Orange roughy

Last updated

Orange roughy
Orange roughy.png
Status iucn3.1 VU.svg
Vulnerable  (IUCN 3.1) [1] (Europe)
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Actinopterygii
Order: Trachichthyiformes
Family: Trachichthyidae
Genus: Hoplostethus
Species:
H. atlanticus
Binomial name
Hoplostethus atlanticus
Collett, 1889

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 bathypelagic, found in cold (3 to 9 °C or 37 to 48 °F), deep (180-to-1,800-metre or 590-to-5,910-foot) 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.

Contents

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 Faroe stamp 251 orange roughy (hoplostethus atlanticus).gif
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.[ citation needed ]

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. The orange roughy also has many predators, like bigger sharks such as goblin sharks and megamouth sharks, and larger fish. Oilfish also sometimes scoop up orange roughy on the ocean floor. [ citation needed ]

Life history

A preserved specimen on display at a museum Hoplostethus atlanticus 02 Pengo.jpg
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.[ citation needed ]

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 a single spawning event. [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 to 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]

Atlantic roughy (Hoplostethus atlanticus) Hoplostethus atlanticus NOAA.jpg
Atlantic roughy (Hoplostethus atlanticus)

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).[ citation needed ]

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.[ citation needed ]

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.[ citation needed ]

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 of its longevity, late maturation and relatively low fecundity, orange roughy stocks tend to recover more slowly 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 [when?] 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.[ citation needed ]

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.[ citation needed ]

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

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.[ citation needed ]

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.[ citation needed ]

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.[ citation needed ]

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.[ citation needed ]

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.[ citation needed ]

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.[ citation needed ]

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.[ citation needed ]

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.[ citation needed ]

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

Related Research Articles

<span class="mw-page-title-main">Antarctic toothfish</span> Species of fish

The Antarctic toothfish, also known as the Antarctic cod, is a large, black or brown fish found in very cold (subzero) waters of the Southern Ocean near Antarctica. It is the largest fish in the Southern Ocean, feeding on shrimp and smaller fish, and preyed on by whales, orcas, and seals. It is caught for food and marketed as Chilean sea bass together with its sister species, the more northerly Patagonian toothfish. Often mistakenly called "Antarctic cod", the Antarctic toothfish belongs to the notothen family (Nototheniidae), a family of fish genera that are abundant near Antarctica.

<span class="mw-page-title-main">Patagonian toothfish</span> Species of fish

The Patagonian toothfish, also known as Chilean sea bass, mero, and icefish, is a species of notothen found in cold waters between depths of 45 and 3,850 m in the southern Atlantic, Pacific, and Indian Oceans and Southern Ocean on seamounts and continental shelves around most Subantarctic islands.

<span class="mw-page-title-main">Beryciformes</span> Order of fishes

The Beryciformes are a poorly-understood order of carnivorous ray-finned fishes consisting of 7 families, 30 genera, and 161 species. They feed on small fish and invertebrates. Beyond this, little is known about the biology of most member species because of their nocturnal habits and deepwater habitats. All beryciform species are marine and most live in tropical to temperate, deepwater environments. Most live on the continental shelf and continental slope, with some species being found as deep as 2,000 m (6,600 ft). Some species move closer to the surface at night, while others live entirely in shallow water and are nocturnal, hiding in rock crevices and caves during the day. Several species are mesopelagic and bathypelagic. Beryciformes' bodies are deep and mildly compressed, typically with large eyes that help them see in darker waters. Colors range from red to yellow and brown to black, and sizes range from 8–61 cm (3.1–24.0 in). Member genera include the alfonsinos, squirrelfishes, flashlight fishes, fangtooth fishes, spinyfins, pineconefishes, redfishes, roughies, and slimeheads. A number of member species are caught commercially, including the alfonsino, the splendid alfonsino, and the orange roughy, the latter being much more economically important. Some species have bioluminescent bacteria contained in pockets of skin or in light organs near the eyes, including the anomalopids and monocentrids.

<span class="mw-page-title-main">Overfishing</span> Removal of a species of fish from water at a rate that the species cannot replenish

Overfishing is the removal of a species of fish from a body of water at a rate greater than that the species can replenish its population naturally, resulting in the species becoming increasingly underpopulated in that area. Overfishing can occur in water bodies of any sizes, such as ponds, wetlands, rivers, lakes or oceans, and can result in resource depletion, reduced biological growth rates and low biomass levels. Sustained overfishing can lead to critical depensation, where the fish population is no longer able to sustain itself. Some forms of overfishing, such as the overfishing of sharks, has led to the upset of entire marine ecosystems. Types of overfishing include growth overfishing, recruitment overfishing, and ecosystem overfishing. Overfishing not only causes negative impacts on biodiversity and ecosystem functioning, but also reduces fish production, which subsequently leads to negative social and economic consequences.

<span class="mw-page-title-main">Fishing industry</span> Economic branch

The fishing industry includes any industry or activity that takes, cultures, processes, preserves, stores, transports, markets or sells fish or fish products. It is defined by the Food and Agriculture Organization as including recreational, subsistence and commercial fishing, as well as the related harvesting, processing, and marketing sectors. The commercial activity is aimed at the delivery of fish and other seafood products for human consumption or as input factors in other industrial processes. The livelihood of over 500 million people in developing countries depends directly or indirectly on fisheries and aquaculture.

<span class="mw-page-title-main">Marine Stewardship Council</span> Fishing certifier

The Marine Stewardship Council (MSC) is a non-profit organisation which aims to set standards for sustainable fishing. Fisheries that wish to demonstrate they are well-managed and sustainable compared to the MSC's standards are assessed by a team of Conformity Assessment Bodies (CABs).

<span class="mw-page-title-main">Slimehead</span> Family of fishes

Slimeheads, also known as roughies and redfish, are mostly small, exceptionally long-lived, deep-sea beryciform fish constituting the family Trachichthyidae. Found in temperate to tropical waters of the Atlantic, Indian, and Pacific Oceans, the family comprises about 50 species in eight genera. Slimeheads are named for the network of muciferous canals riddling their heads.

<span class="mw-page-title-main">Demersal fish</span> Fish that live and feed on or near the bottom of seas or lakes

Demersal fish, also known as groundfish, live and feed on or near the bottom of seas or lakes. They occupy the sea floors and lake beds, which usually consist of mud, sand, gravel or rocks. In coastal waters, they are found on or near the continental shelf, and in deep waters, they are found on or near the continental slope or along the continental rise. They are not generally found in the deepest waters, such as abyssal depths or on the abyssal plain, but they can be found around seamounts and islands. The word demersal comes from the Latin demergere, which means to sink.

The South Tasman Rise is an area of seafloor that lies 550 km south of Hobart, Tasmania in the Southern Ocean where water depths are about 1,500 metres. The South Tasman Rise is also known as the Tasmania Ridge or South Tasmania Ridge. The South Tasman Rise is a sunken landbridge that used to connect Tasmania to Antarctica.

<span class="mw-page-title-main">Environmental impact of fishing</span>

The environmental impact of fishing includes issues such as the availability of fish, overfishing, fisheries, and fisheries management; as well as the impact of industrial fishing on other elements of the environment, such as bycatch. These issues are part of marine conservation, and are addressed in fisheries science programs. According to a 2019 FAO report, global production of fish, crustaceans, molluscs and other aquatic animals has continued to grow and reached 172.6 million tonnes in 2017, with an increase of 4.1 percent compared with 2016. There is a growing gap between the supply of fish and demand, due in part to world population growth.

<i>The End of the Line</i> (book) Book by Charles Clover

The End of the Line: How Overfishing Is Changing the World and What We Eat is a book by journalist Charles Clover about overfishing. It was made into a movie released in 2009 and was re-released with updates in 2017.

The South East Atlantic Fisheries Organisation (SEAFO) is an organization that maintains controls over fishing and fishing related acts in the Southeastern Atlantic Ocean.

<i>Sebastes levis</i> Species of fish

Sebastes levis, the cowcod or cow rockfish, is a species of marine ray-finned fish belonging to the subfamily Sebastinae, the rockfishes, part of the family Scorpaenidae. It is found in the eastern Pacific Ocean.

<span class="mw-page-title-main">Fishing industry in New Zealand</span>

As with other countries, New Zealand's 200 nautical miles exclusive economic zone gives its fishing industry special fishing rights. It covers 4.1 million square kilometres. This is the sixth largest zone in the world, and is fourteen times the land area of New Zealand.

<span class="mw-page-title-main">Friend of the Sea</span> Sustainable seafood organization

Friend of the Sea is a project of the World Sustainability Organization for the certification and promotion of seafood from sustainable fisheries and sustainable aquaculture. It is the only certification scheme which, with the same logo, certifies both wild and farmed seafood.

<span class="mw-page-title-main">Fishing industry in the United States</span>

As with other countries, the 200 nautical miles (370 km) exclusive economic zone (EEZ) off the coast of the United States gives its fishing industry special fishing rights. It covers 11.4 million square kilometres, which is the second largest zone in the world, exceeding the land area of the United States.

<span class="mw-page-title-main">Stock assessment</span> Process used in fisheries management

Stock assessments provide fisheries managers with the information that is used in the regulation of a fish stock. Biological and fisheries data are collected in a stock assessment.

<span class="mw-page-title-main">Chilean jack mackerel</span> Species of fish

The Chilean jack mackerel, sometimes called the Jurel, Inca scad or Peruvian jack mackerel, is a species of jack mackerel in the genus Trachurus of the family Carangidae. Since the 1970s, it has become one of the world's more important commercial fish species. High volumes have been harvested, but the fishery may now be in danger of collapsing.

<i>Hoplostethus</i> Genus of fishes

Hoplostethus is a genus of fish in the slimehead family.

Dianne Margaret Tracey is a New Zealand marine biologist specializing in research on deep-sea fisheries and deep-sea corals at the National Institute of Water and Atmospheric Research (NIWA). She works on the biology of deep water fishes such as orange roughy, and deep sea corals. She was one of the first women in New Zealand to work in fisheries and to work on research vessels and has spent her career advocating and mentoring women in marine science.

References

  1. Collette, B.; Fernandes, P.; Heessen, H.; Herrera, J.; Smith-Vaniz, W.F. (2015). "Hoplostethus atlanticus (Europe assessment)". IUCN Red List of Threatened Species . 2015: e.T155168A45884209. Retrieved 4 May 2024.
  2. 1 2 3 4 5 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.{{cite web}}: CS1 maint: multiple names: authors list (link)
  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. 1 2 3 4 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. Bibcode:1991MarBi.109..197F. 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.{{cite book}}: CS1 maint: location missing publisher (link)
  14. Jacquet, J. L.; Pauly, D. (May 2008). "Trade secrets: Renaming and mislabeling of seafood". Marine Policy. 32 (3): 309–318. Bibcode:2008MarPo..32..309J. CiteSeerX   10.1.1.182.1143 . doi:10.1016/j.marpol.2007.06.007.
  15. Greenpeace International Seafood Red list
  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. [ dead link ]
  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.

Further reading