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Patagonian toothfish
(also known as
Bacalao and Bacalao de profundidad in Chile; Merluza
negra in Argentina and Uruguay; Légine australe in
France; Marlonga-negra in Portugal; and Tandnoting in
Sweden)
Dissostichus
eleginoides
(Smitt,
1898)
(previously
classified as Dissostichus amissus (Gill &
Townsend, 1901) and Macrias amissus (Gill &
Townsend, 1901)) |
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Areas
where Patagonian toothfish have been found |
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Map from
AquaMaps |
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A history of the Patagonian toothfish fishery |
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Today the
Patagonian toothfish (Dissostichus eleginoides)
is the most valuable fishery in Antarctic or sub
Antarctic waters. Commercially and in restaurants it is
sold as Chilean Sea Bass. Prices can exceed $US10 per kilo for
headed, gutted and tailed fish in the main markets in
Japan and the United States. Unlike nearly all other
Antarctic fish, the toothfish can grow to a large size
(just over 2 m long and 100 kg in weight) and this,
together with its high quality white flesh and few
bones, make it highly sought after - particularly given
the growing scarcity of other premium-quality species
from around the world.
This has led in
the last few years to a large-scale illegal fishery,
which attempts to poach fish from the major areas of
distribution of the toothfish around the sub Antarctic
islands and other submarine ridges in the Atlantic and
Indian Ocean sectors of the Southern Ocean. Large
numbers of vessels fishing illegally were first noticed
in 1996 in the western part of the Indian Ocean, but
they soon spread eastwards towards Kerguelen and Heard
Islands where they were seen by Australian and French
licensed vessels in 1997. Although difficult to estimate
reliably, it is thought that illegal catches were very
high in these first couple of years - possibly two to
three times the legal catch of this species from all
sources - and probably caused a significant depletion of
the fish stock in some localities. As a result of
surveillance and arrests by some countries, including
Australia, illegal fishing has declined. It still
however remains a serious problem, with illegal catches
being similar to the level of legal catches in the
1999-2000 season.
Since the start
of fishing activity in sub Antarctic waters in the early
1970s, toothfish had been a minor bycatch species in the
trawl fisheries for marbled rock cod and grey rock cod,
particularly around South Georgia and the Kerguelen
Islands. It was only in 1985 that commercial quantities
of toothfish were discovered at Kerguelen. There had,
however, been a substantial fishery off the Chilean
coast since the mid-1970s, so markets were already
established for this species. Since then, the fishery
for this species developed rapidly and expanded to other
areas, including South Georgia, Marion and Prince Edward
Islands, and Crozet Islands. In 1994 an Australian trawl
fishery began at Macquarie Island, followed by Heard
Island in 1997. Although started as a trawl fishery,
most toothfish is now caught by longline, except for the
Australian fishery and part of the French fishery at
Kerguelen. In the 1999-2000 season, approximately 14,500
tons were caught in the sub Antarctic waters managed by
CCAMLR and a further 11,500 tons were taken outside
CCAMLR waters off Chile, Argentina and the Falkland
Islands.
Patagonian
toothfish is now known to occur throughout the southern
hemisphere in cool temperate and sub Antarctic waters,
from the east and west coasts of South America eastwards
through all of the sub Antarctic islands, submarine
plateaus and seamounts to the Campbell Plateau south of
New Zealand in waters from 300 m to over 2000 m depth.
It probably also occurs in the Pacific sector, but
little exploration has been done there. It is replaced
in the high latitudes close to the coast of Antarctica
by its close relation, the Antarctic toothfish
(Dissostichus mawsoni), for which a fishery is currently
being developed.
Patagonian
toothfish are caught close to the sea bed and most
fishing occurs between 400 m and 1500 m depth. They are
large, active, predatory fish that feed mostly in the
water column on squid and fish, but they have a very
varied diet that can include bottom-living organisms
such as crabs and prawns. Studies on their age and
growth are not yet conclusive, but it appears that they
can live at least 45 years, with males maturing at about
10 years and females at about 12 years. Spawning is
thought to take place in winter (June-July) in depths of
at least 1500 m. Young stages spend some months at least
in surface waters before moving to the sea bed where
they appear to move deeper as they grow. Tagging
experiments suggest, surprisingly for such an apparently
active large species, that fish generally do not move
more than a few tens of miles over a period of several
years. Recently, however, there have been two instances
of tagged fish recaptured at different islands several
hundred miles from their tagging position, so the extent
to which fish interchange between different fishing
grounds is not yet resolved.
Dick Williams
Antarctic Marine Living Resources Program, AAD
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The
Patagonian toothfish (Dissostichus eleginoides)
is a large pelagic predator, belonging to the family
Nototheniidae. It occurs on the shelf and shelf-slope
off islands and banks in the Southern Atlantic, Indian
and Pacific Oceans, notably within the influence of the
Antarctic Circumpolar Current. In the South Atlantic, it
occurs as far south as the South Sandwich Islands; the
closely related species, Dissostichus mawsoni,
occurs further south. D. eleginoides also occurs
off the South American coast from Peru to Cape Horn and
north off Argentine Patagonia.
Fishing began in the 1970s off northern Chile and in the
South Atlantic and South Indian Oceans. To start with,
fishermen used bottom trawling over continental shelves
and caught few toothfish, mostly incidentally while
fishing for other species. Long-lining for toothfish was
developed in northern Chile during the 1980s; and
probably first used at South Georgia in 1986 and off the
Kerguelen and Crozet Islands in the southern Indian
Ocean in 1992. Longlining gave access to deeper waters
along the shelf-break and better returns. Toothfish
catches grew rapidly, with new fisheries developed off
southern Chile, Argentina and the Falkland Islands; and
off Heard, Macquarie and the Prince Edward Islands.
Chile and Russia have been the main catching nations
historically; more recently Argentina and Norway have
become important, but vessels registered in diverse
countries such as Panama and Vanuatu are involved in the
fishery. The toothfish is highly prized in Japan,
selling at US$6.00/kg in mid-1995, and is sold in the
United States under the name of Chilean sea bass – a
prized choice on the restaurant tables of Washington
D.C. and New York.
CCAMLR
fisheries managers estimated the total catch in 1995
around South Georgia and the adjacent Rhine and North
Banks alone at 6171.1 tons. In 1997, they estimated the
catch for the CCAMLR area at 107,000-115,000 tons, of
which 70% was caught illegally.
Patagonian toothfish grow to over 2m long, and live
upwards of 20 years. Absolute fecundity is low at
between 48,000 - 528,900 eggs/individual over the life
history, although relatively high for a notothenid.
Spawning is annual, occurring between June and August
(SC-CCAMLR XI). Size of first spawning is ca. 80 cm for
males and ca. 100 cm for females. Little is known of
their early life history: eggs are considered to be
pelagic and have been found occasionally in the water
column. Larvae and post-larvae have been found only
infrequently, and generally within the upper 50 m of the
water column. Juveniles are found on the continental
shelf at ca.500 m, with increasingly large individuals
along the continental slope in deeper waters. Maximum
depth at which fish have been caught is ca. 2900 m.
Patagonian toothfish display considerable flexibility in
feeding patterns. Diet varies between regions and with
life stage and depth. Juveniles largely eat krill (Euphausia
superba) in Antarctic regions, while adults feed on
cephalopods and other fish (e.g. Champsocephalus
gunnari) feeding on krill, suggesting an ability to
move large distances from the continental shelf. This
evidence is corroborated by their occurrence in sperm
whale stomachs in pelagic waters of the Southern Ocean.
Diet off Chile is almost exclusively of fish, while off
South Georgia benthic crustaceans are present in a large
proportion of full stomachs from fish taken in water
deeper than 1000m. The digestive tract is adapted for
ingesting large items. The proportion of full stomachs
varies between regions and with depth.
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What we
need to know to manage the
fishery |
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Little is known of population structure. Yet most
techniques for assessing fish stocks rely on identifying
isolated populations with no immigration from outside or
migration out. To use these techniques, we therefore
need to know how toothfish move in time and space.
Variations in published growth parameters suggest there
is a population boundary between the southern South
America - Scotia Arc region and the islands of the
Southern Indian Ocean. This evidence is supported by
increasing levels of a disease causing degeneration of
protein (jelly meat) off southern Chile, which has also
appeared off South Georgia but has not been recorded in
fish from the Indian Ocean or northern Chile. Parasite
loadings indicate some isolation between fish
populations found along the north and south coasts of
Chile but also between the Patagonian shelf and South
Georgia.
But
this evidence may be related more to differences in the
environment encountered by older life stages than to
different sources of population recruitment. The
Southern Ocean is circumpolar, connecting the southern
Atlantic, Indian and Pacific Oceans. It is a major site
of production of several water masses, including
Antarctic Surface Water, Antarctic Intermediate Water
and Antarctic Bottom Water, which spread out of the
Antarctic regions to lower latitudes. Mixing with North
Atlantic Deep Water creates Circumpolar Deep Water,
which may form the source of the Common Water of the
Indian and Pacific Oceans. Thus, the Southern Ocean is
not one homogeneous body of water ; it is marked by
considerable change in water masses both vertically and
horizontally and, so close to their origin, the
differences between water masses is very pronounced.
These differences can affect how fast fish grow and the
food they have available – the differences can also
affect their predators. But most importantly, the water
structure may affect how toothfish move.
Within the Southern Ocean, the Antarctic Circumpolar
Current (ACC) moves eastward around the Antarctic
continent. After the ACC passes through the Drake
Passage, the current moves north along the Patagonian
shelf to meet the Brazil Current, after which it travels
eastward across the Atlantic. In the Indian Ocean, the
current passes along the Crozet and Kerguelen Island
groups, to meet the Macquarie Ridge before splitting
into two off the Campbell Plateau south of New Zealand.
Extensive mixing with Pacific Waters occurs until the
current returns to the Drake Passage. Much of the water
transport occurs within three fronts (polar, Antarctic
and continental) which mark large changes in temperature
and salinity. The fast currents at these fronts may also
act as conveyers for transporting toothfish to move
around the Southern Ocean.
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Summary of
Work So Far |
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Sampling longlines
for toothfish
Biologists at
CQFE have developed a multi-stage randomized design to
sample fish caught by commercial longline. Results from
trials indicate that variation at a scale of c500 m
accounted for 76% of all variance in the abundance of
the captured population, while variation between fishing
days accounted for 24%. Most variation in length
composition was captured at scales less than 500 m
(79%). Sampling 16 10-coil lengths of line/day on 36
days of a voyage of 60 days hauling was the optimal
sampling strategy.
Population
structure and growth of toothfish
Stock structure,
critical to good fisheries management, can be inferred
from growth differences between areas – if fish do not
move between areas, differences in temperature and food
availability between the areas will lead to differences
in growth rate. However, if fish move between these
areas, the differences in growth will be homogenized. So
we can test between rival hypotheses of 1) movement
between two areas and 2) no movement between these
areas, by seeing if there are differences in growth –
unless of course the temperature and food regimes
between the areas are so similar that no growth
differences are generated.

Click to
enlarge
Example
of age count from transverse section
of otolith of
Dissostichus elegenoides
Using
the
age estimation developed at CQFE,
we obtained age data from toothfish taken from the
Falkland Islands and South Georgia in the South
Atlantic, and the Kerguelen Islands and Heard Island in
the southern Indian Ocean. We estimated von Bertalanffy
growth parameters for each area, and constructed models
to describe the rival hypotheses of stock mixing and
separation between areas. We then selected between the
models using normal likelihood methods. The growth data
supported the hypothesis of stock separation between the
Falkland Islands and South Georgia, but not between
South Georgia and Kerguelen.
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Stock Assessment
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Click to
enlarge
Demersal longline equipment in the fishery Patagonian
Toothfish
A: The Spanish Manual System
B: The Japanese Manual System
C: The Norwegien Automated System
The development
of longlining techniques for fishing Patagonian
toothfish (Dissostichus eleginoides) led to a
rapid increase in exploitation rate during the early
1990s, which progressively affected fisheries around
southern South America and the Southern Ocean. The level
of illegal fishing was high yet the fish were considered
to be long-lived and slow-growing, indicators of
vulnerability to rapid over-exploitation. But lack of
knowledge of the basic biology of toothfish precluded
the use of an array of powerful population dynamical
techniques commonly used by fisheries managers.
Rigorous
analyses of growth, mortality and population age
structure depend on accurate age data. With age-based
information, the effect of management choices can be
simulated using dynamic pool and age-structured
assessment (ASA) models. Age-structured models can be
used to examine the effect of age-specific vital rates,
allowing managers to ascertain which stages of the life
history cycle are vulnerable to over-exploitation under
a particular set of conditions. Moreover, age-based data
can aid modeling of community interactions, allowing
impacts on other species to be assessed as part of an
ecosystem approach to fisheries management.
But
these methods all rely on accurate and representative
information on age and a single, closed population with
no emigration or immigration. Scientists at CQFE have
been working on techniques to obtain these data and
determine the rates of movement of toothfish.
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Age - Length
Relationships |

Click to enlarge
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Acknowledgments |
Funding for this
research has come from:
United States National Science
Foundation
(Grant
No.
OPP-9614756)
British Antarctic Survey
The work described
on this website was part of a collaboration between
research groups from several nations belonging to the
Convention for the Conservation of Antarctic Marine
Living Resources (CCAMLR).
Collaborating institutions include:
British Antarctic Survey
Museum
National d’Histoire Naturel,
France
Universidad Austral
de Chile
Instituto de
Fomento Pesquero,
Chile
Australian
Antarctic Division
Marine and Coastal
Management,
South Africa
Bundesforschungsanstalt fhr Fischerei,
Germany
New Zealand National Institute of
Water and Atmospheric Research
Falkland Islands Fisheries
Department
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