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Silurus

Silurus is a of freshwater catfishes in the family Siluridae, native to rivers, lakes, and streams across , from to . Comprising approximately 16 recognized , the genus is distinguished by its members' elongated bodies, small dorsal fins with 1–6 rays, and long anal fins with 56–88 rays that are confluent with the notched caudal fin. These typically feature four pairs of barbels, with well-developed maxillary barbels, and pectoral spines that are serrated in males but smooth or weakly serrated in females; they lack an adipose fin and possess 52–74 vertebrae. The etymology of Silurus derives from the Greek silouros, referring to a type of . Systematically, the is divided into two main groups: the cochinchinensis group, found in , and the glanis group, distributed in and , reflecting ecological and morphological variations such as and eye . range in size from small forms like S. microdorsalis (up to 35 cm in total ) to giants such as the (S. glanis), which can exceed 400 cm in total and weigh over 300 kg, making it one of the largest freshwater fishes in the world. Ecologically, Silurus species are primarily benthic and carnivorous, inhabiting diverse environments from fast-flowing torrents to deep lakes, where they often remain hidden during the day and forage at night. Notable species include the Amur catfish (S. asotus) in East Asia, valued in aquaculture and fisheries, and the Tigris catfish (S. triostegus) in the Middle East. Some species, like S. glanis, have been introduced outside their native range, impacting local ecosystems as apex predators. The genus's systematics continue to evolve with ongoing taxonomic revisions, including recent mitogenomic studies identifying cryptic divergence, though the 1989 comprehensive study by Kobayakawa remains a foundational reference.

Taxonomy

Etymology and classification history

The genus name Silurus derives from sílóuros (σίλουρος), referring to a type of or river , a term possibly first applied by ancient authors to species from regions like or and later used for the European (S. glanis) in classical texts such as Pliny's translation of . Carl Linnaeus established the genus Silurus in the 10th edition of Systema Naturae in 1758, placing it within the order Siluriformes and designating Silurus glanis as the based on specimens from rivers. Early taxonomic history included misspellings such as Siluris, treated as an invalid junior synonym, and broader classifications of silurid catfishes under informal groups like "sheatfishes" without clear generic boundaries, reflecting limited understanding of their Eurasian distribution prior to the . A major taxonomic revision occurred in 1989, when Mitsuhiro Kobayakawa's systematic divided the into two phylogenetic groups based on morphological characters like fin structure and barbels, recognizing 13 valid species at the time while describing S. microdorsalis as new and synonymizing others. Subsequent genetic analyses, including a 2024 mitogenomic , have refined this to approximately 14 recognized species, with potential for additional cryptic taxa, confirming Silurus as a monophyletic within the Siluridae. The occupies a position within Siluridae, closely related to genera like Kryptopterus.

Phylogenetic relationships

Silurus belongs to the order Siluriformes and the family Siluridae, a group of Eurasian freshwater catfishes commonly referred to as sheatfishes, distinguished by the absence of an adipose fin and a characteristically elongated body form. Within Siluridae, the Silurus forms a monophyletic , as confirmed by comprehensive mitogenomic analyses involving complete mitochondrial genomes from 109 individuals representing of the genus. These studies, utilizing maximum likelihood and methods, demonstrate strong support for the genus's unity, with bootstrap values exceeding 95% and posterior probabilities near 1.0. Recent studies have identified cryptic diversity within like S. asotus, indicating possible additional taxa pending further taxonomic revision. Sister groups to Silurus within Siluridae include genera such as Kryptopterus, with mitogenomic phylogenies revealing their close relationships based on shared mitochondrial protein-coding genes. Major internal lineage divergences within Silurus occurred during the , approximately 10–15 million years ago, as estimated through relaxed analyses calibrated with fossil priors from the Siluridae fossil record. using the subunit I (COI) gene further corroborates the of Silurus, identifying distinct molecular operational taxonomic units (MOTUs) that highlight cryptic diversity while maintaining genus-level cohesion. Phylogenetic reconstructions reveal subclades within Silurus separating European species, such as the type species Silurus glanis, from Asian counterparts like S. asotus, reflecting biogeographic isolation across . Fossil-calibrated phylogenies indicate the crown age of Silurus from the late Eocene (~38 million years ago) to the present, driven by vicariance events in Eurasian river systems. These estimates, derived from Bayesian time-calibrated trees incorporating fossil calibration points, underscore the genus's evolutionary stability over millions of years.

Description

Morphology

Species of the genus Silurus exhibit a distinctive elongated body form, characterized by a scaleless, naked covered in a slimy layer that aids in protection and through environments. The body is cylindrical anteriorly, tapering to a laterally compressed posterior region, with the positioned far posteriorly, typically originating near the midpoint or beyond of the standard length. This posterior placement contributes to the hydrodynamic profile suited for predation. The anal fin is notably elongated, extending along much of the ventral surface and often nearly reaching or fusing with the caudal fin base, comprising 56–88 soft rays. In contrast, the dorsal fin is small, with 1–6 soft rays and lacking any spines, a distinguishing Silurus from many other siluriform catfishes. The caudal fin is rounded to truncate, providing powerful for bursts of speed. The head is broad and depressed, featuring a large terminal to subterminal equipped with curved teeth on both and a patch of vomerine teeth for grasping prey. Eyes are small and positioned dorsally on the head, reflecting adaptations to low-light conditions where plays a secondary to other senses. Silurus species possess four pairs of barbels—nasal, maxillary, and two mandibular pairs (inner and outer)—which are highly sensitive chemosensory organs covered in , enabling detection of prey in turbid waters. The maxillary barbels are particularly elongated, often extending beyond the pectoral fin base, while mandibular barbels vary slightly in length but serve similar tactile functions. These barbels, along with the slimy skin, underscore the genus's reliance on non-visual sensory modalities. The absence of an adipose fin further defines the morphology, streamlining the body for efficient swimming. Body proportions across Silurus species generally follow a where the head comprises about 20–25% of the standard , though variation exists among reaching sizes from under 50 cm to over 2 m.

Size and variation

in the Silurus display considerable variation in body size, with the largest being S. glanis, which attains a verified maximum total of 2.85 m (as of 2023) and weight of 130 kg, though historical unverified reports claim up to 5 m and 306 kg. Larger in the typically reach average adult lengths of 1 to 1.5 m total , reflecting to diverse freshwater habitats. In contrast, the smallest , S. microdorsalis, reaches a maximum of 35 cm total , with common lengths around 19 cm standard . Growth patterns in Silurus species feature rapid juvenile development, with rates of 10–20 cm per year, reaching 70–130 cm total length in 5–7 years, followed by a marked slowdown after . This biphasic growth is modulated by environmental conditions, including , prey abundance, and , which can accelerate early phases in nutrient-rich systems. Intraspecific and interspecific morphological variations aid in taxonomic distinction, particularly in meristic traits like fin ray counts and barbel proportions. Anal fin ray numbers vary from 56 to 88 rays across the , providing a reliable identifier for species delineation. Barbel lengths relative to head size also differ significantly, with longer barbels in species like S. glanis (up to 200% of head length) compared to shorter ones in smaller congeners. Sexual dimorphism manifests prominently during the breeding season, where males exhibit enlarged pectoral spines with posterior serrations absent in females, enhancing mating interactions. This , observed in multiple , underscores adaptive differences in reproductive without altering overall body proportions substantially.

Distribution and habitat

Geographic range

The genus Silurus is native to , encompassing a broad distribution across and . In , species such as S. glanis () are primarily found in the drainage basins of the Black, Baltic, Caspian, and Aral Seas, extending northward to southern and , as well as the basin from the Maritza and Struma rivers to the Sperchios drainage in and . Asian species occupy diverse river systems, ranging from the River basin in the and northeastern (S. soldatovi) to the River basin in (S. meridionalis) and the River basin in southeastern . Specific distributions highlight regional endemism and specialization within the genus. For instance, S. asotus (Amur catfish) is widespread in , inhabiting rivers and lakes across (Honshu, Shikoku, and Kyushu islands), the Korean Peninsula, , , and the . Recent mitogenomic studies as of 2025 have revealed cryptic divergence within the S. asotus complex, suggesting higher species diversity and potentially refining distribution patterns in . In Southeast Asia, S. cochinchinensis occurs in coastal rivers and basins including the Nam Xam ( tributary) in and , the Chao Phraya in , and the in southern . Endemic species like S. biwaensis are restricted to isolated freshwater bodies, such as in , where they have evolved in relative seclusion. Several Silurus species have established introduced populations beyond their native ranges, often through human-mediated translocations. S. glanis has been widely introduced across , including the (from the in 1853) and (from in 1857), primarily via escapes from facilities and recreational fisheries since the , leading to self-sustaining populations in rivers like the Thames and . These introductions have expanded its range into previously unoccupied western and southern European waters, though ecological impacts vary by site.

Environmental preferences

Species of the genus Silurus inhabit diverse freshwater environments, ranging from fast-flowing torrents to deep lakes and reservoirs, often favoring substrates consisting of , , or for cover and foraging. These are well-adapted to benthic habitats with soft bottoms, often seeking refuge in undercut banks, submerged woody structures, or crevices during the day. Many species exhibit a for depths typically ranging from 1 to 10 meters, though they can occupy waters up to 30 meters deep in reservoirs and lakes. Silurus species demonstrate notable tolerance for low dissolved oxygen levels, enabling survival in hypoxic conditions as low as 1-1.5 mg/L, particularly in warmer waters; this adaptation is facilitated by their ability to access atmospheric oxygen at the surface when necessary. In such murky or turbid waters, they rely on prominent barbels for sensory and prey detection rather than . Certain species, such as S. glanis, occasionally venture into brackish waters, including the and Seas, where they tolerate salinities up to approximately 1.5% for short periods, though they do not complete their full life cycle in fully saline environments. Many Silurus species, particularly in the glanis group, thrive in warm-temperate water conditions, with optimal temperatures between 20-25°C for growth and activity, while tolerating a broader range of 4-30°C. Water pH suitability for these species spans to slightly alkaline levels, from 6.5 to 8.5, aligning with their native Eurasian freshwater ecosystems.

Biology and ecology

Feeding and diet

Species of the genus Silurus, such as the Wels catfish (S. glanis), are carnivorous predators with a broad diet that primarily consists of fish, crustaceans, amphibians, and insects. Larger individuals exhibit opportunistic feeding, preying on semiaquatic vertebrates including birds and small mammals when available. This dietary flexibility allows them to exploit diverse prey in various aquatic environments, with fish often comprising the dominant component, such as tench (Tinca tinca) in some populations. These catfish are primarily nocturnal ambush predators, relying on their system to detect hydrodynamic disturbances from swimming prey in low-visibility conditions. Their four pairs of barbels and acute further aid in prey localization, enabling effective wake-tracking during hunts. Foraging typically involves stationary waiting in cover, such as near structures or submerged vegetation, followed by rapid strikes facilitated by protractile jaws that expand to engulf prey. Ontogenetic shifts in diet are pronounced, with juveniles feeding mainly on invertebrates like insect larvae, small crustaceans, and planktonic organisms during their early benthic phase. As they grow into adults, the diet transitions to larger vertebrate prey, including fish and amphibians, reflecting increased gape size and predatory capability; for instance, individuals over four years old may consume exclusively vertebrates. Seasonal variations influence feeding intensity and prey selection, with higher dietary diversity in spring and summer due to increased invertebrate and spawning fish availability, while winter shows greater stomach fullness from aggregated prey.

Reproduction and development

Species of the genus Silurus, such as the (S. glanis), typically in late spring to summer, from to July, in shallow, areas where water temperatures reach 18–22°C. During this period, males construct nests from or to attract females, engaging in displays that involve circling and nudging. External occurs as females release eggs, which are laid in sticky clusters within the nest; a single female can produce 10,000 to 100,000 eggs, with increasing with body size. Males actively guard the eggs until hatching, fanning them to provide oxygenation, but provide no further after the larvae emerge. Egg incubation lasts approximately 50 hours at 24°C or 2.5–3 days (60 degree-days) at 22–23°C, after which larvae hatch at a length of approximately 8.5 . Newly hatched larvae initially exhibit benthic , remaining motionless on the substrate for the first 2–3 days post-hatching while absorbing their . They then transition to a more active phase, beginning to swim and feed around days 5–6, entering a semi-planktonic stage that lasts about 10–14 days before settling as benthic juveniles. This early development period is marked by high mortality rates, primarily due to predation and environmental stressors. Sexual maturity in Silurus species is generally reached at 3–5 years of age, with males maturing slightly earlier than females; for S. glanis, this corresponds to lengths of 78–87 cm. correlates positively with female size and weight, enabling larger individuals to produce substantially more eggs and support population persistence in suitable habitats.

Species

Extant species

The genus Silurus includes approximately 18 recognized extant of silurid catfishes, primarily inhabiting freshwater systems across and , with a few extending into brackish waters. Recent molecular studies suggest additional cryptic within some , such as up to four molecular operational taxonomic units in S. asotus and two in S. microdorsalis, indicating potential for further taxonomic revisions.
Scientific NameCommon NameDistributionBrief Characteristics
S. aristotelisAristotle's catfishSoutheastern Europe (Greece)Small species reaching 46 cm TL; endemic to the Acheloos River drainage.
S. asotusAmur catfishEast Asia (China, Japan, Korea, Russia, Taiwan, Vietnam)Grows to 130 cm TL; commercially important in aquaculture for its fast growth and tolerance to pond culture, often reaching market size in 1-2 years.
S. biwaensisGiant Lake Biwa catfishJapan (Lake Biwa basin)Attains 118 cm TL; specialized for lacustrine habitats.
S. burmanensisBurmese catfishMyanmar (Inlé Lake)Small, reaching about 25 cm SL; adapted to shallow, vegetated lake environments.
S. caobangensisCao Bang catfishNorthern VietnamRecently described (2015), up to 30 cm TL; inhabits highland rivers with rocky substrates.
S. dakrongensisDakrong catfishNorthern VietnamSimilar to S. caobangensis, reaching 25 cm TL; found in fast-flowing upland streams.
S. duanensisDuanhe catfishChina (Hongshui River)Grows to 40 cm TL; riverine species with preference for middle basin habitats.
S. glanisWels catfishEastern Europe to central Asia (widely introduced elsewhere)Largest species, up to approximately 3 m TL and 150 kg (unverified reports to 5 m); apex predator in large rivers and lakes, known for longevity exceeding 50 years.
S. grahamiGraham's catfishChina (Fuxian Lake)Reaches 43 cm SL; lacustrine form with mottled patterning.
S. lanzhouensisLanzhou catfishChina (upper Yellow River basin)Attains 100 cm TL; adapted to turbid, large river systems with strong currents.
S. lithophilusJapanese common catfishJapan (Lake Biwa and Lake Yogo)Grows to 58 cm TL; lithophilic spawning behavior, preferring rocky lake bottoms.
S. longibarbatusLong-barbeled catfishChina (Hongshui River)Recently described (2019), up to 50 cm TL; notable for elongated barbels in riverine habitats.
S. mentoKunming catfishChina (Dianchi and Yilong Lakes)Reaches 38 cm TL; endemic to highland lakes, with vulnerability to habitat alteration.
S. meridionalisSouthern catfishChina (Yangtze River basin)Grows to 114 cm SL; common in middle river reaches, supports local fisheries.
S. microdorsalisMicrodorsal catfishChina and Korea (Yalu River basin)Small, up to 35 cm TL (though some reports suggest smaller adults around 17 cm SL); characterized by reduced dorsal fin elements.
S. soldatoviSoldatov's catfishRussia and China (Amur River basin)Large, reaching 400 cm TL; euryhaline, tolerating brackish estuaries.
S. tomodaiTomoda's catfishJapan (central Honshu streams)Recently described (2018), up to 51 cm SL; hillstream specialist with flattened body for riffle habitats.
S. triostegusTigris catfishMiddle East (Iraq, Iran, Syria, Turkey; Tigris-Euphrates basin)Attains 99 cm SL; brackish-tolerant, with three dorsal scutes in some populations.

Fossil record

The fossil record of the genus Silurus extends from the to the , with the earliest confirmed occurrences in European deposits dating to approximately 11.6 million years ago. These early fossils primarily consist of isolated bones such as pectoral-fin spines and vertebrae, indicating that the genus had already diversified in freshwater systems by the Sarmatian stage of the . Key extinct species include †S. spinosus, known from late Miocene (Sarmatian) deposits in southeastern , particularly , where it is represented by multiserial denticulations on pectoral-fin spines distinguishing it from extant forms. Another notable extinct in the European record is the late Miocene S. joergi from , while S. soldatovi—now restricted to but formerly widespread—appears in late Miocene to strata across southeastern Europe, suggesting historical range expansions. In , silurid remains attributable to the broader Siluridae family, potentially allied with Silurus, have been recovered from the Middle Sanuki Group in (approximately 15.8 million years ago), featuring 52–53 vertebrae and 61–62 anal fin rays in a specimen of about 92.5 mm standard length. Holocene evidence includes archaeological bones of S. glanis from Belgian sites in the and basins, spanning the Early (around 8200 cal BC) to the late medieval period (early AD), with specimens estimated at 90–200 cm standard length from locations such as Oudenaarde-Donk and Trou de Pont-à-Lesse. These remains confirm the presence of large-bodied individuals in during warmer postglacial periods. Fossils of Silurus species exhibit morphologies closely resembling modern forms, such as robust pectoral spines and vertebral counts, indicating a conservative evolutionary trajectory with minimal major innovations since the Miocene. However, subtle changes, like reductions in denticulations on pectoral-fin spines, occurred over time, potentially aiding ecological adaptations. The record also documents range contractions following the Last Glacial Maximum, with S. glanis persisting in northern refugia like Belgium until post-medieval extinctions likely driven by climatic cooling and human activities.