventricles relax, the ventricular pressure falls, and this causes the closure of the semilunar valves guarding the pulmonary artery and the aorta, which prevents the backflow of blood into the ventricles. The two sounds therefore close the two sets of valves in turn, the atrio-ventricular valves closing at the start of systole and the semilunar valves at the start of diastole, and the interval between lub and dub corresponds to the systole of the ventricles. Their clinical importance is that because each sound is tied to a specific valve event, an abnormal, extra, split or absent sound points to a valve that is not closing properly or to a disturbance in the sequence of the cardiac cycle, which is why the chapter treats the sounds as of clinical diagnostic significance in relation to disorders such as heart failure, meaning the state of the heart when it is not pumping blood effectively enough to meet the needs of the body.
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The standard ECG is a graphical representation of the electrical activity of the heart during a cardiac cycle, obtained with an electro-cardiograph, in which each peak is identified with a letter from P to T that corresponds to a specific electrical activity of the heart. To obtain a standard ECG the patient is connected to the machine with three electrical leads, one to each wrist and to the left ankle, which continuously monitor the heart activity, and for a detailed evaluation of the heart's function multiple leads are attached to the chest region. The tracing has three named components. The P-wave represents the electrical excitation, or depolarisation, of the atria, which leads to the contraction of both the atria, so it is the electrical trigger of the atrial systole that increases the flow of blood into the ventricles by about 30 per cent. The QRS complex represents the depolarisation of the ventricles, which initiates the ventricular contraction; the contraction starts shortly after Q and marks the beginning of the systole, so the QRS complex is the electrical event that opens the ventricular systole and leads to the closure of the tricuspid and bicuspid valves and then to the opening of the semilunar valves. The T-wave represents the return of the ventricles from the excited to the normal state, that is repolarisation, and the end of the T-wave marks the end of systole, so the T-wave closes the ventricular phase and the complex is complete. A standard ECG therefore reads as a small rounded P-wave, a sharp tall QRS complex and a broader T-wave, in that order. The tracing has two important uses. First, by counting the number of QRS complexes that occur in a given time period, one can determine the heart beat rate of an individual, which at rest is about 72 beats per minute. Second, since the ECGs obtained from different individuals have roughly the same shape for a given lead configuration, any deviation from this shape indicates a possible abnormality or disease, which is why the ECG is of great clinical significance and is used in relation to the circulatory disorders described in the chapter, such as hypertension, coronary artery disease and heart failure.
Quick Revision
Memorise these equations — direct application numericals and derivations in CBSE & JEE frequently hinge on these.
Cardiac output
Blood pressure
Lymph flow
Cardiac cycle
Exam Strategy
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FAQ
There are 1 exercise question in this chapter, numbered Ex. Every one is solved step by step on this page in the official NCERT numbering.
The formulas this chapter's questions actually turn on are: Cardiac output, Blood pressure, Lymph flow, Cardiac cycle. They are listed with their expressions in the key formulas section below, and the solved questions show where each one is used.
Very important — the cardiac cycle, cardiac output and the double-circulation question are fixed NEET items, and blood-composition tables are asked in both papers and boards.
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