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Respiratory system

The respiratory system is the integrated network of organs, tissues, and structures responsible for the exchange of oxygen and carbon dioxide between the body and its environment, enabling cellular respiration and the removal of metabolic waste products.^[1] This system facilitates the intake of oxygen-rich air and the expulsion of carbon dioxide, working closely with the circulatory system to transport oxygen to tissues throughout the body and eliminate waste gases via the bloodstream.^[2] In humans, it supports vital processes such as maintaining blood pH balance and providing energy for metabolic functions, with gas exchange occurring every 3 to 5 seconds through nerve-stimulated ventilation.^[2] Anatomically, the respiratory system is divided into the upper and lower respiratory tracts. The upper respiratory tract includes the nose, nasal cavity, mouth, sinuses, pharynx (throat), larynx (voice box), and the upper portion of the trachea (windpipe), which primarily warm, humidify, and filter incoming air to protect the lungs.^[3] The lower respiratory tract comprises the lower trachea, bronchi (large airways branching from the trachea), bronchioles (smaller branching airways), and the lungs themselves, where the majority of gas exchange occurs.^[3] The lungs are a pair of cone-shaped, spongy organs located in the thoracic cavity, with the right lung consisting of three lobes and the left lung two lobes to accommodate the heart; they are enclosed by the pleura, a double-layered membrane that reduces friction during breathing, and supported by the diaphragm muscle below.^[1] Functionally, the respiratory system operates through the processes of ventilation, gas exchange, and transport. During inhalation, the diaphragm and intercostal muscles contract to expand the chest cavity, drawing air through the airways into approximately 480 million alveoli—tiny air sacs in the lungs lined with surfactant to prevent collapse and surrounded by capillaries for diffusion.^[4] Here, oxygen diffuses from the alveoli into the bloodstream, while carbon dioxide diffuses from the blood into the alveoli to be exhaled; this external respiration is complemented by internal respiration, where gases are exchanged between blood and body tissues.^[2] The system also filters out particles and pathogens via mucus and cilia in the airways, and it receives regulatory input from the nervous and immune systems to adjust breathing rate based on activity levels or environmental conditions.^[1]

Overview

Definition and functions

The respiratory system comprises a network of organs and tissues that enable external respiration, defined as the exchange of gases—primarily oxygen and carbon dioxide—between the external environment and the body's internal fluids, such as blood.^[2] This system works in close coordination with the circulatory system to ensure efficient transport of these gases throughout the body.^[5] The primary functions of the respiratory system center on acquiring oxygen to support cellular metabolism and eliminating carbon dioxide, a byproduct of aerobic respiration in cells.^[6] Oxygen uptake fuels energy production via oxidative phosphorylation, while carbon dioxide removal prevents toxic buildup.^[7] Additionally, by regulating carbon dioxide levels, the system contributes to acid-base balance; elevated CO₂ forms carbonic acid, lowering pH, whereas its elimination shifts the bicarbonate buffer equation (CO₂ + H₂O ⇌ H₂CO₃ ⇌ H⁺ + HCO₃⁻) to maintain physiological pH around 7.4.^[8] Beyond gas exchange, the respiratory system supports secondary roles including vocalization, where airflow through laryngeal structures produces sound for communication; olfaction, facilitated by sensory receptors in the nasal passages that detect airborne molecules; and thermoregulation, achieved through evaporative heat loss during exhalation, particularly in panting behaviors.^[9]^[10]^[11] External respiration, occurring at the interface of air and blood, differs from internal respiration, which involves gas exchange between blood and tissue cells to meet metabolic demands.^[12]

Evolutionary origins

The respiratory system's evolutionary origins trace back to the earliest forms of life, where gas exchange occurred via passive diffusion across cell membranes in prokaryotes. In the Last Universal Common Ancestor (LUCA), approximately 3.8 billion years ago, simple prokaryotic cells relied on this diffusion for anaerobic respiration, utilizing metalloproteins to manage gas transport without specialized organs.^[13] The Great Oxidation Event around 2.4 billion years ago, driven by cyanobacterial photosynthesis, enabled the rise of aerobic respiration in prokaryotes, enhancing energy efficiency through oxygen utilization still via membrane diffusion.^[13] Early eukaryotes, emerging around 2 billion years ago through endosymbiosis with α-proteobacteria that became mitochondria, further optimized this process, with oxygen-sensing mechanisms, such as those involving reactive oxygen species, evolving later in eukaryotic lineages around 800 million years ago to regulate aerobic metabolism.^[14]^[15]^[16] As multicellularity evolved in the Metazoa, the limitations of diffusion for larger body sizes necessitated more active transport systems in invertebrates. In arthropods, tracheae emerged around 416 million years ago during the Devonian period, forming a network of branching tubes that deliver oxygen directly to tissues via spiracles, bypassing the circulatory system for efficient gas exchange in terrestrial environments.^[13]^[17] This innovation coincided with the colonization of land and the evolution of flight in insects approximately 350 million years ago.^[13] Concurrently, early chordates developed gills around 500 million years ago as primordial water-breathing organs, featuring thin filaments and secondary lamellae that facilitate countercurrent exchange to extract up to 92% of available oxygen from water.^[17] In vertebrates, the respiratory system advanced with the development of lungs from swim bladders in sarcopterygian fishes approximately 420 million years ago, marking a critical adaptation for air breathing amid fluctuating oxygen levels in shallow waters.^[13] This ventral lung-like structure, initially serving buoyancy, evolved into a respiratory organ in lobe-finned fishes such as lungfishes (Dipnoi), enabling survival in hypoxic conditions and paving the way for tetrapod terrestrialization.^[13] Fossil evidence from Tiktaalik roseae, dated to about 375 million years ago, illustrates this transition as a key intermediate form, possessing both gill arches for aquatic respiration and precursors to lungs, including a robust hyoid-neck apparatus that supported air gulping.^[13]^[18] Key adaptations further diversified vertebrate respiration. In amphibians, cutaneous respiration through moist, permeable skin supplemented lung function, allowing significant oxygen uptake via capillary networks directly beneath the epidermis, a trait retained from early tetrapods to compensate for less efficient lungs.^[19] In birds, unidirectional airflow evolved around 150 million years ago from theropod dinosaur ancestors, utilizing air sacs and a paleopulmonic parabronchial system for continuous gas exchange, far surpassing the bidirectional flow in other vertebrates and supporting high metabolic demands like flight.^[13] These developments highlight convergent evolution across lineages, optimizing oxygen delivery in response to environmental shifts from aquatic to aerial habitats.^[17]

Mammalian Respiratory System

Anatomy

The mammalian respiratory system is anatomically divided into the upper respiratory tract, which conducts and conditions inhaled air, and the lower respiratory tract, which facilitates gas exchange in the lungs. The upper tract includes the nasal cavity, pharynx, and larynx, while the lower tract encompasses the trachea, bronchi, bronchioles, and alveoli. This organization ensures efficient air filtration, humidification, and delivery to the gas exchange surfaces.^[20]^[21] The upper respiratory tract begins with the nasal cavity, a chamber divided by the nasal septum and featuring three turbinates (superior, middle, and inferior) that increase surface area for air warming and humidification. Its mucosa, composed of ciliated pseudostratified columnar epithelium interspersed with goblet cells, secretes mucus to trap particulate matter, while cilia propel this mucus toward the pharynx via the mucociliary escalator, preventing deeper inhalation of debris.^[20]^[21] The pharynx, a muscular tube connecting the nasal and oral cavities to the larynx and esophagus, is divided into nasopharynx, oropharynx, and laryngopharynx regions, all lined with mucous membrane that further aids in filtration and humidification. The larynx, positioned between the pharynx and trachea, consists of nine cartilages—including the thyroid, cricoid, and epiglottis—and is lined with mucosa supporting vocal folds for phonation while maintaining airway patency.^[20]^[21] The lower respiratory tract starts with the trachea, a flexible tube extending from the larynx at the level of the sixth cervical vertebra to the carina (around the fourth or fifth thoracic vertebra), measuring approximately 11-13 cm in length and reinforced by 16-20 C-shaped hyaline **cartilage rings** to prevent collapse. Its inner lining features pseudostratified ciliated columnar epithelium with goblet cells for ongoing mucus production and ciliary clearance. The trachea bifurcates at the carina into the right and left primary bronchi, which branch into secondary (lobar) and tertiary (segmental) bronchi, all supported by irregular cartilage plates and encircled by smooth muscle that modulates airway diameter. These bronchi progressively decrease in size and cartilage content, transitioning into bronchioles—smaller conduits (less than 1 mm in diameter) lacking cartilage but containing smooth muscle and lined with simple cuboidal epithelium, including club cells that secrete protective fluids.^[20]^[21] The terminal bronchioles lead to respiratory bronchioles and finally the alveoli, clustered grape-like air sacs numbering about 480 million in total across both lungs (or approximately 240 million per lung), where gas exchange occurs across a thin blood-air barrier. Alveoli are lined primarily by type I alveolar cells (flat, squamous pneumocytes covering 90-95% of the surface for diffusion) and type II alveolar cells (cuboidal, comprising 5-10% and producing pulmonary surfactant—a phospholipid mixture stored in lamellar bodies that reduces surface tension to prevent collapse).^[20]^[22]^[23] Associated structures support the respiratory tract's positioning and function within the thoracic cavity. The lungs, paired cone-shaped organs, occupy most of the thoracic space: the right lung has three lobes (upper, middle, lower) separated by oblique and horizontal fissures, while the left has two (upper, lower) due to the cardiac notch accommodating the heart. Each lung is enveloped by pleural membranes—a visceral layer adhering to the lung surface and a parietal layer lining the thoracic wall and diaphragm—separated by pleural fluid that minimizes friction during expansion. The diaphragm, a dome-shaped skeletal muscle separating the thoracic and abdominal cavities, serves as the primary ventilator, while intercostal muscles (external for inspiration, internal for expiration) between the ribs elevate and depress the chest wall to alter thoracic volume.^[24] Microscopically, the respiratory epithelium transitions from pseudostratified ciliated columnar in the conducting airways (trachea to bronchioles), featuring goblet cells for mucus and cilia for clearance, to simple squamous in the alveoli for minimal diffusion distance (about 25 nm blood-air barrier). This epithelial diversity optimizes conduction proximally and exchange distally. The vascular supply integrates with this structure via the pulmonary arteries, branching from the right ventricle to deliver deoxygenated blood to alveolar capillaries in a low-oxygen, high-carbon dioxide environment, and pulmonary veins, which collect oxygenated blood and return it to the left atrium; bronchial arteries provide oxygenated systemic blood to nourish the tract's tissues.^[20]^[22]^[24]

Mechanics of breathing

The mechanics of breathing involve the coordinated actions of respiratory muscles to facilitate the movement of air into and out of the lungs through changes in thoracic cavity volume and pressure gradients. During inspiration, the primary process is driven by the contraction of the diaphragm, the chief muscle of respiration, which flattens and descends, increasing the vertical dimension of the thoracic cavity. Simultaneously, the external intercostal muscles elevate the ribs, expanding the anteroposterior and transverse dimensions of the rib cage. This enlargement of the thoracic volume creates a subatmospheric pressure within the pleural space, generating a negative intrapleural pressure that expands the lungs. According to Boyle's law, which states that the pressure and volume of a gas are inversely related at constant temperature (P_1 V_1 = P_2 V_2), the increase in lung volume during inspiration decreases alveolar pressure below atmospheric levels, drawing air into the lungs.^[25] Expiration, in contrast, is primarily passive during quiet breathing, relying on the elastic recoil of the lungs and chest wall to return to their resting state. As the inspiratory muscles relax, the elastic fibers in the lung tissue and the natural tendency of the chest wall to spring outward decrease lung volume, raising alveolar pressure above atmospheric levels and expelling air. This recoil is facilitated by the negative intrapleural pressure maintained throughout the cycle, preventing lung collapse. In forced expiration, such as during exercise or coughing, accessory muscles including the internal intercostals and abdominal muscles (e.g., rectus abdominis and obliques) contract to further compress the abdominal contents, pushing the diaphragm upward and accelerating airflow.^[26] The volumes of air moved during breathing are quantified to assess ventilatory capacity. Tidal volume (TV) represents the normal volume inhaled or exhaled in a single breath at rest, approximately 500 mL in a healthy adult male. Inspiratory reserve volume (IRV) is the additional air that can be inhaled beyond tidal volume, while expiratory reserve volume (ERV) is the extra air that can be exhaled after a normal exhalation. Residual volume (RV) is the air remaining in the lungs after maximal expiration, preventing alveolar collapse. Vital capacity (VC) is the sum of TV, IRV, and ERV, and total lung capacity (TLC) is calculated as VC + RV, typically around 6 liters in adults. These measurements provide insight into overall respiratory efficiency without delving into molecular gas dynamics.^[27] The work of breathing (WOB) quantifies the energy expended to overcome respiratory system resistance and elasticity, essential for maintaining ventilation. It is calculated as the integral of pressure with respect to volume changes (W_{OB} = \int P \, dV), where pressure variations arise from elastic forces and airflow resistance. Key factors include lung and chest wall compliance, which measures volume change per unit pressure (higher compliance reduces work), and airway resistance, influenced by bronchial diameter and mucus. In healthy individuals, WOB accounts for about 1-2% of total oxygen consumption at rest but can rise significantly in disease states like emphysema, where reduced elastic recoil increases the effort required.^[28] Pulmonary surfactant, a phospholipid-protein complex secreted by type II alveolar cells, plays a critical role in minimizing the work of breathing by reducing surface tension at the air-liquid interface in alveoli. Without surfactant, surface tension would cause smaller alveoli to collapse into larger ones due to Laplace's law, which describes the pressure difference across a spherical surface (\Delta P = \frac{2T}{r}, where T is surface tension and r is radius), leading to instability and atelectasis. By dynamically lowering T during expiration, surfactant stabilizes alveoli, enhances compliance, and prevents collapse, thereby optimizing mechanical efficiency.^[29]

Gas exchange

Gas exchange in the mammalian respiratory system occurs primarily through passive diffusion across the alveolar-capillary membrane, where oxygen (O₂) from alveolar air enters the bloodstream and carbon dioxide (CO₂) from blood diffuses into the alveoli for exhalation.^[30] This process is facilitated by the thin, extensive interface between alveolar type I epithelial cells and pulmonary capillary endothelial cells, enabling rapid equilibration of gases between air and blood within approximately 0.75 seconds of transit time through the pulmonary capillaries.^[30] The rate of gas diffusion follows Fick's law, expressed as V = \frac{A \cdot D \cdot \Delta P}{T}, where V is the diffusion rate, A is the surface area available for exchange (approximately 70 m² in adult humans), D is the diffusion coefficient of the gas, \Delta P is the partial pressure gradient across the membrane, and T is the membrane thickness (ranging from 0.2 to 1 μm).^[31] This law underscores how the large surface area and minimal thickness optimize diffusion efficiency, while the partial pressure gradients drive the net movement of gases.^[31] The partial pressure gradients are established by differences between atmospheric air, alveolar gas, and blood. In inspired atmospheric air at sea level, the partial pressure of oxygen (PO₂) is approximately 160 mmHg and that of carbon dioxide (PCO₂) is 0.3 mmHg; in the alveoli, PO₂ drops to about 104 mmHg due to ongoing consumption and mixing with residual air, while PCO₂ rises to 40 mmHg from metabolic production.^[32] In arterial blood, PO₂ equilibrates to 95-100 mmHg and PCO₂ to 40 mmHg, reflecting near-complete diffusion across the membrane under normal conditions.^[33] Once in the blood, oxygen binds to hemoglobin in red blood cells, with the relationship described by the oxygen-hemoglobin dissociation curve, which exhibits a sigmoid shape due to cooperative binding that enhances oxygen loading in the lungs and unloading in tissues.^[34] The curve shifts rightward via the Bohr effect, where decreased pH or increased PCO₂ reduces hemoglobin's oxygen affinity to facilitate tissue delivery; additionally, 2,3-bisphosphoglycerate (2,3-BPG) binds to deoxyhemoglobin, further stabilizing the low-affinity state and promoting oxygen release.^[35]^[34] Carbon dioxide transport from tissues to lungs occurs in three forms: about 70% as bicarbonate ions (HCO₃⁻), 20% bound to hemoglobin as carbaminohemoglobin, and 10% dissolved in plasma.^[36] The bicarbonate form predominates through the carbonic anhydrase-catalyzed reaction in red blood cells: \ce{CO2 + H2O ⇌ H2CO3 ⇌ H+ + HCO3-}, where CO₂ diffuses into erythrocytes, is converted to bicarbonate for exchange with chloride ions (Hamburger shift) to maintain electroneutrality, and then diffuses out to plasma bound to proteins.^[36] Efficient gas exchange requires matching ventilation to perfusion (V/Q ratio), ideally around 0.8 in the lungs overall, to ensure adequate oxygenation without wasted perfusion.^[30] This is regulated by hypoxic pulmonary vasoconstriction, where low alveolar PO₂ triggers constriction of precapillary arterioles in poorly ventilated regions, redirecting blood flow to better-aerated alveoli and minimizing V/Q mismatch.^[37]

Regulation of ventilation

The regulation of ventilation in mammals involves intricate neural and chemical mechanisms that dynamically adjust the rate and depth of breathing to ensure adequate gas exchange and maintain physiological homeostasis. These control systems integrate inputs from the central nervous system, peripheral sensors, and reflexes to respond to changes in metabolic demands, such as those occurring during rest, exercise, or altered blood chemistry. The primary goal is to match alveolar ventilation to metabolic rate, keeping arterial partial pressures of oxygen (PaO₂) and carbon dioxide (PaCO₂) within narrow limits.^[38] Central to this process are the respiratory centers located in the brainstem, which generate and modulate the basic rhythm of breathing. The medullary rhythmicity area, situated in the medulla oblongata, houses the pre-Bötzinger complex, a cluster of neurons essential for initiating the inspiratory phase and establishing the fundamental respiratory rhythm through pacemaker-like activity.^[39] This complex coordinates with the dorsal respiratory group (DRG) for inspiratory drive and the ventral respiratory group (VRG) for both inspiration and expiration. Fine-tuning of the rhythm occurs via pontine centers: the pneumotaxic center in the upper pons limits the duration of inspiration to prevent overinflation and promote expiration, while the apneustic center in the lower pons prolongs inspiration when pneumotaxic input is reduced, ensuring adaptive adjustments to varying conditions.^[40]^[41] Chemical feedback from chemoreceptors provides critical sensory input to these centers, detecting deviations in blood gases and pH to trigger compensatory changes in ventilation. Central chemoreceptors, located on the ventral surface of the medulla, primarily respond to increases in cerebrospinal fluid (CSF) pH, which decreases due to elevated PaCO₂ diffusing across the blood-brain barrier and forming carbonic acid; this hypercapnic stimulus drives hyperventilation to expel excess CO₂.^[42] Peripheral chemoreceptors in the carotid bodies (at the carotid artery bifurcation) and aortic bodies (along the aortic arch) sense arterial PO₂ below approximately 60 mmHg, elevated PCO₂, and decreased pH, rapidly signaling the medullary centers via glossopharyngeal and vagus nerves to increase breathing rate and depth, with a stronger response to hypoxia in acute scenarios.^[38]^[40] A key protective reflex is the Hering-Breuer inflation reflex, mediated by stretch receptors in the smooth muscle of the airways and alveoli. When lung volume increases during inspiration, these receptors activate via the vagus nerve, inhibiting the inspiratory centers in the medulla to terminate inspiration and facilitate expiration, thereby preventing alveolar overdistension and promoting rhythmic breathing.^[43] During exercise, ventilation increases proportionally to metabolic rate—a phenomenon known as exercise hyperpnea—to match heightened oxygen consumption and CO₂ production. This response is primarily triggered by the rise in CO₂ output, which stimulates central and peripheral chemoreceptors, but also involves neural inputs from proprioceptors in exercising muscles (group III and IV afferents) and central command from higher brain centers, ensuring rapid onset of hyperpnea even before significant changes in blood gases occur.^[44]^[45] Ventilation also plays a vital role in acid-base homeostasis, particularly in compensating for metabolic acidosis by inducing hyperventilation to lower PaCO₂ and raise blood pH. This process is governed by the Henderson-Hasselbalch equation, which describes the carbonic acid-bicarbonate buffer system:

\text{pH} = 6.1 + \log_{10} \left( \frac{[\ce{HCO3-}]}{0.03 \times P_{\ce{CO2}}} \right)

Here, reducing P_{\ce{CO2}} through increased ventilation shifts the equilibrium to alleviate acidosis, as detected by chemoreceptors.^[46]^[47]

Additional roles

The mammalian respiratory system serves several non-respiratory functions that contribute to host defense, structural integrity, metabolic homeostasis, communication, thermoregulation, and adaptive responses to environmental stressors. These roles highlight the multifaceted nature of the lungs and airways beyond gas exchange.

Local Defenses

The airways and alveoli employ multiple innate immune mechanisms to protect against inhaled pathogens and particulates. The mucociliary escalator, consisting of ciliated epithelial cells and a overlying mucus layer, traps microbes and debris in the mucus, which is then propelled upward by coordinated ciliary beating toward the pharynx for expulsion via swallowing or coughing.^[48] Alveolar macrophages, resident immune cells within the alveolar spaces, act as sentinels by phagocytosing pathogens, apoptotic cells, and foreign particles, thereby initiating inflammatory responses and maintaining alveolar sterility.^[49] Additionally, pulmonary surfactant contains antimicrobial components such as lysozyme and host defense peptides (e.g., cathelicidins and defensins), which disrupt microbial membranes and enhance local immunity at the air-liquid interface.^[50]

Prevention of Alveolar Collapse

Pulmonary surfactant, a lipid-protein complex secreted by type II alveolar cells, plays a critical role in maintaining lung compliance by reducing surface tension at the air-liquid interface during respiration. Its primary lipid component, dipalmitoylphosphatidylcholine (DPPC), forms a monolayer that dynamically compresses and expands, preventing alveolar collapse (atelectasis) at end-expiration and facilitating efficient lung expansion with minimal energy expenditure.^[51] This biophysical property ensures structural stability, particularly in smaller alveoli prone to instability due to Laplace's law.

Metabolic Functions

The pulmonary endothelium houses angiotensin-converting enzyme (ACE), a key enzyme in the renin-angiotensin system that catalyzes the conversion of angiotensin I to angiotensin II, a potent vasoconstrictor that regulates systemic blood pressure and fluid balance.^[52] This metabolic role positions the lungs as a central processor for circulating peptides, influencing cardiovascular homeostasis independently of gas exchange.

Vocalization

The larynx facilitates sound production essential for communication in mammals. Airflow from the trachea passes through the vocal cords—paired folds of laryngeal tissue—that vibrate due to Bernoulli's principle, wherein subglottic pressure differences cause rapid opening and closing, generating fundamental frequencies modulated by cord tension and length.^[53] This phonation mechanism allows for vocalization ranging from simple calls to complex speech in humans.

Thermoregulation

In many mammals, the respiratory system aids in heat dissipation through panting, a rapid, shallow breathing pattern that increases evaporative cooling from the upper airways and tongue without excessive hyperventilation.^[54] The nasal passages further contribute via countercurrent heat exchange, where warm arterial blood in nasal turbinates transfers heat to cooler venous blood returning from the mucosa, conserving body heat during inhalation while warming inspired air and minimizing respiratory water loss.^[55]

Responses to Hypoxia

The lungs respond directly to alveolar hypoxia through hypoxic pulmonary vasoconstriction (HPV), a localized mechanism where low oxygen tension in pulmonary arterioles triggers smooth muscle contraction, redirecting blood flow from poorly ventilated regions to better-oxygenated areas to optimize ventilation-perfusion matching.^[56] Indirectly, respiratory detection of systemic hypoxia via peripheral chemoreceptors (e.g., carotid bodies) contributes to the hypoxic stimulus that drives renal production of erythropoietin, a hormone stimulating red blood cell formation to enhance oxygen-carrying capacity.^[57]

Variations in Mammals

Aquatic adaptations in cetaceans

Cetaceans, fully aquatic mammals including whales, dolphins, and porpoises, exhibit specialized respiratory adaptations that enable prolonged submersion while facilitating efficient gas exchange upon surfacing. These modifications support dives exceeding 300 meters in species like sperm whales, where hydrostatic pressure compresses the respiratory system to prevent nitrogen uptake and decompression sickness. Central to this is the repositioning and structural enhancement of the nasal passages, alongside physiological mechanisms for oxygen conservation. The blowhole represents a key anatomical adaptation, consisting of a dorsal nasal opening that has migrated posteriorly from the rostrum tip to the top of the head through evolutionary telescoping of the skull.^[58] In odontocetes (toothed whales and dolphins), a single blowhole is equipped with muscular valves and nasal plugs that provide a watertight seal during dives, preventing water ingress while allowing rapid opening for respiration.^[58] Mysticetes (baleen whales) possess paired blowholes separated by a nasal septum, similarly supported by soft tissue and valvular structures that ensure closure under pressure, minimizing energy expenditure for surfacing breaths.^[58] This configuration optimizes hydrodynamic efficiency by positioning the airway atop the head, enabling ventilation with minimal exposure above water. To withstand extreme pressures during deep dives, cetacean lungs demonstrate remarkable tolerance to collapse, facilitated by high thoracic compliance and rib cage flexibility.^[59] The rib cage features reduced bone density and increased elasticity, allowing compression at depths around 70 meters where alveolar collapse begins, with full lung compression occurring up to 300 meters in deep-diving species.^[59] Thickened alveolar walls, abundant elastic fibers, and enhanced pulmonary surfactants reduce surface tension, enabling reversible collapse and re-expansion upon ascent without structural damage.^[59] This adaptation shifts residual air into non-gas-exchanging upper airways, limiting inert gas loading and supporting safe repetitive dives. Oxygen storage is augmented by elevated myoglobin concentrations in skeletal muscles, providing an onboard reserve that extends aerobic dive duration.^[60] Cetacean myoglobin levels are approximately 10–20 times higher than in terrestrial mammals, correlating with protein stability adaptations that maintain function under hypoxia.^[60] This enhancement, evolved since divergence from land ancestors around 50 million years ago, accounts for a significant portion of total body oxygen stores, primarily in locomotory muscles where myoglobin facilitates diffusion to mitochondria during prolonged submersion.^[60] The diving reflex further conserves oxygen through integrated cardiovascular responses triggered by facial immersion in water.^[61] Upon submersion, stimulation of trigeminal nerve receptors in the nasal mucosa induces bradycardia, reducing heart rate by up to 80% via vagal activation to lower cardiac output and oxygen demand.^[61] Concurrently, peripheral vasoconstriction, mediated by sympathetic pathways, redirects blood flow from non-vital tissues like muscles and skin to the brain and heart, maintaining central perfusion under hypoxia.^[61] This reflex, coupled with apnea, prioritizes essential organ oxygenation and is modulated by dive depth and duration. Surfacing for respiration is highly efficient, leveraging large lung volumes and rapid airflow dynamics to maximize gas exchange in brief intervals.^[62] Total lung capacity scales with body mass (approximately 0.135 × body mass^0.92 liters), with vital capacity comprising 80–90% of this volume, allowing near-complete air renewal per breath.^[62] Exhalation, or the "blow," occurs first as a forceful passive recoil driven by elastic thoracic structures, achieving peak flows of 20–160 liters per second and expelling humidified, CO₂-rich air explosively.^[63] Inhalation follows immediately via active diaphragmatic contraction, with inspiratory flows about half the expiratory rate, completing the cycle in fractions of a second and minimizing dead space ventilation.^[63] This sequence supports high respiratory rates during recovery from dives, ensuring rapid reoxygenation.

Unique features in equids and proboscideans

Equids, such as horses, exhibit specialized respiratory adaptations that support high-endurance locomotion, including large nasal turbinates that enhance heat and moisture recovery during intense galloping. These turbinates, richly vascularized, provide an extensive surface area within the nasal cavities for exchanging heat and water vapor with inhaled air, thereby conserving body fluids and minimizing thermal stress in arid or high-exertion environments.^[64] This mechanism is particularly vital during prolonged exercise, where expiratory air warms and humidifies incoming air, reducing evaporative losses that could otherwise impair performance. Additionally, the equine larynx demonstrates notable mobility, enabling it to form a tight seal during swallowing to prevent aspiration of food or liquids into the airway, while dynamically opening to maximal dimensions during inspiration to accommodate high airflow demands.^[64]^[65] Endurance adaptations in equids further include a nasal venous countercurrent exchanger that cools arterial blood en route to the brain, mitigating hyperthermia during exertion. Venous plexuses in the nasal mucosa, cooled by evaporation, transfer heat away from incoming arterial blood via countercurrent flow, preserving cerebral function under thermal load.^[66] Equine lungs reflect this athletic specialization with a vital capacity of approximately 42 liters, roughly eight times that of a human's 5 liters, allowing for substantial tidal volumes—up to 12-15 liters during galloping—to sustain oxygen delivery at peak intensities.^[67]^[64] However, these adaptations also confer vulnerabilities, as exemplified by equine recurrent airway obstruction (RAO), commonly known as heaves, a chronic allergic condition triggered by environmental allergens that causes bronchial inflammation, mucus hypersecretion, and airflow limitation, severely compromising respiratory efficiency in stabled horses.^[68] In proboscideans like elephants, the trunk serves as a multifunctional airway extension, facilitating selective breathing, snorkeling in deep water, and integration with feeding behaviors. This elongated proboscis, containing nasal passages connected directly to the lungs, allows elephants to breathe while submerged up to their head, a capability linked to potential aquatic ancestry and supported by valvular control at the nostrils to prevent water ingress.^[69] The trunk's dual role in respiration and manipulation underscores its evolutionary versatility, enabling efficient gas exchange without disrupting foraging or social activities. Complementing this, elephants possess large lungs scaled to their massive body size to meet baseline oxygen needs despite gravitational constraints on thoracic expansion.^[70] Proboscidean endurance is bolstered by a relatively low mass-specific resting metabolic rate, as expected for large mammals under allometric scaling, which reduces overall oxygen consumption and ventilatory workload during quiescence, with respiratory rates of 4-12 breaths per minute at rest.^[71] Unique pleural adaptations, including a distensible collagen network replacing traditional pleural cavities, further mitigate gravitational stress on the lungs, preventing compression and edema during posture changes or submersion.^[70]

Avian Respiratory System

Anatomical structure

The avian respiratory system features a distinctive anatomical organization centered on rigid lungs and an extensive network of air sacs, optimized for efficient gas exchange during flight. The lungs are small and non-expandable, comprising approximately 1-2% of body mass, similar to the 1-3% in mammals but with a higher density of exchange surfaces that enhance oxygen extraction efficiency.^[72]^[73] A key component is the system of nine interconnected air sacs, divided into cervical (two), clavicular (one, unpaired), thoracic (four: two anterior and two posterior), and abdominal (two) groups. These thin-walled sacs, lacking significant blood vessels, serve as lightweight bellows that facilitate ventilation without participating directly in gas exchange.^[74]^[75] The lungs themselves consist of tubular airways known as parabronchi, which form the primary sites of gas exchange. These parabronchi branch into networks of air capillaries—fine, interconnected tubules where oxygen and carbon dioxide diffusion occur across a thin blood-gas barrier. Unlike the expandable alveoli in mammalian lungs, the avian parabronchi maintain a fixed structure, supporting continuous airflow through the system.^[76]^[73] Blood vessels in the avian lung are arranged in a cross-current configuration, where deoxygenated blood flows perpendicular to the parabronchial airflow, repeatedly encountering fresh air across multiple exchange sites. This setup maintains a favorable partial pressure gradient for oxygen (PO₂), allowing blood to achieve higher oxygenation levels than in the exhaled air.^[76]^[75] Supporting this lightweight anatomy are skeletal adaptations, including the uncinate process—a backward-projecting rib extension that aids in sternal movement—and hollow bones that minimize overall body weight while preserving structural integrity for respiratory function.^[74]

Unidirectional airflow mechanics

The avian respiratory system features unidirectional airflow through the lungs, a key distinction from the bidirectional tidal breathing in mammals, enabling continuous exposure of gas exchange surfaces to fresh air. This flow is achieved over two full respiratory cycles, consisting of two inspirations and two expirations, which together complete the passage of inhaled air through the parabronchi of the lungs. During the first inspiration, fresh air enters the trachea and is directed primarily into the caudal (posterior) air sacs, while simultaneously, deoxygenated air from the lungs begins moving toward the cranial (anterior) air sacs. In the first expiration, air from the caudal air sacs is propelled through the parabronchi for gas exchange, flowing unidirectionally from caudal to cranial regions, and collects in the cranial air sacs. The second inspiration then draws additional fresh air into the caudal air sacs while shifting the now partially exchanged air from the parabronchi into the cranial air sacs. Finally, the second expiration expels the spent air from the cranial air sacs through the trachea to the exterior. This rhythmic, bellows-like action of the air sacs ensures no reversal of flow direction within the lungs, maintaining a steady stream of air across the exchange surfaces.^[77] The precise flow path in this system begins with air entering the trachea, branching into the primary bronchi, and filling the caudal air sacs during inspiration phases. From there, it moves unidirectionally through the parabronchi—narrow, tubular structures within the rigid lungs where gas exchange occurs via cross-current diffusion between air and blood capillaries—before reaching the cranial air sacs. The cranial air sacs then serve as reservoirs, directing the exhaled air back through the trachea and out of the body. This pathway, supported by aerodynamic valving at bronchial junctions rather than physical valves, prevents mixing of fresh and stale air in the exchange regions, ensuring that parabronchi are continuously ventilated with oxygen-rich air throughout both inspiratory and expiratory phases.^[75]^[78] This unidirectional mechanics enhances gas exchange efficiency, allowing birds to extract slightly more oxygen than mammals for equivalent ventilation volumes, primarily due to the elimination of dead space mixing and continuous renewal of air in the parabronchi. In mammals, tidal breathing mixes incoming fresh air with residual exhaled air, reducing effective oxygen availability, whereas the avian system achieves near-complete separation, with extraction efficiencies reaching up to 31% in species like the fish crow compared to 26-30% in mammals such as humans. The theoretical basis for this efficiency in the cross-current model of avian lungs is approximated by the equation for fractional oxygen extraction, F_{\ce{[O2](/page/O2)}} \approx 1 - e^{-[DL](/page/DL) / \dot{V}_A}, where [DL](/page/DL) represents the lung diffusing capacity for oxygen and \dot{V}_A is the alveolar ventilation rate; higher [DL](/page/DL) / \dot{V}_A ratios in birds yield greater extraction without requiring proportional increases in ventilation.^[78]^[79] Respiratory muscles facilitate this asymmetric cycle through coordinated compression and expansion of the air sacs and rib cage. Costal muscles, including external and internal intercostals, drive rib cage expansion during inspiration to inflate the caudal air sacs, while sternal muscles, such as the supracoracoideus and subclavius attached to the keel, contribute to sternum movement for forceful expiration and compression of the cranial air sacs. This asymmetry ensures differential pressure changes that maintain unidirectional flow without reversing direction in the lungs. These mechanics are particularly adapted for flight, reducing overall body buoyancy via lightweight air sacs while supporting elevated metabolic demands; during sustained flight, birds can achieve VO2 max up to 20 times their resting rate, enabling prolonged aerobic activity under hypoxic conditions like high altitudes.^[77]

Reptilian and Amphibian Respiratory Systems

Reptilian lungs and ventilation

Reptilian lungs exhibit significant structural diversity, reflecting adaptations to ectothermic lifestyles and varying metabolic demands. Unicameral lungs, characterized by a single, simple sac-like chamber, are common in snakes and many lizards, such as the tegu lizard (Tupinambis nigropunctatus), where the central lumen is lined with favoli for gas exchange.^[80] In contrast, multicameral lungs feature multiple partitioned chambers formed by incomplete septa, as seen in crocodiles and turtles, which enhance compartmentalization and overall respiratory efficiency.^[80] These septa, often incomplete and vascularized, increase the surface area available for gas exchange without fully dividing the lung into isolated units. Ventilation in reptiles primarily relies on costal movements, but mechanisms differ across taxa. Lizards employ buccal pumping, utilizing the gular region to draw air into the lungs through expansion of the throat and body cavity.^[81] Snakes utilize a hepatic piston mechanism, where contraction of abdominal muscles compresses the liver to expel air and create negative pressure for inspiration. Crocodilians possess a unique diaphragmatic-like muscle, the m. diaphragmaticus, which pulls the liver caudally to expand the thoracic cavity, decoupling ventilation from locomotion and enabling more efficient inspiration.^[81] Reptilian lungs show lower PO₂ gradients compared to mammals, typically 14–28 Torr between expired air and left atrial blood in varanid lizards at rest, attributable to ventilation-perfusion mismatches and modest intrapulmonary shunts (about 2% of cardiac output during exercise).^[80] This reflects their slower metabolic rates as ectotherms. Crocodilians control buoyancy during submersion by shifting the position of their lungs using the diaphragmaticus and other muscles to adjust the center of buoyancy relative to the center of mass.^[82] Ventilation efficiency in reptiles is highly temperature-dependent, with rates following the Q₁₀ effect where metabolic and respiratory rates approximately double for every 10°C rise in body temperature, as observed in crocodiles like Crocodylus porosus (Q₁₀ ≈ 2.68 over 15–35°C).^[83] Multicameral lungs in active species, such as varanids, support higher surface-to-volume ratios, mitigating some inefficiencies from heterogeneous gas distribution.^[80]

Amphibian cutaneous and pulmonary respiration

Amphibians exhibit a bimodal respiratory strategy that integrates cutaneous and pulmonary gas exchange, allowing them to thrive in diverse aquatic and terrestrial environments. Cutaneous respiration occurs through the thin, highly vascularized skin, which is permeable to oxygen (O₂) and carbon dioxide (CO₂), enabling diffusion directly into the bloodstream. This process accounts for 50–100% of total O₂ uptake in many frog species, with extreme cases approaching full reliance on skin breathing during periods of low activity or hypoxia.^[84] In adult amphibians, pulmonary respiration supplements cutaneous exchange via simple, sac-like lungs that possess reduced surface area compared to those of more advanced vertebrates, limiting their efficiency for high metabolic demands. These lungs are unicameral structures, consisting of two elongated chambers connected to the glottis at the mouth base, with minimal internal partitioning. During larval stages, amphibian tadpoles rely on external gills for aquatic gas exchange, which are feathery projections exposed to water and later resorbed during metamorphosis as lungs develop.^[85]^[86] Lung ventilation in adults employs a buccal force pump mechanism, where muscles in the floor of the mouth generate positive pressure to inflate the lungs, distinct from the negative-pressure systems in mammals. The process involves rhythmic compression and expansion of the buccal cavity to draw in and force air into the lungs, often in irregular bouts that maintain lung inflation without active expiration. This pump allows efficient gas renewal despite the lungs' simplicity.^[87] Environmental adaptations enhance respiratory resilience during dormancy. In estivation, species akin to lungfish, such as the Australian goldfields frog (Neobatrachus wilsmorei), reduce metabolic rates by up to 80%, relying on cutaneous diffusion for minimal gas exchange while encased in cocoons to conserve water. Similarly, during hibernation in aquatic habitats, submerged amphibians depend almost entirely on skin respiration to meet low oxygen demands under hypoxic conditions.^[88]^[89] However, the reliance on cutaneous respiration imposes significant limitations on terrestrial activity, as the permeable skin heightens desiccation risk in dry environments, necessitating moist or aquatic habitats for sustained viability. This vulnerability constrains amphibians to humid microclimates, where water loss through the skin does not compromise gas exchange efficiency.^[90]

Fish Respiratory System

Gill structure and function

Fish gills are specialized respiratory organs in aquatic vertebrates, primarily consisting of 4 to 5 gill arches per side of the head, with the first four typically serving respiratory functions and the fifth often non-respiratory. Each gill arch supports a series of primary filaments, which are elongated structures bearing numerous secondary lamellae that form the primary site of gas exchange. These secondary lamellae feature a thin epithelium, approximately 0.5 μm thick, composed of flattened pavement cells that minimize the diffusion distance for oxygen and carbon dioxide across the respiratory surface.^[91]^[92]^[93] The efficiency of oxygen extraction in fish gills relies on a countercurrent exchange system, where water flows over the secondary lamellae in the opposite direction to blood flow within the lamellar capillaries. This arrangement maintains a steep concentration gradient for oxygen diffusion throughout the exchange process, as described by Fick's law of diffusion, which states that the rate of diffusion is proportional to the surface area, diffusion coefficient, and partial pressure difference, divided by the diffusion distance. As a result, fish can achieve 80-90% oxygen extraction from the ventilating water, far exceeding the efficiency of concurrent flow systems.^[94]^[95] Ventilation of the gills occurs through two main mechanisms: ram ventilation, utilized by fast-swimming species where forward motion forces water over the gills, and pump ventilation, involving rhythmic contractions of the buccal and opercular cavities in stationary or slow-moving fish. In pump ventilation, the buccal cavity expands to draw in water and contracts to force it over the gills, while the opercular lid creates a pressure gradient to expel spent water. The total ventilatory flow rate Q is calculated as the product of stroke volume V (the volume of water moved per cycle) and ventilatory frequency f (cycles per unit time), i.e., Q = V \times f, allowing fish to adjust flow based on metabolic demands.^[96] In addition to gas exchange, fish gills integrate ionoregulation through specialized chloride cells, also known as ionocytes, embedded in the filament and lamellar epithelium. These cells actively transport ions such as sodium and chloride to maintain osmotic balance, with seawater fish excreting excess salts and freshwater fish absorbing ions from dilute environments, thereby coupling osmoregulation with respiration without compromising the thin barrier for gas diffusion.^[97] The respiratory efficiency of gills is challenged by the low ambient partial pressure of oxygen (PO₂) in water, typically ranging from 30 to 100 mmHg under natural conditions compared to approximately 160 mmHg in air, necessitating the processing of large volumes of water—often 10 to 20 times the fish's body volume per hour—to meet oxygen demands. This high throughput, enabled by the countercurrent system and ventilatory mechanisms, compensates for the lower oxygen availability in the aqueous medium.^[98]^[99]

Accessory breathing organs

Certain fish species have evolved accessory breathing organs to supplement gill-based aquatic respiration in environments with low dissolved oxygen, such as hypoxic waters or during transitions to air exposure. These structures enable bimodal respiration, allowing oxygen uptake from both water and air, and are particularly prevalent in tropical and subtropical species facing seasonal droughts or stagnant conditions.^[13] In anabantid fishes, such as the betta fish (Betta splendens), the labyrinth organ consists of highly vascularized suprabranchial chambers located above the gills, which facilitate air gulping at the water surface. This organ features intricate, plate-like folds that increase the respiratory surface area, allowing efficient diffusion of oxygen from swallowed air bubbles into the bloodstream. The labyrinth enables these fish to survive in oxygen-poor waters by extracting up to 50-100% of their oxygen needs from air, depending on environmental hypoxia.^[100]^[101] Lungfish (Dipnoi), including species like the African lungfish (Protopterus aethiopicus), possess modified swim bladders that serve as vascularized proto-lungs for aerial oxygen uptake. These lungs, derived from the swim bladder, are paired, sac-like structures lined with a rich capillary network that supports gas exchange during periods of aestivation or low-oxygen aquatic conditions. In normoxic water, lungfish rely primarily on gills for respiration, but under hypoxia, they shift to lung breathing, where the proto-lung can provide nearly all required oxygen while minimizing branchial ventilation.^[102]^[103] Some loaches, such as the weather loach (Misgurnus anguillicaudatus), exhibit gut-based respiration through intestinal diverticula in the posterior intestine, which act as accessory air-breathing sites. These diverticula are thin-walled, vascularized extensions that allow diffusion of oxygen from air swallowed and passed through the gut, particularly in soft-bottom or muddy habitats with severe hypoxia. This adaptation supplements gill function by enabling facultative air breathing, where the intestine can contribute significantly to total oxygen uptake during environmental stress.^[104]^[105] Behavioral adaptations in Amazonian air-breathing fish, such as the tambaqui (Colossoma macropomum), include increased surface access frequency during droughts or hypoxic events, where individuals may gulp air every few minutes to minutes to mitigate oxygen deficits. This surfacing behavior is triggered by environmental cues like low dissolved oxygen levels below 2 mg/L, enhancing survival in seasonally flooded or drying river systems.^[106]^[107] Physiological partitioning in bimodal-breathing fish shifts oxygen uptake dramatically under air exposure or severe hypoxia, with accessory organs often accounting for 80% of total oxygen while gills contribute approximately 20%. This redistribution is mediated by cardiovascular adjustments, such as preferential blood flow to the air-breathing organ, ensuring efficient resource allocation in variable oxygen environments.^[108]^[109]

Invertebrate Respiratory Systems

Tracheal systems in arthropods

The tracheal system in arthropods consists of a network of air-filled tubes that invaginate from the exoskeleton, enabling direct delivery of oxygen to tissues without reliance on a circulatory system.^[13] These structures begin as spiracles, valved external openings typically numbering up to 10 pairs along the thoracic and abdominal segments, which regulate air entry and can close to prevent desiccation.^[13] From the spiracles, primary tracheae branch into progressively finer tubes, including tracheoles with diameters of 0.1–1 μm that terminate at or penetrate individual cells, often near mitochondria for efficient gas exchange.^[110] The walls of tracheae and tracheoles are reinforced by spiral taenidia to maintain patency, and their thin cuticular linings (less than 0.1 μm in tracheoles) facilitate diffusion across a vast surface area.^[110] Ventilation in this system varies by arthropod size and activity level. In small arthropods, such as many mites or inactive insects, gas exchange relies predominantly on passive diffusion driven by concentration gradients, sufficient due to the short distances involved.^[13] Larger insects, including locusts, supplement diffusion with active ventilation through abdominal muscle contractions that pump air in and out, potentially increasing exchange rates up to fourfold during high demand or hypoxia.^[13] Oxygen transport occurs solely via diffusion through the air-filled lumens, bypassing any blood carrier and allowing rapid equilibration directly at tissues.^[110] This efficiency is constrained by Fick's law of diffusion, which limits effective transport distances to less than 1 cm, thereby capping arthropod body sizes and necessitating active mechanisms in bigger species.^[13] A key adaptation in many insects is the discontinuous gas exchange cycle (DGC), which alternates between closed (spiracles shut, minimizing water loss), flutter (rapid spiracle oscillations for selective gas permeation), and open (unidirectional airflow) phases to optimize carbon dioxide release while conserving water.^[111] This pattern, observed across at least five insect orders, evolved independently multiple times and aids regulation in variable environments.^[111] In spiders and scorpions, book lungs represent a transitional form between aquatic gills and fully tracheal systems, featuring stacked lamellae with alternating air-filled and hemolymph channels that support diffusion-based exchange.^[13]

Mantle cavities and other mechanisms in molluscs and annelids

In molluscs, respiration primarily occurs within the mantle cavity, a fluid-filled space enclosed by the mantle tissue that surrounds the visceral mass. Aquatic species, such as bivalves and cephalopods, utilize ctenidia—feather-like gills composed of numerous filaments lined with ciliated epithelial cells—for gas exchange. These structures increase the surface area for oxygen diffusion from water into the hemolymph, while carbon dioxide is expelled.^[112]^[113] Water flow through the mantle cavity in bivalves is directed by the beating of cilia on the ctenidia, creating a unidirectional current that enters via an incurrent siphon and exits through an excurrent siphon, often aided by muscular contractions of the mantle and foot. This ciliary-muscular ventilation ensures efficient oxygenation, with the countercurrent arrangement between water and hemolymph flow in cephalopods like squid maximizing oxygen extraction efficiency.^[114]^[13] In cephalopods, including octopuses, the gills are paired and supported by branchial hearts that pump hemolymph over the respiratory surfaces, supplemented by limited cutaneous respiration through the skin when gills are compromised.^[115] Molluscs employ hemocyanin, a copper-based respiratory pigment dissolved in the hemolymph, which binds oxygen reversibly and is effective in the often oxygen-poor aquatic environments they inhabit.^[116] In terrestrial forms like slugs, the mantle cavity is reduced and vascularized to function as a lung, relying on air diffusion over a moist surface, though this limits efficiency relative to aquatic counterparts due to lower oxygen availability.^[13] In annelids, respiration occurs mainly through cutaneous diffusion across the moist body wall, facilitated by a thin, permeable epidermis richly supplied with capillaries. Earthworms, for instance, derive most of their oxygen needs from skin respiration, with possible minor contributions from the gut or buccal cavity during burrowing.^[117] The dissolved hemoglobin in their blood enhances oxygen transport and storage under low-oxygen conditions.^[118] Polychaete annelids supplement skin diffusion with parapodia—lateral, paddle-like extensions of the body wall that are highly vascularized and increase respiratory surface area. These structures undulate to generate water currents over the body, promoting unidirectional flow for ventilation in aquatic environments, particularly in tube-dwelling species.^[119] Overall, annelid respiratory efficiency is lower than in active aquatic molluscs, constrained by reliance on passive diffusion and environmental moisture.^[118]

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Mechanisms of unidirectional flow in parabronchi of avian lungs
The dorsobronchial flow was shown to be unidirectional in both respiratory phases, leading from the mesobronchus through the dorsobronchi to the parabronchi.
[65]
Comparative Physiology of Lung Complexity: Implications for Gas Exchange | Physiology | American Physiological Society
### Summary of Reptilian Lung Types and Related Features
[66]
Evolution and Functional Differentiation of the Diaphragm Muscle of ...
In crocodiles, piston action of the diaphragmaticus muscle against the liver increases the thoracic volume and decouples ventilation from locomotion restraints ...
[67]
Metabolic Rate, Q10 and Respiratory Quotient (RQ) in Crocodylus ...
Metabolic Rate, Q10 and Respiratory Quotient (RQ) in Crocodylus porosus, and Some Generalizations about Low RQ in Reptiles · Abstract · Journal History.
[68]
(PDF) Skin Breathing in Amphibians - ResearchGate
Nov 16, 2014 · Cutaneous gas exchange can fulfill routinely 0% to 100% of O2 uptake and 20% to 100% of CO2 excretion (1). Amphibians pay a price for this: They ...
[69]
Respiratory System – Comparative Vertebrate and Human Anatomy
... amphibians and probably maintained an aquatic larval phase reliant on gills for respiration. ... gills as larvae and then lungs as adults. Some amphibians, ...<|separator|>
[70]
The Life Cycle of Amphibians | Biology for Non-Majors II
With frogs and toads, the external gills of the newly hatched tadpole are covered with a gill sac after a few days, and lungs are quickly formed. Front legs ...
[71]
Ventilatory Mechanisms of the Amphibian, Xenopus Laevis
Jun 1, 1979 · The buccal cavity is used as a pump to fill the lungs, and in ranids and bufonids two ventilation patterns, renewing gas in the lungs or in the ...ABSTRACT · INTRODUCTION · MATERIALS AND METHODS · RESULTS
[72]
Metabolic depression and Na + /K + gradients in the aestivating ...
During aestivation the metabolic rate of the Australian goldfields frog Neobatrachus wilsmorei was reduced by 80% from its standard metabolic rate.
[73]
Pulmonary and cutaneous O2 gas exchange: a student laboratory ...
Mar 1, 2013 · Many aquatic frogs are renowned for their cutaneous gas exchange capacity, where often the majority of CO2 is excreted across the skin.
[74]
Amphibians Exhibit Extremely High Hydric Costs of Respiration
Sep 17, 2024 · Amphibians are known for being vulnerable to rapid desiccation, in part because they rely on thin, permeable skin for cutaneous respiration.
[75]
WFS 550 Fish Physiology - Gill Structure
All modern fishes have four respiratory gill arches and a 5th non-respiratory arch on each side of the buccal cavity.Missing: 4-5 thin
[76]
Gill - an overview | ScienceDirect Topics
The gills of teleosts consist of gill arches, filaments and lamellae. In adults, the lamellae are considered the definitive site of respiratory gas exchange ...
[77]
New developments on gill innervation: insights from a model ...
Aug 1, 2008 · The filaments and lamellae are covered by a thin epithelium composed of several cell types that perform such processes as gas exchange, ion ...<|separator|>
[78]
[PDF] Dissolved Oxygen - Eyes on the Bay - Maryland.gov
The countercurrent exchange system gives fish an 80-90% efficiency in acquiring oxygen. Part II: Investigation #2 How does temperature affect dissolved oxygen? ...
[79]
Lecture 20/gas exchange I
Countercurrent flow is very powerful strategy for maximizing exchange; look for it later in the semester. Q. Which variables in Fick's law do these features ...
[80]
[PDF] Techniques in Whole Animal Respiratory Physiology
Ventilation volume is the total volume of water forced over the gills. Ventilatory frequency is the frequency of buccal or opercular movements, and ventilatory ...
[81]
Structure and Function in the Gills of Freshwater Fishes
This review focuses on the structure and function of the chloride cell in freshwater teleosts and summarizes recent advances related to its role in ionic ...
[82]
4. Dissolved Oxygen - CHEMICAL FEATURES OF WATER
At an atmospheric pressure of 760 mm Hg (NTP) the partial pressure of oxygen (pO2) will be 159 mm Hg i.e.. At 100% air saturation solubility of oxygen at 30°C ...
[83]
Dissolved Oxygen - Environmental Measurement Systems
According to Henry's Law, the dissolved oxygen content of water is proportional to the percent of oxygen (partial pressure) in the air above it 13.
[84]
Cardiorespiratory physiological phenotypic plasticity in developing ...
Aug 4, 2017 · Although both species use labyrinth organs for air breathing, these two air breathing fishes live and reproduce in distinctly different habitats ...
[85]
[PDF] Cardio-respiratory ontogeny and the transition to bimodal respiration ...
Blue gouramis are obligatory air breathing fish that possess a labyrinth-like structure that serves as the air breathing organ. Gouramis were reared for up to ...
[86]
[PDF] Circulation and Respiration in Lungfishes (Dipnoi)
ABSTRACT This paper reviews the cardiorespiratory morphology and physiology of the living lungfishes, in the special context of their highly effective use of ...
[87]
The Origin and Evolution of the Surfactant System in Fish
Lungs and swim bladders have different ontogenetic origins and can be used either for buoyancy or as an accessory respiratory organ.
[88]
The Structure of Digestive Tract Coordinating Digestion and ... - NIH
May 25, 2024 · The weatherloach, Misgurnus anguillicaudatus, is a facultative air-breathing teleost fish, which employs its partial digestive tract as an ...Missing: diverticula | Show results with:diverticula
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[PDF] fishes that breathe air with their gut - Towson University
Aerial ventilation in GAB fishes is driven primarily by oxygen partial pressure of the water (PO2) and possibly also by metabolic demand. The effect of aerial.
[90]
Do air-breathing fish suffer branchial oxygen loss in hypoxic water?
Sep 13, 2023 · Many teleost fish resort to air-breathing in hypoxic and warm tropical waters and this ability has evolved independently more than 80 times [1].
[91]
Increasing Temperatures Enhance Hypoxic Encounters in the Amazon
Elevated temperatures cause an increase in metabolic activity, reduce oxygen solubility in water, and therefore are expected to stimulate air-breathing. This ...
[92]
Hypoxia tolerance and partitioning of bimodal respiration in the ...
Using newly developed bimodal intermittent-closed respirometry, the partitioning of oxygen consumption in normoxia and hypoxia was investigated in P.
[93]
Morphometric partitioning of the respiratory surface area and ...
Bimodal breathing (i.e., oxygen uptake from the water by gills and from the air by an air-breathing organ) has evolved many times among teleost fishes.
[94]
Tracheole - an overview | ScienceDirect Topics
The tracheal system is a 'direct-delivery' respiratory system, allowing the movement of respiratory gases between the atmosphere and cells without requiring an ...
[95]
Discontinuous Gas Exchange in Insects: Is It All in Their Heads?
Since the insect's cuticle is largely impermeable to gas diffusion, this “tracheal system” opens to the environment through spiracles, small pores located along ...
[96]
Phylum Mollusca | manoa.hawaii.edu/ExploringOurFluidEarth
Molluscs breathe with gills called ctenidia that sit in a cavity between the mantle and body mass (Fig. 3.57). In some molluscs, most notably bivalves like ...
[97]
Respiratory Organs of Phylum Mollusca and Its Modification
Aquatic molluscs respire through ctenidia. These are the comb-like outgrowths of the mantle and are located within the mantle cavity.
[98]
Part 2 - Basic bivalve biology: taxonomy, anatomy and life history
The prominent gills or ctenidia are a major characteristic of lamellibranchs. They are large leaf-like organs that are used partly for respiration and partly ...
[99]
Perfused Gills Reveal Fundamental Principles of pH Regulation and ...
Mar 20, 2017 · The octopus gill is capable of regulating ammonia (NH3/ NH 4 + ) homeostasis by the accumulation of ammonia at low blood levels (<260 μM) and ...<|separator|>
[100]
Molluscan hemocyanin: structure, evolution, and physiology - PMC
Most molluscs have blue blood because their respiratory molecule is hemocyanin, a type-3 copper-binding protein that turns blue upon oxygen binding.
[101]
Describe the respiratory system structure in an earthworm. - CK-12
The process of respiration in an earthworm involves the diffusion of oxygen from the environment into the moist skin, where it is picked up by the hemoglobin ...
[102]
[PDF] Annelida - Smithsonian Institution
Respiratory pigments, such as hemoglobin, chlorocruorin, or hemerythrin, may be found in the blood plasma, in coelomic fluid, in corpuscles, and in tissues such ...
[103]
28.4 Phylum Mollusca and Annelida – General Biology
In aquatic gastropods, the mantle cavity encloses the gills (ctenidia), but in land gastropods, the mantle itself is the major respiratory structure, acting as ...28.4 Phylum Mollusca And... · Class Gastropoda · Phylum Annelida<|separator|>