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Distribution

provided by FAO species catalogs
Western North Atlantic from the Gulf of Maine. Eastern Atlantic, from Ireland, Bay of Biskay, Azores to off the Cape of South Africa; Durban (Indian Ocean) and Pacific Ocean South of Australia, around New Zealand and Chilean waters.

Benefits

provided by FAO species catalogs
Not uncommon but so far none of the species considered important commercially but flesh highly esteemed. Caught incidentally in bottom trawls. The total catch reported for this species to FAO for 1999 was 36 636 t. The countries with the largest catches were New Zealand (23 780 t) and Australia (7 553 t).

Brief Summary

provided by FAO species catalogs
Bathypelagic species,from depths of 180 to 1.500 m, most abundant between 400 and 900 m.Feeds crustaceans and fish have found in the stomachs of various specimens. Practically nothing is known about the reproduction. A ripe female measuring 451 mm standard length has been taken in September off Rockland, Maine.

Diagnostic Description

provided by FAO species catalogs
Body oval, deep an remarkably compressed. Head large, about 3 times in standard length. Eye small, about 23% of head; no spines on opercular or post-temporal bones. Teeth minute, in bands; vomer toothless in large specimens. Enlarged scales in abdominal midline sometimes present, sometimes not. Lateral line with 31 scales enlarged, bearing a low spine. Dorsal fin with 5-6 spines and 15-18 soft rays. Anal fin with 3 spines and 10-12. Pectoral fin with 19-20. Gillrakers with 6 + 1 + 13-14. Colour dark orange, red on head and body; opercular membranes black; branchiostegals red outside, black inside; anus black; fins bright orange; membranes of spinous dorsal black; inside of buccal cavity black.

References

  • Lloris, D. - 1986. Ictiofauna demersal y aspectos biogeográficos de la costa sudoccidental de África (SWA/Namibia). Monogr. Zool. Mar., 1: 9-432 pp.
  • Maul, G. E. - 1986. Soleidae. In: P.J.P. Whitehead et al., (eds.). Fishes of the North-eastern Atlantic and the Mediterranean (FNAM). Unesco, Paris, vol. III: 1308-1324.
  • Maul, G. E. - 1990. Soleidae. In: J.C. Quero et al., (eds.) Check-list of the fishes of the eastern tropical Atlantic (CLOFETA). Unesco, Portugal, vol. II: 620-622.
  • Nakamura, I. - 1986. Trachichthyidae. In: I. Nakamura; T. Inada; M. Takeda; H. Hatanaka (eds.). Important Fishes trawled off Patagonia. Japan mar. Fish. Resource Res. Center: 164-165.

Size

provided by FAO species catalogs
About 70 cm; common 20-35 cm.

Trophic Strategy

provided by Fishbase
Found on the continental slope (Ref. 75154). Orange roughy feed opportunistically on bentho-pelagic and meso-pelagic fish, crustaceans, and squid. Juveniles feed mainly on crustaceans whereas adults prefer fish and squids. They appear to have moderately high rates of food consumption (Ref. 27075). Dietary changes may be linked to modifications in morphology with growth (Ref. 27076). Little is known of the larvae and juveniles, which do not appear to aggregate (Ref. 6390).
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Morphology

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Dorsal spines (total): 4 - 6; Dorsal soft rays (total): 15 - 19; Analspines: 3; Analsoft rays: 10 - 12
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Migration

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Oceanodromous. Migrating within oceans typically between spawning and different feeding areas, as tunas do. Migrations should be cyclical and predictable and cover more than 100 km.
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Life Cycle

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Orange roughy are synchronous annual spawners (Ref. 7030). They form dense spawning aggregations over sea hills and slopes. Eggs and sperms are shed into the water at the same time. Individual males appear to spawn over a 1-2 week period and females spawn for up to 1 week. Little is known of the larvae and juveniles.
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Diagnostic Description

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Bright brick-red in color, mouth and gill cavity bluish black (Ref. 4181). Ventral scutes: 19-25.
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Biology

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Inhabits deep, cold waters over steep continental slopes, ocean ridges and sea-mounts. Shallow range of usual occurrence from Ref. 27121. Appears to be dispersed over both rough bottoms and steep, rough grounds where it feeds on crustaceans and fish. In New Zealand, the main prey include mesopelagic and benthopelagic prawns, fish, and squid, with other organisms such as mysids, amphipods and euphausiids occasionally being important (Ref. 9072). Juveniles feed mainly on crustaceans (Ref. 27075, 27076). Grows very slowly and is one of the longest lived fish species known. Based on parasite and trace-element analyses, orange roughy is a sedentary species with little movement between fish-management zones (Ref. 27089). Little is known of the larvae and juveniles which are probably confined to deep water (Ref. 27088). The fishery targets sporadically formed dense spawning and non-spawning aggregations. Marketed fresh and frozen; eaten steamed, fried, microwaved and baked (Ref. 9988). Because of severe overfishing the species has been listed as threatened by the Australian Government in 2006.
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Importance

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fisheries: highly commercial; price category: medium; price reliability: reliable: based on ex-vessel price for this species
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Hoplostethus atlanticus ( German )

provided by wikipedia DE

Hoplostethus atlanticus, auch Kaiserbarsch, Orange Roughy oder Granatbarsch genannt, ist ein relativ großer Tiefseefisch. Er kommt in kalten (3–9 °C), tiefen (bathypelagisch, ca. 180–1800 m) Gewässern des Westatlantiks (nördlich von Neuschottland), Ostatlantiks (von Island bis Marokko, Namibia bis Südafrika), zwischen Neuseeland und Australien sowie im Ostpazifik vor Chile vor.[1]

Merkmale

Der Granatbarsch ist mit einer maximalen Größe (inklusive Schwanzflosse) von 75 cm und einem maximalen Gewicht von 7 kg der bisher größte bekannte Vertreter der Trachichthyiformes. Jedoch haben die meisten kommerziell gefangenen Exemplare standardmäßig nur eine Größe von 30 bis 40 cm Hoplostethus atlanticus ist auffällig ziegelrot gefärbt, das Innere des Mauls und das Innere der Kiemen ist schwarzblau. Die Schuppen sind klein und unregelmäßig angeordnet.[1]

Von anderen, ähnlich gefärbten Fischen kann Hoplostethus atlanticus durch seinen großen verknöcherten Kopf, die kleinen, unregelmäßig angeordneten Schuppen und die zahlreichen Schuppen am Bauch unterschieden werden.[2]

Der Orange Roughy ist bekannt dafür, dass er sehr alt (bis ca. 150 Jahre) werden soll und sein fortpflanzungsfähiges Alter erst mit ca. 30–35 Jahren erreicht.[3] Diese Angaben sind allerdings umstritten; über den wirklichen Lebenszyklus der Tiere ist wenig bekannt. Sollten sie stimmen, sind viele der heute gefischten Exemplare vor dem Ersten Weltkrieg geschlüpft. Die Bestände dürften sich dann äußerst langsam erholen und unter Beibehaltung derzeitiger Fangmengen rasch erschöpft sein.[3] Welche Rolle der Granatbarsch im Ökosystem der Tiefsee spielt und welche Folgen sein Verschwinden für andere Arten hat, ist bislang nicht ausreichend geklärt. Sicher ist, dass er in Schwärmen lebt, die alle Altersstufen umfassen und weite Wanderungen unternehmen. Dabei folgen sie eventuell Tiefseeströmungen.

Fischerei

 src=
Hoplostethus atlanticus
 src=
Die Fangraten für den Orange Roughy weltweit

Der Fisch ist für die Tiefseefischerei von großer Bedeutung und wird häufig im Handel als Speisefisch angeboten. Er wird auch in Deutschland verkauft, aber vor allem in Großbritannien, den USA, in China und Australien gegessen.[3] Seine ziegelrote Farbe schwächt sich nach dem Tod zu einem gelblichen Orange ab. Der Granatbarsch kann maximal 75 cm lang und 7 kg schwer werden. Jedoch haben die meisten kommerziell gefangenen Exemplare standardmäßig nur eine Größe von 30–40 cm.

Im Jahr 2007 verboten die Regierungen von Neuseeland und Australien die Orange-Roughy-Fischerei auf unbestimmte Zeit, da die Bestände kollabiert waren.[4] Nachdem die beiden Staaten ein Überwachungs- und Erholungsprogramm einführten, erhielt die Orange-Roughy-Fischerei Ende 2016 die MSC-Zertifizierung und der Fisch darf wieder gefangen werden.[5]

Einzelnachweise

  1. a b Hoplostethus atlanticus auf Fishbase.org (englisch)
  2. Geoffrey Tingley und Dr Matthew Dunn: Global review of orange roughy (Hoplostethus atlanticus), their fisheries, biology and management. FAO, Fisheries and Aquaculture Technical Paper No. 622. Rom, 2018, Seite 4 u. 5. PDF
  3. a b c Robert Kunzig: Die Jagd am Unterwasserberg. In: folio.nzz.ch. Folio Neue Zürcher Zeitung, 1. Juli 2007, abgerufen am 16. Februar 2017.
  4. Anja Franzenburg: Fangverbot für Fische. In: greenpeace.de. Greenpeace, 3. Dezember 2007, abgerufen am 16. Februar 2017.
  5. MSC-Zertifizierung für den neuseeländischen Granatbarsch. (Nicht mehr online verfügbar.) In: msc.org. Marine Stewardship Council, 12. September 2016, archiviert vom Original am 16. Februar 2017; abgerufen am 16. Februar 2017.  src= Info: Der Archivlink wurde automatisch eingesetzt und noch nicht geprüft. Bitte prüfe Original- und Archivlink gemäß Anleitung und entferne dann diesen Hinweis.@1@2Vorlage:Webachiv/IABot/www.msc.org
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Hoplostethus atlanticus: Brief Summary ( German )

provided by wikipedia DE

Hoplostethus atlanticus, auch Kaiserbarsch, Orange Roughy oder Granatbarsch genannt, ist ein relativ großer Tiefseefisch. Er kommt in kalten (3–9 °C), tiefen (bathypelagisch, ca. 180–1800 m) Gewässern des Westatlantiks (nördlich von Neuschottland), Ostatlantiks (von Island bis Marokko, Namibia bis Südafrika), zwischen Neuseeland und Australien sowie im Ostpazifik vor Chile vor.

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Búrfiskur ( Faroese )

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Faroe stamp 251 orange roughy (hoplostethus atlanticus).gif

Búrfiskur (frøðiheiti - Hoplostethus atlanticus) verður til støddar uml. 70 cm. Hann er hávaksin við stórum høvdi, hægstur (1/3 av longdini) beint aftan fyri høvdið. Kjafturin er stórur, svartur innan og stendur á skák. Hann hevur fleiri píkar á høvdinum, og roðslan eftir strikuni er beinakend og á hesum fiskaslagi størri enn annars. Liturin á kroppinun er fagurt reyðgulur, og høvdið reytt. Í Norðuratlanshavi er hann undir Íslandi og suður til Biskayavíkina og við Azorurnar. Annars livir hann á sunnaru hálvu. Við New Zealand, Australia og Tasmania eru tað í fleiri ár fiskaðar stórar nøgdir av búrfiski. Á okkara leiðum er hann fyri tað mesta fingin djúpari enn 600 m og oftast fram við brøttum hellingum og fram við tindum í sjónum. Á sunnaru hálvu veksur fiskurin sera spakuliga, og í Australia rokna fiskifrøðingar við, at bert uml. 3% av samlaðu stovnunum kunnu fiskast árliga, uttan at stovnurin minkar.

Kelda

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Búrfiskur: Brief Summary ( Faroese )

provided by wikipedia emerging languages
Faroe stamp 251 orange roughy (hoplostethus atlanticus).gif

Búrfiskur (frøðiheiti - Hoplostethus atlanticus) verður til støddar uml. 70 cm. Hann er hávaksin við stórum høvdi, hægstur (1/3 av longdini) beint aftan fyri høvdið. Kjafturin er stórur, svartur innan og stendur á skák. Hann hevur fleiri píkar á høvdinum, og roðslan eftir strikuni er beinakend og á hesum fiskaslagi størri enn annars. Liturin á kroppinun er fagurt reyðgulur, og høvdið reytt. Í Norðuratlanshavi er hann undir Íslandi og suður til Biskayavíkina og við Azorurnar. Annars livir hann á sunnaru hálvu. Við New Zealand, Australia og Tasmania eru tað í fleiri ár fiskaðar stórar nøgdir av búrfiski. Á okkara leiðum er hann fyri tað mesta fingin djúpari enn 600 m og oftast fram við brøttum hellingum og fram við tindum í sjónum. Á sunnaru hálvu veksur fiskurin sera spakuliga, og í Australia rokna fiskifrøðingar við, at bert uml. 3% av samlaðu stovnunum kunnu fiskast árliga, uttan at stovnurin minkar.

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Orange roughy

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The orange roughy (Hoplostethus atlanticus), also known as the red roughy, slimehead and deep sea perch, is a relatively large deep-sea fish belonging to the slimehead family (Trachichthyidae). The UK Marine Conservation Society has categorized orange roughy as "vulnerable to exploitation". It is found in 3 to 9 °C (37 to 48 °F), deep (bathypelagic, 180-to-1,800-metre (590 to 5,910 ft)) waters of the Western Pacific Ocean, eastern Atlantic Ocean (from Iceland to Morocco; and from Walvis Bay, Namibia, to off Durban, South Africa), Indo-Pacific (off New Zealand and Australia), and in the eastern Pacific off Chile. The orange roughy is notable for its extraordinary lifespan, attaining over 200 years. It is important to commercial deep-trawl fisheries. The fish is a bright, brick-red color, fading to a yellowish-orange after death.

Like other slimeheads, orange roughy is slow-growing and late to mature, resulting in a very low resilience, making them extremely susceptible to overfishing. Many stocks (especially those off New Zealand and Australia, which were first exploited in the late 1970s), became severely depleted within 3–20 years, but several have subsequently recovered to levels that fisheries management believe are sustainable, although substantially below unfished populations.

Description

Fish in the Faroe Islands:
Orange roughy, Hoplostethus atlanticus
Faroese stamp issued: 7 Feb 1994
Artist: Astrid Andreasen

The orange roughy is not a vertically slender fish. Its rounded head is riddled with muciferous canals (part of the lateral line system), as is typical of slimeheads. The single dorsal fin contains four to six spines and 15 to 19 soft rays; the anal fin contains three spines and 10 to 12 soft rays. The 19 to 25 ventral scutes (modified scales) form a hard, bony median ridge between the pelvic fins and anus. The pectoral fins contain 15 to 18 soft rays each; the pelvic fins are thoracic and contain one spine and six soft rays; the caudal fin is forked. The interior of the mouth and gill cavity is a bluish black; the mouth itself is large and strongly oblique. The scales are ctenoid and adherent. The lateral line is uninterrupted, with 28 to 32 scales whose spinules or 'ctenii' largely obscure the lateral line's pores. The eyes are large.

The orange roughy is the largest known slimehead species at a maximum standard length (a measurement that excludes the tail fin) of 75 cm (30 in) and a maximum weight of 7 kg (15 lb). The average commercial catch size is commonly between 35 and 45 centimetres (14 and 18 in) in length, again, varying by area.

Life history

A preserved specimen on display at a museum

Orange roughy are generally sluggish and demersal; they form aggregations with a natural population density of up to 2.5 fish per m2, now reduced to about 1.0 per m2. These aggregations form in and around geologic structures, such as undersea canyons and seamounts, where water movement and mixing is high, ensuring dense prey concentrations. The aggregations are not necessarily for spawning or feeding; the fish are thought to cycle through metabolic phases (active or feeding and inactive or resting) and seek areas with ideal hydrologic conditions to congregate during each phase. They lose almost all pigmentation while inactive, when they are very approachable. Predators include large, deep-roving sharks, cutthroat eels, merluccid hakes, and snake mackerels.

When active, juveniles feed primarily on zooplankton such as mysid shrimp, euphausiids (krill), mesopelagic and benthopelagic fish, amphipods, and other crustaceans; mature adults consume smaller fish, predominantly of the Butterflyfish and Lanternfish families, and squid, which make up to 20% of their diet. The diet of the orange roughy is depth-related, with adult diets inversely related to that of juveniles. For example, juvenile consumption of crustaceans is lowest at 900 metres (3,000 ft) but increases with depth, while crustaceans in the adult diet peak at 800–1,000 metres (2,600–3,300 ft) and decrease with depth. The consumption of fish is the opposite: juvenile consumption decreases with depth while adult consumption increases. This inverse feeding pattern may be an example of resource-partitioning to avoid intraspecific competition for the available food at depths where prey is less abundant. The orange roughy's metabolic phases are thought to be related to seasonal variations in prey concentrations. The inactive phase conserves energy during lean periods. Orange roughy can live for over 200 years.[2]

Reproduction

Orange roughy are oceanodromous (wholly marine), pelagic spawners: that is, they migrate several hundred kilometers between localized spawning and feeding areas each year and form large spawning aggregations (possibly segregated according to gender) wherein the fish release large, spherical eggs 2.0–2.5 millimetres (0.079–0.098 in) in diameter, made buoyant by an orange-red oil globule) and sperm en masse directly into the water. The fertilized eggs, (and later larvae) are planktonic, rising to around 200 m (660 ft) to develop, with the young fish eventually descending to deeper waters as they mature. Orange roughy are also synchronous, shedding sperm and eggs at the same time. The time between fertilization and hatching is thought to be 10 to 20 days; fecundity is low, with each female producing only 22,000 eggs per kg of body weight, less than 10% of the average for other species of fish. Females rarely produce more than 90,000 eggs in one lifetime.[3] Spawning may last up to three weeks and starts around June or July. Orange roughy are very slow-growing and do not begin to breed until they are at least 20 years old, when they are around 30 cm (12 in) in length.[4]

The maturation age used in stock assessments ranges from 23–40 years,[5][6] which limits population growth/recovery, because each new generation takes so long to start spawning.[5]

Lifespan

When commercial fishing of orange roughy began in the 1970s, they were thought to live for only 30 years.[2] Since the 1990s, however, there is clear evidence that this species lives to an exceptional age. Early estimates of 149 years were determined via radiometric dating of trace isotopes found in an orange roughy's otolith (ear bone);[7] counting by the growth rings of orange roughy otoliths gave estimated ages of 125 to 156 years.[8] One specimen caught 1500 km east of Wellington in 2015 was estimated to be over 230 years old.[2] Orange roughy caught near Tasmania have been aged at 250 years.[2] The orange roughy is the longest-lived commercial fish species, and does not breed every year, which has important implications for its conservation status.[9]

Consumption

The flesh is firm with a mild flavour; it is sold skinned and filleted, fresh or frozen.[10] This species was first given the common name "Orange Roughy" by scientists in New Zealand in 1975 following the discovery of large aggregations during a deep-water research cruise.[11][12][13] A large scale fishery for orange roughy subsequently developed around New Zealand, and imports into the United States increased where it was renamed from the less gastronomically appealing "slimehead" through a U.S. National Marine Fisheries Service program during the late 1970s that identified underused species that should be renamed to make them more marketable.[14]

Historically, the United States has been the largest consumer of orange roughy, however, in recent years, the market for orange roughy in China has increased significantly. In 2014, the U.S. imported around 1,455 tonnes (4.4 million lb) (mainly fillets) from New Zealand, China, Peru and Indonesia. In 2015, China imported at least 4,000 tonnes (8.8 million lb) (mainly whole fish).

A number of major food retailers have established seafood sustainability policies to reassure customers that they are stocking sustainable seafood. These policies often involve partnering with non-governmental organizations to define criteria for seafood that may be stocked. In addition, a number of ecolabels exist to help retailers and consumers identify seafood that has been independently assessed against a robust, scientific standard. One of the best known such programmes is that of the Marine Stewardship Council.

In 2010, Greenpeace International added orange roughy (deep sea perch) to its seafood red list, which contains fish generally sourced from unsustainable fisheries.[15]

A 2003 joint report by the TRAFFIC Oceania and World Wildlife Foundation Endangered Seas Program argues, "probably no such thing [exists] as an economically viable deep-water fishery that is also sustainable."[16] However, others have argued that deepwater fisheries can be managed sustainably provided that it is recognized that sustainable yields are low and catches are set accordingly.[17][18]

Because of its longevity, the orange roughy accumulates large amounts of mercury in its tissues, having a range of 0.30–0.86 ppm compared with an average mercury level of 0.086 ppm for other edible fish.[19] Based on average consumption and the recommendations of a National Marine Fisheries Service study, in 1976 the FDA set the maximum safe mercury level for fish at 1 ppm.[20] Regular consumption of orange roughy can have adverse effects on health.[21][22] Compared to most edible fish, orange roughy is a very poor source of omega-3 fatty acids, averaging less than 3.5 g/kg.

Fisheries

Orange roughy fisheries exist in New Zealand, Australia and Namibia.[5] Annual global catches began in 1979 and increased significantly to a high of over 90,000 tonnes in the late 1980s. These high catch levels quickly decreased as stocks were fished down. For many stocks, the lack of understanding of the biological characteristics meant that they were overfished. By the end of the 1990s, three of the eight New Zealand orange roughy fisheries had collapsed and were closed.[2] Because its longevity, late maturation and relatively low fecundity, orange roughy stocks tend to recover slower than most other species.[5][23]

A number of orange roughy stocks live outside the jurisdiction of any particular nation, making it more challenging to limit overall catches. The South Pacific Regional Fisheries Management Organisation[24] (SPRFMO) and the South Indian Ocean Fisheries Agreement[25] have orange roughy stocks that are managed within their jurisdictions. These organizations have made progress toward collecting better information on total orange roughy catches and also with setting catch limits for fisheries on the high seas. For example, SPRFMO limited orange roughy catches and effort from 2007.[26]

Orange roughy is fished almost exclusively by bottom trawling. This fishing method has been heavily criticized by environmentalists for its destructive nature. This, combined with heavy commercial demand, has focused criticism from both environmentalists and media.[27][28][29]

New Zealand fisheries

New Zealand currently operates the largest orange roughy fisheries in the world, with a total catch of over 8,500 tonnes in the 2014 calendar year. This accounts for 95% of the total estimated catch of orange roughy. Exports of orange roughy provided an estimated revenue to New Zealand of NZ$53 million (US$37M) in 2015.

Fisheries in New Zealand are managed through the Quota Management System (QMS), under which individuals or companies own quota shares for a stock of a particular species or species group. For each stock, a Total Allowable Catch (TAC) is set that maintains the stock at or above a level that can produce the maximum sustainable yield or that will move the stock toward that level. Orange roughy has been managed within the QMS since 1986.

The Ministry for Primary Industries is responsible for the implementation of the QMS and its enabling legislation, the Fisheries Act 1996.

Historical

Fishery farming of orange roughy was initiated in the mid-1970s, but full exploitation did not begin until 1979. There was no regulation of these early catches, and records indicate that they were very high. For many fisheries, management settings allow for a "fishing down" period during which the biomass is reduced to a level that will provide the maximum sustainable yield. For example, a fishery with a hypothetical unfished biomass of 100,000 tonnes will be allowed to be fished down to a biomass of 40,000 tonnes (assuming that this is the biomass that provides for the maximum sustainable yield) over a number of years. The rate of this "fish-down" can vary depending on the objectives of the fishery, but catches would then be more strictly controlled to maintain the biomass at around 40,000 tonnes.

For the New Zealand orange roughy fisheries, productivity parameters and resulting estimates of unfished biomass were incorrectly estimated in the first decade of the fishery. Catch limits exceeded recommended estimates of sustainable yields for a subsequent decade and catches were estimated to have exceeded those catch limits because of burst nets, escape windows in nets and lost gear. Catch limits were reduced in the mid-1990s, although they were increased again following indications that stocks had begun to rebuild. This was later found not to be the case and a number of fisheries were closed completely or had catch limits reduced to one tonne to allow the stocks to rebuild.

In one New Zealand fishery, the Total Allowable Catch (TAC) was reduced in 2008 from 1,470 tonnes to 914 tonnes, but this reduction was challenged in court. In February 2008, the High Court overturned the new quota, ruling that the Minister of Fisheries did not have the legal power to set quotas for ORH1. This was because of a strict interpretation of the Fisheries Act that required an accurate estimation of the biomass that could support the maximum sustainable yield. As a result of this decision, the Fisheries Act 1996 was amended to allow TACs to be set based on the best available information in the absence of an estimate of the biomass that could support the maximum sustainable yield.

Current situation (2016)

The New Zealand fishing industry contracted a pre-assessment of selected orange roughy fisheries against the Marine Stewardship Council (MSC) Fisheries Standard in 2009. Following the pre-assessment, the industry representative body (Deepwater Group Ltd) put four orange roughy fisheries into Fishery Improvement Plans (FIPs) to deliver improvements in the fisheries that would enable them to meet the certification requirements of the MSC. These FIPs are public and have been monitored by the Sustainable Fisheries Partnership.

In 2014, Bayesian model-based stock assessments were completed for four of New Zealand's main orange roughy stocks, one of which had been closed to fishing since 2000. The stock assessments used data collected by research surveys carried out by research organizations and the fishing industry. A key factor was the use of new acoustic technology, developed by the fishing industry, in recent surveys. The multi-frequency acoustic optical system (AOS) enables scientists to differentiate the types of fish acoustically ‘seen’ during the survey and works on slopes that previously made effective surveying impossible in some areas. The AOS also has the potential to allow scientists to see in real-time video, what is being measured by the survey. Other research-derived data were also critical to the success of the stock assessments, notably age-frequencies from improved ageing methods.

The 2014 stock assessments,[30] which were subject to a robust peer review process, indicated that three of the stocks had recovered enough to sustain increased catches. The TACs for these stocks were subsequently increased. The fourth stock was estimated to be at a low stock status and the TAC was reduced by over 40% to allow the stock to rebuild.

In addition, an industry sponsored Management Strategy Evaluation[31] was completed that provided an estimate of the biomass that could support the maximum sustainable yield (≈25–27% of the unfished biomass). Based on this output, the fishing industry agreed to aim to maintain the orange roughy stocks within a management target range of 30–50% of the unfished biomass. Further to this, a Harvest Control Rule was agreed that would define what catch limits should be given an estimate of stock status. Catch limits for those fisheries are currently consistent with the outputs of the agreed Harvest Control Rule. In May 2014, three orange roughy fisheries entered full assessment against the Marine Stewardship Council Fisheries Standard.

Australian fisheries

The Australian orange roughy fishery was not discovered until the 1970s, but by 2008, the biomass of some stocks remained high while others was estimated to be down to 10% of the unfished level after years of commercial fishing.[32] It was the first commercially sought fish to appear on Australia's threatened species list because of overfishing.[33] By late 2017, a number of Australian orange roughy fisheries had been re-opened.[34]

In July 2020, a leading US-based MSC consultancy (conformity assessment body or CAB) acting for a group of Australian eastern zone orange roughy quota holders, released a scoring report recommended that the orange roughy eastern zone stock be given Marine Stewardship Council accreditation, scoring the fishery and its management highly (289/300) in each of the three assessment principles. However, environmental groups the Australian Marine Conservation Society and World Wildlife Fund raised late objections. MSC's decision to allow objections from these two eNGOs who did not engage in the more than year long process in contravention of the MSC Standard is seen by many as raising questions about the independence and credibility of the standard itself.

The Arbitrator issued her decision in three iterations in early 2021 each following representations from the Appellants, CAB and Fishery Client. During the process the Australian Minister for fisheries wrote to the MSC explaining that although orange roughy was listed under Australia's EPBC Act (1999) that it was also managed under the Fisheries Management Act(1991) and Fisheries Administration Act (1991) and that the commercial take of orange roughy allowed continued recovery and that it is listed in a section of the EPBC Act that allowed this commercial take. However, the Arbitrator found that her view was that the standard could not have intended threatened species to be certified and that the goal for threatened species should be zero catch. Further, that because orange roughy was listed under the EPBC Act that it should be considered as an endangered, threatened and protected (ETP) species as part of MSC Principle 2 and could therefore not also be considered as a target or subject stock under Principle 1.

In her second decision (February 2021) the Arbitrator summarised her decision by stating, "This particular stock is, according to the CAB and I have no reason within my limited remit, to disagree with this view, well managed and currently sustainably fished in terms of the prevailing science. I do acknowledge therefore that the remand decision will be all the more unwelcome by the CAB and the fishery client. However, the difficulty, in my view, lies in the narrow terms of the Standard when read against the Australian ETP legislation. It is not open to me to go beyond my interpretation, in light of any views I might have on the otherwise sustainability of the stock and the suitability of the unit of assessment for certification. The remedy to this lies outside of this process in seeking a change either to the Australian legislation or clarity in the Standard.

The Fishery Client subsequently withdrew the stock from assessment. Documents from the objection process can be found here https://fisheries.msc.org/en/fisheries/australia-orange-roughy-eastern-zone-trawl/@@assessments.

The precedent set by this decision has raised questions about the future of MSC in Australia given that a number of fish species involved in existing MSC certificates are listed under the EPBC Act. The current apparent incompatibility of the MSC Standard and Australian legislation is one reason why the MSC system has been so slow to develop in Australia and that Australian consumers have little recognition of the MSC brand.

See also

References

  1. ^ Collette, B., Fernandes, P., Heessen, H., Herrera, J. & Smith-Vaniz, W.F. 2015. Hoplostethus atlanticus. The IUCN Red List of Threatened Species 2015: e.T155168A45884209. Downloaded on 24 September 2021.
  2. ^ a b c d e Evans, Kate (Nov–Dec 2019). "The 230-year-old fish". New Zealand Geographic. 160.
  3. ^ Environment, jurisdiction=Commonwealth of Australia; corporateName=Department of the. "Hoplostethus atlanticus — Orange Roughy, Deep-sea Perch, Red Roughy". www.environment.gov.au.
  4. ^ Bulman, C.M.; Koslow, J.A. (June 1992). "Diet and food consumption of a deep-sea fish, orange roughy Hoplostethus atlanticus (Pisces: Trachichthyidae), off southeastern Australia". Marine Ecology Progress Series. 82: 115–129. Bibcode:1992MEPS...82..115B. doi:10.3354/meps082115.
  5. ^ a b c d Branch, Trevor (2001). "A review of orange roughy Hoplostethus atlanticus fisheries, estimation methods, biology and stock structure". South African Journal of Marine Science. 23: 181–203. doi:10.2989/025776101784529006.
  6. ^ "Managing risk and uncertainty in deep-sea fisheries: lessons from Orange Roughy" (PDF). Traffic.org. Retrieved 13 October 2017.
  7. ^ Fenton, G.E; Short, S.A.; Ritz, D.A. (June 1991). "Age determination of orange roughy, Hoplostethus atlanticus (Pisces: Trachichthyidae) using 210 Pb: 226 Ra disequilibria". Marine Biology. 109 (2): 197–202. doi:10.1007/BF01319387. ISSN 0025-3162. S2CID 84942308.
  8. ^ "Diary from the deep: part 3". Bbc.co.uk. 2 December 2011. Archived from the original on 2017-11-25. Retrieved 2018-12-15.
  9. ^ Kilvert, Nick (5 July 2020). "Orange roughy fishery report recommends 'sustainable seafood' status - but is slammed by conservation groups". ABC News. Australian Broadcasting Corporation. Retrieved 5 July 2020.
  10. ^ "Science fact sheet: Orange Roughy - delicacy from the deep". Archived from the original on 2007-07-09. Retrieved 2007-08-17.
  11. ^ Batson, P. B. (2003). Deep New Zealand : blue water, black abyss. Kim Westerskov. Christchurch, N.Z.: Canterbury University Press. ISBN 1-877257-09-5. OCLC 52201441.
  12. ^ Johnson, David (2004). Hooked : the story of the New Zealand fishing industry. Jenny Haworth. Christchurch, N.Z.: Hazard Press for the Fishing Industry Association. ISBN 1-877270-64-4. OCLC 57574484.
  13. ^ Pankhurst, Tim (2017). Roughy on the rise : the story of New Zealand's most controversial fishery. Wellington, Aotearoa New Zealand. ISBN 978-0-947493-40-0. OCLC 987574122.
  14. ^ Jacquet, J. L.; Pauly, D. (May 2008). "Trade secrets: Renaming and mislabeling of seafood". Marine Policy. 32 (3): 309–318. CiteSeerX 10.1.1.182.1143. doi:10.1016/j.marpol.2007.06.007.
  15. ^ "Greenpeace Seafood Red list". greenpeace.org.
  16. ^ Lack, M., Short, K. & Willock, A., 2003. Managing risk and uncertainty in deep-sea fisheries:lessons from orange roughy, TRAFFIC Oceania and WWF Australia, Sydney.
  17. ^ Clark, M.R. 2001. Are deepwater fisheries sustainable? – the example of orange roughy (Hoplostethus atlanticus) in New Zealand. Fisheries Research, 51: 123–135.
  18. ^ Sissenwine, M.P. & Mace, P.M. 2007. Can deep water fisheries be managed sustainably? In: Report and documentation of the Expert Consultation on Deep-sea Fisheries in the High Seas. Bangkok, Thailand, 21–23 November 2006. FAO Fisheries Report. No. 838. Rome, FAO. 2007. pp. 61–112.
  19. ^ Canada, Health (9 March 2007). "Updating the Existing Risk Management Strategy for Mercury in Retail Fish – Canada.ca". Hc-sc.gc.ca. Retrieved 13 October 2017.
  20. ^ "Seafood Network Information Center". Archived from the original on 2012-11-23. Retrieved 2012-10-22.
  21. ^ "Techno-economic data on Mercury and major compounds" (PDF). Rsde.ineris.fr. June 13, 2006. Archived from the original (PDF) on 27 January 2009. Retrieved 13 October 2017.
  22. ^ ""Mercury: how much is safe?". Green Left. June 24, 1998. An average woman weighing 60 kilograms can ingest 60 x 0.1 = 6 micrograms of mercury per day without exceeding the EPA reference dose. If each gram of fish contains 0.2 micrograms of mercury, our average woman could only eat 6/0.2 = 30 grams of fish per day without exceeding the EPA reference dose". Greenleft.org. 6 September 2016. Retrieved 13 October 2017.
  23. ^ "Case for trawl ban 'overwhelming'". News.bbc.co.uk. 15 November 2006. Retrieved 13 October 2017.
  24. ^ "South Pacific Regional Management Organisation". sprfmo.int.
  25. ^ "FAO Fisheries & Aquaculture – Regional fishery bodies (RFB)". fao.org.
  26. ^ "Archived copy" (PDF). Archived from the original (PDF) on 2015-06-04. Retrieved 2016-05-10.{{cite web}}: CS1 maint: archived copy as title (link)
  27. ^ Roberts, C.M. (2002). Deep impact: the rising toll of fishing in the deep sea. Trends In Ecology and Evolution 17(5): 242-245
  28. ^ NRC (National Research Council) (2002). Effects of trawling and dredging on seafloor habitat. National Academy of Sciences, Washington DC
  29. ^ Morgan, L.E., Norse, E.A., Roger, A.D., Haedrich, R.L. & Maxwell, S.M. 2005. Why the world needs a time-out on high-seas bottom trawling. The Deep Sea Conservation Coalition. 14pp.
  30. ^ "Archived copy". Archived from the original on 2016-02-16. Retrieved 2016-05-10.{{cite web}}: CS1 maint: archived copy as title (link)
  31. ^ [1]
  32. ^ "Orange roughy: Down and out: An unsustainable seafood choice from a destructive trawl fishery". Archived from the original on 2008-07-20. Retrieved 2009-01-31.
  33. ^ "Trawled fish on endangered list – Environment – Specials – smh.com.au". Smh.com.au. 10 November 2006. Retrieved 13 October 2017.
  34. ^ "Orange roughy decision shows changes are needed – Scoop News". Scoop.co.nz. Retrieved 13 October 2017.
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Orange roughy: Brief Summary

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The orange roughy (Hoplostethus atlanticus), also known as the red roughy, slimehead and deep sea perch, is a relatively large deep-sea fish belonging to the slimehead family (Trachichthyidae). The UK Marine Conservation Society has categorized orange roughy as "vulnerable to exploitation". It is found in 3 to 9 °C (37 to 48 °F), deep (bathypelagic, 180-to-1,800-metre (590 to 5,910 ft)) waters of the Western Pacific Ocean, eastern Atlantic Ocean (from Iceland to Morocco; and from Walvis Bay, Namibia, to off Durban, South Africa), Indo-Pacific (off New Zealand and Australia), and in the eastern Pacific off Chile. The orange roughy is notable for its extraordinary lifespan, attaining over 200 years. It is important to commercial deep-trawl fisheries. The fish is a bright, brick-red color, fading to a yellowish-orange after death.

Like other slimeheads, orange roughy is slow-growing and late to mature, resulting in a very low resilience, making them extremely susceptible to overfishing. Many stocks (especially those off New Zealand and Australia, which were first exploited in the late 1970s), became severely depleted within 3–20 years, but several have subsequently recovered to levels that fisheries management believe are sustainable, although substantially below unfished populations.

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Hoplostethus atlanticus ( Spanish; Castilian )

provided by wikipedia ES

El reloj anaranjado o reloj del Atlántico es la especie Hoplostethus atlanticus,[2]​ un pez marino de la familia traquictiídeos, distribuida por el este y noroeste del océano Atlántico, sur del océano Pacífico y océano Índico.[3]

Importancia para el hombre

Es una especie inofensiva, muy pescada y ampliamente comercializada.[3]​ Los barcos de pesca los localizan esporádicamente formando densos cardumenes; se puede encontrar en el mercado fresco o congelado, siendo normal que se cocine frito o al horno.[4]

Anatomía

Aunque se han descrito capturas mucho mayores la longitud máxima es normalmente de unos 40 cm.[5]​ En la aleta dorsal tiene de 4 a 6 espinas y 15 a 19 radios blandos, mientras que en la aleta anal hay 3 espinas y 10 a 12 radios blandos; el color es rojo-ladrillo brillante, con las cavidades de boca y agallas de color azulado.[5]

Hábitat y biología

Es un pez batipelágico y oceanódromo, que vive sedentario pegado al sustrato a una gran profundidad normalmente entre 400 y 900 m,[6]​ normalmente en aguas frías del talud continental, en cordilleras oceánicas y otros relieves altos marinos, donde vive disperso alimentándose de crustáceos y otros peces.[3]

El crecimiento es muy lento, siendo uno de los peces más longevos que existen con un espécimen capturado con una edad de 149 años.[7]​ Muy poco se sabe sobre sus larvas y juveniles, que habitan probablemente en aguas abisales.[8]

Referencias

  1. "Hoplostethus atlanticus". En FishBase (Rainer Froese y Daniel Pauly, eds.). Consultada en mayo de 2010. N.p.: FishBase, 2010.
  2. Sistema Integrado de Información Taxonómica. «Hoplostethus atlanticus (TSN 166139)» (en inglés).
  3. a b c Maul, G.E., 1986. "Trachichthyidae". p. 749-752. En P.J.P. Whitehead, M.-L. Bauchot, J.-C. Hureau, J. Nielsen y E. Tortonese (eds.) Fishes of the north-eastern Atlantic and the Mediterranean. UNESCO, París. Vol. 2.
  4. Frimodt, C., 1995. "Multilingual illustrated guide to the world's commercial coldwater fish". Fishing News Books, Osney Mead, Oxford, Inglaterra. 215 p.
  5. a b Heemstra, P.C., 1986. "Trachichthyidae". p. 410-413. En M.M. Smith y P.C. Heemstra (eds.) Smiths' sea fishes. Springer-Verlag, Berlín.
  6. Maul, G.E., 1990. "Trachichthyidae". p. 620-622. En J.C. Quéro, J.C. Hureau, C. Karrer, A. Post y L. Saldanha (eds.) Check-list of the fishes of the eastern tropical Atlantic (CLOFETA). JNICT, Lisboa; SEI, París; y UNESCO, París. Vol. 2.
  7. Fenton, G.E., S.A. Short y D.A. Ritz, 1991. "Age determination of orange roughy Hoplostethus atlanticus (Pisces: Trachichthyidae) using 210 Pb/226Ra disequilibria". Mar. Biol. 109:197-202.
  8. Jordan, A.R. y B.D. Bruce, 1993. "Larval development of three roughy species complexes (Pisces: Trachichthyidae) from southern Australian waters, with comments on the occurrence of orange roughy Hoplostethus atlanticus". Fish. Bull. 91:76-86.

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Hoplostethus atlanticus: Brief Summary ( Spanish; Castilian )

provided by wikipedia ES

El reloj anaranjado o reloj del Atlántico es la especie Hoplostethus atlanticus,​ un pez marino de la familia traquictiídeos, distribuida por el este y noroeste del océano Atlántico, sur del océano Pacífico y océano Índico.​

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Erloju-arrain laranja ( Basque )

provided by wikipedia EU

Erloju-arrain laranja (Hoplostethus atlanticus) Hoplostethus generoko animalia da. Arrainen barruko Trachichthyidae familian sailkatzen da.

Banaketa

Espezie hau Agulhasko itsaslasterran aurki daiteke.

Erreferentziak

  1. Froese, Rainer & Pauly, Daniel ed. (2006), Hoplostethus atlanticus FishBase webgunean. 2006ko apirilaren bertsioa.

Ikus, gainera

(RLQ=window.RLQ||[]).push(function(){mw.log.warn("Gadget "ErrefAurrebista" was not loaded. Please migrate it to use ResourceLoader. See u003Chttps://eu.wikipedia.org/wiki/Berezi:Gadgetaku003E.");});
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Erloju-arrain laranja: Brief Summary ( Basque )

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Erloju-arrain laranja (Hoplostethus atlanticus) Hoplostethus generoko animalia da. Arrainen barruko Trachichthyidae familian sailkatzen da.

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Hoplostèthe orange ( French )

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Hoplostethus atlanticus

L'hoplostèthe orange, hoplostèthe rouge ou poisson-montre (Hoplostethus atlanticus) est une espèce de poissons de la famille des Trachichthyidae. L'hoplostèthe orange vit dans tous les océans entre 900 et 1 800 m de profondeur. Il a une longévité potentielle d'au moins 149 ans[1] et il n'atteint sa maturité sexuelle qu'entre 20 et 30 ans. Avec une longueur maximale de 75 cm pour 7 kg, c'est le plus grand de sa famille.

Commercialisé sous le nom d'empereur, il fait l'objet d'une importante exploitation commerciale, mais en raison de son faible recrutement, ses populations tendent à diminuer. De nombreux stocks, en particulier ceux de la Nouvelle-Zélande et de l'Australie, qui ont été exploités dans les années 1970, ont déjà été décimés ; les stocks de substitution récemment découverts s'épuisent rapidement.

Description

 src=
Dessin d'un hoplostèthe orange.

L'hoplostèthe orange est rouge lorsqu'il est vivant, mais devient progressivement orange, une fois mort. C'est la plus grande espèce de la famille des Trachichthyidés, avec une longueur maximale de 75 cm et un poids maximum de 7 kg[2]. La taille moyenne des captures commerciales est située entre 35 et 45 cm de longueur[3],[4].

Sa tête arrondie est criblée de canaux muqueux, ce qui est typique des Trachichthyidés. L'unique nageoire dorsale est composée de quatre à six épines et de 15 à 19 rayons mous ; la nageoire anale comporte trois épines et 10 à 12 rayons mous. Les 19 à 25 écailles ventrales (écailles modifiées) forment une crête osseuse médiane entre les nageoires pelviennes et l'anus. Les nageoires pectorales ont 15 à 18 rayons mous chacune ; les nageoires pelviennes sont thoraciques et possèdent une épine et six rayons mous ; la nageoire caudale est fourchue. L'intérieur de la bouche et la cavité branchiale sont d'un noir bleuté, la bouche elle-même est grande et fortement oblique. Les écailles sont cténoïdes et adhérentes[5],[6].

Biologie et écologie

L'hoplostèthe orange est généralement inactif et démersal, il forme de grands bancs d'une densité moyenne de 2,5 poissons par mètre carré, maintenant réduit à environ 1 par mètre carré à cause de la surpêche. Ces agrégats se forment dans et autour des structures géologiques, telles que les canyons sous-marins et les monts sous-marins, où les courants assurent un apport de proies abondant. Ce n'est pas nécessairement pour frayer ou s'alimenter qu'ils se réunissent : ces agrégats assurent une protection pendant les périodes d'inactivité. En effet, le cycle biologique de l'hoplostèthe orange traverse des phases métaboliques distinctes, d'activité consacrées à l'alimentation, et d'inactivité et de repos, durant laquelle ils perdent la quasi-totalité de leur pigmentation et sont vulnérables. Les bancs recherchent, en fonction de chaque phase, les zones possédant les conditions hydrologiques les plus favorables à ces rassemblements. Les prédateurs de l'hoplosthète orange comprennent certains requins, des anguilles égorgées, des merlus et l'escolier serpent.

Alimentation

 src=
Un hoplostèthe orange conservé dans le formol.

Lorsqu'il est actif, il se nourrit principalement de zooplancton tel que les mysidacés (en) et les euphausiacés, de poissons mésopélagiques et benthopélagiques, d'amphipodes, de petits céphalopodes, de crustacés et autres. La consommation alimentaire journalière a été estimée à 0,91 % du poids corporel pour les juvéniles et 1,15 % du poids corporel pour les adultes[7]. Les phases métaboliques de l'hoplostèthe orange sont censées être liées aux variations saisonnières de l'abondance des proies. La phase inactive permet d'économiser leur énergie pendant les périodes de vaches maigres[8],[9].

Reproduction

L'hoplostèthe orange est océanodrome : il effectue des migrations de plusieurs centaines de kilomètres entre le lieu de ponte et les aires d'alimentation chaque année, mais il n'existe aucune preuve directe de ces migrations. Des preuves indirectes sont données par le pourcentage de femelles reproductrices au sein d'un banc[10]. Il forme de grandes agrégations lors de la période du frai (parfois séparées selon le sexe) durant laquelle les poissons libèrent des œufs sphériques (2,25 mm de diamètre), dans une substance huileuse orange-rouge, et le sperme directement dans l'eau. Les œufs fécondés (et plus tard les larves) sont planctoniques, remontent à environ 200 mètres de profondeur ; puis les alevins redescendent dans des eaux plus profondes à mesure qu'ils grandissent. L'hoplostèthe orange est également synchrone, l'excrétion du sperme et des œufs se fait simultanément. Le temps entre la fécondation et l'éclosion est estimé entre 10 et 20 jours ; la fécondité est faible, avec chaque femelle ne produisant que 22 000 œufs par kilogramme de poids corporel, ce qui est inférieur de 10 % à la moyenne des autres espèces de poissons. En outre, la ponte peut durer jusqu'à 2-3 semaines et commence autour de juin ou juillet. La croissance de l'hoplostèthe orange est très lente ; il n'atteint sa maturité sexuelle qu'entre 20 et 30 ans[11]. Son faible taux de croissance s'explique probablement par un taux de prédation faible et la rareté des proies dans les grandes profondeurs[9]. Il fait partie des espèces caractérisées par leur sénescence négligeable[12]. L’individu le plus âgé observé avait 149 ans, âge calculé par datation radiométrique des isotopes de ses otolithes[2],[13].

Répartition et habitat

 src=
Un hoplostèthe orange dans son milieu naturel.

L'hoplostèthe orange vit à des profondeurs allant d'une centaine de mètres à près de 2 000 mètres, mais il est couramment pêché entre 900 et 1 800 mètres. Il fréquente le milieu et le bas du talus continental et les dorsales océaniques. La température de son environnement est comprise entre 4 et 7 °C. Il fréquente les récifs coralliens d'eau froide, où il trouve refuge[14].

On le trouve dans les eaux du monde entier, mais surtout dans l'océan Atlantique, l'océan Indien et l'océan Pacifique. Dans l'océan Pacifique occidental, dans l'est de l'océan Atlantique (à partir de l'Islande jusqu'au Maroc, et de la Namibie jusqu'à l'Afrique du Sud), dans l'Indo-Pacifique (au large de la Nouvelle-Zélande, de l'Australie) et au large du Chili, dans le Pacifique oriental[8],[15].

Étymologie et dénominations

Hoplostethus provenant du grec ancien, construit à partir de 'όπλον' (hoplo) signifiant « arme » et de 'στῆθος' (stêthos) signifiant « poitrine ». Atlanticus fait référence à l'océan Atlantique où les premiers spécimens ont été pêchés[6]. Le terme hoplostèthe est donc une francisation du nom scientifique du genre Hoplostethus[16]. Mais le second « h » n'ayant pas une utilité phonétique, il est souvent enlevé, ce qui donne « hoplostète »[15].

Le terme « poisson-montre » est issu de l'apparence de la tête du poisson. Elle est ronde et dispose de nombreux canaux muqueux apparents, rappelant les rouages d'une montre. Son nom commercial « empereur » a été instauré dans les années 1980 avec la commercialisation de ce poisson[17].

Taxinomie

L'hoplostèthe orange fut décrit pour la première fois par Robert Collett en 1889 sous le nom Hoplostethus atlanticus[15]. Depuis, le taxon n'a pas changé, cependant certains auteurs orthographient « atlanticum » au lieu de « atlanticus »[6].

Ce taxon connaît quelques synonymes :

  • Hoplostethus atlanticum Richard, 1910
  • Leiogaster atlanticus var. spinulosus Roule, 1916
  • Hoplostethus gilchristi Smith, 1935
  • Hoplostethus islandicus Kotthaus, 1952

L'hoplostèthe orange et l'homme

Pêche

 src=
Capture mondiale d'hoplostèthes orange entre 1975 et 2010.

L'hoplostèthe orange est très commun et sa chair est réputée délicieuse. Il fait l'objet d'une pêche importante au large de l’Europe occidentale, et aussi mais surtout au Sud de l'Australie et de la Nouvelle-Zélande. Bien que déjà consommé en Nouvelle-Zélande dès les années 1960, l'empereur a commencé à être pêché massivement par d'autres pays à partir des années 1980, époque où de grands bancs ont été découverts au-dessus des guyots et autres monts sous-marins. Dans les années 1990, les prises atteignaient 50 000 tonnes par an[9]. Les pêcheurs industriels ont commencé à prendre des centaines de tonnes par jour, provoquant une dangereuse chute des stocks. En effet ce poisson, aux effectifs de dédoublement supérieurs à 14 ans, pourrait bien disparaître rapidement si une pêche excessive continue à se pratiquer. Un moratoire sur la pêche de ce poisson pourrait être créé chez les pays concernés par cette surpêche[18].

L'âge de maturation utilisé dans les évaluations des stocks varie entre 23 et 40 ans, ce qui limite la vitesse du recrutement, étant donné que chaque nouvelle génération prend beaucoup de temps pour commencer la ponte[14].

État de conservation et mesures de gestion ou de protection

 src=
Un hoplostèthe orange conservé dans le formol.

Toutes les espèces de grand fond se reproduisent très tardivement et sont exposées à la surexploitation et la surpêche.

Une étude a montré dans les années 1990 (à l'ouest de l'Angleterre) sur des poissons vivant en profondeur en bordure du plateau continental que la réduction de leur biomasse à la suite de la pêche au chalut se fait très rapidement (en quelques années), mais d'une manière plus ou moins marquée selon d'espèce (dans ce cas par exemple l'hoplostèthe orange a plus rapidement et fortement décliné que le grenadier de roche coryphaenoides rupestris[19]

Les mesures de conservation consistent à appliquer des limites de capture, et d'inscrire les diverses espèces menacées d'extinction sur des listes tenues par les gouvernements et les associations environnementales. Selon la Seafood Watch (États-Unis), la Royal Forest and Bird Protection Society of New Zealand, la Marine Conservation Society (Royaume-Uni), les consommateurs devraient fortement éviter cette espèce. L'hoplostèthe orange est l'espèce la plus pêchée en Nouvelle-Zélande, il représente 17,2 % du total des exportations de poissons. Lorsque la biomasse d'origine est arrivé à 30 %, les quotas ont été fixés. Le rendement maximal durable a été fixé à 1 200 tonnes par an, mais en 2005, ce quota a été jugé trop élevé[20].

En 2010, Greenpeace International a ajouté l'hoplostèthe orange à sa liste rouge, qui contient des poissons qui font l'objet d'une pêche non-durable[21],[22].

Utilisation alimentaire

La chair de l'hoplostèthe orange est ferme avec une douce saveur ; il est vendu en filets sans peau, frais ou congelés. En raison de sa longévité, il bioaccumule de grandes quantités de mercure dans ses tissus[23]. Sa consommation régulière peut avoir des effets néfastes sur la santé[24].

Voir aussi

Références taxinomiques

Notes et références

  • (en) Cet article est partiellement ou en totalité issu de l’article de Wikipédia en anglais intitulé .
  1. Collectif (trad. Michel Beauvais, Marcel Guedj, Salem Issad), Histoire naturelle [« The Natural History Book »], Flammarion, mars 2016, 650 p. (ISBN 978-2-0813-7859-9), Hoplostèthe orange page 338
  2. a et b G.E Fenton, S.A. Short et D.A. Ritz, « Age determination of orange roughy, Hoplostethus atlanticus (Pisces: Trachichthyidae) using 210 Pb: 226 Ra disequilibria », Marine Biology, Berlin/Heidelberg, Springer, vol. 109, no 2,‎ juin 1991, p. 197–202 (ISSN et , DOI , lire en ligne)
  3. B.-J. Muus, J.-G. Nielsen, P. Dahlström et B. Olesen Nyström, Guide des poissons de la mer et de la pêche, Delachaux et Niestlé, mars 2005 (ISBN 2-603-01455-2)
  4. FAO, « Species Fact Sheets : Hoplostethus atlanticus », septembre 2010
  5. « Managing risk and uncertainty in deep-sea fisheries: lessons from Orange Roughy »
  6. a b et c Albert Ier de Monaco, Résultats des campagnes scientifiques accomplies sur son yacht par Albert Ier, prince souverain de Monaco, 1896, 17-19 p. (lire en ligne)
  7. (en) C.M. Bulman et J.A. Koslow, « Diet and food consumption of a deep-sea fish, orange roughy Hoplostethus atlanticus (Pisces: Trachichthyidae), off southeastern Australia. », Marine Ecology Progress Series,‎ 1992 (DOI , lire en ligne)
  8. a et b J.-C. Quéro et P. Porché, Les poissons de mer, Gisserot, 2009 (ISBN 2755800674)
  9. a b et c John R. Paxton, William N. Eschmeyer et J.-J. Vayne (trad. Marc Baudoux), Les poissons, Bordas, coll. « Encyclopédie des animaux », 1995 (ISBN 2-04-027019-1)
  10. (en) R. I. C. C. Francis et M. R. Clark, « Inferring spawning migrations of orange roughy (Hoplostethus atlanticus) from spawning ogives », Marine and Freshwater Research,‎ 2002 (DOI , lire en ligne)
  11. (en) M.R. Clark, D.J. Fincham et D.M. Tracey, « Fecundity of orange roughy (Hoplostethus atlanticus) in New Zealand Waters. », New Zealand Journal of Marine and Freshwater Research,‎ 1994 (DOI , lire en ligne)
  12. (en) Caleb Finch, « Variations in Senescence and Longevity Include the Possibility of Negligible Senescence », Journal of Gerontology : BIOLOGICAL SCIENCES,‎ 1998
  13. Orange Roughy
  14. a et b Gouvernement australien (The Department of Sustainability, Environment, Water, Population and Communities), « Hoplostethus atlanticus — Orange Roughy, Deep-sea Perch, Red Roughy » (consulté le 11 avril 2012)
  15. a b et c (fr+en) Référence FishBase :
  16. Georges Cuvier et Achille Valenciennes, Histoire naturelle des poissons, 1829, 469-478 p. (lire en ligne)
  17. DGCCRF, « Poisson », septembre 2010
  18. UICN, « Deep-water fisheries » (consulté le 6 octobre 2012)
  19. Lorance P (1998) Structure du peuplement ichtyologique du talus continental à l'ouest des îles Britanniques et impact de la pêche. Cybium, 22(4), 309-331.
  20. [PDF]the Orange Roughy Management Company, « Industry management within the New Zealand quota management system », septembre 2010
  21. [PDF]Greenpeace International, « Species Fact Sheet New Zealand orange roughy », septembre 2010
  22. Greenpeace International, « Greenpeace International Seafood Red list », septembre 2010
  23. INERIS, « Mercure et principaux composés », 13 juillet 2006
  24. BIPC, « Mise à jour de la stratégie de gestion des risques actuelle en matière de présence de mercure dans le poisson vendu au détail »
La version du 21 octobre 2012 de cet article a été reconnue comme « bon article », c'est-à-dire qu'elle répond à des critères de qualité concernant le style, la clarté, la pertinence, la citation des sources et l'illustration.
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Hoplostèthe orange: Brief Summary ( French )

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Hoplostethus atlanticus

L'hoplostèthe orange, hoplostèthe rouge ou poisson-montre (Hoplostethus atlanticus) est une espèce de poissons de la famille des Trachichthyidae. L'hoplostèthe orange vit dans tous les océans entre 900 et 1 800 m de profondeur. Il a une longévité potentielle d'au moins 149 ans et il n'atteint sa maturité sexuelle qu'entre 20 et 30 ans. Avec une longueur maximale de 75 cm pour 7 kg, c'est le plus grand de sa famille.

Commercialisé sous le nom d'empereur, il fait l'objet d'une importante exploitation commerciale, mais en raison de son faible recrutement, ses populations tendent à diminuer. De nombreux stocks, en particulier ceux de la Nouvelle-Zélande et de l'Australie, qui ont été exploités dans les années 1970, ont déjà été décimés ; les stocks de substitution récemment découverts s'épuisent rapidement.

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Hoplostethus atlanticus ( Italian )

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Hoplostethus atlanticus (Collet, 1889), comunemente conosciuto come pesce specchio atlantico o pesce specchio[1]) è un pesce d'acqua salata appartenente alla famiglia Trachichthyidae.

Distribuzione e habitat

Il pesce specchio atlantico è diffuso nell'oceano Atlantico, nell'Indiano, nel Pacifico occidentale. Non vive nel mar Mediterraneo. Vive sulla scarpata continentale o sulla piana abissale a profondità da 180 a 1809 metri[2].

Descrizione

La testa è molto grande e tozza, ricca di pieghe e ossa sporgenti, la bocca è girata verso l'alto, dotata di piccoli denti disposti in file. Il corpo è ovaloide, molto compresso ai fianchi, con peduncolo caudale allungato. Le pinne sono arrotondate, rette da grossi raggi. La pinna caudale è bilobata.

La livrea è molto semplice: tutto il corpo è rosso, con sfumature che variano dall'arancio al rosso carminio. L'interno della bocca e delle branchie è bluastro[2].

Raggiunge una lunghezza massima di 75 cm per 7 kg, più comunemente la taglia arriva a 40 cm[2].

Biologia

È uno dei pesci ossei dalla vita più lunga: sono stati pescati esemplari di 149 anni[2].

Riproduzione

La biologia della specie è poco nota, si crede che i giovanili vivano in acque profonde. L'accrescimento è molto lento[2].

Alimentazione

H. atlanticus si nutre di crostacei (anfipodi, eufausiacei e gamberetti), cefalopodi e di pesci. Gli esemplari giovanili predano piccoli crostacei[2].

Predatori

È preda abituale di Ruvettus pretiosus, Diastobranchus sp. e Merluccius merluccius[3].

Pesca

Ha una notevole importanza per la pesca commerciale in certe aree. Nel 2006 è stata dichiarata specie minacciata dal governo australiano a causa della sovrapesca[2].

Note

  1. ^ Denominazione obbligatoria in Italia per tutti i membri del genere Hoplostethus ai sensi del DM 31 gennaio 2008
  2. ^ a b c d e f g (EN) Hoplostethus atlanticus, su FishBase. URL consultato il 27.08.2014.
  3. ^ (EN) Sommario dei predatori da Fishbase

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Hoplostethus atlanticus: Brief Summary ( Italian )

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Hoplostethus atlanticus (Collet, 1889), comunemente conosciuto come pesce specchio atlantico o pesce specchio) è un pesce d'acqua salata appartenente alla famiglia Trachichthyidae.

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Keizerbaars ( Dutch; Flemish )

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Vissen

De keizerbaars of oranje zaagbuikvis (Hoplostethus atlanticus) is een straalvinnige vis uit de familie van zaagbuikvissen (Trachichthyidae) en behoort derhalve tot de orde van slijmkopvissen (Beryciformes).

Kenmerken

Het lichaam is oranjerood. Hij heeft een grote stompe kop en kaken met kleine, in stroken bijeen geplaatste tanden. De vis kan maximaal 75 cm lang worden.

Verspreiding en leefgebied

Hoplostethus atlanticus is een zoutwatervis. De vis prefereert een diepwaterklimaat en heeft zich verspreid over de drie belangrijkste oceanen van de wereld (Grote, Atlantische en Indische Oceaan) aan de randen van het continentaal plat en op de diepzeebodem. De diepteverspreiding is 180 tot 1809 m onder het wateroppervlak.

Relatie tot de mens

Hoplostethus atlanticus is voor de visserij van groot commercieel belang. In de hengelsport wordt er weinig op de vis gejaagd. Omdat de soort lang leeft, traag volwassen wordt en relatief weinig nakomelingen heeft, is ze erg kwetsbaar voor overbevissing.

Externe link

Bronnen, noten en/of referenties
  • Froese, R., D. Pauly. en redactie. 2005. FishBase. Elektronische publicatie. www.fishbase.org, versie 06/2005.
  • David Burnie (2001) - Animals, Dorling Kindersley Limited, London. ISBN 90-18-01564-4 (naar het Nederlands vertaald door Jaap Bouwman en Henk J. Nieuwenkamp).
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Keizerbaars: Brief Summary ( Dutch; Flemish )

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De keizerbaars of oranje zaagbuikvis (Hoplostethus atlanticus) is een straalvinnige vis uit de familie van zaagbuikvissen (Trachichthyidae) en behoort derhalve tot de orde van slijmkopvissen (Beryciformes).

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Gardłosz atlantycki ( Polish )

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Gardłosz atlantycki[potrzebny przypis] (Hoplostethus atlanticus) – gatunek ryby z rodziny gardłoszowatych (Trachichthyidae).

Występowanie

Zamieszkuje głębokie wody, poniżej stoku kontynentalnego, grzbiety i rowy oceaniczne ok. 800 do 1800 m p.p.m. Występuje we wszystkich oceanach z wyjątkiem Arktycznego.

Charakterystyka

Młode żywią się skorupiakami, dorosłe także rybami. Bardzo ceniony i ekskluzywny przysmak.[potrzebny przypis] Poławiane włokami dennymi na stokach oceanicznych w okolicach Nowej Zelandii i Australii przez cały rok, na północno-zachodnim Atlantyku od stycznia do marca.

Rośnie bardzo wolno, dorasta do 60 cm, maksymalnie do 75 cm, żyje do 150 lat[6].

Przypisy

  1. Hoplostethus atlanticus, w: Integrated Taxonomic Information System (ang.).
  2. R. Collett. Diagnoses de poissons nouveaux provenant des campagnes de "L’Hirondelle." III.— Description d’une espèce nouvelle du genre Hoplostethus. „Bulletin de la Société Zoologique de France”. 14, s. 306, 1889 (fr.).
  3. L. Roule. Notice préliminaire sur quelques espèces nouvelles ou rares des poissons provenant des croisières de S. A. S. le Prince de Monaco. „Bulletin de l’Institut Océanographique de Monaco”. 320, s. 15, 1916 (fr.).
  4. J.L.B. Smith. New and little known fishes from South Africa. „Records of the Albany Museum Grahamstown”. 4, s. 182, 1935 (ang.).
  5. A. Kotthaus. Hoplostethus islandicus, nov. spec. (Acanthopterygia, Abt. Beryciformes, Familie Trachichthyidae) aus den südisländischen Gewässern. „Helgoländer wissenschaftliche Meeresuntersuchungen”. 4 (1), s. 66, 1952 (niem.).
  6. R. Froese & D. Pauly: Hoplostethus atlanticus Collett, 1889 (ang.). FishBase (version: 10/2017). [dostęp 2018-03-13].
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Gardłosz atlantycki: Brief Summary ( Polish )

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Gardłosz atlantycki[potrzebny przypis] (Hoplostethus atlanticus) – gatunek ryby z rodziny gardłoszowatych (Trachichthyidae).

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Hoplostethus atlanticus ( Portuguese )

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Hoplostethus atlanticus Collett, 1889, conhecido pelo nome comum de peixe-relógio, é um peixe do oceano profundo pertencente à família Trachichthyidae (traquictiídeos), distribuída pelo leste e noroeste do Oceano Atlântico, pelo sul do Oceano Pacífico e pelo Oceano Índico.[2]

Anatomia

Apesar de existirem referências à captura de espécimes de maior dimensão, a espécie tem um comprimento máximo aproximado de 40 cm.[3] Na barbatana dorsal tem de 4 a 6 espinhas e 15 a 19 raios flexíveis, enquanto que na barbatana anal tem 3 espinhas e 10 a 12 rios flexíveis. A cor é vermelho alaranjado, brilhante, com as cavidades da boca e guelras de cor azulada[3] .

Habitat e biologia

É um peixe batipelágico e oceanódromo, que vive sedentário junto ao substrato a uma grande profundidade, normalmente entre 400 e 900 m,[4] normalmente nas águas frias do talude continental, nas cordilheiras oceânicas e outros relevos altos marinhos, onde vive disperso, alimentando-se de crustáceos e de outros peixes[2] .

O crescimento é muito lento, sendo um dos peixes mais longevos conhecidos, com um espécimen capturado com uma idade de 149 anos.[5] Sabe-se pouco sobre as suas larvas e juvenis, que habitam provavelmente em águas abissais.[6]

A espécie é alvo de uma importante pescaria comercial, sendo amplamente comercializada na Austrália, Japão, Nova Zelândia, Europa e América do Norte[2] , fresco ou congelado, sendo consumido frito ou assado.[7] Os barcos de pesca localizam esporadicamente densos cardumes da espécie.

Notas

  1. Hoplostethus atlanticus — Orange Roughy, Deep-sea Perch, Red Roughy, Species Profile and Threats Database, Department of the Environment and Heritage, Australia.
  2. a b c Maul, G.E., 1986. "Trachichthyidae". p. 749-752. En P.J.P. Whitehead, M.-L. Bauchot, J.-C. Hureau, J. Nielsen y E. Tortonese (eds.) Fishes of the north-eastern Atlantic and the Mediterranean. UNESCO, París. Vol. 2.
  3. a b Heemstra, P.C., 1986. "Trachichthyidae". p. 410-413. En M.M. Smith y P.C. Heemstra (eds.) Smiths' sea fishes. Springer-Verlag, Berlín.
  4. Maul, G.E., 1990. "Trachichthyidae". p. 620-622. En J.C. Quéro, J.C. Hureau, C. Karrer, A. Post y L. Saldanha (eds.) Check-list of the fishes of the eastern tropical Atlantic (CLOFETA). JNICT, Lisboa; SEI, París; y UNESCO, París. Vol. 2.
  5. Fenton, G.E., S.A. Short y D.A. Ritz, 1991. "Age determination of orange roughy Hoplostethus atlanticus (Pisces: Trachichthyidae) using 210 Pb/226Ra disequilibria". Mar. Biol. 109:197-202.
  6. Jordan, A.R. y B.D. Bruce, 1993. "Larval development of three roughy species complexes (Pisces: Trachichthyidae) from southern Australian waters, with comments on the occurrence of orange roughy Hoplostethus atlanticus". Fish. Bull. 91:76-86.
  7. Frimodt, C., 1995. "Multilingual illustrated guide to the world's commercial coldwater fish". Fishing News Books, Osney Mead, Oxford, Inglaterra. 215 p.

Referências

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Hoplostethus atlanticus: Brief Summary ( Portuguese )

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Hoplostethus atlanticus Collett, 1889, conhecido pelo nome comum de peixe-relógio, é um peixe do oceano profundo pertencente à família Trachichthyidae (traquictiídeos), distribuída pelo leste e noroeste do Oceano Atlântico, pelo sul do Oceano Pacífico e pelo Oceano Índico.

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Atlantisk soldatfisk ( Swedish )

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Atlantisk soldatfisk (Hoplostethus atlanticus) är en djuphavsfisk som framför allt lever utanför Atlantens kuster, men också i Stilla havet och Indiska oceanen. Den kallas också atlantsoldatfisk.[2]

Utseende

Den atlantiska soldatfisken är orangeröd med flera slemfyllda gropar på huvudet.[2] Största längd är 75 cm, även om den vanligen inte blir mycket längre än 40 cm.[3] Den kan leva upp till en uppskattad ålder av 149 år,[3] som har tagits fram genom radiologisk undersökning av en hörselsten[4]. Det är sällan fisken blir så gammal; de större exemplaren brukar vara omkring 75 år gamla.[2]

Vanor

Arten är en djuphavsfisk som lever på ett djup mellan 300 och 1 700 m, där den lever av fisk, bläckfisk och räkor.[2] Litet är känt om dess fortplantning[3], men den blir könsmogen vid ungefär 35 års ålder.[5]

Utbredning

Arten lever i västra Stilla havet, östra Atlanten från Island till Marocko och från Namibia till Sydafrika, västra Atlanten utanför Nova Scotia, södra centrala Indiska oceanen till vattnen utanför utanför Nya Zeeland och Australien samt i östra Stilla havet utanför Chile.[3]

Kommersiell användning

Arten fiskas flitigt utanför Nya Zeeland och södra Australien.[2] På grund av kraftigt överfiske förklarades den för hotad av den australiska regeringen 2006[3], och WWF avråder från konsumtion av den.[5].

Se även

Referenser

  1. ^ Hoplostethus atlanticus (Collett, 1889)” (på engelska). ITIS. http://www.itis.gov/servlet/SingleRpt/SingleRpt?search_topic=TSN&search_value=166139. Läst 10 september 2010.
  2. ^ [a b c d e] Muus, Bent J; Nielsen, Jørgen G; Svedberg, Ulf (1999). Havsfisk och fiske i Nordvästeuropa. Stockholm: Prisma. sid. 154. ISBN 91-518-3505-3
  3. ^ [a b c d e] Luna, Susan M. (20 april 2010). Hoplostethus atlanticus Collett, 1889 Orange roughy” (på engelska). Fishbase. http://www.fishbase.org/Summary/speciesSummary.php?id=334. Läst 9 september 2010.
  4. ^ G. E. Fenton, S. A. Short & D. A. Ritz (1 februari 1991). ”Age determination of orange roughy, Hoplostethus atlanticus (Pisces: Trachichthyidae) using 210Pb:226Ra disequilibria” (på engelska). Marine Biology (Springer) 2: sid. 197-202. ISSN 15729753. http://www.springerlink.com/content/q4878h1m8jh84282/. Läst 9 september 2010.
  5. ^ [a b] ”Djuphavsfiskar som bör undvikas”. WWF. 2008. http://www.wwf.se/v/hav-kust/havets-m/1133548-djuphavsfiskar-som-bor-undvikas. Läst 9 september 2010.

Externa länkar

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Atlantisk soldatfisk: Brief Summary ( Swedish )

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Atlantisk soldatfisk (Hoplostethus atlanticus) är en djuphavsfisk som framför allt lever utanför Atlantens kuster, men också i Stilla havet och Indiska oceanen. Den kallas också atlantsoldatfisk.

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Хоплостет помаранчевий ( Ukrainian )

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Хоплостет помаранчевий: Brief Summary ( Ukrainian )

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Hoplostethus atlanticus ( Vietnamese )

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Cá tráp cam (Danh pháp khoa học: Hoplostethus atlanticus) là một loài cá biển trong họ Trachichthyidaetrong tiếng Anh nó còn được gọi là Orange Roughy. Loài cá Hoplostethus atlanticus bị cạn kiệt về số lượng do nạn khai thác quá mức. Các chuyên gia nói rằng phải mất nhiều thập kỉ mới khôi phục được số lượng loài này lại như cũ.

Khai thác

Loài cá biển sâu ngày càng là những món đặc sản bị khai thác nặng nề, chủ yếu là do con người thiếu cá ngừ để bắt và ăn vì thế hiện naybuộc phải ăn những phiên bản cá đột biến kỳ dị. Nó không phải là con cá bình thường đã bị tra tấn bằng cách lột da khi còn sống. Chúng ta ăn thịt của con cá này, nhưng khi chúng còn sống, đó là một trong những con cá bị săn đuổi nhất. Các đầu bếp thích Orange Roughy, giống như những loài cá biển sâu khác, ít nhất là 100 tuổi vì vòng đời của nó rất nhậm.

Chú thích

Tham khảo

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Hoplostethus atlanticus: Brief Summary ( Vietnamese )

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Cá tráp cam (Danh pháp khoa học: Hoplostethus atlanticus) là một loài cá biển trong họ Trachichthyidaetrong tiếng Anh nó còn được gọi là Orange Roughy. Loài cá Hoplostethus atlanticus bị cạn kiệt về số lượng do nạn khai thác quá mức. Các chuyên gia nói rằng phải mất nhiều thập kỉ mới khôi phục được số lượng loài này lại như cũ.

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Атлантический большеголов ( Russian )

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Царство: Животные
Подцарство: Эуметазои
Без ранга: Вторичноротые
Подтип: Позвоночные
Инфратип: Челюстноротые
Группа: Рыбы
Группа: Костные рыбы
Подкласс: Новопёрые рыбы
Инфракласс: Костистые рыбы
Надотряд: Колючепёрые
Серия: Berycida
Отряд: Trachichthyiformes
Подотряд: Трахихтиевидные
Семейство: Большеголовые
Род: Hoplostethus
Вид: Атлантический большеголов
Международное научное название

Hoplostethus atlanticus Collett, 1889

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ITIS 166139NCBI 96778EOL 206716

Атлантический большеголов, или атлантический слизнеголов, или исландский берикс[1] (лат. Hoplostethus atlanticus) — вид крупных глубоководных лучепёрых рыб семейства большеголовых (Trachichthyidae). По сведениям Общества охраны моря (Marine Conservation Society), является видом, находящимся под угрозой[2].

Описание

Атлантический большеголов живёт в холодной воде (от 3 до 9 °C) на глубине от 180 до 1800 метров в Атлантическом, Тихом и Индийском океанах. Известен большой продолжительностью жизни. Максимальный зафиксированный (хотя и поставленный под сомнение) возраст — 149 лет. Является объектом глубоководной траулерной рыбной ловли. При жизни имеет красновато-кирпичный цвет, после смерти — желтовато-оранжевый. Рост очень медленный, созревание позднее.

 src=
Изображение рыбы на марке Фарерских островов. Худ. Астрид Андреасен

Примечания

  1. Решетников Ю. С., Котляр А. Н., Расс Т. С., Шатуновский М. И. Пятиязычный словарь названий животных. Рыбы. Латинский, русский, английский, немецкий, французский. / под общей редакцией акад. В. Е. Соколова. — М.: Рус. яз., 1989. — С. 215. — 12 500 экз.ISBN 5-200-00237-0.
  2. Hoplostethus atlanticus — Orange Roughy, Deep-sea Perch, Red Roughy, Species Profile and Threats Database, Department of the Environment and Heritage, Australia. (англ.)
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Атлантический большеголов: Brief Summary ( Russian )

provided by wikipedia русскую Википедию

Атлантический большеголов, или атлантический слизнеголов, или исландский берикс (лат. Hoplostethus atlanticus) — вид крупных глубоководных лучепёрых рыб семейства большеголовых (Trachichthyidae). По сведениям Общества охраны моря (Marine Conservation Society), является видом, находящимся под угрозой.

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大西洋胸棘鯛 ( Chinese )

provided by wikipedia 中文维基百科
二名法 Hoplostethus atlanticus
Collett, 1889

大西洋胸棘鯛胸棘鯛屬的一,分布於全球各大洋熱帶至溫帶海域,棲息深度180-1809公尺,體長可達75公分,棲息在大陸坡、海脊等深水域,屬肉食性,以魚類甲殼類片腳類等為食,可做為食用魚。

大西洋胸棘鯛的大規模商業捕撈始於1970年代,但由於過度捕撈,其數量迅速下降。現在新西蘭是這種魚的主要產地,現在絕大多數大西洋胸棘鯛都是在此捕撈的。[1]

参考文献

  1. ^ Case for trawl ban 'overwhelming'. News.bbc.co.uk. 15 November 2006 [13 October 2017].

擴展閱讀

 src= 維基物種中有關大西洋胸棘鯛的數據

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大西洋胸棘鯛: Brief Summary ( Chinese )

provided by wikipedia 中文维基百科

大西洋胸棘鯛是胸棘鯛屬的一,分布於全球各大洋熱帶至溫帶海域,棲息深度180-1809公尺,體長可達75公分,棲息在大陸坡、海脊等深水域,屬肉食性,以魚類甲殼類片腳類等為食,可做為食用魚。

大西洋胸棘鯛的大規模商業捕撈始於1970年代,但由於過度捕撈,其數量迅速下降。現在新西蘭是這種魚的主要產地,現在絕大多數大西洋胸棘鯛都是在此捕撈的。

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オレンジラフィー ( Japanese )

provided by wikipedia 日本語
Nuvola apps important orange.svg

この記事には複数の問題があります改善ノートページでの議論にご協力ください。

  • 出典がまったく示されていないか不十分です。内容に関する文献や情報源が必要です。2013年8月
  • 正確性に疑問が呈されています。2013年8月
オレンジラフィー Orange roughy.png
オレンジラフィー Hoplostethus atlanticus
分類 : 動物界 Animalia : 脊索動物門 Chordata 亜門 : 脊椎動物亜門 Vertebrata : 条鰭綱 Actinopterygii : キンメダイ目 Beryciformes : ヒウチダイ科 Trachichthyidae : ヒウチダイ属 Hoplostethus : オレンジラフィーH. atlanticus 学名 Hoplostethus atlanticus
Collett, 1889 和名 オレンジラフィー 英名 Orange roughy

オレンジラフィー(学名:Hoplostethus atlanticus )は、ヒウチダイ科の魚類である。

形態[編集]

左右が平たい体型をしている。最大は55センチメートル程度。頭部の皮膚は多孔性である。

生態[編集]

水深100メートルから1500メートルくらいの深海に生息している底生魚である。

分布[編集]

大西洋太平洋インド洋

資源として[編集]

食用の高級白身魚として欧米や現地で食されている。 オーストラリアニュージーランドでは重要な水産物の一つでもある。ニュージーランドでは1980年代に輸出品目として深海魚に注目が集まり、チャタム諸島に好漁場が見つかった事から乱獲された。一般的に深海魚の成長性及び再生産性は高くないため、1990年代には漁獲量が制限される事態になるなど資源としての持続性の維持には注意が必要となる。

皮下には消化出来ない脂(ワックスエステル)を蓄えているため食用においてはこの部分を切り落とす必要がある。 このワックスエステルは精製されオレンジラフィー油として化粧品などに利用されており、医薬部外品原料規格においても「オレンジラフィー油」として登録されるなど日本国内では食用よりもオレンジラフィー油の方が馴染み深い魚と思われる。


執筆の途中です この項目は、魚類に関連した書きかけの項目です。この項目を加筆・訂正などしてくださる協力者を求めていますPortal:生き物と自然/プロジェクト:生物)。  src= ウィキメディア・コモンズには、オレンジラフィーに関連するメディアがあります。
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オレンジラフィー: Brief Summary ( Japanese )

provided by wikipedia 日本語

オレンジラフィー(学名:Hoplostethus atlanticus )は、ヒウチダイ科の魚類である。

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오렌지라피 ( Korean )

provided by wikipedia 한국어 위키백과

오렌지라피납작금눈돔목 납작금눈돔과의 물고기이다.

특징

Faroe stamp 251 orange roughy (hoplostethus atlanticus).gif

오렌지라피의 머리는 둥글다. 1개의 등지느러미에는 4~6개의 등뼈와 15~19개의 연조가 들어있다. 항문지느러미에는 3개의 등뼈와 10-12개의 연조가 있다. 19-25개의 복부 모비늘은 지느러미항문 사이에 딱딱한 골반 중간 능선을 형성한다. 가슴지느러미는 각각 15-18개의 연조를 포함한다. 골반지느러미는 흉부에 있으며 1개의 등뼈와 6개의 연조를 포함한다. 꼬리지느러미는 갈라진다. 입과 아가미 구멍의 내부는 푸르스름한 검은색이다. 입 자체는 크고 크게 기울어져 있다. 비늘은 딱딱하고 끈적거린다. 오렌지라피의 눈은 크다.

오렌지라피의 최대 표준 몸길이는 75cm이고 최대 몸무게는 7kg이다.

참고 자료

  • Earle, Sylvia. 2009. The World is Blue. 내셔널 지오그래픽. ISBN 1-4262-0541-4
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Diet

provided by World Register of Marine Species
Feeds on prawns, mysids, amphipods, euphausiids and fishes including cardinalfish and lanternfish

Reference

North-West Atlantic Ocean species (NWARMS)

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Distribution

provided by World Register of Marine Species
from the Davis Strait west of the Southern tip of Greenland to the Labrador shelf and north east Newfoundland shelf and the Grand Banks

Reference

North-West Atlantic Ocean species (NWARMS)

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Habitat

provided by World Register of Marine Species
Inhabits deep, cold waters over steep continental slopes, ocean ridges and sea-mounts. Appears to be dispersed over both rough bottoms and steep, rough grounds where it feeds on crustaceans and fish.

Reference

North-West Atlantic Ocean species (NWARMS)

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Habitat

provided by World Register of Marine Species
nektonic

Reference

North-West Atlantic Ocean species (NWARMS)

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Habitat

provided by World Register of Marine Species
Known from seamounts and knolls

Reference

Stocks, K. 2009. Seamounts Online: an online information system for seamount biology. Version 2009-1. World Wide Web electronic publication.

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