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Pharaoh cuttlefish

The Pharaoh cuttlefish (Sepia pharaonis, recently reclassified as Acanthosepion pharaonis) is a medium- to large-sized cephalopod in the family Sepiidae, characterized by a broad, dorsoventrally flattened mantle, prominent eyes, internal cuttlebone for buoyancy regulation, and specialized skin chromatophores enabling rapid color and pattern changes for camouflage, hunting, and communication.^[1]^[2] Native to the tropical and subtropical Indo-West Pacific, it inhabits shallow benthic and epibenthic environments such as sand flats, seagrass beds, and coral reefs, typically at depths of 0–40 m but ranging up to 130 m, often migrating vertically to hunt at night.^[1]^[2] Adults grow to a maximum mantle length of 43 cm (males) or 33 cm (females), with weights up to 5 kg, and exhibit semelparous reproduction where mature individuals form spawning aggregations, females deposit clusters of 300–600 eggs on substrata after internal fertilization, and both sexes die post-reproduction following a lifespan of about 240 days.^[1]^[3] This species is an ambush predator, primarily feeding on crustaceans like crabs and shrimp, small fish, and occasionally other cephalopods or even conspecifics through cannibalism, using jet propulsion, ink ejection, and arm-flapping behaviors for capture and escape.^[1]^[2] Its distribution spans from the Red Sea and Persian Gulf eastward through the Arabian Sea, Andaman Sea, and to the western Pacific including Taiwan and Australia, with occasional records in the Mediterranean via Lessepsian migration.^[1]^[2]^[3] Commercially significant, S. pharaonis supports artisanal and industrial fisheries, aquaculture operations, and the aquarium trade across its range, particularly in the Gulf of Oman and Andaman Sea, where it is abundant and landed at sizes of 15–20 cm.^[1] Despite this importance, the species is assessed as Data Deficient (2009) by the IUCN Red List due to insufficient data on population trends, with potential threats including overfishing, habitat degradation, and ocean acidification.^[1]^[4]

Taxonomy and nomenclature

Scientific classification

The Pharaoh cuttlefish is classified within the kingdom Animalia, phylum Mollusca, class Cephalopoda, subclass Coleoidea, superorder Decapodiformes, order Sepiida, suborder Sepiina, family Sepiidae, and genus Acanthosepion.^[5] Its binomial name is Acanthosepion pharaonis (Ehrenberg, 1831), originally described as Sepia pharaonis in 1831 based on specimens from the Red Sea.^[6]

Taxonomic Rank	Name
Kingdom	Animalia
Phylum	Mollusca
Class	Cephalopoda
Subclass	Coleoidea
Superorder	Decapodiformes
Order	Sepiida
Suborder	Sepiina
Family	Sepiidae
Genus	Acanthosepion
Species	A. pharaonis

This classification reflects a recent reclassification from the genus Sepia to Acanthosepion in 2023, based on analyses of gladius (pen) and rostral characters that delineate Acanthosepion as a distinct clade within Sepiidae, incorporating S. pharaonis and related taxa.^[7] Phylogeographic analyses based on partial mitochondrial 16S rRNA sequences indicate that A. pharaonis comprises a species complex with five distinct clades across the Indo-Pacific (e.g., Gulf of Aden/Red Sea, northern Indian Ocean, etc.), showing deep phylogenetic divergence that suggests cryptic speciation influenced by historical oceanographic barriers, though further morphological and genetic studies are needed to formally delimit species boundaries.^[8] Historically, S. pharaonis has undergone taxonomic revisions, including synonymy with several nominal species due to overlapping morphological traits in early descriptions. Recognized synonyms include Sepia formosana S. S. Berry, 1912; Sepia framea Ortmann, 1891; Sepia hulliana (Iredale, 1926); Sepia rouxii A. d'Orbigny, 1842; Sepia singalensis E. S. Goodrich, 1896; Sepia tigris M. Sasaki, 1929; Sepia torosa Ortmann, 1888; and Sepia ursulae (Cotton, 1929), many of which were later consolidated into the pharaonis complex based on type specimen re-examinations and molecular data.^[6]

Etymology and synonyms

The species epithet pharaonis in the scientific name Sepia pharaonis derives from the Latin pharao, referring to the ancient Egyptian pharaohs, a naming choice tied to the species' description from specimens collected in the Gulf of Suez, a region historically linked to pharaonic Egypt due to its prevalence there.^[6] The genus name Sepia originates from the Ancient Greek σήπια (sēpía), meaning "cuttlefish," in reference to the cephalopod's ink, which was extracted and used as a reddish-brown pigment in classical art and writing.^[9] The current genus name Acanthosepion (established as a subgenus by Rochebrune in 1884 and elevated to genus in 2023) derives from the Greek akantha (spine or thorn) and sēpion (cuttlefish), referring to the characteristic long, pointed spine on the posterior end of the cuttlebone in species of this group.^[7] Sepia pharaonis was first described by the German naturalist Christian Gottfried Ehrenberg in 1831, based on material from an expedition to Egypt and surrounding areas, marking it as one of the earliest documented cuttlefish species from the Red Sea.^[10] The original publication appeared in Symbolae physicae, a work documenting new or little-known invertebrates from the expedition's collections.^[6] Over time, the species has accumulated several junior synonyms due to regional variations and historical misidentifications, including Sepia formosana S. S. Berry, 1912; Sepia framea Ortmann, 1891; Sepia hulliana (Iredale, 1926); Sepia rouxii A. d'Orbigny, 1842; Sepia singalensis E. S. Goodrich, 1896; Sepia tigris M. Sasaki, 1929; Sepia torosa Ortmann, 1888; and Sepia ursulae (Cotton, 1929).^[6] In contemporary taxonomy, Sepia pharaonis is considered a junior synonym, with the accepted name shifted to Acanthosepion pharaonis (Ehrenberg, 1831) following phylogenetic revisions that elevated subgeneric distinctions within the Sepiidae family.^[5]

Physical characteristics

Morphology and size

The Pharaoh cuttlefish (Sepia pharaonis) exhibits a typical cephalopod body plan, characterized by a soft-bodied, bilaterally symmetrical structure with a prominent muscular mantle that encloses the internal organs and the distinctive cuttlebone, a rigid, calcareous internal shell used for buoyancy regulation and support. The mantle is elongated and tapered posteriorly, housing the gills and funnel (siphon) within the mantle cavity, while the head bears eight shorter arms and two longer tentacles, all lined with suckers for manipulation and prey capture. The siphon, a muscular tube, enables rapid jet propulsion by expelling water, facilitating both locomotion and escape responses. Additionally, the species possesses large, well-developed eyes with W-shaped pupils, adapted for high-acuity vision in low-light environments typical of their benthic habitats.^[11]^[12] Adults can attain a maximum mantle length of 43 cm (males) or 33 cm (females), with total lengths reaching approximately 80 cm from the anterior tentacles to the posterior fin margin, and body weights up to 5 kg, though common sizes in fisheries range from 15 to 25 cm mantle length; regional variations occur, with smaller maxima reported (e.g., 36 cm along the Gujarat coast, India).^[1]^[13] The cuttlebone, a key diagnostic feature, measures on average 21.8 cm in length for males (range 14–30 cm) and 20.7 cm for females (range 16–24 cm), with a characteristic broad, plate-like posterior callosity. These dimensions vary regionally, with larger individuals reported from the Indian coast compared to the Persian Gulf.^[14]^[12] Sexual dimorphism is evident in size and reproductive structures, with males generally larger than females—reaching global maximum mantle lengths of 43 cm versus 33 cm in females—though regional studies report smaller sizes (e.g., 30 cm males versus 22–25 cm females in the Persian Gulf and Gujarat), and possessing a specialized hectocotylus on the left ventral arm, modified with enlarged suckers and a sperm groove for spermatophore transfer during mating. The tentacles feature clubs with up to six enlarged suckers in the medial rows, aiding in precise handling.^[12]^[14]^[1] Growth rates differ between captive and wild conditions, reflecting environmental influences on development. In captivity, S. pharaonis hatchlings start at 8 mm mantle length and can achieve 168 mm mantle length within 210 days, with daily growth peaking at 1.2 mm during mid-juvenile stages. In the wild, growth is slower, attaining approximately 115 mm mantle length by six months, influenced by factors such as prey availability and temperature.^[15]

Coloration and camouflage mechanisms

The skin of the Pharaoh cuttlefish (Sepia pharaonis) features specialized cellular components that enable rapid and versatile coloration changes. Chromatophores, pigment-containing organs, are present at densities of up to 200 per square millimeter, allowing for quick shifts from pale white to dark brown tones through expansion and contraction of their radial muscles. These include yellow, red, and brown pigments that contribute to a broad palette for blending with substrates.^[16] Underlying the chromatophores are iridophores and leucophores, which provide structural coloration. Iridophores consist of stacked reflectin protein plates that generate iridescent effects through thin-film interference, reflecting light in hues like blue, green, or silver to enhance pattern subtlety. The S. pharaonis genome encodes 12 reflectin gene copies, including unique variants, supporting this tunable iridescence for environmental matching. Leucophores, spherical cells that diffusely scatter ambient light, produce bright white reflections to create high-contrast elements or mimic bright backgrounds, ensuring visibility balance from various angles.^[17] These components facilitate multiple camouflage strategies. Background matching involves uniform or mottled patterns where chromatophores and leucophores adjust to replicate substrate tones and brightness, such as sandy seafloors. Disruptive coloration employs bold contrasts, like passing cloud or zebra-like stripes, generated by selective chromatophore expansion to break up the body outline and confuse predators. Motion camouflage is achieved through papillae—muscular skin projections that alter texture; these can protrude or undulate in under a second to mimic wavy algae or rough corals during movement. The Pharaoh cuttlefish also employs mimicry for defense and predation. Adults exhibit arm-flapping mimicry of hermit crabs, raising and darkening the first pair of arms to simulate eyes while flapping the second and third pairs to imitate jointed legs, often lightening surrounding skin for a shell-like appearance; this behavior aids stealthy approaches during hunting.^[18]^[19] Neural control orchestrates these adaptations directly from the brain, bypassing hormonal delays for instantaneous responses. Visual input from the retina processes through the optic and lateral basal lobes to the chromatophore lobes, where motor neurons innervate skin effectors; this pathway enables chromatophore expansion in approximately 100 milliseconds and papillae adjustments in less than a second, driven by real-time environmental cues.

Distribution and habitat

Geographic range

The Pharaoh cuttlefish (Sepia pharaonis) is native to the tropical and subtropical waters of the Indo-West Pacific, with its range extending from the Red Sea and East Africa eastward to southern Japan and northern Australia.^[11]^[20] This distribution encompasses latitudes from approximately 35°N to 30°S and longitudes from 30°E to 150°E, primarily along coastal and neritic zones.^[21] Within its native range, the species is particularly abundant in the western Indian Ocean, including the Red Sea, Persian Gulf, and coastal waters of East Africa, as well as the Arabian Sea and Bay of Bengal up to India.^[22]^[23] It is notably absent from the eastern Pacific Ocean, where no established populations have been recorded.^[24] As a Lessepsian migrant, S. pharaonis has indications of presence in the Mediterranean Sea via the Suez Canal, with the first cuttlebone recorded in 2001 from the Bitter Lakes and large numbers washing ashore along the Israeli coast in 2003, though no living specimens have been confirmed.^[25]^[26] In some native regions, such as the Arabian Sea coast of Oman and Iranian waters of the Persian Gulf, local populations have shown declines attributed to overfishing, though comprehensive global population estimates remain unavailable.^[27]^[28]

Habitat preferences and migrations

The Pharaoh cuttlefish, Sepia pharaonis, inhabits shallow coastal waters ranging from 0 to 130 meters in depth, with a preference for depths of 10 to 40 meters in regions such as the Andaman Sea and Gulf of Thailand.^[2] It favors soft substrata like sandy or muddy bottoms, which allow for burrowing and concealment during the day.^[4] These conditions support its benthic lifestyle, where individuals often embed themselves partially in the sediment to rest.^[15] This species thrives in tropical to subtropical marine environments with temperatures typically between 24.6°C and 29.1°C (mean 28.1°C) and salinities of 30 to 40 ppt, with an optimal salinity around 30 psu for embryonic development. Such water conditions are prevalent in its Indo-West Pacific range, enabling active metabolism and growth.^[4] S. pharaonis exhibits seasonal migrations between inshore and offshore waters, often moving toward coastal areas with the advancement of the monsoon season.^[22] Off the coast of India, adults undertake offshore movements in depths of 60 to 86 meters for spawning, particularly during peak periods from October to April. Additionally, individuals perform daily vertical migrations, rising higher in the water column at night.^[2] Preferred microhabitats include seagrass beds, edges of coral reefs, and estuarine areas, where the species can exploit structural complexity for shelter.^[4] These environments provide a mix of soft sediments and vegetation, facilitating camouflage adaptations to muddy substrates.^[15]

Biology and behavior

Feeding ecology

The Pharaoh cuttlefish (Sepia pharaonis) is an opportunistic feeder with a diet dominated by fishes and crustaceans, supplemented by mollusks and occasionally other cephalopods. Stomach content analyses from specimens along the Gujarat coast of the northeastern Arabian Sea reveal that fishes constitute the primary prey group, accounting for approximately 68% of the index of relative importance (IRI), followed by crustaceans at 19.8%, mollusks at 6.1%, and cephalopods at lower proportions.^[29] This composition reflects its generalist predation on available benthic and epibenthic organisms, including small crabs, shrimp, mysids, and teleost fishes such as gobies and anchovies. As an ambush predator, S. pharaonis primarily forages in shallow coastal waters, relying on camouflage to blend with sandy or seagrass substrates during hunts. It exhibits heightened activity at night, when it emerges from daytime hiding spots to stalk prey, though juveniles begin active hunting as early as 8 mm mantle length upon hatching.^[2] For elusive targets, it employs jet propulsion to pursue and close distances rapidly, augmenting its typical stationary ambush strategy.^[30] Hunting in S. pharaonis follows a characteristic three-phase strike sequence: attention, positioning, and seizure. In the attention phase, the cuttlefish uses dynamic skin patterns and binocular vision to detect and fixate on moving prey, often initiating with a unique arm-flapping display where the first pair of arms is raised and darkened to mimic a threat or lure. During positioning, it maneuvers tentacles to align at an optimal distance—typically around 0.6 times its mantle length for moving targets—while maintaining camouflage.^[31] The seizure phase involves a rapid tentacular strike, where specialized tentacles extend to ensnare prey with suckers, followed by retraction to the mouth for consumption via beak and radula; if the strike fails, it may switch to a "jump-on" pounce using all arms for closer-range capture.^[31] This method leverages the tentacles' club-like tips, which feature adhesive suckers distinct from the ambulatory arms.^[32] Ecologically, S. pharaonis serves as a mid-level predator in Indo-Pacific benthic communities, exerting top-down control on crustacean and small fish populations to maintain balance in demersal food webs. Its predation pressure on abundant crustaceans, such as shrimp and crabs, helps regulate these groups' densities in coastal ecosystems, while its own role as prey for larger fish and sharks underscores its position in trophic dynamics.

Reproduction and development

The Pharaoh cuttlefish (Sepia pharaonis) exhibits a mating system characterized by high sperm competition, where males engage in agonistic displays and guarding behaviors to secure mating opportunities.^[3] Larger males typically dominate through visual displays, such as transverse black line patterns on the mantle and raised arms to express antagonism toward rivals, while smaller "sneaker" males opportunistically attempt to mate.^[33] Winners of these contests often escort paired females, maintaining close proximity to prevent interference during copulation and subsequent egg-laying periods.^[3] Both males and females are promiscuous, mating multiple times over the reproductive season, which spans spring and summer in their native range.^[2] Copulation occurs via internal fertilization in a face-to-face posture, lasting approximately 4-5 minutes per bout.^[3] The male uses a specialized arm, the hectocotylus, to transfer spermatophores directly to the female's buccal membrane, where sperm are stored in seminal receptacles for later use.^[2] This process allows females to fertilize eggs as they are laid, with males often repeating transfers during the extended spawning phase to maximize paternity.^[34] Following mating, females lay eggs in clusters attached to hard substrata such as coral or rocks, typically in shallow coastal waters.^[3] Each cluster contains 300–600 eggs, with females producing multiple batches over several weeks, resulting in a total fecundity of 75–1,525 eggs per individual depending on size and condition.^[35] Egg-laying involves a three-phase sequence: the female retracts and fists her arms to extrude eggs (lasting about 30 seconds), blows water from her funnel to position them, and deposits them while encapsulating each in a protective, ink-darkened capsule using mucoid secretions.^[3] Incubation lasts 2-4 weeks, varying with temperature (22-31 days at 18-25°C), during which eggs remain adhered and guarded indirectly by the female's site selection.^[3] Embryonic development progresses through approximately 30 stages, beginning with cleavage shortly after fertilization and advancing to organogenesis, including blastulation, gastrulation, and formation of the mantle, arms, and cuttlebone.^[3] By stage 30, the external yolk sac is absorbed, and embryos exhibit eye pigmentation and chromatophore development.^[3] Hatchlings emerge at approximately 8 mm mantle length, fully formed with functional arms and jet propulsion, immediately adopting a benthic lifestyle by adhering to substrata and seeking hideouts for camouflage and foraging.^[2] Sexual maturity is reached at around 120 mm mantle length for females typically within 4–7 months.^[35]^[2] The species' lifespan is typically 6-12 months, with adults dying post-spawning.^[2]

Regeneration and other adaptations

The Pharaoh cuttlefish (Sepia pharaonis) exhibits remarkable limb regeneration capabilities and has been well-studied for this trait alongside Sepia officinalis.^[36] This process restores functional structures, including chromatophores, suction cups, and normal morphology, enabling full social and predatory utility within approximately 39 days, at which point the regenerated appendage reaches about 95% of its original length.^[36] Regeneration proceeds through a series of predictable stages involving dedifferentiation of existing cells into a proliferative blastema, followed by cell proliferation and redifferentiation to reconstruct complex tissues like musculature and nervous elements. This ability enhances survival in environments where physical damage from predators or conspecific interactions is common. Genomic and transcriptomic studies of S. pharaonis reveal molecular features supporting rapid healing and disease resistance, contributing to its suitability for aquaculture. The species demonstrates strong overall disease resistance, including tolerance to common mariculture pathogens, through robust immune responses that mitigate infections.^[37] Specifically, it exhibits resistance to bacterial infections such as those caused by Vibrio species via innate immune mechanisms, including antimicrobial peptides in haemocytes and ink secretions that inhibit bacterial growth, such as Vibrio alginolyticus.^[38] Transcriptomic analyses post-stress, including ink ejection, highlight upregulated genes related to immunity and coagulation, underscoring adaptive physiological resilience.^[39] Sensory adaptations in S. pharaonis include advanced visual capabilities tailored for predation, featuring a highly developed optic lobe and retinal structure that enable precise tracking of moving prey. This allows for ballistic interception strategies, where the cuttlefish predicts and strikes at future prey positions despite sensorimotor delays.^[40] Complementing this, ink ejection serves as a primary defense mechanism against threats, releasing a melanin-rich cloud that confuses predators and contains antimicrobial compounds to deter secondary infections during escape.^[41] Behaviorally, S. pharaonis maintains social hierarchies through agonistic displays that extend beyond reproductive contexts, such as establishing dominance in foraging groups or territorial disputes. These include multimodal signals like arm waving and postural changes to signal threat levels, escalating from subtle warnings to overt aggression, thereby reducing physical confrontations and conserving energy.

Human interactions

Commercial uses and aquaculture

The pharaoh cuttlefish (Sepia pharaonis) supports significant commercial fisheries across its range, particularly in the Philippines, India, and the Arabian Sea region off Oman, where it is harvested using bottom trawlers, traps, and hand lines.^[42]^[43]^[44] In the Arabian Sea off Oman, it constitutes approximately 70% of cephalopod landings, with average annual yields of around 4,612 metric tons recorded in 2001–2002 and a maximum sustainable yield estimated at 9,608 metric tons.^[42] Off India's southwest coast near Vizhinjam, the species forms a key component of hook-and-line fisheries, with an average annual standing stock of 636 metric tons as estimated in a 1978–1980 study.^[43] In the Philippines, it is among the most commonly fished cuttlefish species, contributing to regional cephalopod exports, though specific annual catch figures remain aggregated with other species.^[44] The species is primarily exploited for human consumption, with dried shredded meat and roe processed for local and export markets, particularly in Southeast Asia where it features in regional cuisines such as stir-fries and soups.^[45]^[46] Its ink has historical significance as a source of sepia pigment for artistic applications, derived from melanin-rich secretions used in dyes and inks since ancient times.^[47]^[48] Aquaculture efforts for S. pharaonis have advanced through laboratory and semi-closed systems, enabling rearing from eggs to marketable size—reaching an average of 521 g and 168 mm mantle length in 210 days—using simple recirculating setups with mysids and shrimp as initial feed.^[15] Multi-generational culture has been achieved over five consecutive generations in controlled environments, demonstrating feasibility for large-scale production and adaptation to formulated feeds during weaning at dorsal mantle lengths of 24 mm or more.^[49]^[50] The species' high-quality reference genome, which highlights unique genetic features like expanded reflectin genes, supports potential domestication and selective breeding for aquaculture enhancement.^[51]

Conservation status and threats

The Pharaoh cuttlefish (Sepia pharaonis) is classified as Data Deficient on the IUCN Red List, with the assessment last updated in 2009 as of the 2025-1 version due to insufficient data on population trends and distribution to determine decline or extinction risk.^[1]^[4] This status reflects the lack of comprehensive global surveys, though localized studies indicate declining trends in native ranges such as the Arabian Sea and parts of the Indian coast, where recruitment overfishing has reduced abundance.^[52] In overfished regions like the eastern Arabian Sea off India, catch rates have shown seasonal variability but overall pressure from targeted fisheries, leading to concerns over stock sustainability. Major threats to the species include overfishing, particularly through aggregation devices and bottom trawling that target spawning aggregations, resulting in recruitment overfishing in key native habitats.^[53] Bycatch in trawl fisheries exacerbates mortality, as cuttlefish are often captured unintentionally during operations in shallow coastal waters across the Indo-West Pacific.^[54] Habitat loss from coastal development, including urbanization and pollution in tropical inshore areas, further pressures populations by degrading essential benthic environments for juveniles and adults.^[55] The species' range expansion into the Mediterranean Sea as a Lessepsian migrant via the Suez Canal exposes it to additional local fishing pressures and potential competition, though specific impacts remain understudied. Conservation measures are limited but include management efforts in India, such as policy guidelines from the Central Marine Fisheries Research Institute to regulate fish aggregating device use and prevent overexploitation of spawning stocks.^[52] Research into sustainable aquaculture is advancing, with successful larval rearing protocols developed to support commercial culture and alleviate wild harvest pressure, particularly in high-demand regions like Southeast Asia. Broader strategies, such as bycatch reduction devices in trawls, have been recommended globally to mitigate incidental capture.^[54]

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[35]
Physiological, biochemical and molecular responses of Sepia ...
Apr 18, 2021 · This species is characterized by rapid growth, short life span, tolerance to crowding and human handling, resistance to diseases and feeding ...
[36]
Antimicrobial and cytotoxic activities of flavonoid and phenolics ...
Aug 12, 2024 · S. pharaonis ink ethanolic extract showed a promising cytotoxic potency against various cell lines and a remarkable antimicrobial action against different ...
[37]
A transcriptome resource for pharaoh cuttlefish (Sepia pharaonis ...
When the genomic sequences were not available, transcriptome sequencing could provide a comprehensive understanding of regulatory mechanisms involved in ...Missing: healing | Show results with:healing
[38]
Visual Attack on the Moving Prey by Cuttlefish - Frontiers
Jun 17, 2020 · To successfully seize a moving prey, the predator must be able to compensate for any inherent sensorimotor delay before initiating the visual ...
[39]
Continuous Inking Affects the Biological and Biochemical ... - Frontiers
We investigated the effects of continuous ink release on survival, behavior, and biochemical characteristics of cuttlefish Sepia pharaonis and tried to ...<|separator|>
[40]
(PDF) Biology and stock assessment of the pharaoh cuttlefish, Sepia ...
Aug 5, 2025 · A study on the biology, population parameters and stock assessment of the pharaoh cuttlefish Sepia pharaonis Ehrenberg, 1831 was carried out from the Arabian ...
[41]
[PDF] bulletin 37 - Eprints@CMFRI
The average annual stock oi Sepia pharaonis in. Vizhinjam area where it supports a good fishery, is high, 636 t and females form 54% of the population. The ...
[42]
[PDF] Phylogeography of the Pharaoh Cuttle Sepia pharaonis ... - OpenSIUC
... Sepia pharaonis is actually a complex of at least three species. To evaluate this possibility, we collected tissue samples from Sepia pharaonis from throughout.
[43]
Pharaoh cuttlefish (Sepia pharaonis) - JungleDragon
It is a commonly fished species of cuttlefish in the Philippines, as well as the most economically important cuttlefish in the northern Indian Ocean. Off the ...
[44]
Cuttlefish - Species | Sydney Fish Market
Various species are imported, mainly from South East Asia, whole (cleaned, frozen and dried), as 'steaks', 'cuttle crackers' and shredded. Recipes. Black ...
[45]
First multi-generation culture of the tropical cuttlefish Sepia ...
Aug 7, 2025 · The pharaoh cuttlefish, Sepia pharaonis Ehrenberg, 1831, is a commercially fished species found from Japan to East Africa. Previous ...
[46]
[PDF] Enzymatic hydrolysis as an approach to produce alternative protein ...
Mar 27, 2020 · The various valuable constituents in their ink have been used over millennia for practical and commercial purposes.<|separator|>
[47]
[PDF] inflammatory activity of sepia pharaonis ink extract in different ...
T K.,2021). Reduced dose of sepia pharaonis liver oil enhanced the immune response and decreased the inflammatory mechanism of formalin-induced and ...
[48]
First multi-generation culture of the tropical cuttlefish Sepia ...
Size at hatching wasmeasured for fourth generation (G4) hatchlings; the mean weight athatching was 0.103 g and the mean mantle length was 6.4mm.
[49]
Optimum weaning method for pharaoh cuttlefish, Sepia pharaonis ...
Nov 4, 2020 · The optimal weaning protocols for cuttlefish juvenile are as follows: a dorsal mantle length of 24.0 mm or more, the feeding frequency of 4 meals/day and the ...
[50]
Pharaoh Cuttlefish, Sepia pharaonis, Genome Reveals Unique ...
Feb 14, 2021 · Sepia pharaonis, the pharaoh cuttlefish, is a commercially valuable cuttlefish species across the southeast coast of China and an important ...
[51]
[PDF] Policy guidance on cuttlefish fishery using Fish Aggregating Devices
Recruitment overfishing of Sepia pharaonis along the eastern. Arabian Sea. • Decrease in free-school cuttlefish abundance. • Increase in marine debris as result ...
[52]
Can an aggregation-fishery be responsible for recruitment ...
The pharaoh cuttlefish, Sepia pharaonis is the major targeted cuttlefish resource in the study area. ... Annual cuttlefish fishing trends, catch rates, size ...
[53]
Cuttlefish conservation: a global review of methods to ameliorate ...
Nov 24, 2022 · A global review of methods to ameliorate unwanted fishing mortality and other anthropogenic threats to sustainability.
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Threats | CCI - Cuttlefish Conservation Initiative
Eggs have a smaller chance of hatching due to habitat loss and current potting practices. Young individuals are being potentially over-fished after migration ...