The fishery for Patagonian toothfish (Dissostichus eleginoides) in Subarea 48.3 began in the 1980s and expanded rapidly during the early 1990s, when considerable illegal, unreported and unregulated (IUU) catches were also taken (Table 1). The initial fishery also caused high rates of incidental bird mortality, with relatively large numbers of albatrosses and petrels attracted to the baited hooks and being caught and drowned. In response to these issues, CCAMLR introduced strict regulations designed to reduce bird by catch. These regulations, including seasonal closures, streamer lines, line-weighting regimes and night-setting requirements, greatly reduced bird by-catch in this fishery. The current toothfish fishery uses demersal longlines in which lines of baited hooks are deployed close to the sea floor at depths down to 2,250 m.
The limits on the fishery for D. eleginoides in Subarea 48.3 for the forthcoming season are defined in Conservation Measure 41-02.
In 2020, 5 vessels participated in this fishery.
In 2004, CCAMLR agreed to subdivide Subarea 48.3 into three Management Areas (A, B and C; Fig. 1) defined in Conservation Measure 41-02, Annex 41-02/A.
In 1998, the fishery was restricted to the winter months (1 May to 31 August) to minimise interactions with foraging birds during their breeding season. Since 2010, CCAMLR has applied a gradual extension to the season, accompanied by a number of seabird bycatch limits in those extension periods, the season is now from 16 April to 14 September as set out in Conservation Measure 41-02.
Reported catches of Dissostichus eleginoides are shown in Table 1. In this fishery, the catch of D. eleginoides reached a maximum of 7493 tonnes in 2003. In 2020, 1884 tonnes of D. eleginoides were caught.
Season | Number of vessels | Catch limit (tonnes) | Catch | Estimated IUU catch (tonnes) |
---|---|---|---|---|
1980 | 1 | 64 |
|
|
1981 | 1 | 7 |
|
|
1984 | 1 | 3 |
|
|
1986 | 1 | 7 |
|
|
1987 | 1 | 130 |
|
|
1988 | 4 | 584 |
|
|
1989 | 3 | 3577 |
|
|
1990 | 2 | 5023 |
|
|
1991 | 1 | 270 |
|
|
1992 | 19 | 3500 | 3986 | 3066 |
1993 | 19 | 3350 | 4018 | 4019 |
1994 | 4 | 1300 | 639 | 4780 |
1995 | 13 | 2800 | 3082 | 1674 |
1996 | 13 | 4000 | 3297 | 0 |
1997 | 10 | 5000 | 3724 | 0 |
1998 | 9 | 3300 | 2848 | 146 |
1999 | 12 | 3500 | 3660 | 667 |
2000 | 16 | 5310 | 5067 | 1015 |
2001 | 16 | 4500 | 3916 | 196 |
2002 | 17 | 5820 | 5453 | 3 |
2003 | 19 | 7810 | 7493 | 0 |
2004 | 16 | 4420 | 4460 | 0 |
2005 | 9 | 3050 | 3030 | 23 |
2006 | 10 | 3556 | 3546 | 0 |
2007 | 10 | 3554 | 3539 | 0 |
2008 | 12 | 3920 | 3862 | 0 |
2009 | 11 | 3920 | 3382 | 0 |
2010 | 9 | 3000 | 2518 | 0 |
2011 | 6 | 3000 | 1732 | 0 |
2012 | 7 | 2600 | 1836 | 0 |
2013 | 7 | 2600 | 2094 | 0 |
2014 | 7 | 2400 | 2180 | 0 |
2015 | 6 | 2400 | 2195 | 0 |
2016 | 6 | 2750 | 2196 | 0 |
2017 | 6 | 2750 | 2195 | 0 |
2018 | 6 | 2600 | 1950 | 0 |
2019 | 6 | 2600 | 2124 | 0 |
2020 | 5 | 2327 | 1884 |
|
Annual catch limits for by-catch species groups are defined in Conservation Measures 41-02 and 33-01. If the by-catch of skates or macrourids exceeds 1 tonne in any one haul or set, then the fishing vessel must move at least 5 nautical miles away for a period of at least five days.
Catches of by-catch species groups (macrourids, skates (Rajids) and other species), their respective catch limits and number of skates released alive are summarised in Table 2.
Season | Catch Limit (tonnes) | Reported Catch (tonnes) | Catch Limit (tonnes) | Reported Catch (tonnes) | Number Released | Catch Limit (tonnes) | Reported Catch (tonnes) |
---|---|---|---|---|---|---|---|
1985 | 0 | 0 | 0 | 4 | 0 | 0 | <1 |
1986 | 0 | <1 | 0 | 9 | 0 | 0 | <1 |
1987 | 0 | <1 | 0 | 3 | 0 | 0 | <1 |
1988 | 0 | <1 | 0 | <1 | 0 | 0 | <1 |
1989 | 0 | <1 | 0 | 11 | 0 | 0 | <1 |
1990 | 0 | <1 | 0 | <1 | 0 | 0 | <1 |
1991 | 0 | 1 | 0 | 4 | 0 | 0 | <1 |
1992 | 0 | <1 | 0 | 2 | 0 | 0 | <1 |
1993 | 0 | 2 | 0 | <1 | 0 | 0 | <1 |
1994 | 0 | <1 | 0 | 12 | 0 | 0 | <1 |
1995 | 0 | 12 | 0 | 90 | 0 | 0 | <1 |
1996 | 0 | 32 | 0 | 54 | 0 | 0 | <1 |
1997 | 0 | 33 | 0 | 43 | 0 | 0 | 2 |
1998 | 0 | 21 | 0 | 13 | 0 | 0 | 1 |
1999 | 0 | 21 | 0 | 19 | 0 | 0 | <1 |
2000 | 0 | 18 | 0 | 12 | 0 | 0 | 2 |
2001 | 0 | 21 | 0 | 27 | 0 | 0 | 1 |
2002 | 0 | 50 | 0 | 25 | 0 | 0 | 5 |
2003 | 0 | 74 | 0 | 37 | 0 | 0 | 10 |
2004 | 221 | 30 | 221 | 6 | 0 |
|
3 |
2005 | 152 | 121 | 152 | 8 | 0 |
|
19 |
2006 | 177 | 136 | 177 | 7 | 21056 |
|
35 |
2007 | 177 | 129 | 177 | 4 | 9265 |
|
26 |
2008 | 196 | 161 | 196 | 12 | 19558 |
|
36 |
2009 | 196 | 110 | 196 | 22 | 23709 |
|
33 |
2010 | 150 | 70 | 150 | 7 | 15810 |
|
16 |
2011 | 150 | 74 | 150 | 4 | 12832 |
|
9 |
2012 | 130 | 54 | 130 | 2 | 13503 |
|
9 |
2013 | 130 | 59 | 130 | 2 | 14005 |
|
11 |
2014 | 120 | 61 | 120 | 3 | 12969 |
|
15 |
2015 | 120 | 56 | 120 | 2 | 10937 |
|
10 |
2016 | 138 | 64 | 138 | 2 | 14960 |
|
14 |
2017 | 138 | 54 | 138 | 3 | 12916 |
|
16 |
2018 | 130 | 107 | 130 | 4 | 21235 |
|
29 |
2019 | 130 | 107 | 130 | 3 | 23817 |
|
41 |
2020 | 116 | 87 | 116 | 3 | 23610 |
|
47 |
A preliminary assessment of skate populations in Subarea 48.3 using a surplus production model implemented in a Bayesian framework was presented in 2007 (WG-SAM-07/11), at which time it was considered that there were insufficient data to inform the assessment. Nevertheless, these preliminary results suggested that the by-catch limit in Subarea 48.3 for rajids would be considered sustainable.
A skate tagging program has been under way since 2006 in Subarea 48.3 and a preliminary assessment of skates in Subarea 48.3 using tagging data was presented in 2014 (WG-FSA-14/48). This assessment indicated a stable biomass. Using the same skate tagging programme, a stock status and population assessment of the Antarctic starry skate (Amblyraja georgiana) in Subarea 48.3 was presented in 2018 (WG-FSA-18/27). These results indicated that the longline fishery for toothfish does not appear to have resulted in a decline in the population of A. georgiana and at present has low by-catch rates of exploitation.
Recent genetic analysis of skates (Amblyraja spp.) (WG-FSA-18/73) suggests that skates caught as by-catch from CCAMLR subareas 48.3 and 48.4 that were identified as A. georgiana, A. georgiana sp. anon and A. taaf do not represent distinct, reproductively isolated species. Rather, these different morphological forms of Amblyraja appear to be interbreeding members from two geographically differentiated stocks, one occurring around South Georgia and the other around the South Sandwich Islands (Subarea 48.4).
As Conservation Measure 22-06 does not apply to this subarea there are no CCAMLR VMEs or VME Risk Areas designated in Subarea 48.3. There are fishery-specific restrictions in place to mitigate the impact of the fishery on vulnerable marine ecosystems (VMEs), including benthic communities and benthos such as seamounts, hydrothermal vents and cold-water corals.
A summary of seabird mortality in the longline fishery in Subarea 48.3 in recent years is shown in Table 3. The three most common species injured or killed in the fishery since 2005 were southern giant petrel (Macronectes giganteus), white-chinned petrel (Procellaria aequinoctialis) and black-browed albatross (Thalassarche melanophris).
The requirements of Conservation Measure 25-02 ‘Minimisation of the incidental mortality of birds in the course of longline fishing or longline fishing research in the Convention Area’ apply to this fishery in addition to the seasonal closure and the night-setting requirements described in Conservation Measure 41-02.
The risk level in this fishery in Subarea 48.3 is category 5 (high) (SC CAMLR-XXX, Annex 8, paragraph 8.1).
Season | Macronectes giganteus | Procellaria aequinoctialis | Thalassarche melanophris | Other |
---|---|---|---|---|
1992 | 4 | |||
1995 | 122 | 597 | 39 | 176 |
1996 | 5 | 102 | 297 | 291 |
1997 | 13 | 198 | 253 | 122 |
1998 | 37 | 8 | 6 | |
1999 | 1 | 42 | 62 | 5 |
2000 | 1 | 1 | ||
2001 | 1 | |||
2003 | 2 | 1 | 1 | |
2004 | 1 | |||
2005 | 1 | |||
2009 | 1 | 1 | ||
2010 | 2 | |||
2011 | 1 | |||
2012 | 1 | 1 | ||
2013 | 1 | 1 | ||
2014 | 77 | |||
2015 | 1 | |||
2016 | 30 | |||
2017 | 19 | 1 | ||
2018 | 1 | 22 | 1 | 1 |
2019 | 1 | |||
2020 | 1 |
A summary of mammal mortalities associated with longline fishing in Subarea 48.3 is given in Table 4.
Season | Arctocephalus gazella | Hydrurga leptonyx | Leptonychotes weddellii | Mirounga leonina | Otariidae, Phocidae | Physeter catodon |
---|---|---|---|---|---|---|
1995 | 1 | |||||
1996 | 1 | 1 | ||||
1997 | 3 | |||||
1998 | 1 | |||||
2004 | 1 | |||||
2007 | 2 | |||||
2009 | 1 | 1 | ||||
2012 | 1 | |||||
2014 | 1 |
There has been no reported evidence of IUU fishing activities in Subarea 48.3 since 2006 (Table 1).
The collection of biological data is conducted in accordance to Conservation Measure 23-05. The collection of biological data as part of the CCAMLR Scheme of International Scientific Observation (SISO) includes representative samples of length, weight, sex and maturity stage, as well as collection of otoliths for age determination of the target and most frequently taken by-catch species.
Recent length frequency distributions for catches of D. eleginoides in Subarea 48.3 are shown in Figure 2. These length frequency distributions are unweighted; they have not been adjusted for factors such as the size of the catches from which they were collected. The interannual variability exhibited in the figure may reflect changes in the fished population but is also likely to reflect changes in the gear used, the number of vessels in the fishery and the spatial and temporal distributions of fishing.
Tagging of D. eleginoides is conducted at a rate of 1.3 fish per tonne in this fishery; a total of 60971 D. eleginoides have been tagged and released and 10836 have been recaptured, 10124 of which were released in this area (Table 5).
Season | Tagged | 2004 | 2005 | 2006 | 2007 | 2008 | 2009 | 2010 | 2011 | 2012 | 2013 | 2014 | 2015 | 2016 | 2017 | 2018 | 2019 | 2020 | Total |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
2004 | 3218 | 25 | 97 | 129 | 116 | 109 | 51 | 36 | 31 | 16 | 4 | 16 | 9 | 9 | 6 | 6 | 2 | 3 | 665 |
2005 | 3949 | 23 | 194 | 155 | 148 | 121 | 86 | 45 | 24 | 39 | 26 | 17 | 19 | 25 | 11 | 10 | 5 | 948 | |
2006 | 4889 | 31 | 227 | 197 | 146 | 132 | 73 | 51 | 52 | 43 | 20 | 13 | 22 | 16 | 12 | 12 | 1047 | ||
2007 | 4782 | 41 | 239 | 172 | 139 | 82 | 64 | 56 | 51 | 36 | 21 | 30 | 17 | 16 | 14 | 978 | |||
2008 | 4632 | 61 | 235 | 150 | 107 | 81 | 79 | 69 | 48 | 49 | 43 | 35 | 38 | 14 | 1009 | ||||
2009 | 3506 | 19 | 138 | 71 | 67 | 66 | 60 | 52 | 32 | 40 | 22 | 29 | 16 | 612 | |||||
2010 | 2966 | 12 | 72 | 62 | 48 | 55 | 39 | 40 | 32 | 19 | 17 | 17 | 413 | ||||||
2011 | 2909 | 18 | 98 | 89 | 81 | 64 | 59 | 48 | 32 | 42 | 25 | 556 | |||||||
2012 | 3027 | 19 | 118 | 98 | 79 | 73 | 53 | 37 | 33 | 36 | 546 | ||||||||
2013 | 3356 | 17 | 126 | 89 | 93 | 90 | 53 | 63 | 37 | 568 | |||||||||
2014 | 3563 | 34 | 126 | 129 | 106 | 72 | 70 | 48 | 585 | ||||||||||
2015 | 3718 | 15 | 170 | 143 | 98 | 119 | 83 | 628 | |||||||||||
2016 | 3515 | 35 | 194 | 111 | 107 | 109 | 556 | ||||||||||||
2017 | 3486 | 41 | 169 | 140 | 127 | 477 | |||||||||||||
2018 | 3381 | 27 | 154 | 119 | 300 | ||||||||||||||
2019 | 3159 | 24 | 169 | 193 | |||||||||||||||
2020 | 2915 | 43 | 43 | ||||||||||||||||
Total | 60971 | 10124 |
In January-February 2019, the UK undertook a random stratified bottom trawl survey of South Georgia and Shag Rocks (see WG-FSA-2019/20). The survey used the same trawl gear and survey design as previous UK surveys in Subarea 48.3 (see WG-FSA-15/26 and WG-FSA-17/44). The 2019 survey covered the whole shelf area, covering depths of 100-350m. The primary aim of the survey was to estimate stocks of mackerel icefish (Champsocephalus gunnari) but juvenile D. eleginoides were also captured. Numbers and lengths of D. eleginoides provide an index of recruitment for stock assessments.
Dissostichus eleginoides were caught in 28 of the 73 hauls in the 2019 survey and were, as in previous surveys, present in greatest numbers around the eastern and western ends of the Shag Rocks shelf. Toothfish ranged in length from 18 to 117 cm, with evidence of a 1+ cohort with a mode at 18-26 cm.
All toothfish vessels in Subarea 48.3 carry a CCAMLR scientific observer who collects a range of data on toothfish and common by-catch, including conversion factors, length frequencies, weights and maturity. Toothfish otoliths are collected by observers for an ageing program that provides length-at-age data for assessments. Observers also record whale occurrence at the vessel during hauling; data which is then used to model depredation rates which are included in the stock assessment. Observers work with vessels to tag toothfish and skates and collate recapture data.
Dissostichus eleginoides in Subarea 48.3 are genetically distinct from those found on the Patagonian shelf (FAO Area 41). The stock, occurring within Management Areas A, B and C, is genetically separate from fish taken in the extreme north and west of Subarea 48.3 and the assessments consider only the stock within Management Areas A, B and C (further details of the stock assessment are provided in the Stock Assessment Annex).
Assessment of the Patagonian toothfish (D. eleginoides) in Subarea 48.3 indicates that the current status of the stock is at 50% of B0. Spawning biomass has been relatively constant in recent years (WG-FSA-19/28).
The stock of D. eleginoides in Subarea 48.3 was assessed using an age-structured, two-fleet, CASAL integrated stock assessment model (WG-FSA-19/28).
Assessments are reviewed biennially, the last assessment was in 2019.
A recent summary of the potential impacts of climate change on Southern Ocean fisheries (FAO 2018) highlights the following key points:
The Antarctic region is characterized by complex interaction of natural climate variability and anthropogenic climate change that produce high levels of variability in both physical and biological systems, including impacts on key fishery taxa such as Antarctic krill.
The impact of anthropogenic climate change in the short-term could be expected to be related to changes in sea ice and physical access to fishing grounds, whereas longer-term implications are likely to include changes in ecosystem productivity affecting target stocks.
There are no resident human populations or fishery-dependent livelihoods in the Commission for the Conservation of Antarctic Marine Living Resources (CCAMLR) Area, therefore climate change will have limited direct implications for regional food security. However, as an “under-exploited” fishery, there is potential for krill to play a role in global food security in the longer term.
The institutional and management approach taken by CCAMLR, including the ecosystem-based approach, the establishment of large marine protected areas, and scientific monitoring programmes, provides measures of resilience to climate change.
There is no formal evaluation of the impacts of climate change and environmental variability available for this particular fishery.