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Catshark

Catsharks are small to medium-sized sharks belonging to the family Scyliorhinidae within the Carcharhiniformes, distinguished by their elongated, cat-like eyes equipped with a and a bottom-dwelling . This is the largest family of sharks, encompassing around 160 species across 17 genera, with many species rarely exceeding 1 meter in length, though the maximum recorded size reaches about 1.6 meters. They inhabit a wide range of benthic environments in temperate and tropical seas worldwide, from shallow coastal waters and intertidal zones to depths greater than 2,000 meters on continental and insular slopes. Physically, catsharks feature a body covered in placoid scales, five slits (with the fifth positioned over the pectoral base), two small spineless fins located posteriorly on the body, and an anal . Their mouths are positioned forward but not fully under the , and most lack prominent nasal barbels, though exceptions exist in like Poroderma. These sharks are generally slow-moving and non-migratory, with many exhibiting nocturnal behavior; some species, such as swell sharks in the genus Cephaloscyllium, can inflate their stomachs with air or water as a defense mechanism. Biologically, catsharks are predominantly oviparous, with about 90% of laying eggs encased in tough, rectangular capsules often equipped with tendrils for attachment to substrates like or rocks, facilitating prior to deposition. A smaller number are ovoviviparous, retaining eggs internally until hatching. Their diet consists mainly of small fishes, crustaceans, mollusks, and other , with feeding strategies ranging from bottom to predation. While harmless to humans, many catsharks hold ecological importance as predators in marine food webs and some economic value in fisheries, though certain face threats from and degradation, leading to vulnerable or near-threatened statuses for several taxa.

Taxonomy and classification

Families and genera

The term "catshark" collectively refers to small sharks in the order assigned to five main families, encompassing approximately 160 characterized by their elongated cat-like eyes and bottom-dwelling habits. As of 2024, updates include the addition of new species like Apristurus ovicorrugatus in Pentanchidae. The family Scyliorhinidae, known as true catsharks, includes the majority of shallow-water and is now restricted to three genera with about 36 following recent revisions: Cephaloscyllium (swellsharks, 18 ), Poroderma (2 ), and Scyliorhinus (16 , including the nursehound S. stellaris). Pentanchidae, the deepwater catsharks, comprises around 90 species across 10 genera, such as (ghost catsharks, approximately 39 species), (sawtail catsharks, 18 species), and (11 species); this family was historically subsumed within Scyliorhinidae but elevated based on distinct morphological traits like the absence of supraorbital crests. Atelomycteridae, the coloured catsharks, features about 12 species in two subfamilies and genera including (6 species) and (4 species); it was revalidated and split from Scyliorhinidae using molecular and morphological evidence to reflect its unique ectodermal pit distribution and coloration patterns. Pseudotriakidae, the false catsharks, contains 5 species in three genera: Pseudotriakis, Gollum, and Planonasus, distinguished by continuous labial furrows and deep-sea adaptations. Proscylliidae, the finback catsharks, includes 7 species in three genera: Ctenacis, Eridacnis, and Proscyllium, noted for their slender bodies and rudimentary nictitating membranes. A phylogenetic study utilizing 143 morphological characters and NADH2 sequences confirmed the of these families and most genera, driving updates like the redefinition of Apristurus and the addition of subfamilies within Pentanchidae (Halaelurinae and Galeinae), enhancing understanding of catshark diversity.

and

The "catshark" originates from a linguistic evolution in post-medieval vernaculars, where the Latin term catulus (meaning "" or "young ") was misinterpreted or adapted into words evoking "" in , such as (cat) and gatto (cat). This shift appeared in early ichthyological texts, including Guillaume Rondelet's 1554 description as Chat rochier and Ippolito Salviani's 1558 Pescie Gatto, reflecting a misapplication of descriptors to these sharks' small size and bottom-dwelling habits rather than their ocular features. Although popularly attributed to the sharks' large, reflective, cat-like eyes, historical analysis confirms the name's canine roots, with English usage emerging in the 18th century alongside . In nomenclature, catsharks were initially classified by in his 1758 Systema Naturae under the order Selachii (a broad grouping for cartilaginous fishes) and the genus Squalus, with species like Squalus canicula (now the lesser spotted catshark, Scyliorhinus canicula) named using binomial descriptors emphasizing diminutive canine traits (canicula from Latin for "little dog"). The family Scyliorhinidae, established by in 1862, derives its name from the genus Scyliorhinus (Blainville, 1816), combining Greek skýlion (small dog or whelp, alluding to dogfish-like qualities) and rhī́nē (rasp or file, referring to the rough, denticle-covered skin), though some interpretations link it to rhīs (nose) for the tapered snout. Modern binomial nomenclature applies this system across genera, exemplified by Scyliorhinus canicula for the widespread northeast Atlantic species. Common names vary regionally, with many populations of Scyliorhinus referred to as "dogfish" due to overlapping historical descriptors, leading to frequent confusion with true dogfishes of the family (e.g., spurdogs like Squalus acanthias). In fisheries contexts, terms like "ground shark" or "rock salmon" (a for S. canicula in markets) further obscure distinctions, as catsharks inhabit benthic grounds but differ taxonomically from other ground sharks. Synonymy issues stem from early misclassifications, such as Linnaeus's Squalus catulus (1758), a junior synonym of Scyliorhinus canicula arising from redundant canine epithets. In deepwater taxa, genera like Apristurus (family Pentanchidae, formerly lumped with Scyliorhinidae) were historically termed "black catsharks" based on uniform dark coloration, but recent phylogenetic revisions specify them by depth ranges (e.g., 400–2000 m) to resolve ambiguities with shallower Scyliorhinus species.

Phylogenetic relationships

The families collectively referred to as catsharks belong to the order , commonly known as ground sharks, where they occupy a basal position relative to other families such as (houndsharks). This order is characterized by shared morphological traits including a and a caudal fin with a ventral lobe longer than the dorsal lobe. Phylogenetic analyses indicate that the crown group of originated in the , with divergence times estimated at approximately 192 million years ago (95% highest posterior density interval: 175–207 Ma), aligning with the period's onset around 201–145 Ma. Molecular evidence from studies utilizing (mtDNA) and nuclear genes has elucidated key splits within , including the separation of Pentanchidae (deep-sea catsharks) from Scyliorhinidae. A 2012 analysis of NADH dehydrogenase 2 (ND2) mtDNA sequences across diverse elasmobranchs supported the basal positioning of scyliorhinids and highlighted paraphyletic patterns in related families, reinforcing earlier morphological frameworks. Complementary work by Maisey (2012) integrated paleontological data with molecular phylogenies, emphasizing the evolutionary divergence of catshark lineages from triakids around 150–190 million years ago during the . Shirai's 1992 cladistic analysis of skeletal and muscular characters further established the monophyly of while positioning Scyliorhinidae as a foundational , with subsequent molecular validations confirming these interrelationships. In broader phylogenetic trees of , Proscylliidae (finback catsharks) occupies the most basal position, followed by Scyliorhinidae, with and more derived families like Carcharhinidae branching later. The of Scyliorhinidae has been affirmed by genomic analyses in the , including mitogenomic studies that resolve internal relationships using complete mitochondrial genomes and nuclear markers, demonstrating cohesive genetic clustering distinct from neighboring families. These trees underscore catsharks' primitive traits, such as egg-laying reproduction, as plesiomorphic within the order. The fossil record of catshark-like forms dates to the , with articulated skeletons from representing early around 150 million years ago, though definitive Scyliorhinidae fossils appear in the (~100 Ma). Notable examples include Paracarcharias from deposits of , , featuring dental morphologies akin to modern catsharks, providing evidence of their persistence through the . This record aligns with molecular divergence estimates, illustrating a gradual diversification from ancestors.

Physical characteristics

Morphology and anatomy

Catsharks in the family Scyliorhinidae exhibit an elongated, slender body shape that tapers at both ends, often slightly depressed, facilitating efficient movement through aquatic environments. The body features two s positioned posteriorly, typically with the first dorsal fin originating over or behind the pelvic fin bases, and both lacking spines, a characteristic distinguishing them from many other families. An is present, contributing to , while the caudal fin is asymmetrical with a long upper lobe and a shorter lower lobe featuring a subterminal notch. The head of catsharks is relatively narrow to moderately broad, with a that varies from short and bluntly rounded to moderately long and pointed, often lacking lateral flaps. Eyes are large and cat-like, positioned dorsolaterally as horizontal ovals, equipped with a rudimentary for protection but without subocular pockets. Sensory adaptations include nasal barbels (prominent in some genera, such as Poroderma) and, in many , nasoral grooves connecting the nostrils to the mouth, enhancing chemosensation; spiracles, moderately large and positioned below the eyes, aid in water intake for respiration. Additional sensory structures encompass for detecting electric fields and a system for mechanoreception, with olfactory rosettes providing a well-developed . The skeletal system is entirely cartilaginous, hardened by calcified deposits, providing flexibility and lightness compared to bony structures in other , which supports agile swimming and reduces overall body weight. Muscular arrangements include well-developed trunk and appendicular musculature, with specific units in the cephalic region integrating feeding and sensory functions, though detailed muscular differentiation varies across . Respiratory adaptations feature five pairs of slits on the sides of the head, increasing in size posteriorly in some genera, without extension onto the surface or screens. Spiracles supplement ventilation by allowing to enter directly, particularly useful in low-oxygen benthic habitats, while buccopharyngeal denticles line the mouth and pharyngeal regions, offering protection against abrasion during feeding. Some species, such as those in deeper waters, exhibit enlarged branchial regions to cope with hypoxic conditions.

Size variations and growth

Catsharks display considerable variation in adult size across species, with most attaining total lengths (TL) of 20–100 cm. Representative examples include the small-spotted catshark (Scyliorhinus canicula), which reaches a maximum of approximately 100 cm TL, and the blackmouth catshark (Galeus melastomus), typically growing to 70–80 cm TL. At the extremes, deepwater species such as certain Apristurus max out at 30–50 cm TL, while larger shallow-water species like the nursehound (Scyliorhinus stellaris) can exceed 170 cm TL. Growth in catsharks is generally slow, with annual increments of 0.5–2 cm in later stages, as indicated by von Bertalanffy growth parameters (e.g., growth coefficient K ≈ 0.20 year⁻¹ for S. canicula). occurs at 30–60 cm , varying by ; for instance, S. canicula males mature at about 43 cm and females at 45 cm , often after 6–7 years. ranges from 10 to 30 years, with tag-recapture studies confirming lifespans exceeding 12 years in S. canicula and up to 20+ years in related through vertebral validation. Sexual dimorphism is prevalent, with females typically larger than males at maturity and exhibiting extended growth post-maturity. curves, estimated via counts of annual vertebral bands, reveal sex-specific trajectories; in S. canicula, females surpass males in asymptotic length, reaching 5–10 cm greater maximum sizes. Factors such as depth and influence size attainment, with deepwater consistently smaller (e.g., Bythaelurus reaching a maximum of 30–76 cm TL) compared to shallower-water . Latitudinal effects are evident in like S. canicula, where Mediterranean populations achieve larger sizes than those at higher latitudes, potentially due to temperature-driven growth differences.

Coloration and camouflage

Catsharks in the family Scyliorhinidae exhibit a diverse array of coloration patterns that primarily serve adaptive purposes in their respective habitats, often featuring mottled browns, grays, or darker tones interspersed with spots, saddles, or bars. For instance, the lesser spotted catshark (Scyliorhinus canicula) displays a grayish-brown surface adorned with numerous small, dark spots and subtle saddles, contrasting with a pale ventral side, which aids in blending with sandy or rocky seabeds. Similarly, in the genus Atelomycterus, such as the catshark (A. marmoratus), possess more vivid patterns including bold black spots outlined in white against a brownish background, providing disruptive among coral structures. These patterns vary across genera, with deeper-water forms like the filetail catshark (Parmaturus xaniurus) showing uniform gray-brown dorsally without prominent markings, suited to dimly lit slopes. A key camouflage mechanism in catsharks is , where the dorsal surface is darker to match the shadowed underwater environment from above, while the lighter ventral side mimics the brighter light, reducing visibility to predators in benthic or midwater settings. In addition, many species incorporate bio, particularly in deeper waters, where pigments absorb and re-emit it as green fluorescence that enhances their mottled patterns. For example, in the chain catshark (Scyliorhinus retifer) and swellshark (Cephaloscyllium ventriosum), this green glow intensifies the contrast of spots and saddles under low-light conditions, potentially aiding concealment by matching ambient light spectra. This fluorescent enhancement is chemically derived from brominated metabolites in the skin, which not only produce the glow but also contribute to the overall pigmentation. Ontogenetic changes in coloration are common among scyliorhinid catsharks, with juveniles typically displaying more vivid and contrasting patterns that fade or become more subdued as mature, reflecting shifts in use or predation pressures. In many species, early life stages feature bolder spots or saddles for in areas, which homogenize with growth to suit broader ranges. These transformations underscore the adaptive flexibility of catshark pigmentation, aligning visual traits with developmental ecology across the .

Distribution and habitat

Global range

Catsharks, belonging to the family Scyliorhinidae, exhibit a across temperate and tropical s worldwide, inhabiting , , and Pacific basins from shallow coastal waters to deep-sea environments. This broad range spans multiple biogeographic provinces, with species documented on continental shelves and slopes across all major systems except the polar and regions in significant numbers. Recent taxonomic revisions have reduced the family to 37 species across 3 genera (as of November 2025), unevenly distributed, with higher diversity in the compared to . Many genera show regional biases, such as Scyliorhinus, which predominates in the Northern Hemisphere's temperate waters of the eastern Atlantic and , where species like the (Scyliorhinus canicula) range from to . Other genera extend into the western Atlantic and eastern Pacific. is particularly pronounced in isolated or deep-sea regions, contributing to the family's . High rates underscore the role of oceanographic barriers in . Most catshark species are sedentary, with limited large-scale migrations, though some coastal forms exhibit seasonal movements tied to temperature or prey availability. In the Mediterranean, for instance, populations of show restricted dispersal influenced by historical glacial refugia, maintaining genetic structure over small scales.

Habitat preferences

Catsharks, members of the family Scyliorhinidae, predominantly exhibit benthic and demersal lifestyles, residing on or near the seafloor in a variety of coastal and shelf ecosystems. They favor substrates such as rocky reefs, beds, and soft sediments including sand, mud, and gravel, which provide ample cover and foraging opportunities. For instance, the (Scyliorhinus canicula) thrives in shallow coastal waters up to 400 m deep, commonly over sandy or muddy bottoms in the northeastern Atlantic. These sharks often associate with structural features for shelter, hiding in crevices, caves, or among algae during inactive periods. Species in the genus Cephaloscyllium, such as the swellshark (Cephaloscyllium ventriosum), actively inflate their bodies with water or air to wedge tightly into rocky crevices or caves, enhancing security against predators. This behavior underscores their preference for complex reef habitats that offer microhabitats for resting and egg deposition. Catsharks generally require moderate marine conditions, with levels around 30–35 and temperatures ranging from 5–25°C, varying by species and geographic distribution. Temperate species like S. canicula prefer 14–19°C and salinities near 35 in coastal environments. They also co-occur with other benthic in shared dens or overlapping habitats, such as with the Eledone cirrhosa and various crustaceans, where resource partitioning allows coexistence in and sedimentary areas.

Depth and environmental adaptations

Catsharks exhibit a wide range of depth distributions, with species primarily inhabiting shallower coastal waters from 0 to 200 meters, while some extend to mesopelagic depths up to 1,500 meters or more. This vertical stratification reflects evolutionary adaptations to gradients, where the flexible, of catsharks provides inherent , allowing tissues to withstand hydrostatic pressures up to 450 atmospheres without structural collapse, unlike rigid bony skeletons in fishes. Physiological mechanisms enable catsharks to thrive in these environments, including elevated concentrations in their blood and tissues for , which maintains cellular under high and conditions common in deep waters. Deep-dwelling species possess enlarged livers rich in low-density oils, comprising up to 20% of body weight, which provide and reduce energy expenditure on locomotion in the absence of a . Additionally, in these sharks exhibit high oxygen affinity, facilitating efficient oxygen uptake in low-oxygen deep-sea waters, with some species demonstrating exceptional tolerance comparable to the most resilient fishes. Catsharks also display resilience to environmental stressors such as temperature fluctuations and , critical for survival in variable deep-sea conditions. Recent deep-sea research, including expeditions identifying new in waters at depths over 1,000 meters, has highlighted specialized sensory adaptations in these catsharks for navigating extreme environments, though direct associations with hydrothermal vents remain under investigation in ongoing studies.

Biology and ecology

Diet and feeding habits

Catsharks are carnivorous predators with diets dominated by benthic and small fishes, reflecting their opportunistic in coastal and shelf environments. The (Scyliorhinus canicula), a common shallow-water , primarily consumes crustaceans such as and , alongside small demersal fishes and occasional mollusks, with stomach content analyses revealing crustaceans comprising up to 38% of the diet by numerical abundance and fishes around 53%. In deeper-water like the (Galeus melastomus), decapod crustaceans remain a key component (46% by index of relative importance), but cephalopods, euphausiids, and mesopelagic fishes contribute significantly as secondary prey. Feeding strategies among catsharks emphasize predation, where individuals often lie in wait on the seafloor during the day, relying on before striking at passing prey, particularly during nocturnal activity peaks. They capture prey using a combination of biting and feeding, facilitated by protrusion that enhances intraoral and allows rapid enclosure of targets within the gape. This modulation of feeding enables effective predation on mobile and evasive fishes, with smaller catsharks exhibiting greater reliance on for elusive prey. As mid-level predators, catsharks occupy trophic levels typically ranging from 3.5 to 4.0, positioning them as mesopredators that regulate lower trophic tiers while facing predation from larger elasmobranchs. Dietary composition shifts with , season, and habitat depth; juveniles and smaller individuals preferentially target like mysids and euphausiids, transitioning to more fishes as they grow, while seasonal variations reflect prey availability. Stomach content studies highlight depth-related differences, with shallow-water species deriving over 70% of their diet from in some populations, compared to deeper conspecifics or related taxa incorporating more pelagic fishes (up to 50% or higher). These patterns underscore the trophic plasticity of catsharks, enabling adaptation to varying environmental conditions.

Reproduction and development

Catsharks (family Scyliorhinidae) are predominantly oviparous, with females laying eggs encased in leathery capsules known as mermaid's purses, which feature tendrils for attachment to substrates such as , rocks, or to prevent drifting. These egg cases are typically deposited one per , though some species exhibit multiple , retaining several in each uterus simultaneously. occurs via the males' claspers, paired appendages on the pelvic fins that deliver during , a process observed year-round in many tropical and subtropical species but with seasonal peaks in temperate ones, such as winter and summer breeding activity in the (Galeus melastomus). Embryonic development within the egg case is direct, with the absorbing the completely before , resulting in fully formed, juveniles without a prolonged yolk-sac larval stage. Incubation periods vary by species and environmental conditions, typically ranging from 4 to 12 months; for example, the (Scyliorhinus canicula) hatches after 5-6 months at temperate temperatures, while the larger (Scyliorhinus stellaris) requires 9-12 months. Hatchlings emerge at lengths of 8-15 cm, depending on the species, and are immediately capable of predatory feeding and dispersal. Fecundity in catsharks generally ranges from 10 to 50 eggs per female annually, increasing with female size and species; the produces 29-62 eggs per year, while larger congeners like the may lay more due to greater ovarian capacity. Egg production is often continuous but modulated by environmental cues, contributing to the family's relatively high reproductive output among oviparous elasmobranchs.

Behavior and social interactions

Catsharks in the family Scyliorhinidae exhibit predominantly nocturnal or crepuscular activity patterns, with increased movement and foraging occurring at night while they rest during the day. For instance, the small-spotted catshark (Scyliorhinus canicula) shows higher activity levels and larger activity spaces at night (mean speed of 79 ± 41 m/h and activity space of 0.13 ± 0.04 km²) compared to daytime (activity space of 0.09 ± 0.02 km²), often remaining inactive at midday possibly through buccal pumping while sheltered in crevices or caves. Similarly, the swellshark (Cephaloscyllium ventriosum) rests motionless in rocky dens during daylight hours and becomes active at night to hunt, aligning with its ambush predation strategy. Locomotion in catsharks relies on a combination of axial undulation for steady and pectoral movements for precise maneuvering and . In like the , steady swimming involves anguilliform body undulation, with pectoral angling to generate and control during cruising or turns. This -based maneuvering allows for agile navigation over complex benthic habitats. In the swellshark genus (Cephaloscyllium), slow, weak swimming is supplemented by pectoral adjustments, enabling the to hover or position itself effectively for prey ambushes. Catsharks are generally solitary, showing no evidence of complex social hierarchies, though juveniles may aggregate when familiar with one another and adults occasionally form loose groups in areas of high prey density. Adult small-spotted catsharks, for example, display high site fidelity and residency without grouping tendencies, with females exhibiting stronger philopatry than males. In contrast, juvenile S. canicula form non-random aggregations driven by familiarity, increasing social attraction indices but not necessarily group sizes, suggesting a role in reducing predation risk during early life stages. Swellsharks (C. ventriosum) are typically solitary but may congregate in caves or high-prey reef areas, without observed dominance structures. Antipredator behaviors in catsharks emphasize camouflage, immobility, and physical defenses rather than aggression. Many species, including the , employ a freeze response when detecting threats, remaining motionless to blend with the and avoid detection by larger predators like other sharks. In the swellshark genus (Cephaloscyllium), individuals curve their bodies into a U-shape and gulp water or air into the stomach to inflate up to double their size, making them difficult to swallow and deterring predators. These responses to threats, such as approaching larger elasmobranchs, highlight adaptations suited to their benthic lifestyle.

Conservation and human interactions

Threats and vulnerabilities

Catsharks, belonging to the Scyliorhinidae, face significant threats from in commercial fisheries, particularly demersal trawls and gillnets targeting species. In the Northeast Atlantic, species such as the (Scyliorhinus canicula) are commonly captured as incidental catch, comprising a notable proportion of discards due to their abundance in coastal and shelf habitats. Although many individuals exhibit high post-release survivorship, the cumulative mortality from repeated captures contributes to population stress, especially for smaller-bodied species with limited escape capabilities. Habitat degradation poses another major vulnerability, primarily through that disrupts benthic environments like rocky reefs and beds essential for catshark shelter and deposition. This method physically damages structures, reducing available areas and increasing exposure to predators. Additionally, coastal development and , including chemical contaminants, adversely affect case integrity and embryonic development, as catsharks are oviparous and rely on protective capsules for . Climate change exacerbates these risks, with ocean warming and acidification altering physiological processes in catsharks. Experimental studies on the demonstrate that combined warming and acidification impair embryonic growth, hatching success, and early juvenile metabolism, potentially reducing recruitment rates. Furthermore, rising temperatures may shift distributions poleward, disrupting established ranges and increasing overlap with intensified grounds. Overfishing represents a direct threat, as some catshark species are targeted or retained for fishmeal, bait, and aquarium trade, compounded by their k-selected life history traits including slow growth and low fecundity. In regions like the Mediterranean, intense exploitation has led to regional declines, classifying certain populations as vulnerable despite global assessments often rating the family as least concern overall. This vulnerability is heightened by their limited mobility and dependence on stable habitats, making recovery challenging without reduced fishing pressure.

Conservation measures

Conservation efforts for catsharks are guided primarily by assessments from the International Union for Conservation of Nature (IUCN), which classify many species in the family Scyliorhinidae as due to insufficient data on population trends, distribution, and threats. For instance, the (Scyliorhinus canicula), one of the most abundant and widely distributed species, is rated Least Concern, reflecting its resilience across coastal waters of the Northeast Atlantic and Mediterranean. In contrast, deepwater species such as the yellowspotted catshark (Scyliorhinus capensis) are assessed as Near Threatened (assessed 01 August 2019), underscoring their vulnerability to habitat disturbance and in deeper oceanic zones. Regulatory measures have been enacted to mitigate impacts on catshark populations, particularly in regions with intensive fishing. The introduced a comprehensive deep-sea fisheries in 2016, prohibiting below 800 meters in EU waters to safeguard vulnerable marine ecosystems, including habitats frequented by deepwater catsharks. In 2022, the closed 87 areas to all bottom-contact fishing gears, representing about 7% of EU waters and further protecting deep-sea habitats used by catsharks. While no catshark species are currently listed under the (CITES), broader protections for elasmobranchs, such as those for rare deep-sea taxa in families like Atelomycteridae, are advocated through regional agreements to prevent unregulated trade. These policies aim to reduce incidental capture, a key threat briefly noted in vulnerability assessments, by enforcing gear restrictions and closed seasons in high-risk areas. Research initiatives play a crucial role in informing strategies for catsharks. The International Council for the Exploration of the Sea (ICES) on Elasmobranch Fishes (WGEF) conducted population monitoring in 2023, including tagging studies to track movements and abundance of like S. canicula, revealing limited patterns that support targeted protection efforts. Additionally, programs for breeding have been established, such as those at the Zoo Aquarium, where coral catsharks (Atelomycterus marmoratus) have been successfully reared since 2010 to bolster captive populations and for potential reintroduction. Success stories demonstrate the efficacy of protected areas in catshark recovery. In the Mediterranean, the establishment of marine protected areas (MPAs) post-2010, such as those under the Barcelona Convention, has led to observed increases in elasmobranch densities, including catsharks, by restricting activities and allowing regeneration. These MPAs have contributed to localized population rebounds, providing models for expanding conservation networks across catshark ranges.

Role in fisheries and aquaria

Catsharks are harvested in commercial fisheries primarily in and for their and skins, contributing to local and regional markets. In European waters, species such as the (Scyliorhinus canicula) hold moderate commercial importance, with catches targeted for human and processed products. In , Indo-Pacific catsharks like the catshark (Chiloscyllium punctatum) are caught for similar uses, often as part of broader elasmobranch fisheries. The represents a significant market for and , including catsharks, with focused on intra-regional . Several catshark species are popular in public aquaria due to their small size, bottom-dwelling habits, and relative ease of care, making them suitable for educational displays. The bamboo catshark is frequently featured in touch pools at facilities such as the and the , where visitors can interact with these docile animals to learn about shark biology. Similarly, the is commonly displayed in aquarium tanks across and for its adaptability to captivity. Captive breeding programs for elasmobranchs, including catsharks like coral and small-spotted species, are implemented in aquaria to support sustainable exhibits and reduce reliance on wild captures, employing reproductive technologies such as . Sustainable practices in catshark fisheries emphasize low-impact methods and eco-labeling to ensure long-term viability. Programs like the certify shark fisheries that minimize and adhere to science-based quotas, applying to some catshark-harvesting operations in as part of broader elasmobranch management. These initiatives promote alternatives to , such as selective gear and stock assessments, while aquarium breeding reduces demand for wild specimens. Catsharks hold cultural significance in coastal communities, serving as bait in targeted fisheries and contributing to traditional shark-derived products. In some Asian regions, shark species including catsharks are incorporated into folk medicines for purported health benefits, though scientific validation is limited. Ecotourism opportunities allow divers to observe catsharks in their natural habitats, fostering public appreciation and supporting conservation awareness without direct handling.

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