biology in focus - chapter 34

CAMPBELL BIOLOGY IN FOCUS

Urry • Cain • Wasserman • Minorsky • Jackson • Reece

Lecture Presentations by Kathleen Fitzpatrick and Nicole Tunbridge

34Circulation and Gas Exchange

Overview: Trading Places

The resources that animal cells require, such as nutrients and O2, enter the cytoplasm by crossing the plasma membrane

In unicellular organisms, these exchanges occur directly with the environment

Most multicellular organisms rely on specialized systems that carry out exchange with the environment and transport materials through the body

Gills are an example of a specialized exchange system in animals O2 diffuses from the water into blood vessels

CO2 diffuses from blood into the water

Internal transport and gas exchange are functionally related in most animals

Figure 34.1

Concept 34.1: Circulatory systems link exchange surfaces with cells throughout the body

Small, nonpolar molecules such as O2 and CO2 move between cells and their immediate surroundings by diffusion

Diffusion time is proportional to the square of the distance travelled

Diffusion is only efficient over small distances

In small or thin animals, cells can exchange materials directly with the surrounding medium

In most animals, cells exchange materials with the environment via a fluid-filled circulatory system

Gastrovascular Cavities

Some animals lack a circulatory system Some cnidarians, such as jellies, have elaborate

gastrovascular cavities A gastrovascular cavity functions in both digestion

and distribution of substances throughout the body The body wall that encloses the gastrovascular

cavity is only two cells thick Flatworms have a gastrovascular cavity and a flat

body shape to optimize diffusional exchange with the environment

Figure 34.2

Gastrovascularcavity

Open and Closed Circulatory Systems

A circulatory system has a circulatory fluid, a set of interconnecting vessels, and a muscular pump, the heart

Several basic types of circulatory systems have arisen during evolution, each representing adaptations to constraints of anatomy and environment

All circulatory systems are either open or closed In insects, other arthropods, and some molluscs,

circulatory fluid bathes the organs directly in an open circulatory system

In an open circulatory system, there is no distinction between circulatory fluid and interstitial fluid, and this general body fluid is called hemolymph

Figure 34.3

Branch vesselsin each organ

Tubular heart

Hemolymph in sinuses

(a) An open circulatory system

(b) A closed circulatory system

HeartBlood

Dorsal vessel(main heart)

Auxiliaryhearts

Ventral vessels

Interstitialfluid

Figure 34.3a

Tubular heart

Hemolymph in sinuses

(a) An open circulatory system

In closed circulatory systems the circulatory fluid called blood is confined to vessels and is distinct from interstitial fluid

These systems are found in annelids, most cephalopods, and all vertebrates

One or more hearts pump blood through the vessels Chemical exchange occurs between blood and

interstitial fluid and between interstitial fluid and body cells

Figure 34.3b

Branch vesselsin each organ

(b) A closed circulatory system

HeartBlood

Dorsal vessel(main heart)

Auxiliaryhearts

Ventral vessels

Interstitialfluid

Organization of Vertebrate Circulatory Systems

Humans and other vertebrates have a closed circulatory system called the cardiovascular system

The three main types of blood vessels are arteries, veins, and capillaries

Blood flow is one-way in these vessels

Arteries branch into arterioles and carry blood away from the heart to capillaries

Networks of capillaries called capillary beds are the sites of chemical exchange between the blood and interstitial fluid

Venules converge into veins and return blood from capillaries to the heart

Arteries and veins are distinguished by the direction of blood flow, not by O2 content

Vertebrate hearts contain two or more chambers Blood enters through an atrium and is pumped out

through a ventricle

Single Circulation

Bony fishes, rays, and sharks have single circulation with a two-chambered heart

In single circulation, blood leaving the heart passes through two capillary beds before returning

Figure 34.4

Lungand skincapillaries

Body capillaries

Gill capillaries

(a) Single circulation: fish

Heart:

(b) Double circulation:amphibian

Systemiccapillaries

Pulmocutaneous circuit

Artery

Ventricle (V)Atrium (A)

Oxygen-rich bloodOxygen-poor blood

Right Left

Systemic circuit

Lungcapillaries

(c) Double circulation:mammal

Systemiccapillaries

Pulmonary circuit

Right Left

Systemic circuit

Figure 34.4a

Body capillaries

Gill capillaries

(a) Single circulation: fish

Heart:

Artery

Ventricle (V)Atrium (A)

Double Circulation

Amphibians, reptiles, and mammals have double circulation

Oxygen-poor and oxygen-rich blood is pumped separately from the right and left sides of the heart

Having both pumps within a heart simplifies coordination of the pumping cycle

Figure 34.4b

Lungand skincapillaries

(b) Double circulation:amphibian

Systemiccapillaries

Pulmocutaneous circuit

Right Left

Systemic circuit

Figure 34.4c

KeyOxygen-rich bloodOxygen-poor blood

Lungcapillaries

(c) Double circulation:mammal

Systemiccapillaries

Pulmonary circuit

Right Left

Systemic circuit

In reptiles and mammals, oxygen-poor blood flows through the pulmonary circuit to pick up oxygen through the lungs

In amphibians, oxygen-poor blood flows through a pulmocutaneous circuit to pick up oxygen through the lungs and skin

Oxygen-rich blood delivers oxygen through the systemic circuit

Double circulation maintains higher blood pressure in the organs than does single circulation

Evolutionary Variation in Double Circulation

Some vertebrates with double circulation are intermittent breathers

These animals have adaptations that enable the circulatory system temporarily to bypass the lungs

Frogs and other amphibians have a three-chambered heart: two atria and one ventricle

The ventricle pumps blood into a forked artery that splits the ventricle’s output into the pulmocutaneous circuit and the systemic circuit

When underwater, blood flow to the lungs is nearly shut off

Turtles, snakes, and lizards have a three-chambered heart: two atria and one ventricle

Their circulatory system allows control of relative amounts of blood flowing to the lungs and body

In alligators, caimans, and other crocodilians a septum divides the ventricle

A connection to atrial valves can temporarily shunt blood away from the lungs, as needed

Mammals and birds have a four-chambered heart with two atria and two ventricles

The left side of the heart pumps and receives only oxygen-rich blood, while the right side receives and pumps only oxygen-poor blood

There is no mechanism to vary relative blood flow to the lungs and body

Mammals and birds are endotherms and require more O2 than ectotherms

Concept 34.2: Coordinated cycles of heart contraction drive double circulation in mammals

The mammalian cardiovascular system meets the body’s continuous demand for O2

Mammalian Circulation

Blood begins its flow with the right ventricle pumping blood to the lungs via the pulmonary arteries

The blood loads O2 and unloads CO2 in the capillary beds of the lungs

Oxygen-rich blood from the lungs enters the heart at the left atrium via the pulmonary veins and is pumped through the aorta to the body tissues by the left ventricle

The aorta provides blood to the heart through the coronary arteries

Diffusion of O2 and CO2 takes place in the capillary beds throughout the body

Blood returns to the heart through the superior vena cava (blood from head, neck, and forelimbs) and inferior vena cava (blood from trunk and hind limbs)

The superior vena cava and inferior vena cava flow into the right atrium

Animation: Path of Blood Flow

Figure 34.5

Capillaries ofabdominal organsand hind limbs

Capillariesof right lung

Superiorvena cava

Pulmonaryartery

PulmonaryveinRight atriumRight ventricleInferior vena cava

Capillariesof left lung

Pulmonary artery

Pulmonaryvein

Left atriumLeft ventricle

Capillaries ofhead andforelimbs

Aorta9

The Mammalian Heart: A Closer Look

A closer look at the mammalian heart provides a better understanding of double circulation

When the heart contracts, it pumps blood; when it relaxes, its chambers fill with blood

One complete sequence of pumping and filling is called the cardiac cycle

Atria have relatively thin walls and serve as collection chambers for blood returning to the heart

The ventricles are more muscular and contract much more forcefully than the atria

The volume of blood each ventricle pumps per minute is called the cardiac output

Figure 34.6

Atrioventricular(AV) valve

Semilunarvalve

Pulmonary artery

Rightatrium

Right ventricle

Pulmonary artery

Left atrium

Left ventricle

Atrioventricular(AV) valve

Semilunarvalve

Figure 34.7-1

Atrial andventriculardiastole

0.4sec

Figure 34.7-2

Atrial systole andventricular diastole

0.4sec

0.1sec

Figure 34.7-3

Atrial systole andventricular diastole

Ventricular systole and atrial diastole

0.4sec

0.3 sec

0.1sec

The heart rate, also called the pulse, is the number of beats per minute

The stroke volume is the amount of blood pumped in a single contraction

Cardiac output depends on both the heart rate and stroke volume

Four valves prevent backflow of blood in the heart The atrioventricular (AV) valves separate each

atrium and ventricle The semilunar valves control blood flow to the

aorta and the pulmonary artery

The “lub-dup” sound of a heart beat is caused by the recoil of blood against the AV valves (lub) then against the semilunar (dup) valves

Backflow of blood through a defective valve causes a heart murmur

Maintaining the Heart’s Rhythmic Beat

Some cardiac muscle cells are autorhythmic, meaning they contract without any signal from the nervous system

The sinoatrial (SA) node, or pacemaker, sets the rate and timing at which all other cardiac muscle cells contract

The SA node produces electrical impulses that spread rapidly through the heart and can be recorded as an electrocardiogram (ECG or EKG)

Figure 34.8-1

Signals (yellow)from SA nodespreadthrough atria.

SA node(pacemaker)

Figure 34.8-2

SA node(pacemaker)

1 Signals aredelayedat AV node.

AV node

Figure 34.8-3

SA node(pacemaker)

Bundlebranchespass signalsto heart apex.

AV node

Bundlebranches Heart

apexECG

Figure 34.8-4

SA node(pacemaker)

Bundlebranchespass signalsto heart apex.

Signalsspreadthroughoutventricles.

AV node

Bundlebranches Heart

Purkinjefibers

Impulses from the SA node travel to the atrioventricular (AV) node

At the AV node, the impulses are delayed and then travel to the Purkinje fibers that make the ventricles contract

The pacemaker is regulated by two portions of the nervous system: the sympathetic and parasympathetic divisions

The sympathetic division speeds up the pacemaker The parasympathetic division slows down the

pacemaker The pacemaker is also regulated by hormones and

temperature

Concept 34.3: Patterns of blood pressure and flow reflect the structure and arrangement of blood vessels

The physical principles that govern movement of water in plumbing systems also apply to the functioning of animal circulatory systems

Blood Vessel Structure and Function

A vessel’s cavity is called the central lumen The epithelial layer that lines blood vessels is called

the endothelium The endothelium is smooth and minimizes resistance

to blood flow

Capillaries have thin walls, the endothelium and its basal lamina, to facilitate the exchange of substances

Arteries and veins have an endothelium, smooth muscle, and connective tissue

Arteries have thicker walls than veins to accommodate the high pressure of blood pumped from the heart

Figure 34.9

Connectivetissue

Smoothmuscle

Connectivetissue

Smoothmuscle

Endothelium Endothelium

Artery Vein

Red bloodcells

Basal lamina

Capillary

Red blood cell

Capillary

ArterioleVenule

Valve100 m

Figure 34.9a

Connectivetissue

Smoothmuscle

Connectivetissue

Smoothmuscle

EndotheliumEndothelium

Artery Vein

Basal lamina

Capillary

ArterioleVenule

Figure 34.9b

Artery Vein

Red bloodcells

Figure 34.9c

Red blood cell

Capillary

Blood Flow Velocity

Blood vessel diameter influences blood flow Velocity of blood flow is slowest in the capillary

beds, as a result of the high resistance and large total cross-sectional area

Blood flow in capillaries is necessarily slow for exchange of materials

Figure 34.10

Systolicpressure

Diastolicpressure

4,0002,000

Blood Pressure

Blood flows from areas of higher pressure to areas of lower pressure

Blood pressure exerts a force in all directions

Changes in Blood Pressure During the Cardiac Cycle

Systole is the contraction phase of the cardiac cycle Pressure at the time of ventricle contraction is called

systolic pressure Diastole is the the relaxation phase of the cardiac

cycle; diastolic pressure is lower than systolic

Maintenance of Blood Pressure

Blood pressure is determined by cardiac output and peripheral resistance due to constriction of arterioles

Vasoconstriction is the contraction of smooth muscle in arteriole walls; it increases blood pressure

Vasodilation is the relaxation of smooth muscles in the arterioles; it causes blood pressure to fall

Vasoconstriction and vasodilation help maintain adequate blood flow as the body’s demands change

Nitric oxide is a major inducer of vasodilation The peptide endothelin is an important inducer of

vasoconstriction

Fainting is caused by inadequate blood flow to the head

Animals with long necks require a higher systolic pressure to pump blood against gravity

Gravity is a consideration for blood flow in veins, particularly in the legs

One-way valves in veins prevent backflow of blood Blood returns to the heart through contraction of

smooth muscle in the walls of veins and venules and by contraction of skeletal muscles

Figure 34.11

Direction of bloodflow in vein(toward heart)

Valve (open)

Valve (closed)

Skeletal muscle

Capillary Function

Blood flows through only 5–10% of the body’s capillaries at a time

Capillaries in major organs are usually filled to capacity

Blood supply varies in many other sites

Two mechanisms alter blood flow in capillary beds Vasoconstriction or vasodilation of the arteriole that

supplies a capillary bed Precapillary sphincters, rings of smooth muscle at the

capillary bed entrance, open and close to regulate passage of blood

Critical exchange of substances takes place across the thin walls of the capillaries

Blood pressure tends to drive fluid out of the capillaries

The difference in solute concentration between blood and interstitial fluid (the blood’s osmotic pressure) opposes fluid movement from the capillaries

Blood pressure is usually greater than osmotic pressure

Net loss of fluid from capillaries occurs in regions where blood pressure is highest

Fluid Return by the Lymphatic System

The lymphatic system returns fluid, called lymph, that leaks out from the capillary beds

Lymph has a very similar composition to interstitial fluid

The lymphatic system drains into veins in the neck Valves in lymph vessels prevent the backflow of

Figure 34.12Interstitialfluid

Lymphaticvessel

Bloodcapillary

Tissue cells

Lymph nodeMasses ofdefensivecells

Lymphaticvessels

Lymph nodes

Peyer’s patches(small intestine)

Appendix(cecum)

Thymus(immunesystem)

AdenoidTonsils

Spleen

Lymph vessels have valves to prevent backflow Lymph nodes are organs that filter lymph and play

an important role in the body’s defense Edema is swelling caused by disruptions in the flow

of lymph The lymphatic system also plays a role in harmful

immune responses, such as those responsible for asthma

Concept 34.4: Blood components function in exchange, transport, and defense

With open circulation, the fluid that is pumped comes into direct contact with all cells and has the same composition as interstitial fluid

The closed circulatory systems of vertebrates contain blood, which can be much more highly specialized

Blood Composition and Function

Blood is a connective tissue consisting of cells suspended in a liquid matrix called plasma

The cellular elements occupy about 45% of the volume of blood

Video: Leukocyte Rolling

Figure 34.13

Separatedbloodelements

Solvent forcarrying othersubstances

Plasma 55% Cellular elements 45%

Constituent Major functions

Osmotic balance,pH buffering,and regulationof membranepermeability

Ions (bloodelectrolytes)SodiumPotassiumCalciumMagnesiumChlorideBicarbonate

Osmotic balance,pH buffering

Clotting

Defense

Fibrinogen

Plasma proteinsAlbumin

Immunoglobulins(antibodies)

Substances transported by bloodNutrients (such as glucose, fattyacids, vitamins)Waste products of metabolismRespiratory gases (O2 and CO2)Hormones

Functions

Leukocytes (white blood cells)

Transportof O2 and some CO2

Cell typeNumber

per L (mm3)of blood

Basophils Lymphocytes

Eosinophils

Neutrophils Monocytes

Platelets

Erythrocytes (red blood cells)

250,000–400,000

5,000,000– 6,000,000

Bloodclotting

5,000–10,000 Defenseandimmunity

Figure 34.13a

Solvent for carrying othersubstances

Plasma 55%Constituent Major functions

Osmotic balance, pH buffering,and regulation of membranepermeability

Ions (blood electrolytes)SodiumPotassiumCalciumMagnesiumChlorideBicarbonate

Osmotic balance, pH buffering

Clotting

Defense

Fibrinogen

Plasma proteinsAlbumin

Immunoglobulins(antibodies)

Substances transported by bloodNutrients (such as glucose, fatty acids, vitamins)Waste products of metabolismRespiratory gases (O2 and CO2)Hormones

Figure 34.13b

Cellular elements 45%

Functions

Leukocytes (white blood cells)

Transport of O2 and some CO2

Cell type Numberper L (mm3) of blood

Basophils Lymphocytes

Eosinophils

Neutrophils Monocytes

Platelets

Erythrocytes (red blood cells)

250,000–400,000

5,000,000–6,000,000

Blood clotting

5,000–10,000 Defense andimmunity

Plasma

Blood plasma is about 90% water Among its solutes are inorganic salts in the form of

dissolved ions, sometimes called electrolytes Plasma proteins influence blood pH, osmotic

pressure, and viscosity Particular plasma proteins function in lipid transport,

immunity, and blood clotting

Cellular Elements

Blood contains two classes of cells Red blood cells (erythrocytes) transport O2

White blood cells (leukocytes) function in defense

Platelets, a third cellular element, are fragments of cells that are involved in clotting

Figure 34.14

Stem cells(in bone marrow)

BasophilsLymphocytes

Eosinophils

Neutrophils

MonocytesPlatelets

Erythrocytes

Myeloidstem cells

Lymphoidstem cells

B cells T cells

Erythrocytes Red blood cells, or erythrocytes, are by far the most

numerous blood cells They contain hemoglobin, the iron-containing

protein that transports O2

Each molecule of hemoglobin binds up to four molecules of O2

In mammals, mature erythrocytes lack nuclei

Sickle-cell disease is caused by abnormal hemoglobin that polymerizes into aggregates

The aggregates can distort an erythrocyte into a sickle shape

Through a person’s life, multipotent stem cells replace the worn-out cellular elements of blood

Erythrocytes circulate for about 120 days before they are replaced

Stem cells that produce red blood cells and platelets are located in red marrow of bones like the ribs, vertebrae, sternum, and pelvis

Leukocytes There are five major types of white blood cells, or

leukocytes They function in defense by engulfing bacteria and

debris or by mounting immune responses against foreign substances

They are found both in and outside of the circulatory system

Platelets Platelets are fragments of cells and function in

blood clotting

Blood Clotting

Coagulation is the formation of a solid clot from liquid blood

A cascade of complex reactions converts inactive fibrinogen to fibrin, which forms the framework of a clot

A blood clot formed within a blood vessel is called a thrombus and can block blood flow

Figure 34.15

PlateletPlateletplug

Collagenfibers

PlateletsClotting factors from:

Damaged cellsPlasma (factors include calcium, vitamin K)

Fibrin

Thrombin

Fibrinogen

Prothrombin

Enzymatic cascade

Fibrin clot

Fibrin clotformation

Red blood cell 5 m

Figure 34.15a

PlateletPlateletplug

Collagenfibers

PlateletsClotting factors from:

Damaged cellsPlasma (factors include calcium, vitamin K)

Fibrin

Thrombin

Fibrinogen

Prothrombin

Enzymatic cascade

Fibrin clot

Fibrin clotformation

Figure 34.15b

Fibrin clot

Red blood cell 5 m

Cardiovascular Disease

Cardiovascular diseases are disorders of the heart and the blood vessels

Cardiovascular diseases account for more than half the deaths in the United States

Cholesterol, a steroid, helps maintain normal membrane fluidity

Low-density lipoprotein (LDL) delivers cholesterol to cells for membrane production

High-density lipoprotein (HDL) scavenges excess cholesterol for return to the liver

Risk for heart disease increases with a high LDL to HDL ratio

Inflammation is also a factor in cardiovascular disease

Atherosclerosis, Heart Attacks, and Stroke

One type of cardiovascular disease, atherosclerosis, is caused by the buildup of fatty deposits within arteries

A fatty deposit is called a plaque; as it grows, the artery walls become thick and stiff and the obstruction of the artery increases

Figure 34.16

Endothelium

Plaque

Blood clot

A heart attack, or myocardial infarction, is the death of cardiac muscle tissue resulting from blockage of one or more coronary arteries

Coronary arteries supply oxygen-rich blood to the heart muscle

A stroke is the death of nervous tissue in the brain, usually resulting from rupture or blockage of arteries in the head

Angina pectoris is caused by partial blockage of the coronary arteries and may cause chest pain

Risk Factors and Treatment of Cardiovascular Disease

A high LDL to HDL ratio increases the risk of cardiovascular disease

The proportion of LDL relative to HDL is increased by smoking and consumption of trans fats and decreased by exercise

Drugs called statins reduce LDL levels and risk of heart attacks

Inflammation plays a role in atherosclerosis and thrombus formation

Aspirin inhibits inflammation and reduces the risk of heart attacks and stroke

Hypertension (high blood pressure) contributes to the risk of heart attack and stroke

Hypertension can be reduced by dietary changes, exercise, medication, or some combination of these

Concept 34.5: Gas exchange occurs across specialized respiratory surfaces

Gas exchange is the uptake of molecular O2 from the environment and the discharge of CO2 to the environment

Partial Pressure Gradients in Gas Exchange

Partial pressure is the pressure exerted by a particular gas in a mixture of gases

For example, the atmosphere is 21% O2, by volume, so the partial pressure of O2 (PO2

) is 0.21 the

atmospheric pressure

Partial pressures also apply to gases dissolved in liquid, such as water

When water is exposed to air, an equilibrium is reached in which the partial pressure of each gas is the same in the water and the air

A gas always undergoes net diffusion from a region of higher partial pressure to a region of lower partial pressure

Respiratory Media

O2 is plentiful in air, and breathing air is relatively easy

In a given volume, there is less O2 available in water than in air

Obtaining O2 from water requires greater energy expenditure than air breathing

Aquatic animals have a variety of adaptations to improve efficiency in gas exchange

Figure 34.17

Coelom

Tube foot

(b) Sea star(a) Marine worm

Parapodium (functions as gill)

Figure 34.17a

(a) Marine worm

Figure 34.17b

(b) Sea star

Respiratory Surfaces

Gas exchange across respiratory surfaces takes place by diffusion

Respiratory surfaces tend to be large and thin and are always moist

Respiratory surfaces vary by animal and can include the skin, gills, tracheae, and lungs

Gills in Aquatic Animals

Gills are outfoldings of the body that create a large surface area for gas exchange

Ventilation is the movement of the respiratory medium over the respiratory surface

Ventilation maintains the necessary partial pressure gradients of O2 and CO2 across the gills

Aquatic animals move through water or move water over their gills for ventilation

Fish gills use a countercurrent exchange system, where blood flows in the opposite direction to water passing over the gills

Blood is always less saturated with O2 than the water it meets

Countercurrent exchange mechanisms are remarkably efficient

Figure 34.18

Lamella

Water flow

Countercurrent exchange

O2-poor blood

Gill filaments

Operculum

Gillarch

Waterflow

Gill arch

Bloodvessels

O2-rich blood

Blood flow

PO2 (mm Hg)

in blood

PO2 (mm Hg) in water

Netdiffusionof O2

140 110 80 50 30

150 120 90 60 30

Tracheal Systems in Insects

The tracheal system of insects consists of a network of air tubes that branch throughout the body

The tracheal system can transport O2 and CO2 without the participation of the animal’s open circulatory system

Larger insects must ventilate their tracheal system to meet O2 demands

Figure 34.19 Tracheoles Muscle fiberMitochondria

Tracheae

Air sacs

External opening

Airsac Tracheole

Trachea

Bodycell

Figure 34.19a

Tracheoles Muscle fiberMitochondria

Lungs are an infolding of the body surface, usually divided into numerous pockets

The circulatory system (open and closed) transports gases between the lungs and the rest of the body

The use of lungs for gas exchange varies among vertebrates that lack gills

Mammalian Respiratory Systems: A Closer Look

A system of branching ducts conveys air to the lungs Air inhaled through the nostrils is warmed,

humidified, and sampled for odors The pharynx directs air to the lungs and food to the

stomach Swallowing tips the epiglottis over the glottis in the

pharynx to prevent food from entering the trachea

Air passes through the pharynx, larynx, trachea, bronchi, and bronchioles to the alveoli, where gas exchange occurs

Exhaled air passes over the vocal cords in the larynx to create sounds

Cilia and mucus line the epithelium of the air ducts and move particles up to the pharynx

This “mucus escalator” cleans the respiratory system and allows particles to be swallowed into the esophagus

Gas exchange takes place in alveoli, air sacs at the tips of bronchioles

Oxygen diffuses through the moist film of the epithelium and into capillaries

Carbon dioxide diffuses from the capillaries across the epithelium and into the air space

Animation: Gas Exchange

Figure 34.20

Bronchiole

Bronchus

Right lungTrachea(Esophagus)Larynx

Pharynx

(Heart)

Terminalbronchiole

Leftlung

Nasalcavity

Capillaries

Alveoli

Dense capillary bedenveloping alveoli(SEM)

Branch ofpulmonary vein(oxygen-richblood)

Branch of pulmonary artery (oxygen-poorblood)

Diaphragm

Figure 34.20a

Bronchiole

Bronchus

Right lungTrachea(Esophagus)Larynx

Pharynx

(Heart)

Leftlung

Nasalcavity

Diaphragm

Figure 34.20b

Terminalbronchiole

Capillaries

Alveoli

Branch ofpulmonary vein(oxygen-richblood)

Branch of pulmonary artery (oxygen-poorblood)

Figure 34.20c

Dense capillary bedenveloping alveoli (SEM)

Alveoli lack cilia and are susceptible to contamination Secretions called surfactants coat the surface of

the alveoli Preterm babies lack surfactant and are vulnerable to

respiratory distress syndrome; treatment is provided by artificial surfactants

Figure 34.21

Deaths fromother causes

RDS deaths

Body mass of infant<1,200 g >1,200 g

(n 9) (n 0) (n 29) (n 9)

Results

Concept 34.6: Breathing ventilates the lungs

The process that ventilates the lungs is breathing, the alternate inhalation and exhalation of air

An amphibian such as a frog ventilates its lungs by positive pressure breathing, which forces air down the trachea

Birds have eight or nine air sacs that function as bellows that keep air flowing through the lungs

Air passes through the lungs of birds in one direction only

Passage of air through the entire system—lungs and air sacs—requires two cycles in inhalation and exhalation

How a Mammal Breathes

Mammals ventilate their lungs by negative pressure breathing, which pulls air into the lungs

Lung volume increases as the rib muscles and diaphragm contract

The tidal volume is the volume of air inhaled with each breath

Animation: Gas Exchange

Figure 34.22

Inhalation:Diaphragm contracts

(moves down).

Diaphragm

Exhalation:Diaphragm relaxes

(moves up).

Airinhaled.

Airexhaled.

Rib cageexpands asrib musclescontract.

Rib cage getssmaller asrib musclesrelax.

The maximum tidal volume is the vital capacity After exhalation, a residual volume of air remains

in the lungs Each inhalation mixes fresh air with oxygen-depleted

residual air

As a result, the maximum PO2 in alveoli is

considerably less than in the atmosphere

Control of Breathing in Humans

In humans, the main breathing control center consists of neural circuits in the medulla oblongata, near the base of the brain

The medulla regulates the rate and depth of breathing in response to pH changes in the cerebrospinal fluid

The medulla adjusts breathing rate and depth to match metabolic demands

Figure 34.23-1

Homeostasis:Blood pH of about 7.4

Stimulus:Rising level of CO2in tissues lowers

blood pH.

Figure 34.23-2

Carotidarteries

blood pH.

Sensor/controlcenter:

AortaCerebro-spinalfluid

Medullaoblongata

Figure 34.23-3

Carotidarteries

Response:Signals frommedulla to ribmuscles anddiaphragmincrease rateand depth ofventilation.

blood pH.

Medullaoblongata

Figure 34.23-4

Carotidarteries

Response:Signals frommedulla to ribmuscles anddiaphragmincrease rateand depth ofventilation.

CO2 leveldecreases. Stimulus:

Rising level of CO2in tissues lowers

blood pH.

Medullaoblongata

Sensors in the aorta and carotid arteries monitor O2 and CO2 concentrations in the blood

These sensors exert secondary control over breathing

Concept 34.7: Adaptations for gas exchange include pigments that bind and transport gases

The metabolic demands of many organisms require that the blood transport large quantities of O2 and CO2

Coordination of Circulation and Gas Exchange

Blood arriving in the lungs has a low PO2 and a high

PCO2 relative to air in the alveoli

In the alveoli, O2 diffuses into the blood and CO2 diffuses into the air

In tissue capillaries, partial pressure gradients favor diffusion of O2 into the interstitial fluids and CO2 into the blood

Specialized carrier proteins play a vital role in this process

Animation: O2 Blood to Tissues

Animation: O2 Lungs to Blood

Animation: CO2 Blood to Lungs

Animation: CO2 Tissues to Blood

Figure 34.24

Alveolarepithelialcells

Alveolarspaces

Alveolarcapillaries

Inhaled airExhaled air

Pulmonaryveins

Systemicarteries

Pulmonaryarteries

Systemicveins

Systemiccapillaries

CO2 O2

Body tissuecells

O2 CO2

120 27

O2 CO2

160 0.2

O2 CO2

104 40

O2 CO2

<40 >45

Respiratory Pigments

Respiratory pigments circulate in blood or hemolymph and greatly increase the amount of oxygen that is transported

A variety of respiratory pigments have evolved among animals

These mainly consist of a metal bound to a protein

The respiratory pigment of almost all vertebrates and many invertebrates is hemoglobin

A single hemoglobin molecule can carry four molecules of O2, one molecule for each iron- containing heme group

Hemoglobin binds oxygen reversibly, loading it in the gills or lungs and releasing it in other parts of the body

Figure 34.UN01

Hemoglobin

Hemoglobin binds O2 cooperatively

When O2 binds one subunit, the others change shape slightly, resulting in their increased affinity for oxygen

When one subunit releases O2, the others release their bound O2 more readily

Cooperativity can be demonstrated by the dissociation curve for hemoglobin

Figure 34.25

pH 7.4

PO2 (mm Hg)

pH 7.2

Hemoglobinretains lessO2 at lower pH(higher CO2

concentration

Tissuesat restPO2

(mm Hg)

Tissues duringexercise

O2 unloadedto tissues

during exercise

O2 unloadedto tissuesat rest

(b) pH and hemoglobin dissociation(a) PO2 and hemoglobin dissociation

at pH 7.4

0100806040200 100806040200

Figure 34.25a

Tissuesat restPO2

(mm Hg)

Tissues duringexercise

O2 unloadedto tissues

during exercise

O2 unloadedto tissuesat rest

(a) PO2 and hemoglobin dissociation

at pH 7.4

0100806040200

CO2 produced during cellular respiration lowers blood pH and decreases the affinity of hemoglobin for O2; this is called the Bohr shift

Hemoglobin also assists in preventing harmful changes in blood pH and plays a minor role in CO2 transport

Figure 34.25b

pH 7.4

PO2 (mm Hg)

pH 7.2

Hemoglobinretains lessO2 at lower pH(higher CO2

concentration

(b) pH and hemoglobin dissociation

0100806040200

Carbon Dioxide Transport

Most of the CO2 from respiring cells diffuses into the blood and is transported in blood plasma, bound to hemoglobin or as bicarbonate ions (HCO3

Respiratory Adaptations of Diving Mammals

Diving mammals have evolutionary adaptations that allow them to perform extraordinary feats For example, Weddell seals in Antarctica can remain

underwater for 20 minutes to an hour For example, elephant seals can dive to 1,500 m and

remain underwater for 2 hours

These animals have a high blood to body volume ratio

Deep-diving air breathers can store large amounts of O2

Oxygen can be stored in their muscles in myoglobin proteins

Diving mammals also conserve oxygen by Changing their buoyancy to glide passively Decreasing blood supply to muscles Deriving ATP in muscles from fermentation once

oxygen is depleted

Figure 34.UN02a

Plasma LDL cholesterol (mg/dL)

uals 30

03002502001501000

Individuals with an inactivating mutation in one copyof PCSK9 gene (study group)

Figure 34.UN02b

Plasma LDL cholesterol (mg/dL)

uals 30

03002502001501000

Individuals with two functional copies of PCSK9 gene (control group)

Figure 34.UN03

Alveolarepithelialcells

Pulmonaryarteries

Systemicveins

Pulmonaryveins

Systemicarteries

Systemiccapillaries

Alveolarcapillaries

Alveolarspaces

Exhaled air Inhaled air

Body tissue

Figure 34.UN04

PO2 (mm Hg)

)Mother

100806040200

biology in focus - chapter 34

Science

biology in focus chapter one

biology in focus chapter 4

biology in focus - chapter 17

06 biology special focus evolution

biology in focus - chapter 13

biology in focus - chapter 23

biology in focus - chapter 22

biology in focus - chapter 30

biology in focus - chapter 40

biology in focus - chapter 35

biology in focus chapter 2

bnl focus #34

biology in focus - chapter 31

biology in focus - chapter 39

primary focus: mitochondria biology - astellas

biology in focus - chapter 29

biology in focus - chapter 8

biology in focus - chapter 16

biology in focus - chapter 43

biology in focus - chapter 33