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Fish anatomy

Fish anatomy encompasses the structural organization of fishes, a diverse paraphyletic group of aquatic vertebrates characterized by a notochord or vertebral column, gills for respiration, paired fins for locomotion, and typically a body covered in scales for protection. These features enable fishes to efficiently navigate, hunt, and survive in varied aquatic environments, from shallow streams to abyssal depths.^[1] Most fishes are ectothermic, relying on external environmental temperatures to regulate body heat, and exhibit remarkable morphological diversity across their approximately 37,000 species, including adaptations like streamlined bodies for fast swimming or flattened forms for bottom-dwelling.^[2]^[3]^[4] The external anatomy of fishes includes several key features that facilitate movement, sensory perception, and defense. Prominent among these are the fins: unpaired dorsal and anal fins provide stability and directional control, while the caudal (tail) fin generates thrust for propulsion; paired pectoral and pelvic (ventral) fins assist in steering, braking, and maneuvering.^[5] The body is often covered by cycloid or ctenoid scales, which reduce drag and offer armor against predators, though exceptions exist such as scaleless species like catfish.^[3] Sensory structures include the lateral line system, a series of mechanoreceptors along the sides that detects water movements and pressure changes for navigation and prey detection; nares (nostrils) for olfaction; prominent eyes for vision in low-light conditions; and a mouth equipped with teeth or jaws adapted to specific diets. Gills, covered by an operculum, extract oxygen from water passed over them.^[5]^[6] Internally, fish anatomy supports essential physiological processes tailored to aquatic life. The skeletal system features a flexible backbone that supports muscles and maintains shape without bearing full body weight against gravity, complemented by lighter bones than those in terrestrial vertebrates.^[7] The circulatory system includes a two-chambered heart that pumps deoxygenated blood to the gills for oxygenation before distribution to the body, ensuring efficient oxygen delivery in water.^[7] Digestive organs vary by diet but commonly include a stomach for initial breakdown, liver for bile production and detoxification, pyloric caeca for nutrient absorption, and intestines for further processing; herbivorous or carnivorous adaptations influence organ size and structure.^[8]^[6] The swim bladder, a gas-filled organ in most bony fishes, regulates buoyancy to maintain depth without constant swimming effort.^[3] Reproductive organs (gonads) produce eggs or sperm, often in large quantities suited to external fertilization in water. Kidneys filter waste and maintain osmotic balance against the surrounding medium, a critical adaptation for freshwater or marine species. The brain, though relatively small, coordinates sensory input and basic behaviors, with variations in size among species reflecting ecological niches.^[8]^[7]

Overall Body Plan

Body Shape and Proportions

Fish body shapes exhibit significant diversity, reflecting adaptations to diverse aquatic environments and locomotor demands. The fusiform shape, resembling a spindle or torpedo, is prevalent among pelagic species and optimized for high-speed cruising in open water. This streamlined form reduces drag by minimizing the cross-sectional area and smoothing the transition from head to tail, enabling efficient thrust generation primarily through tail undulation. Examples include tunas (Thunnus spp.) and barracudas (Sphyraena spp.), where the body tapers gradually to a narrow caudal peduncle, enhancing hydrodynamic performance during sustained swimming.^[9]^[10] In contrast, depressed body shapes are dorso-ventrally flattened, facilitating close association with the substrate in benthic habitats. Such forms, seen in flatfishes like flounders (Paralichthys spp.) and frogfishes (Antennariidae), allow for effective camouflage and ambushing of prey while minimizing resistance when gliding over the bottom. Laterally compressed shapes predominate in reef-associated fishes, promoting agility in cluttered environments; angelfish (Pomacanthidae) exemplify this with their tall, thin profiles that support rapid turns and acceleration via pectoral fin steering. Elongated or anguilliform shapes, as in eels (Anguillidae), feature extended trunks for sinuous, low-energy locomotion through confined spaces like reefs or riverbeds.^[9]^[11] Body proportions, defined by the relative lengths of head, trunk, and tail regions, further tune these shapes for locomotor efficiency and buoyancy. In fusiform species, the head typically comprises about 20-25% of total length, the trunk 50-60%, and the tail 20-25%, creating a balanced profile that optimizes the ratio of thrust to drag for steady swimming. This configuration shifts in specialized forms; for instance, deep-bodied compressed fishes like angelfish have proportionally shorter heads and tails relative to an expanded trunk, aiding maneuverability but increasing drag at high speeds. Elongated eels feature a small head (less than 10% of total length), an elongated trunk (around 25-40%), and a long tail (over 50%), favoring flexibility over speed.^[12]^[13]^[14] These proportions influence wave propagation during undulatory swimming, where longer trunks amplify posterior thrust while shorter heads reduce frontal resistance, contributing to overall energy economy in movement. Buoyancy adaptations, such as neutral body density paired with these shapes, prevent sinking or floating, allowing sustained positioning in the water column.^[12]^[13]

Segmentation and Regionalization

The body of a fish is typically divided into three primary regions: the head, trunk, and tail, each serving distinct functional roles in survival and locomotion. The head, extending from the snout to the posterior margin of the operculum, houses the cranium and major sense organs, facilitating feeding, respiration, and environmental perception. The trunk, spanning from the operculum to the anus, contains the visceral organs and supports the pectoral and pelvic girdles, providing stability and housing metabolic functions. The tail, or caudal region, begins at the anus and includes the caudal fin supported by modified vertebrae, primarily responsible for propulsion during swimming. This regionalization arises from embryonic segmentation through somites, paired blocks of mesoderm that form along the notochord and differentiate into structures like the vertebral column and musculature.^[15] In adult fish, this developmental process manifests as myomeres, segmented muscle blocks arranged in a zigzag pattern along the body axis, which enable undulatory swimming by contracting sequentially from head to tail.^[15] These myomeres support the functional division, with anterior segments aiding in head movements for prey capture and sensing, while posterior segments drive tail oscillations for thrust generation.^[15] Variations in segmentation occur across fish groups, reflecting evolutionary adaptations. Agnathans, such as lampreys and hagfishes, lack true vertebrae and exhibit rudimentary or absent segmentation in their axial skeleton, relying instead on a persistent notochord for support without the discrete somite-derived divisions seen in jawed fishes.^[16] In contrast, teleosts—comprising most modern bony fishes—display advanced regionalization, particularly in the tail, where homocercal tails predominate; these are symmetrical, with the vertebral column terminating at the fin base, optimizing efficient propulsion and maneuverability.^[17] Functionally, these regions integrate to enhance fitness: the head's sensory array, including eyes, nares, and lateral line, detects stimuli for navigation and predation, while the tail's myomeres and fin generate the majority of forward thrust in undulatory swimmers.^[4] The trunk bridges these, accommodating buoyancy via the swim bladder and stability through girdle attachments, with vertebral elements providing flexible support across regions.

Integumentary System

Skin Structure

The skin of fish serves as a multifunctional integumentary barrier, consisting primarily of two main layers: the epidermis and the dermis. The epidermis forms the outermost layer, a stratified squamous epithelium that is typically thin and avascular, containing specialized cells such as mucous cells (goblet cells) that secrete a protective mucus layer.^[4] These mucous cells are abundant throughout the epidermal layer, producing glycoproteins that contribute to the slime coat enveloping the fish.^[18] Beneath the epidermis lies the dermis, a thicker connective tissue layer composed mainly of collagen fibers arranged in a dense stratum compactum and a looser stratum spongiosum. The dermis provides structural support and houses chromatophores, pigment cells responsible for coloration and camouflage through expansion or contraction of pigment granules.^[19] These chromatophores, including melanophores, xanthophores, and iridophores, are embedded primarily in the upper dermal layers and enable rapid color changes for environmental adaptation.^[4] Mucous secretions from the epidermis play critical roles in lubrication, reducing friction during swimming, and forming a physical and chemical barrier against pathogens. This mucus layer inhibits microbial adhesion and contains antimicrobial peptides and enzymes that neutralize invading organisms, enhancing overall disease resistance.^[20]^[21] Structural variations exist across fish taxa; for instance, most teleosts possess skin overlaid with scales, while species in the order Siluriformes, such as channel catfish (Ictalurus punctatus), exhibit scaleless skin with a thicker, more robust epidermis to compensate for the absence of dermal armor.^[22]^[23] Additionally, the fish skin incorporates sensory functions, with taste buds embedded primarily in the epidermis of the head, barbels, and body surface, allowing chemosensory detection of food and environmental cues. These taste buds, innervated by cranial nerves, are particularly numerous in bottom-dwelling species like catfish, aiding in foraging by sensing dissolved amino acids.^[24]^[25]

Scales and Coverings

Fish scales are dermal structures that form a protective covering over the body of most fish species, embedded in the dermis and providing a flexible yet durable integumentary layer.^[4] These scales vary widely across fish taxa, reflecting evolutionary adaptations to diverse aquatic environments, and are primarily composed of mineralized tissues derived from bone or tooth-like materials.^[26] Placoid scales, characteristic of cartilaginous fishes such as sharks and rays, resemble small teeth or denticles embedded in the skin. They consist of an outer layer of enameloid—a hypermineralized, enamel-like substance—surrounding a core of dentine, with a central pulp cavity containing blood vessels and nerves.^[27] This composition provides rigidity and sharpness, aiding in hydrodynamic efficiency by reducing drag.^[28] Ganoid scales, found in primitive bony fishes like gars (Lepidosteidae) and bichirs (Polypteridae), are thick, rhomboid plates that form a heavy armor. Their multilayered structure includes an outermost shiny layer of ganoine, an acellular hypermineralized tissue analogous to enamel; a middle layer of dentine; an underlying isopedine layer of orthogonally arranged collagen fibers resembling plywood; and an innermost bony base.^[29] This arrangement confers exceptional puncture resistance while allowing limited flexibility.^[30] In contrast, the majority of modern bony fishes (teleosts) possess elasmoid scales, which are thinner and more flexible. Cycloid scales, typical of many soft-rayed fishes like salmonids, are round or oval with smooth posterior margins and consist of a superficial bony layer rich in calcium-based salts overlying a fibrous stratum of collagen fibers.^[27] Ctenoid scales, common in spiny-rayed teleosts such as perches, differ by featuring comb-like projections (ctenii) of bone on their exposed posterior edges, enhancing grip on slippery surfaces during locomotion, while sharing the same basic calcium-mineralized and collagenous composition.^[31] Many fish scales exhibit concentric growth rings, or annuli, formed by seasonal variations in growth rates, with wider rings indicating faster summer growth and narrower ones reflecting slower winter periods.^[32] By counting these annuli under magnification, researchers can accurately estimate a fish's age, a technique widely applied in fisheries management for species like bluegill sunfish.^[33] Some fish lack true scales, relying instead on alternative coverings. Sturgeons (Acipenseridae) possess large, bony scutes—dermal plates primarily composed of calcium-based minerals—arranged in five longitudinal rows along the body, providing robust armor against predation.^[34] Hagfishes (Myxinidae), primitive jawless fishes, have naked skin devoid of scales or scutes, featuring a loose, multilayered dermis rich in collagen that secretes copious slime for defense.^[35] Scales primarily function in physical protection, shielding the underlying skin from abrasion, injury, and predators through their overlapping arrangement and mineralized composition.^[4] Additionally, they contribute to camouflage; iridophores—dermal cells containing reflective guanine platelets—often underlie or integrate with scales to produce iridescent colors that disrupt outlines and match environmental backgrounds, enhancing concealment in teleosts like zebrafish.^[36]

Skeletal System

Axial Skeleton

The axial skeleton in fishes forms the central supportive framework along the longitudinal body axis, comprising the cranium and vertebral column, which together protect vital structures such as the brain and spinal cord while enabling flexibility for locomotion. This endoskeletal component arises from mesodermal tissues and varies between cartilaginous (chondrichthyans) and bony (osteichthyans) fishes, with the latter often featuring ossified elements for enhanced rigidity. In advanced fishes, the axial skeleton replaces the embryonic notochord as the primary structural support, facilitating undulatory swimming movements.^[37] The vertebral column consists of a series of individual vertebrae that extend from the skull to the tail, typically numbering 30–60 in teleost fishes depending on species. Each vertebra includes a cylindrical centrum, often amphicoelous in teleosts with concave anterior and posterior faces to accommodate the persistent notochord remnants and allow flexibility. Dorsally, a neural arch with a spinous process encloses and protects the spinal cord, while ventrally, haemal arches and spines form in caudal vertebrae to shield the caudal blood vessels and provide muscle attachment sites; in abdominal regions, parapophyses extend laterally to support ribs. These features enable the column to resist compressive forces during swimming, with variations such as reduced centra in some elasmobranchs where cartilage predominates. The axial skeleton also offers attachment for epaxial and hypaxial muscles, supporting body undulation.^[38]^[39]^[40] The cranium, or skull, is divided into the neurocranium (braincase) and splanchnocranium (visceral skeleton). The neurocranium forms a cartilaginous or bony enclosure for the brain, olfactory organs, and inner ear, with dermal bones roofing the skull in bony fishes to provide additional protection. The splanchnocranium includes the mandibular and hyoid arches that support the jaws and gills, derived from pharyngeal pouches. Jaw suspension mechanisms vary among fishes. Many chondrichthyans, including sharks, exhibit hyostylic suspension, where the palatoquadrate (upper jaw) connects primarily to the hyomandibula, enhancing bite force and allowing protrusion for predatory feeding.^[41] Most bony fishes also exhibit hyostylic suspension, with the upper jaw connecting indirectly to the cranium through the hyomandibula bone, enabling greater jaw protrusion and versatility in prey capture. The skull roof, comprising flat bones like the frontals and parietals, overlies the neurocranium and integrates with sensory structures.^[42] Evolutionarily, the fish axial skeleton traces back to agnathans (jawless fishes), where a persistent notochord provided axial support with minimal ossification, as seen in lampreys and hagfishes lacking true vertebrae. In gnathostomes (jawed vertebrates), selective pressures for enhanced mobility and protection led to the development of ossified centra and arches, regionalizing the column into cervical, trunk, and caudal segments; this transition involved neural crest contributions to cranial elements and somitic mesoderm for vertebrae, marking a key innovation in vertebrate diversification.^[43]^[44]

Appendicular Skeleton

The appendicular skeleton of fishes comprises the bony or cartilaginous elements that support the paired pectoral and pelvic fins as well as the unpaired dorsal, anal, and caudal fins, facilitating locomotion, stability, and maneuverability in aquatic environments. In bony fishes (Osteichthyes), this skeleton is primarily ossified, while in cartilaginous fishes (Chondrichthyes) it remains largely cartilaginous. The paired fin girdles anchor these structures to the body, with radials extending from the girdles to support the fin rays, whereas unpaired fins articulate directly with the axial skeleton via specialized proximal elements. The pectoral girdle in bony fishes consists of three main dermal bones: the cleithrum, which forms the posterior ventral plate; the coracoid, a ventral endochondral bone; and the scapula, a dorsal endochondral bone. These elements fuse ventrally at the midline and articulate laterally with four proximal radials that extend into the fin base, allowing flexible movement of the pectoral fin. The pelvic girdle, positioned more posteriorly, features a similar but reduced structure, often comprising paired puboischiac bars (ventral coracoid-like elements) and ischiopubis bones that connect to the body wall via connective tissue rather than direct skeletal fusion, with radials supporting the pelvic fin rays. These girdles provide attachment points for muscles that control fin abduction and adduction.^[45]^[46]^[47] Fin rays, or lepidotrichia in teleost bony fishes, are paired, segmented, and branched dermal structures composed of bone that bifurcate distally to form the fin web, articulating with distal radials for flexibility during swimming. In contrast, ceratotrichia in sharks and other chondrichthyans are unsegmented, keratinized collagen filaments that provide tensile support without ossification, embedding into the fin membrane and attaching to basal cartilaginous elements. For unpaired fins, the dorsal and anal fins are supported by pterygiophores—rod-shaped proximal bones that insert between consecutive neural (dorsal) and haemal (ventral) spines of the vertebral column, with each pterygiophore expanding distally to articulate with fin rays or spines. The caudal fin skeleton includes modified haemal elements such as hypurals (fused ventral plates supporting ventral rays), the parhypural, and uroneurals (elongated neural arches supporting dorsal rays), forming a fan-like array that enhances thrust generation.^[48]^[49]^[50]^[51] A notable variation occurs in perciform fishes and other acanthomorphs, where the anterior portions of the dorsal and anal fins feature isolated, rigid spines derived from modified lepidotrichia, serving a defensive role by deterring gape-limited predators through erection and locking mechanisms that increase the fish's apparent size and profile. These spines often precede softer ray-supported sections and are innervated for rapid deployment.^[52]^[53]

Muscular System

Myomeres and Muscle Layers

The axial musculature of fish varies across taxa but is primarily composed of myomeres, which are segmental blocks of muscle arranged longitudinally along the body axis. In teleost fishes, these myomeres exhibit a characteristic W-shaped configuration in cross-section, formed by the folding of muscle sheets separated by connective tissue septa known as myosepta.^[54] This geometry allows for efficient transmission of force during undulatory swimming, where waves of contraction propagate along the body to generate thrust, ensuring uniform strain distribution across the muscle fibers despite complex three-dimensional deformations.^[55] In chondrichthyans, myomeres are also W-shaped but integrated with a more robust cartilaginous skeleton, while in agnathans like lampreys, they are simpler chevron-shaped without a clear epaxial/hypaxial division. Within each myomere, muscle fibers are differentiated into red and white types in bony fishes, enabling varied locomotor demands. Red fibers, located peripherally near the skin, are slow-oxidative and rich in mitochondria and myoglobin, supporting sustained, aerobic swimming through efficient oxygen utilization and fatigue resistance.^[56] In contrast, white fibers occupy the deeper core of the myomere and are fast-glycolytic, relying on anaerobic metabolism for rapid, burst contractions such as escape responses, though they fatigue quickly due to lactic acid buildup.^[56] This regionalization optimizes energy use, with red fibers powering cruise swimming and white fibers enabling high-speed maneuvers.^[57] The myomeres are divided into dorsal epaxial and ventral hypaxial layers by the horizontal myoseptum in most vertebrates, which facilitates antagonistic bending of the body. Epaxial muscles, positioned above the septum, contract to elevate the vertebral column and produce dorsal curvature, while hypaxial muscles below the septum induce ventral bending for propulsion. These layers attach to the axial skeleton, including the vertebral centra, neural spines, and notochord, allowing coordinated torque generation during locomotion. Jaw and opercular musculature includes the adductor mandibulae complex, which powers mouth closure and biting in teleost fishes. This multi-segmented muscle (divisions A1–Aω) originates from the cranium and suspends to the lower jaw, generating forceful adduction essential for prey capture.^[58] In certain lineages, myomeres have undergone modifications into electric organs, adapting the axial musculature for electrogenic functions. In electric fishes like mormyrids and most gymnotids, electrocytes derive from modified deep lateral myomeres during ontogeny, transforming contractile tissue into bioelectric generators for navigation, communication, and predation while retaining a myogenic origin confirmed by developmental markers; however, in apteronotid gymnotids, electric organs are neurogenic.^[59]

Fin Musculature

The musculature of fish fins is broadly categorized into intrinsic and extrinsic components, with the intrinsic muscles residing within the fin structure to control ray movements and the extrinsic muscles connecting the pectoral and pelvic girdles to the axial body wall for broader positioning and propulsion support.^[60] Intrinsic muscles typically consist of layered abductors, adductors, and arrectors that enable fine-tuned adjustments, while extrinsic muscles, including hypaxial and epaxial extensions, provide anchorage and power transmission from the trunk. This arrangement allows fins to function as versatile control surfaces during swimming, maneuvering, and stability maintenance.^[61] In the pectoral fins of many teleost fishes, intrinsic musculature features superficial and deep adductor and abductor layers that insert onto the fin rays, facilitating rowing-like motions for slow-speed locomotion and station-holding. These muscles, often organized into multiple bundles, permit elevation, depression, protraction, and retraction of the fin, with abductors primarily responsible for spreading the rays outward and adductors for folding them inward.^[62] Extrinsic muscles, such as those originating from the cleithrum and linking to the scapular processes, integrate fin action with body undulations by anchoring the girdle to the myosepta and vertebral column. The pectoral fin rays, composed of lepidotrichia, serve as attachment points for these muscles, enabling coordinated force generation.^[63] Teleost fins exhibit specialized ray muscle arrangements where intrinsic fibers, including helicoidal bands along the ray segments, allow independent control of each lepidotrichium for undulating or oscillating motions. These muscles operate bilaterally to abduct, adduct, spread, or collapse the fin web, providing precise hydrodynamic control essential for agile navigation in varied environments.^[64] In contrast, median fins like the dorsal and anal often have simpler musculature with hypochordal and epichordal lobes derived from axial extensions, though ray-specific control remains prominent in advanced teleosts. Specializations in pectoral fin musculature are evident in flying fishes (Exocoetidae), where lateral extensor muscles are hypertrophied to extend the enlarged fins for gliding, while medial flexor muscles enable rapid furling upon water re-entry.^[65] This adaptation enhances aerial propulsion, supporting sustained glides of several meters.^[65] Such modifications highlight evolutionary divergence in fin musculature for multifunctional locomotion.^[66]

Sensory Systems

Visual System

The visual system of fish is adapted to function effectively in aquatic environments, where light propagation differs significantly from air due to refraction and absorption in water. The fish eye shares basic structural similarities with other vertebrates but exhibits specialized features for underwater vision, including a cornea with limited refractive power because its index of refraction is close to that of water, relying primarily on the lens for focusing light. The lens is typically spherical and rigid, enabling accommodation through forward and backward movement rather than shape change, which allows fish to adjust focus for near or far objects. The retina lines the back of the eye and contains photoreceptor cells: rods for low-light sensitivity and cones for color discrimination and high-acuity vision in brighter conditions.^[24] In diverse habitats, fish eyes show remarkable adaptations to optimize vision. Deep-sea species often possess tubular eyes, elongated structures that increase the eye's length relative to its diameter, enhancing light collection and sensitivity in dim, blue-shifted light at depths where red wavelengths are absent. For instance, the barreleye fish (Macropinna microstoma) features a transparent, dome-shaped head enclosing tubular eyes that can rotate to scan upward for bioluminescent prey. Conversely, reef-dwelling fish like those in the family Pomacentridae exhibit advanced color vision with multiple cone types sensitive to ultraviolet, blue, green, and red spectra, aiding in mate selection and foraging among colorful corals. These adaptations reflect evolutionary tuning to local light environments, with rod-dominated retinas in low-light species and cone-rich retinas in well-lit shallows.^[67] Many fish enhance low-light vision with a tapetum lucidum, a reflective layer behind the retina composed of guanine crystals or other pigments that bounces unabsorbed light back through the photoreceptors for a second chance at detection, producing the "shiny eye" effect in nocturnal species. Pupil morphology varies: round pupils in many species allow maximal light intake, while horizontal or slit-shaped pupils in others improve contrast and reduce glare in shallow, variable-light waters. Vision field configuration also differs by ecology; predatory fish like the northern pike (Esox lucius) have forward-directed eyes providing binocular overlap for depth perception and accurate strikes, whereas prey species such as herring (Clupea harengus) position eyes laterally for a near-360-degree panoramic view to detect threats. These features collectively enable fish to navigate, hunt, and evade in their submerged world.^[68]^[69]

Lateral Line System

The lateral line system is a mechanosensory network in fish that detects vibrations, water movements, and pressure gradients in the surrounding aquatic environment. This system consists of specialized sensory organs called neuromasts, which are distributed across the head, trunk, and tail fin. Each neuromast functions as a discrete transducer, containing clusters of hair cells whose stereocilia are embedded in a gelatinous cupula that protrudes into the water or canal fluid. When water flows over the cupula, it deflects the stereocilia, triggering depolarization in the hair cells and generating afferent signals to the central nervous system.^[70] Neuromasts are categorized into superficial and canal types based on their location and sensitivity profiles. Superficial neuromasts, also known as pit organs or free neuromasts, lie exposed on the skin surface, often embedded within the epidermis, and are highly responsive to local accelerations and higher-frequency water movements near the fish's body. In contrast, canal neuromasts are housed within subdermal, fluid-filled canals that open to the exterior via pores, providing protection and enhanced sensitivity to lower-frequency, longer-wavelength stimuli such as distant pressure waves; these canals follow specific patterns, including the main trunk line along the body and cephalic lines on the head. The entire system is innervated by branches of cranial nerves, primarily the facial (VII), glossopharyngeal (IX), and vagus (X) nerves, which originate from dedicated lateral line ganglia and convey sensory information to the brainstem.^[70]^[71] The lateral line system plays critical roles in various behaviors essential for survival. It enables schooling by allowing fish to sense hydrodynamic signals from nearby conspecifics, facilitating synchronized swimming and rheotaxis. For predator avoidance, it detects approaching threats through the propagation of water disturbances, while prey localization relies on the detection and tracking of dipole-like sources generated by small organisms' movements. These functions are particularly vital in low-visibility conditions, where visual cues are limited.^[72]^[72] In some electroreceptive fish, such as certain cartilaginous and non-teleost bony species, the lateral line placodes also give rise to ampullary organs, which detect weak electric fields produced by prey or environmental sources; these are distinct from the mechanosensory neuromasts and function in electrolocation rather than hydrodynamic sensing.^[73]

Other Sensory Organs

Fish possess olfactory organs adapted for detecting chemical cues dissolved in water, primarily through paired nares that lead to an olfactory rosette. The nares, located on the snout, serve as external openings that allow water to flow into the nasal cavity without direct connection to the mouth or respiratory system.^[74] Inside, the olfactory rosette consists of multiple lamellae or folds lined with olfactory epithelium containing receptor neurons that bind odorants, enabling acute smell for foraging, navigation, and reproduction.^[74] This structure varies in complexity across species, with more lamellae generally correlating to greater olfactory sensitivity in environments rich in chemical signals.^[74] Taste in fish is mediated by taste buds distributed not only in the oral cavity but also across the body surface, allowing direct sampling of environmental chemicals. In species like catfish (family Ictaluridae), specialized barbels—elongated, fleshy appendages around the mouth—bear dense concentrations of taste buds to explore substrates for food.^[75] These taste buds, embedded in the epithelium, detect amino acids, nucleotides, and other solutes, with some species possessing hundreds of thousands of taste buds distributed across the body surface and barbels to support their bottom-feeding lifestyle. Whole-body distribution of taste buds, particularly in siluriform and cypriniform fishes, enhances detection of palatable or toxic substances during feeding.^[76] Electroreception in certain fish, notably elasmobranchs like sharks and rays, occurs via the ampullae of Lorenzini, gel-filled canals opening as pores on the head and ventral surface. These organs detect weak electric fields generated by prey muscle activity or bioelectric signals, with sensitivity down to 5 nanovolts per centimeter.^[77] The ampullary structure includes a sensory epithelium at the base that transduces voltage gradients into neural impulses, aiding in prey localization even in turbid waters or when visual and olfactory cues are obscured.^[78] This sensory modality complements mechanoreception from the lateral line for precise orientation toward hidden targets.^[78]

Respiratory System

Gill Arches and Filaments

In bony fishes, the gills are supported by four pairs of gill arches located on each side of the head, with each arch bearing a holobranch composed of two hemibranchs—one anterior and one posterior row of filaments—allowing for efficient structural support within the protected pharyngeal cavity.^[4] In contrast, sharks and other elasmobranchs typically possess five gill arches per side, where each arch supports hemibranchs separated by complete interbranchial septa, resulting in exposed gill structures without a unified protective covering.^[79] Extending from these arches are numerous gill filaments, which serve as the primary lamellae and project perpendicularly to increase the respiratory surface; each filament is further subdivided into secondary lamellae, thin, plate-like folds that vastly expand the available area for interaction with water while maintaining structural integrity through supporting rods.^[80] These secondary lamellae are densely packed along the filaments, forming a compact yet expansive array that optimizes the gill's overall architecture.^[81] Attached to the inner edges of the gill arches are gill rakers, comb-like projections that vary in form and density depending on diet; in planktivorous species such as menhaden or herring, the rakers are elongated and numerous, forming a fine mesh that effectively filters microscopic prey from the incoming water stream without impeding flow.^[82] In the operculum-covered gills of bony fishes, this filtration occurs as part of the buccal pumping mechanism, where expansion of the buccal cavity draws water inward through the mouth while the opercula flare outward, followed by contraction that forces water across the gills and out via the opercular slits.^[4] A rich vascular supply threads through the filaments and lamellae to support these structures.^[80]

Gill Circulation and Gas Exchange

In fish gills, blood circulation facilitates gas exchange through a highly efficient countercurrent flow system, where deoxygenated blood from the body enters the afferent branchial arteries and flows through the gill arches into the filaments and lamellae in the opposite direction to the exiting water stream.^[83] This arrangement maintains a consistent concentration gradient for oxygen diffusion across the thin gill epithelium, allowing fish to extract 50-90% of available oxygen from water, far surpassing the efficiency of concurrent flow systems.^[80] Oxygen diffuses from the water into the blood capillaries within the lamellae, while carbon dioxide moves in the reverse direction, driven by partial pressure differences.^[82] The gill capillaries, lined by specialized pillar cells, are critical for maintaining structural integrity and optimizing blood flow during respiration. Pillar cells, unique to fish gills, form paired, contractile structures that span the lamellae, preventing capillary collapse or ballooning under varying blood pressures and directing blood primarily into the efferent filaments for venous return.^[84] These cells also contain cytoplasmic plates that create narrow channels for blood passage, enhancing turbulence and diffusion efficiency while minimizing diffusion distances to about 0.5-1 micrometer.^[85] Beyond gas exchange, gill circulation supports ion regulation through chloride cells, also known as ionocytes, embedded in the gill epithelium. In marine fish, these cells actively secrete chloride ions into seawater via apical channels, creating an electrical gradient that drives passive sodium extrusion to combat osmotic influx; in freshwater species, they facilitate ion uptake to counter dilution.^[86] This osmoregulatory function is hormonally modulated and integral to maintaining internal salt balance.^[87] Certain fast-swimming fish, such as tunas and billfishes, exhibit adaptations like ram ventilation, where continuous forward motion forces water over the gills without buccal pumping, relying on streamlined mouth and opercular structures to sustain high-volume flow.^[88] This passive mechanism supports elevated oxygen demands during sustained speeds but requires structural reinforcements, such as gill fusions, to prevent deformation.^[89]

Circulatory System

Heart Morphology

The fish heart is a linear, tubular or saccular organ typically consisting of four sequential chambers arranged in series: the sinus venosus, atrium, ventricle, and bulbus arteriosus (or conus arteriosus in some species). The sinus venosus is a thin-walled, compliant sac that receives deoxygenated blood from the systemic veins via the ductus Cuvier and hepatic veins, serving as a low-pressure reservoir before propelling it into the atrium.^[90] The atrium, a moderately muscular chamber, contracts to pass blood through the atrioventricular (AV) valve into the thick-walled, spongy ventricle, which provides the primary pumping force due to its compact myocardial layer. In teleosts, the final chamber is the elastic bulbus arteriosus, a distensible structure that dampens pressure fluctuations and directs blood toward the ventral aorta for oxygenation in the gills.^[91] Valves ensure unidirectional blood flow through these chambers. The AV valve, composed of fibrous cusps guarded by endocardial tissue, prevents backflow from the ventricle to the atrium during ventricular systole. In species with a conus arteriosus, such as elasmobranchs, additional pocket-like valves line it to regulate outflow and minimize regurgitation; the bulbus arteriosus in teleosts is typically valveless.^[90] The entire heart is enclosed within a fibrous pericardial sac, which provides structural support and limits excessive expansion while allowing limited movement during contraction. Fish hearts exhibit myogenic control, where rhythmic contractions originate intrinsically from specialized pacemaker cells in the sinus venosus and myocardium, independent of neural input for basic rhythmicity, though modulated by autonomic innervation.^[92] This contrasts with neurogenic hearts in certain invertebrates, where beats depend entirely on extrinsic nerve impulses.^[93] In cyclostomes, such as lampreys and hagfish, the heart retains a primitive configuration with a single atrium, though hagfish often lack a distinct atrial compartment, relying more on a simple sinus venosus-ventricle arrangement.^[94] These variations reflect evolutionary adaptations, with the overall design facilitating efficient propulsion of deoxygenated blood to the gills in a single-circuit system.^[95]

Vascular Patterns

In fish, the vascular patterns form a single, closed circulatory loop that distributes oxygenated blood from the gills throughout the body via the dorsal aorta, a major elastic artery running longitudinally along the dorsal region.^[96] This aorta arises from the efferent branchial arteries of the gill arches, which serve as the primary site for oxygen uptake, and it supplies systemic tissues with oxygen-rich blood under relatively low pressure compared to higher vertebrates.^[97] The dorsal aorta gives rise to numerous branches, including segmental arteries that supply the myomeres and body wall, epibranchial arteries to the head and brain, and mesenteric arteries to the viscera, ensuring targeted perfusion to muscles, organs, and peripheral tissues.^[98] A key feature of fish vascular anatomy is the presence of portal systems, which allow for secondary capillary filtration before blood returns to the heart. The renal portal system collects deoxygenated blood primarily from the caudal vein and posterior body via paired posterior cardinal veins, directing it through a network of renal capillaries in the kidneys for additional processing and filtration before returning to the heart via efferent renal veins and the posterior cardinal veins.^[99] This system receives contributions from segmental flank veins in most species, enhancing renal clearance of metabolites from the lower body. Complementing this, the hepatic portal vein gathers nutrient-laden blood from the gastrointestinal tract, spleen, and pancreas, routing it through extensive sinusoidal capillaries in the liver for detoxification, nutrient storage, and processing prior to entry into the systemic circulation via hepatic veins to the sinus venosus.^[97] Fish lack a true lymphatic system with dedicated lymph nodes, instead relying on a rudimentary network of lymph vessels that parallel the blood vasculature and facilitate fluid return from tissues without specialized nodal filtration.^[100] The spleen functions as the primary blood filtration organ, receiving arterial supply from the coeliac-mesenteric artery and filtering erythrocytes, pathogens, and debris through its ellipsoidal and melanomacrophage structures before venous drainage joins the hepatic portal system.^[101] Capillary beds represent the terminal exchange networks in fish vascular patterns, embedded within skeletal muscles, skin, fins, and visceral organs to enable diffusion of oxygen, nutrients, and waste.^[96] These thin-walled vessels, often arranged in parallel arrays in active tissues like red muscle, optimize gas and metabolite transfer under the low-pressure gradient of the single-circuit system, with venous return converging through cardinal and portal veins back toward the heart.^[99]

Digestive System

Oral Cavity and Jaws

The oral cavity of fish encompasses the space bounded by the jaws, lips, oral valve, and buccal walls, serving as the primary site for food ingestion and initial prey manipulation. In most bony fish (teleosts), the jaws form a kinetic mechanism that allows independent movement of the upper and lower elements relative to the cranium, facilitating precise capture strategies such as biting or suction feeding. This kinetic suspension, often linked to the hyostylic or amphistylic cranial attachments, enables the upper jaw to protrude forward, aligning the mouth directly with approaching prey to maximize strike efficiency.^[102]^[103] Teleost jaws exhibit diverse morphologies adapted to feeding ecologies, with the upper jaw comprising the premaxilla and maxilla that can slide and rotate via ligaments and joints. Protrusion in these species, such as in cichlids, involves coordinated cranial elevation, lower jaw depression, and suspensorium rotation, often extending the jaw by up to 30-50% of head length to generate hydrodynamic forces during suction. Complementing the oral jaws, many teleosts possess pharyngeal jaws—derived from modified gill arches in the throat—that function in secondary processing, including grinding tough prey like mollusks or exoskeletons through opposing dentition. These pharyngeal structures operate independently, suspended by muscles without direct bony links to the skull, allowing simultaneous oral capture and pharyngeal mastication.^[104]^[105]^[106] Fish teeth embedded in the jaws vary widely in form to suit dietary needs, with predatory species typically bearing conical or pointed teeth for piercing and holding elusive prey, as seen in sharks and many teleosts. In contrast, filter-feeding fish often have villiform teeth—small, brush-like projections—that aid in straining plankton or small particles without damaging them, promoting efficient particulate capture. Tooth replacement follows a polyphyodont pattern in most fish, where teeth are continuously shed and regenerated in a wave-like sequence from the lingual to labial side, ensuring functional dentition throughout life; this process varies by species, with some exhibiting alternating pits and teeth along the jaw.^[107]^[108]^[109] The buccal cavity expands rapidly during feeding through lowering of the hyoid and elevation of the neurocranium, creating negative pressure that draws water and prey inward via suction. An oral valve, formed by folds of tissue at the mouth's anterior edge and often augmented by fleshy lips, seals the cavity to maintain pressure gradients and prevent water escape, enhancing flow velocities toward the prey. This expansion can increase buccal volume by factors of 2-4 times in a fraction of a second, with lips providing additional flexibility in species like labrids for precise sealing during ram-suction hybrid strikes.^[110]^[111] Specialized adaptations in the oral cavity and jaws highlight evolutionary innovation for extreme environments, such as in deep-sea anglerfish (Lophiiformes), where the jaws are immensely distensible—capable of engulfing prey larger than the fish's body—and equipped with an esca, a bioluminescent lure dangling from a modified dorsal spine to attract victims in perpetual darkness. These jaws employ a gape-and-suck mechanism, with strong lower jaw musculature generating suction to pull lured prey into a maw lined with inward-curving, needle-like teeth that prevent escape. Such features underscore the oral region's role in integrating sensory deception with mechanical capture for survival in nutrient-scarce habitats.^[112]^[113]^[114]

Alimentary Canal

The alimentary canal in fishes begins with the esophagus, a short, muscular, and distensible tube that transports food from the pharynx to the stomach or directly to the intestine in species lacking a stomach.^[115] Its wall consists of longitudinal and circular muscle layers overlaid by stratified squamous or columnar epithelium, facilitating rapid passage of ingested material through peristaltic contractions.^[115] In species such as cyprinids, the esophagus is notably short and joins directly to a long intestine, reflecting adaptations to their diet.^[116] Many teleost fishes possess a stomach, typically divided into a cardiac region anteriorly for initial storage and mechanical breakdown of food, and a pyloric region posteriorly for further mixing with gastric secretions before entry into the intestine.^[117] The stomach is absent in some groups, such as certain cypriniforms and siluriforms, where digestion relies more heavily on intestinal processes.^[116] At the pyloric-duodenal junction, a muscular valve or mucosal fold regulates the flow of chyme into the intestine.^[115] The intestine varies significantly in length and structure, generally shorter in carnivorous species (typically 0.2-2.5 times body length) to expedite processing of protein-rich diets, and longer in herbivores (up to 10-20 times body length or more) with coiled configurations to enhance fermentation and nutrient extraction from plant material.^[118]^[116] In elasmobranchs like sharks and rays, the intestine features a distinctive spiral valve, a coiled mucosal fold that increases absorptive surface area without elongating the gut and slows digesta transit for improved nutrient uptake.^[119] Pyloric caeca, finger-like blind sacs numbering from a few to over 100, project from the anterior intestine near the pylorus in many teleosts, significantly expanding the absorptive area for sugars, amino acids, and dipeptides while secreting digestive enzymes. The posterior intestine, or rectum, is a short, straight segment separated from the anterior intestine by an ileo-rectal valve in many species, characterized by longitudinal mucosal folds that aid in water reabsorption and fecal compaction.^[115] It terminates at the anus, a ventrally positioned opening typically located just anterior to the anal fin base, through which undigested waste is expelled.^[120] In elasmobranchs, the anus opens into a cloaca shared with the urinary and reproductive systems.^[116]

Accessory Digestive Organs

In fish, the liver is a multilobular organ located ventral to the stomach and intestine, serving multiple roles in digestion and metabolism. It produces bile, a greenish fluid containing bile salts, bilirubin, and cholesterol, which emulsifies fats to facilitate their enzymatic breakdown in the intestine. This bile is synthesized by hepatocytes and transported via hepatic ducts to the gall bladder in most teleost species, where it is concentrated and stored until released into the duodenum in response to the presence of dietary lipids. The liver also functions in glycogen storage, converting excess glucose from the diet into glycogen for energy reserves, a process critical for maintaining metabolic homeostasis during fasting or activity.^[121] The pancreas in fish is typically a diffuse structure rather than a compact gland, often embedded within the mesenteries surrounding the anterior intestine and pyloric region, integrating closely with the digestive tract. Its exocrine component consists of acinar cells that secrete a variety of digestive enzymes, including trypsin, chymotrypsin, amylase, and lipase, which are delivered via pancreatic ducts to the intestine to hydrolyze proteins, carbohydrates, and lipids, respectively. The endocrine portion comprises clusters of islets of Langerhans scattered within or near the exocrine tissue; these islets contain alpha cells producing glucagon to elevate blood glucose and beta cells secreting insulin to lower it, thereby regulating carbohydrate metabolism in coordination with hepatic functions. This dual exocrine-endocrine organization supports efficient nutrient processing adapted to the fish's diet and environment.^[122]^[123] The spleen, while primarily a hematopoietic and immune organ, is anatomically associated with the digestive system in fish, often lying along the dorsal surface of the stomach or intestine within the peritoneal cavity. It acts as a blood filter, with macrophages in its red pulp phagocytizing damaged erythrocytes, debris, and pathogens from the circulation, thereby maintaining blood quality and contributing to immune surveillance. In many species, the spleen also supports erythropoiesis, producing red blood cells, and its proximity to the gut allows it to respond to ingested antigens.^[124] Intestine-associated glands in fish primarily include mucous-secreting goblet cells embedded in the epithelial lining of the intestinal mucosa, which produce a protective mucus layer to lubricate food passage, shield against abrasion, and maintain an optimal pH for enzymatic activity. These unicellular glands are abundant in the mid- and hindgut, with their secretion composition varying by species and diet—acidic mucins in carnivores for antimicrobial defense and neutral mucins in herbivores for lubrication. Additionally, the diffuse exocrine pancreatic tissue often integrates directly with the intestinal wall, providing localized enzyme release to enhance nutrient absorption without a centralized duct system.^[125]^[123]

Excretory and Osmoregulatory System

Kidney Structure

In teleost fish, the functional adult kidney is primarily mesonephric, developing from the embryonic mesonephros and extending as an elongated structure along the dorsal coelomic cavity, often divided into an anterior head kidney (derived from the pronephros) and a posterior trunk kidney. The head kidney retains some pronephric characteristics but primarily serves hematopoietic and endocrine roles, while the trunk kidney handles excretion and osmoregulation through numerous nephron units.^[126]^[127] The basic nephron in fish consists of a renal corpuscle and a renal tubule, enabling filtration of blood plasma and selective reabsorption of ions and water. The renal corpuscle features a glomerulus—a tuft of capillaries enclosed by Bowman's capsule—where ultrafiltration occurs, driven by hydrostatic pressure from the renal arteries branching off the dorsal aorta. The filtrate then passes through the renal tubule, which includes a short neck segment, proximal tubule for bulk reabsorption of glucose, amino acids, and ions, distal tubule for fine-tuning ion balance, and collecting ducts that merge to form larger efferent tubules. This structure allows for efficient processing of large plasma volumes, with nephrons arranged in lobules separated by interstitial tissue containing melanomacrophages.^[128]^[127]^[129] Kidney structure varies significantly between freshwater and marine fish to adapt to osmoregulatory demands. Freshwater teleosts possess large, compact kidneys with abundant glomeruli and well-developed tubules, facilitating the production of copious dilute urine (up to 20% of body weight daily) to eliminate excess water gained osmotically across the gills and skin while reabsorbing essential salts. In contrast, marine teleosts have smaller, more diffuse kidneys with fewer glomeruli—some species, like the goosefish, are entirely aglomerular, relying on peritubular secretion for filtration—and produce small volumes of isotonic urine high in urea and divalent ions to conserve water in a hyperosmotic environment. These adaptations highlight the kidney's role in maintaining internal ion balance, with vascular supply from segmental renal arteries ensuring efficient perfusion for filtration.^[130]^[131]^[128] Urine from the nephrons collects in efferent tubules that drain into the mesonephric (Wolffian) ducts, paired structures running the length of the kidney that serve dual roles in excreting urine and conveying gametes in both sexes.^[127]^[126]

Urinary and Reproductive Ducts

In teleost fishes, the urinary system connects to the kidneys via paired archinephric ducts, which transport urine to a urinary bladder present in many species for temporary storage before excretion.^[4] This bladder, located ventrally near the posterior body cavity, varies in size and capacity; for instance, in yellow perch (Perca flavescens), it forms a small sac that rapidly expels urine to maintain osmotic balance in freshwater environments. Absent in some marine teleosts adapted for high-salinity conditions, the bladder's presence aids in volume regulation where reabsorption of water occurs.^[132] The urogenital sinus in teleosts serves as a common chamber where urinary and reproductive outflows converge before exiting via a single urogenital pore on a papilla posterior to the anus.^[4] In females, the urinary bladder often integrates with the oviducts to form this sinus, facilitating the release of eggs alongside urine, while in males, sperm ducts (vasa deferentia) join the urinary pathway internally but maintain separation to prevent mixing. This arrangement is typical in oviparous species, whereas viviparous teleosts like surfperches exhibit fully independent urinary and spermatic ducts with distinct openings on the papilla, supporting internal fertilization without urinary interference.^[133] Oviducts in oviparous teleosts typically develop as extensions of the ovarian cavity or from posterior peritoneal folds, transporting ova directly to the urogenital sinus without true Müllerian duct homology. In contrast, sperm ducts in males are derived from anterior kidney regions modified into vasa efferentia and deferentia, which elongate posteriorly to deliver spermatozoa separately from urine in advanced teleosts.^[132] These ducts ensure efficient gamete transport during spawning, with separation enhancing sperm viability by avoiding dilution.^[134] In chondrichthyans, such as sharks and rays, a cloaca functions as the unified terminal chamber for urinary, digestive, and reproductive tracts, opening externally between the pelvic fins.^[135] Lacking a urinary bladder, urine flows directly from the opisthonephric kidneys via mesonephric ducts into a urogenital sinus within the cloaca, where it mixes minimally with other effluents before expulsion through a papilla.^[136] The urogenital sinus, particularly in males, expands to store spermatozoa from the deferens ducts, aiding in internal fertilization, while female oviducts route ova through the cloaca independently of urinary flow.^[135] This cloacal structure reflects the group's evolutionary retention of a primitive vertebrate excretory-reproductive integration.^[137]

Buoyancy and Sound Systems

Swim Bladder

The swim bladder, also known as the gas bladder or air bladder, is a gas-filled organ located in the dorsal body cavity of most bony fishes (Osteichthyes), enabling precise control of buoyancy to maintain neutral hydrostatic equilibrium without constant swimming effort.^[138] It originates embryonically as a dorsal outpocketing of the foregut (esophagus), with its wall layers homologous to those of the alimentary canal, reflecting its evolutionary derivation from an ancestral lung-like structure in early sarcopterygians.^[79] This organ is absent in many bottom-dwelling (benthic) species, such as certain darters and loaches, where negative buoyancy aids substrate adherence and energy conservation in low-flow environments.^[139] Structurally, the swim bladder consists of a thin-walled, bilobed sac lined with epithelium and connective tissue, filled primarily with oxygen (up to 90% in some species) and smaller amounts of nitrogen, carbon dioxide, and other gases. In physostomous fishes (e.g., salmonids like Oncorhynchus spp.), it remains connected to the esophagus via a pneumatic duct, allowing direct gas intake or expulsion by gulping air at the surface.^[138] Conversely, in the more derived physoclistous condition (e.g., perciforms like Perca spp.), the pneumatic duct is lost or obliterated, and gas regulation occurs exclusively through blood circulation via specialized gas glands and the rete mirabile—a countercurrent multiplier system of densely packed arterial and venous capillaries (e.g., ~50,000 pairs in eels) that facilitates gas diffusion across a minimal 1–2 µm barrier.^[138]^[140] The rete mirabile secretes gases by elevating partial pressures (e.g., increasing PO₂ by 7–8 times through countercurrent exchange and lactate-induced acidification), enabling bladder inflation even at depths exceeding 1000 m where ambient pressure compresses gases.^[140]^[141] The primary function of the swim bladder is hydrostatic regulation, where volume adjustments via gas secretion or resorption counterbalance the fish's density against water, minimizing energy expenditure for vertical migration—critical for pelagic species that exploit prey layers at varying depths.^[138] It also contributes to sound resonance, acting as a vibrating chamber that amplifies low-frequency sounds for production and enhances hearing sensitivity, though detailed auditory linkages are specialized in certain taxa.^[142] In physoclistous forms, the rete mirabile's efficiency ensures sustained buoyancy without surface access, underscoring its adaptive role in diverse aquatic habitats.^[140]

Weberian Apparatus

The Weberian apparatus is a specialized auditory structure unique to otophysan fishes, comprising a chain of small ossicles that link the swim bladder to the inner ear, thereby enhancing hearing sensitivity through the transmission of sound-induced vibrations. This apparatus functions as a mechanical coupling, allowing the swim bladder to act as a pressure detector for underwater sound waves, which are then relayed via the ossicles to the perilymphatic spaces of the ear. Found exclusively in the Otophysi superorder, which includes over 10,000 species such as carps (Cypriniformes) and catfishes (Siluriformes), the Weberian apparatus represents a key evolutionary innovation that extends auditory capabilities beyond those of non-otophysan fishes.^[143]^[144]^[145] The apparatus consists of four primary ossicles: the scaphium, claustrum, intercalarium, and tripus, which form a serial chain derived from modifications of the neural arches and parapophyses of the anterior vertebrae. The scaphium attaches to the prootic bone of the cranium near the inner ear, while the claustrum lies between the scaphium and intercalarium; the intercalarium connects these to the tripus, which is the largest ossicle and extends from the complex vertebra (vertebra 1 or 2) to contact the swim bladder's anterior wall via ligaments and a thin tunica externa. These ossicles, often numbering 1–4 depending on the species, operate in analogy to the mammalian middle ear bones, amplifying and directing vibrations from bladder wall displacements to the saccule and utricle of the inner ear.^[144]^[146]^[147] Evolutionarily, the Weberian apparatus originated in the early Cretaceous from serial homology among the first four vertebrae, with the tripus evolving from the parapophysis of vertebra 3 or 4, and the scaphium from the neural arch of vertebra 1, enabling otophysans to exploit acoustic cues for predator avoidance, foraging, and communication in freshwater environments. This modification likely arose once in the otophysan lineage, serving as a synapomorphy that distinguishes the group. In terms of auditory performance, the apparatus boosts sensitivity by 20–30 dB across frequencies of approximately 100–5000 Hz in species like the goldfish (Carassius auratus) and various catfishes, with peak thresholds as low as 70–80 dB re 1 µPa in the 500–2000 Hz range, far surpassing the ~500 Hz limit of fishes lacking this structure.^[146]^[148]^[145]

Reproductive System

Male Reproductive Organs

In teleost fishes, the primary male reproductive organs are the paired testes, which are typically elongated, bilobed structures suspended from the dorsal body wall by the mesorchium. These organs are enclosed in a fibrous tunica albuginea and subdivided into lobules by connective tissue septa that radiate inward from the capsule. The lobular organization is characteristic of most teleosts, facilitating the compartmentalized process of gamete production.^[149]^[150] Spermatogenesis in the testes occurs within discrete cysts, where cohorts of germ cells at synchronized developmental stages—ranging from spermatogonia to spermatozoa—are enveloped by supportive Sertoli cells. These cysts form along the lobule walls and release mature spermatozoa into the central lumens upon completion of spermiation, a process involving the phagocytosis of residual cytoplasmic material by Sertoli cells. In species from temperate regions, testicular activity is often seasonal, with spermatogenic cycles aligning to environmental factors like photoperiod and temperature, leading to gonadal recrudescence in autumn or winter and regression post-spawning.^[151]^[149]^[152] Mature spermatozoa from the testicular lobules are collected by a network of efferent ducts originating from the rete testis and channeled into the main sperm duct, a single or paired tube that extends posteriorly along the length of the testis. This sperm duct lacks an epididymis in most teleosts and transports sperm to the urogenital region, where it may merge with the urinary system to form a common outlet.^[149]^[153] Accessory structures associated with the male reproductive system are generally underdeveloped in teleosts compared to other vertebrates, with minimal glandular tissue dedicated to seminal fluid production. However, in certain groups such as catfishes (Siluriformes), paired seminal vesicles attached to the testes secrete a mucoid fluid rich in glycoproteins and steroid conjugates, which enhances sperm motility and provides pheromonal cues during spawning. These secretions are stored in the sperm duct and released sparingly to avoid diluting sperm concentration.^[154]^[155] In chondrichthyan fishes (sharks, rays, and chimaeras), the male reproductive organs include paired testes embedded in an epigonal organ for immune support, connected to elongated efferent ducts that lead to seminal vesicles and a glandular Squalus gland for fluid secretion. Sperm is stored in the mesonephric ducts before transfer via paired claspers—rigid, grooved extensions of the pelvic fins that function as intromittent organs for internal fertilization.^[136] Hermaphroditism occurs in approximately 2% of fish species, including some wrasses (Labridae), where individuals possess both ovarian and testicular tissue. Sequential hermaphroditism predominates in many wrasses, such as the bluehead wrasse (Thalassoma bifasciatum), which is protogynous: initial-phase females or small males can transition to territorial males, with the ovary transforming into a functional testis through atrophy of ova and proliferation of testicular lobules. Primary males develop testes directly, while secondary males exhibit anatomically distinct gonads with residual ovarian lamellae. Simultaneous hermaphroditism is rarer but present in species like the cleaner wrasse (Labroides dimidiatus), where bilateral gonads contain interspersed testicular and ovarian regions, allowing concurrent gamete production and pair spawning with egg trading behaviors. In both forms, the male components retain the lobular testicular structure typical of gonochoristic teleosts.^[156]^[157]^[158]

Female Reproductive Organs

The female reproductive organs in fish primarily consist of the ovaries and associated oviducts, which facilitate oogenesis, yolk deposition, and egg release. In most teleost fish, the ovaries are paired, elongated structures located in the dorsal body cavity, attached to the mesentery and containing numerous ovarian lamellae where oocyte development occurs. These ovaries produce eggs through oogenesis, a process involving primary oocyte growth followed by vitellogenesis, during which yolk proteins derived from vitellogenin—synthesized in the liver and transported to the ovaries—accumulate to nourish developing embryos. Vitellogenesis is critical for ovarian maturation, enabling the formation of lipid- and protein-rich yolk that supports early larval development post-hatching. Ovulation marks the culmination of oocyte maturation, where fully grown eggs are released from the ovarian follicles into the central ovarian lumen. In teleosts, this process typically occurs in cycles synchronized with environmental cues, such as temperature and photoperiod, leading to periodic spawning events. The oviducts, often short and paired in teleosts, serve as conduits for transporting ovulated eggs from the ovaries to the exterior via the urogenital opening, often integrating with urinary ducts for shared passage. In species with external fertilization, such as most teleosts, the oviducts facilitate the release of unfertilized eggs into the water, where sperm entry occurs primarily through the micropyle—a narrow canal in the egg chorion—ensuring monospermy. Fish eggs exhibit diverse morphologies adapted to reproductive strategies, broadly categorized as pelagic or demersal. Pelagic eggs, produced by many marine species like herring, are buoyant due to oil droplets, allowing them to float in the water column for wide dispersal. In contrast, demersal eggs, common in freshwater and some coastal species such as salmon, are denser and often adhesive, sinking to the substrate where they attach to vegetation or rocks for protection. Chondrichthyan fish, including sharks, display advanced reproductive diversity; many are viviparous, with ovaries releasing oocytes into elongated oviducts where fertilization occurs internally, and embryos develop within a specialized uterus nourished via yolk-sac placentation or uterine secretions until live birth. Spawning patterns in female fish vary between single events and batch spawning, reflecting adaptations to environmental stability and predation risks. Single spawning involves the release of all mature eggs in one discrete event, typical in semelparous species like Pacific salmon that die post-reproduction. Batch spawning, prevalent in iteroparous reef fish such as groupers, entails multiple ovulations over an extended season, with ovaries retaining reserves of previtellogenic oocytes that mature sequentially, thereby spreading reproductive effort and enhancing offspring survival odds.

Nervous System

Central Nervous System

The central nervous system (CNS) of fish comprises the brain and spinal cord, which integrate sensory information and coordinate motor responses essential for survival in aquatic environments. Unlike in mammals, the fish brain is relatively small compared to body size but exhibits specialized regionalization adapted to sensory priorities such as olfaction and vision. The brain is divided into forebrain (prosencephalon), midbrain (mesencephalon), and hindbrain (rhombencephalon), with each region processing distinct functions.^[159] The telencephalon, part of the forebrain, primarily handles olfaction and consists of paired cerebral hemispheres with attached olfactory bulbs that receive direct input from the nasal organs, enabling detection of chemical cues in water.^[160] In the hindbrain, the cerebellum coordinates locomotion and maintains balance during swimming by integrating proprioceptive and vestibular inputs.^[161] Adjacent to it, the medulla oblongata regulates vital autonomic functions, including heart rate and respiration, while serving as a relay between the brain and spinal cord. The midbrain's optic tectum dominates visual processing, acting as the primary center for integrating retinal inputs and multimodal sensory data to guide behaviors like prey capture and obstacle avoidance.^[162] The spinal cord extends continuously from the medulla, forming a tubular structure that transmits neural signals along the body axis and gives rise to segmental nerves through paired dorsal (sensory) and ventral (motor) roots, which unite to form mixed spinal nerves innervating muscles and sensory organs.^[159] Prominent identified neurons within the CNS include the Mauthner cells, a pair of large reticulospinal neurons located in the medulla oblongata of the hindbrain; their axons cross the midline and descend contralaterally through the spinal cord to activate a rapid C-start escape response upon sudden stimuli, such as predator approaches.^[163]

Peripheral Nervous System

The peripheral nervous system (PNS) in fish comprises the cranial nerves, spinal nerves, and associated ganglia that transmit sensory and motor signals between the central nervous system and the body's peripheral structures, enabling responses to environmental stimuli and internal regulation.^[164] In bony fishes (teleosts), the PNS is adapted for aquatic life, with specialized components for sensory detection in water, such as the lateral line system.^[165] Fish possess 10 pairs of cranial nerves, numbered I through X, which originate from the brainstem and forebrain to innervate the head, gills, and associated sensory organs.^[166] These nerves include sensory, motor, and mixed types, with a unique acustico-lateralis component in many species for mechanosensory and electrosensory functions. For instance, the glossopharyngeal nerve (IX) primarily innervates the gills, carrying sensory information from gill arches and taste buds while providing motor control to pharyngeal muscles.^[167] Similarly, the vagus nerve (X) extends to visceral organs, with multiple roots that innervate the gills via its anterior branches and supply parasympathetic innervation to the heart, gut, and other viscera through its posterior branches.^[167] Spinal nerves emerge metamerically from the spinal cord along the body, with each nerve formed by the fusion of dorsal (sensory) and ventral (motor) roots that join distal to the spinal cord.^[165] These mixed nerves branch to innervate muscles, skin, and fins, with autonomic components diverging to regulate visceral functions. The autonomic nervous system in teleosts includes sympathetic chains formed by paired paravertebral ganglia linked longitudinally along the trunk, providing adrenergic innervation to cardiovascular and other systems, while parasympathetic outflow occurs mainly via cranial nerves like the vagus.^[168] Fish also feature an enteric nervous system, consisting of the myenteric plexus within the gut wall, which autonomously coordinates gastrointestinal motility independent of central input.^[169] Sensory ganglia associated with the PNS include dorsal root ganglia along the spinal cord for somatic sensation and specialized cranial ganglia for aquatic sensory systems. Notably, the anterior and posterior lateral line ganglia house cell bodies of afferent neurons that innervate neuromasts in the lateral line, detecting water movements and vibrations for navigation and predator avoidance.^[170]

Endocrine and Immune Systems

Endocrine Glands

The endocrine glands in fish, particularly teleosts, regulate a wide array of physiological processes including growth, metabolism, reproduction, osmoregulation, and stress responses through the secretion of hormones directly into the bloodstream. Unlike in mammals, many fish endocrine structures are diffuse or integrated with other organs, reflecting evolutionary adaptations to aquatic environments. Key glands include the pituitary, thyroid, ultimobranchial bodies, interrenal and chromaffin tissues in the head kidney, endocrine pancreas, corpuscles of Stannius, pineal gland, urophysis, and gonads, each producing specific hormones that coordinate bodily functions.^[171] The pituitary gland, situated ventrally to the hypothalamus and connected via an infundibular stalk, consists of two main parts: the adenohypophysis (anterior pituitary) and neurohypophysis (posterior pituitary). The adenohypophysis secretes several tropic hormones, including growth hormone (GH) from somatotropes, which promotes somatic growth and metabolism, and thyroid-stimulating hormone (TSH) from thyrotropes, which regulates thyroid function.^[172] The neurohypophysis stores and releases neurohormones such as arginine vasotocin (AVT), the fish homolog of antidiuretic hormone (ADH), which aids in osmoregulation and cardiovascular control, along with isotocin, akin to oxytocin.^[173] In teleosts, the pituitary's structure is more compact than in higher vertebrates, with direct innervation influencing hormone release.^[174] The thyroid gland in fish is typically diffuse, consisting of follicles scattered throughout the pharyngeal region and derived evolutionarily from the endostyle of ancestral chordates, which facilitates iodine uptake for hormone synthesis. It produces thyroxine (T4) and triiodothyronine (T3), essential for metamorphosis, growth, and metabolism, with TSH from the pituitary stimulating its activity.^[175] Distinct from the thyroid, the ultimobranchial glands, located near the esophagus or in the transverse septum between the heart and liver, are the primary source of calcitonin in fish—a hypocalcemic peptide hormone that lowers blood calcium levels by inhibiting bone resorption and promoting renal calcium excretion. These glands, derived from the last pharyngeal pouch, exhibit follicular or cord-like structures indicative of endocrine function and are responsive to hypercalcemia, with their activity potentially modulated by pituitary influences.^[176] In teleost fish, the adrenal homolog is not a discrete organ but comprises interrenal and chromaffin tissues embedded within the head kidney, the anterior portion of the renal system. The interrenal tissue, analogous to the mammalian adrenal cortex, forms clusters of steroidogenic cells around posterior cardinal veins and synthesizes corticosteroids such as cortisol, which mediate stress responses, carbohydrate metabolism, and immune modulation.^[177] Adjacent chromaffin cells, homologous to the adrenal medulla, produce catecholamines including adrenaline and noradrenaline, facilitating rapid stress-induced changes in blood pressure, heart rate, and energy mobilization.^[178] This integration with the head kidney allows coordinated endocrine and excretory functions in a compact structure. The endocrine pancreas in fish, often organized as discrete Brockmann bodies separate from the exocrine tissue, consists of islets containing alpha cells that secrete glucagon to raise blood glucose levels, beta cells producing insulin to lower glucose, and delta cells releasing somatostatin to inhibit other islet hormones. These structures are typically located along the intestinal tract or spleen and are crucial for carbohydrate metabolism and energy homeostasis in response to feeding and environmental changes.^[179] Unique to teleost fish, the corpuscles of Stannius are small, paired endocrine glands attached to the posterior kidney that secrete stanniocalcin-1 (STC-1), a hormone that inhibits gill calcium uptake and promotes phosphate excretion to maintain calcium-phosphate balance, particularly important in freshwater environments where calcium influx is high.^[180] The pineal gland, located on the dorsal midline of the brain, functions both as a photoreceptor and endocrine organ in fish, producing melatonin in response to light-dark cycles to regulate circadian rhythms, seasonal reproduction, and stress responses. In many species, it directly perceives light through pinealocytes, integrating photoperiod information for physiological synchronization.^[181] The urophysis, part of the caudal neurosecretory system in the terminal spinal cord, consists of neurosecretory Dahlgren cells whose axons terminate in a neurohemal organ that releases urotensins into the bloodstream. Urotensin I (corticotropin-releasing factor-like) and urotensin II regulate osmoregulation, cardiovascular function, and stress adaptation, with the urophysis playing a key role in ion and water balance.^[182] Gonadal steroids, produced by the testes and ovaries under regulation by pituitary gonadotropins, include androgens like testosterone, estrogens such as 17β-estradiol, and progestogens including 17α,20β-dihydroxy-4-pregnen-3-one, which drive gametogenesis, sexual differentiation, and reproductive behaviors in teleosts. These steroids are synthesized via cholesterol-derived pathways in gonadal interstitial cells, with levels fluctuating seasonally to synchronize spawning.^[183]

Immune Organs and Responses

The immune system in fish comprises both innate and adaptive components, adapted to their aquatic environment and ectothermic physiology. Primary lymphoid organs, where immune cells originate and mature, include the thymus and kidney. The thymus develops early in fish ontogeny and serves as the site for T-lymphocyte maturation, housing thymocytes that undergo selection processes to generate a functional T-cell repertoire.^[184] In teleost fish, the anterior or head kidney functions as the principal hematopoietic organ, producing leukocytes including B and T lymphocytes, granulocytes, and monocytes through ongoing hematopoiesis throughout life.^[185] Unlike in mammals, fish hematopoiesis is not confined to bone marrow but is prominently featured in the kidney, supporting both innate and adaptive immunity.^[186] Secondary lymphoid organs facilitate antigen encounter and immune response amplification. The spleen acts as a blood-filtering structure, containing melanomacrophage centers that aggregate pigments, debris, and pathogens to initiate humoral and cellular responses; these centers are particularly prominent in species like salmonids and cyprinids.^[184] Gut-associated lymphoid tissue (GALT), distributed along the intestinal mucosa, includes lymphoid aggregates and intraepithelial lymphocytes that sample luminal antigens, contributing to mucosal immunity against enteric pathogens.^[187] Fish lack organized lymph nodes, relying instead on diffusion of antigens through these organs for immune activation.^[188] Innate immune responses in fish provide immediate defense through physical and chemical barriers, as well as cellular and humoral factors. The skin and gills, as primary interfaces with the environment, are coated in mucus rich in lysozyme—an enzyme that degrades bacterial cell walls—and antimicrobial peptides that inhibit microbial colonization.^[186] The complement system, activated via classical, alternative, or lectin pathways, opsonizes pathogens and lyses cells, with components like C3 being conserved across fish species for broad-spectrum protection.^[189] Phagocytic cells such as macrophages and neutrophils further engulf invaders, releasing reactive oxygen species. Adaptive immunity in fish is antibody-dominated, with immunoglobulin M (IgM) as the predominant isotype in serum and mucosal secretions, mediating pathogen neutralization and opsonization; IgT (or IgZ in some species) specializes in gut immunity.^[188] T-cell responses, including cytotoxic and helper functions, mature in the thymus and coordinate with B cells in the kidney and spleen, though memory formation is less robust than in higher vertebrates.^[184] In aquaculture, vaccination exploits these mechanisms by inducing specific IgM production and protective memory, as seen in commercial vaccines against viral hemorrhagic septicemia in salmon, enhancing survival rates without lymph node equivalents.^[189]

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Morphohistology of the Digestive Tract of the Damsel Fish Stegastes ...
The intestine has anterior, medium, and posterior portions (Figure 2). Ventrally, the rectum ends at the anus situated in front of the anal fin. Details are ...
[116]
Zebrafish: An Important Tool for Liver Disease Research - PMC
We review how studies of zebrafish have advanced our understanding of inherited and acquired liver diseases as well as liver cancer and regeneration.Comparative Liver Structure... · Metabolic And Fatty Liver... · Liver Cancer
[117]
Anatomy of the endocrine pancreas in actinopterygian fishes and its ...
The present study is the first comprehensive survey on the anatomy of the endocrine pancreas (diffuse versus compact) across 322 actinopterygian species in 39 ...
[118]
WFS 550 Fish Physiology - Digestive System
The structural components of a fish's digestive system include the mouth, teeth and gill rakers, esophagus, stomach, pylorus, pyloric caeca, pancreatic tissue.Missing: spiral valve
[119]
Structural and Functional Aspects of the Spleen in Molly Fish ...
In fish, larger macrophage aggregations or MMCs are normally found in the lymphatic system and other organs, and it has been suggested that they are involved ...
[120]
Morphology, Histology, and Histochemistry of the Digestive Tract of ...
Mar 5, 2023 · The digestive tract of fish is anatomically composed of a long hollow tube, and as in other vertebrates, it is functionally in charge of ...Missing: position | Show results with:position
[121]
Head Kidney - an overview | ScienceDirect Topics
Posterior to the pronephros develops a second kidney, the mesonephros, which co-opts the pronephric duct as its conduit to drain urine to the cloaca.
[122]
Fish Model of Renal Regeneration and Development | ILAR Journal
Oct 1, 2001 · The tubule grows out and fuses with the pronephric excretory duct, which eventually becomes the mesonephric or Wolffian duct. Secondary and ...
[123]
An update on the evolutionary origin of aglomerular kidney with ...
The kidney of fish contains numerous nephrons, each of which is divided into the renal corpuscle and renal tubules. This glomerular structure is the filtration ...
[124]
Morphological and functional characteristics of the kidney of ...
Morphological studies have revealed that the renal tubules of marine cartilaginous fishes are highly elaborate and show unique features compared with those of ...
[125]
Osmoregulation in fish Mechanisms and clinical implications
Histologically, fish kidneys are highly variable, and, overall, the marine fishes have smaller and fewer glomeruli than freshwater fishes [11]. The kidneys of ...
[126]
WFS 550 Fish Physiology - Osmoregulation/Kidney Function
In fish, the tubule is divided into a Bowman's capsule that surrounds the glomerulus, followed by a series of segments (proximal I, proximal II, distal, and ...
[127]
Fish sperm biology in relation to urogenital system structure
Jul 1, 2019 · Morphology of the urogenital system has evolved during fish speciation. Urine has no impact on sperm biology in hagfishes, lampreys and elasmobranchs.
[128]
External reproductive structures of male Surfperches (Embiotocidae ...
Nov 24, 2021 · The urinary duct and spermatic ducts were independent structures associated with the papilla and each had their own external opening. Our ...
[129]
Fish sperm biology in relation to urogenital system structure
Apr 20, 2019 · In contrast, urinary and sperm ducts in the more evolved Teleostei are completely separate, and sperm and urine are not mixed before being ...
[130]
Reproductive Anatomy of Chondrichthyans: Notes on Specimen ...
Jun 25, 2021 · The cloaca is located between the pelvic fins, usually near the origin of the claspers. In some species, the cloaca is enveloped by two cloacal ...
[131]
Reproductive Anatomy of Chondrichthyans: Notes on Specimen ...
Both the urogenital sinus and the deferens ducts are capable of storing a large amount of sperm. The urogenital sinus opens to the exterior through the ...
[132]
Class Chondrichthyes – The Biology Classroom - UBC Blogs
Jan 25, 2017 · This leads to a cloaca – an opening for the urinary, digestive, and reproductive systems (one hole for all!)
[133]
Swim Bladder - an overview | ScienceDirect Topics
Physostomous fish maintain the connection of the swim bladder-esophagus all through the adult stage (Fig. 2.16), whereas physoclistous fish lose the pneumatic ...
[134]
extreme swimbladder sexual dimorphism in the South Asian torrent ...
The swimbladder plays an important role in buoyancy regulation but is typically reduced or even absent in benthic freshwater fishes that inhabit fast flowing ...
[135]
The rete mirabile: a possible control site for swimbladder function
Apr 15, 2023 · In physoclist fish a countercurrent system, the rete mirabile, is used to concentrate gases for the filling of the swimbladder under elevated ...
[136]
THE SECRETION OF OXYGEN INTO THE SWIM-BLADDER OF ...
It is concluded that carbon dioxide brought into the swim-bladder is liberated from blood by the addition of lactic acid. The rete mirabile must act to multiply ...
[137]
Fish Sound Production: The Swim Bladder - VCU Scholars Compass
Sep 11, 2023 · The swim bladder is a major sound-producing organ in fishes. It also functions in hearing and is responsible for most returns from sonar.
[138]
Ontogenetic Development of Weberian Ossicles and Hearing ...
Apr 12, 2011 · The Weberian apparatus of otophysine fishes facilitates sound transmission from the swimbladder to the inner ear to increase hearing sensitivity.
[139]
Diversity in Fish Auditory Systems: One of the Riddles of Sensory ...
Otophysans possess a chain of 1-4 Weberian ossicles that function in ... (A) Swim bladder, Weberian ossicles (tripus, intercalarium, scaphium, and ...
[140]
Size matters: diversity in swimbladders and Weberian ossicles ...
May 15, 2008 · Otophysine fish possess Weberian ossicles, which connect the swimbladder to the inner ear and improve hearing ability.
[141]
[PDF] Origin, Evolution and Homologies of the Weberian Apparatus
The Weberian apparatus is a mechanical device improving audition, consisting of a double chain of ossicles joining the air bladder to the inner ear.
[142]
Finite element modelling of sound transmission in the Weberian ...
Jan 10, 2024 · The Weberian ossicles mechanically couple vibrations of the gas bladder induced by sound pressure to the fluid filled sac of the inner ear, ...
[143]
Finite element modelling of sound transmission in the Weberian ...
Jan 10, 2024 · We conclude that the Weberian apparatus's resonance frequency can explain zebrafish's best hearing frequency, and their biomechanical characteristics are not ...
[144]
Comparative testicular structure and spermatogenesis in bony fishes
In most bony fishes, testes are paired elongated organs, attached to the dorsal wall of the body by a mesorchium. But, in some species there is a single testis, ...Testis Types Of Bony Fishes · Tubular Testis Type · Germ Cells During...
[145]
Reproductive system - Fish Necropsy Manual
The fish reproductive system includes gonads (testes in males, ovaries in females) and ducts. Male testes are usually white, while female ovaries are saccular.
[146]
Structural evidence for two different testicular types in teleost fishes
Sperm development in teleosts is cystic, cysts being comprised of Sertoli-cell processes. In both testicular types described, Sertoli cells phagocytize ...
[147]
Seasonal Effects on Female Fecundity and Male Sperm Availability ...
Oct 1, 2011 · Fish species from temperate climates exhibit seasonal variation in reproduction triggered by abiotic variables such as day length and ...
[148]
Development of the Genital Duct System in the Protandrous Black ...
Feb 2, 2011 · In gonochoristic teleosts, the sperm ducts and oviducts of the male fish and female fish are considered as an extension of testis and ovary, ...
[149]
9. THE TESTES
Testes are a pair of elongated structures composed of branching seminiferous tubules embedded in the stroma.9.1 Morphology · 9.2 Cellular Source Of... · 9.3 Androgenic Steroids<|separator|>
[150]
Male reproductive system as sex pheromone producer in teleost fish
Feb 1, 1992 · In African catfish, Clarias gariepinus, the male reproductive organ system consists of two paired structures, the testis and the seminal vesicle ...
[151]
Hermaphroditism in fishes: an annotated list of species, phylogeny ...
May 7, 2020 · Here we present an annotated list of hermaphroditic fish species from a comprehensive review and careful re-examination of all primary literature.
[152]
Brain regions controlling courtship behavior in the bluehead wrasse
Nov 20, 2023 · Bluehead wrasses are diandric, protogynous (female-to-male) sequential hermaphrodites that form an elaborate social hierarchy. Three distinctive ...
[153]
A social basis for the development of primary males in a sex ... - NIH
In some sex-changing fishes, the testes of primary males appear anatomically similar to those of non-sex-changing species, whereas the testes of secondary males ...
[154]
[PDF] Fish Brains: Anatomy, Functionality, and Evolutionary Relationships
The forebrain is divided into paired olfactory bulbs, ventrally attached to the telencephalic hemispheres, dorsally covering the Diencephalon (the “between-.
[155]
[PDF] Fish brains: evolution and environmental relationships
The telencephalon consists of paired cerebral hemispheres with olfactory bulbs attached to the rostral hemispheres in most fish.
[156]
WFS 550 Fish Physiology - Neural Control
The primary function of the cerebellum is muscle coordination and swimming. The medulla oblongata serves as a relaying center between the spinal cord and ...
[157]
[PDF] The Optic Tectum in Fishes - ResearchGate
The optic tectum forms the roof of the midbrain and is the primary visual center in fishes. The retina and input from other sensory modalities (auditory, ...
[158]
Direct activation of the Mauthner cell by electric field pulses drives ...
Escape responses in fish are initiated by the Mauthner cells, giant reticulospinal neurons with unique specializations for swift responses (Faber and Korn 1978) ...
[159]
Nervous and Sensory Systems - ScienceDirect.com
The central nervous system (CNS) and sensory systems of “primitive” fishes have received considerable attention, and these studies provide crucial insights into ...
[160]
Nervous system and the sensory organs
The nerves, which are the essential part of the peripheral nervous system, are formed of bundles of fibres surrounded by connective tissue. They transmit ...
[161]
On the Course and Origin of Cranial Nerves in the Teleost Fish ...
By horseradish peroxidase (HRP) labelling the course and origin of the II-X cranial nerves are identified in the teleost fish Gnathonemus petersii.
[162]
Central Projections and Motor Nuclei of the Facial ... - PubMed
The sensory and motor nuclei of the VIIth, IXth, and Xth cranial nerves of Gnathonemus petersii were studied by anterograde and retrograde axoplasmatic ...
[163]
Comparative anatomy of the autonomic nervous system - PubMed
The autonomic nervous system shows similarities across vertebrates, with increasing complexity from fish to tetrapods. Segmental ganglia are incomplete in ...<|control11|><|separator|>
[164]
Zebrafish: A Model Organism for Studying Enteric Nervous System ...
Zebrafish lack the muscularis mucosa and submucosal plexus. In addition, the enteric neurons are not organized in ganglia, but rather as individual cells ( ...
[165]
ZFIN zebrafish anatomy
Hair cells are innervated by lateral line nerves; cell bodies of afferent neurons sit in cranial anterior and posterior lateral line ganglia. Three types of ...
[166]
Endocrine Gland - an overview | ScienceDirect Topics
1.23 shows the main endocrine organs of a teleost fish, which include the pituitary gland, the thyroid gland, the head kidneys, the gastrointestinal tract ...
[167]
[PDF] Endocrine Glands of Fish The glands that secrete their products into ...
The thyroid glands in sharks and higher teleosts are diffused in nature. ... The ultimo-branchial gland is under the control of pituitary gland. The Sex ...
[168]
[PDF] Hormones and Social Behaviour of Teleost Fish - ISE
As in other vertebrates, the fish pituitary gland consists of two types of tissue, the adenohypophysis and neurohypophysis, and the secretion of the ...
[169]
Pituitary multi-hormone cells in mammals and fish - ScienceDirect.com
It is composed of two main parts: the anterior (adenohypophysis) and the posterior pituitary (neurohypophysis). ... (TSH), prolactin (PRL), and growth hormone (GH) ...Missing: ADH | Show results with:ADH
[170]
The Role of the Thyroid Axis in Fish - Frontiers
In this review, we discuss the roles of the thyroid axis in fish and its contributions to growth and development, metamorphosis, reproduction, osmoregulation, ...
[171]
Calcitonin and ultimobranchial glands in fishes - Wiley Online Library
Ultimobranchial bodies in fishes contain follicles or cords of cells which show features of endocrine secretion. Hypocalcemic activities are present in the ...
[172]
Histopathological evaluation of the interrenal gland (adrenal ... - NIH
Jul 9, 2022 · The trunk or tail kidney does not have any steroidogenic or chromaffin tissues, however, the renal units and the lymphoid tissues, MMC, and ...
[173]
Adrenocortical and Adrenomedullary Homologs in Eight Species of ...
Steroidogenic cells are always confined to the head kidney. During development chromaffin and steroidogenic cells appear early after hatching in the pronephric ...
[174]
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[175]
Immune System of Fish: An Evolutionary Perspective - IntechOpen
... fish immune system. The kidney (head and middle), thymus and spleen are the largest lymphoid organ in teleost fishes. The development sequence of lymphoid ...
[176]
A Comparison of the Innate and Adaptive Immune Systems in ...
This review will discuss and compare components of both the innate and adaptive immune systems in Gnathostomes, particularly in Chondrichthyes (cartilaginous ...
[177]
Main Components of Fish Immunity: An Overview of the Fish ... - MDPI
The main cellular constituents of the fish immune system are macrophages, granulocytes, dendritic cells, NK cells, and cytotoxic T cells.
[178]
Development of Fish Immunity and the Role of β-Glucan in ... - NIH
The fish adaptive immune response takes place thanks to the presence of well-developed and functionally specialized structures and organs, like in higher ...
[179]
Unique Features of Fish Immune Repertoires - NIH
With respect to fish B lymphocytes, cells expressing, respectively, IgT or IgM are specialized in mucosal versus systemic immunity, reminding the roles of IgA ...
[180]
A Review of Immune System Components, Cytokines, and ...
This review provides a generalized overview of the innate and adaptive arms of the fish immune system, and provides highlights of recently published work in ...