| Year | Iceland_Winter | Norway_Winter | Faroes_Winter | Greenland_Winter | Total_Winter | Iceland_Sum.Aut | Norway_Sum.Aut | Faroes_Sum.Aut | Greenland_Sum.Aut | EU_Sum.Aut | Total_Sum.Aut | Total |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1964 | 8.6 | 0.0 | 0.0 | 0.0 | 8.6 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 8.6 |
| 1965 | 49.7 | 0.0 | 0.0 | 0.0 | 49.7 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 49.7 |
| 1966 | 124.5 | 0.0 | 0.0 | 0.0 | 124.5 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 124.5 |
| 1967 | 97.2 | 0.0 | 0.0 | 0.0 | 97.2 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 97.2 |
| 1968 | 78.1 | 0.0 | 0.0 | 0.0 | 78.1 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 78.1 |
| 1969 | 170.6 | 0.0 | 0.0 | 0.0 | 170.6 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 170.6 |
| 1970 | 190.8 | 0.0 | 0.0 | 0.0 | 190.8 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 190.8 |
| 1971 | 182.9 | 0.0 | 0.0 | 0.0 | 182.9 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 182.9 |
| 1972 | 276.5 | 0.0 | 0.0 | 0.0 | 276.5 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 276.5 |
| 1973 | 440.9 | 0.0 | 0.0 | 0.0 | 440.9 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 440.9 |
| 1974 | 461.9 | 0.0 | 0.0 | 0.0 | 461.9 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 461.9 |
| 1975 | 457.1 | 0.0 | 0.0 | 0.0 | 457.1 | 3.1 | 0.0 | 0.0 | 0.0 | 0.0 | 3.1 | 460.2 |
| 1976 | 338.7 | 0.0 | 0.0 | 0.0 | 338.7 | 114.4 | 0.0 | 0.0 | 0.0 | 0.0 | 114.4 | 453.1 |
| 1977 | 549.2 | 0.0 | 24.3 | 0.0 | 573.5 | 259.7 | 0.0 | 0.0 | 0.0 | 0.0 | 259.7 | 833.2 |
| 1978 | 468.4 | 0.0 | 36.2 | 0.0 | 504.6 | 497.5 | 154.1 | 3.4 | 0.0 | 0.0 | 655.0 | 1159.6 |
| 1979 | 521.7 | 0.0 | 18.2 | 0.0 | 539.9 | 442.0 | 124.0 | 22.0 | 0.0 | 0.0 | 588.0 | 1127.9 |
| 1980 | 392.1 | 0.0 | 0.0 | 0.0 | 392.1 | 367.4 | 118.7 | 24.2 | 0.0 | 17.3 | 527.6 | 919.7 |
| 1981 | 156.0 | 0.0 | 0.0 | 0.0 | 156.0 | 484.6 | 91.4 | 16.2 | 0.0 | 20.8 | 613.0 | 769.0 |
| 1982 | 13.2 | 0.0 | 0.0 | 0.0 | 13.2 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 13.2 |
| 1983 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 133.4 | 0.0 | 0.0 | 0.0 | 0.0 | 133.4 | 133.4 |
| 1984 | 439.6 | 0.0 | 0.0 | 0.0 | 439.6 | 425.2 | 104.6 | 10.2 | 0.0 | 8.5 | 548.5 | 988.1 |
| 1985 | 348.5 | 0.0 | 0.0 | 0.0 | 348.5 | 644.8 | 193.0 | 65.9 | 0.0 | 16.0 | 919.7 | 1268.2 |
| 1986 | 341.8 | 50.0 | 0.0 | 0.0 | 391.8 | 552.5 | 149.7 | 65.4 | 0.0 | 5.3 | 772.9 | 1164.7 |
| 1987 | 500.6 | 59.9 | 0.0 | 0.0 | 560.5 | 311.3 | 82.1 | 65.2 | 0.0 | 0.0 | 458.6 | 1019.1 |
| 1988 | 600.6 | 56.6 | 0.0 | 0.0 | 657.2 | 311.4 | 11.5 | 48.5 | 0.0 | 0.0 | 371.4 | 1028.6 |
| 1989 | 609.1 | 56.0 | 0.0 | 0.0 | 665.1 | 53.9 | 52.7 | 14.4 | 0.0 | 0.0 | 121.0 | 0.0 |
| 1990 | 612.0 | 62.5 | 12.3 | 0.0 | 686.8 | 83.7 | 21.9 | 5.6 | 0.0 | 0.0 | 111.2 | 798.0 |
| 1991 | 202.4 | 0.0 | 0.0 | 0.0 | 202.4 | 56.0 | 0.0 | 0.0 | 0.0 | 0.0 | 56.0 | 258.4 |
| 1992 | 573.5 | 47.6 | 0.0 | 0.0 | 621.1 | 213.4 | 65.3 | 18.9 | 0.5 | 0.0 | 298.1 | 919.2 |
| 1993 | 489.1 | 0.0 | 0.0 | 0.5 | 489.6 | 450.0 | 127.5 | 23.9 | 10.2 | 0.0 | 611.6 | 1101.2 |
| 1994 | 550.3 | 15.0 | 0.0 | 1.8 | 567.1 | 210.7 | 99.0 | 12.3 | 2.1 | 0.0 | 324.1 | 891.2 |
| 1995 | 539.4 | 0.0 | 0.0 | 0.4 | 539.8 | 175.5 | 28.0 | 0.0 | 2.2 | 0.0 | 205.7 | 745.5 |
| 1996 | 707.9 | 0.0 | 10.0 | 5.7 | 723.6 | 474.3 | 206.0 | 17.6 | 15.0 | 60.9 | 773.8 | 1497.4 |
| 1997 | 774.9 | 0.0 | 16.1 | 6.1 | 797.1 | 536.0 | 153.6 | 20.5 | 6.5 | 47.1 | 763.6 | 1561.5 |
| 1998 | 457.0 | 0.0 | 14.7 | 9.6 | 481.3 | 290.8 | 72.9 | 26.9 | 8.0 | 41.9 | 440.5 | 921.8 |
| 1999 | 607.8 | 14.8 | 13.8 | 22.5 | 658.9 | 83.0 | 11.4 | 6.0 | 2.0 | 0.0 | 102.4 | 761.3 |
| 2000 | 761.4 | 14.9 | 32.0 | 22.0 | 830.3 | 126.5 | 80.1 | 30.0 | 7.5 | 21.0 | 265.1 | 1095.4 |
| 2001 | 767.2 | 0.0 | 10.0 | 29.0 | 806.2 | 150.0 | 106.0 | 12.0 | 9.0 | 17.0 | 294.0 | 1061.2 |
| 2002 | 901.0 | 0.0 | 28.0 | 26.0 | 955.0 | 180.0 | 118.7 | 0.0 | 13.0 | 28.0 | 339.7 | 1294.7 |
| 2003 | 585.0 | 0.0 | 40.0 | 23.0 | 648.0 | 96.5 | 78.0 | 3.5 | 2.5 | 18.0 | 198.5 | 846.5 |
| 2004 | 478.8 | 15.8 | 30.8 | 17.5 | 542.9 | 46.0 | 34.0 | 0.0 | 12.0 | 0.0 | 92.0 | 634.9 |
| 2005 | 594.1 | 69.0 | 19.0 | 10.0 | 692.0 | 9.0 | 0.0 | 0.0 | 0.0 | 0.0 | 9.0 | 701.1 |
| 2006 | 193.0 | 8.0 | 30.0 | 7.0 | 238.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 238.0 |
| 2007 | 307.0 | 38.0 | 19.0 | 12.8 | 376.8 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 376.8 |
| 2008 | 149.0 | 37.6 | 10.1 | 6.7 | 203.4 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 203.4 |
| 2009 | 15.1 | 0.0 | 0.0 | 0.0 | 15.1 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 15.1 |
| 2010 | 110.6 | 28.3 | 7.7 | 4.7 | 150.7 | 5.4 | 0.0 | 0.0 | 0.0 | 0.0 | 5.4 | 156.1 |
| 2011 | 321.8 | 30.8 | 19.5 | 13.1 | 385.2 | 8.4 | 58.5 | 0.0 | 5.2 | 0.0 | 72.1 | 457.3 |
| 2012 | 576.2 | 46.2 | 29.7 | 22.3 | 674.4 | 9.0 | 0.0 | 0.0 | 1.0 | 0.0 | 10.0 | 684.4 |
| 2013 | 454.0 | 40.0 | 30.0 | 17.0 | 541.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 541.0 |
| 2014 | 111.4 | 6.2 | 8.0 | 16.1 | 141.7 | 0.0 | 30.5 | 0.0 | 5.3 | 9.7 | 45.5 | 187.2 |
| 2015 | 353.6 | 50.6 | 29.9 | 37.9 | 471.9 | 0.0 | 0.0 | 0.0 | 2.5 | 0.0 | 2.5 | 474.4 |
| 2016 | 101.1 | 58.2 | 8.5 | 3.3 | 171.1 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 171.1 |
| 2017 | 196.8 | 60.4 | 15.0 | 27.4 | 299.8 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 299.8 |
| 2018 | 186.3 | 74.5 | 14.3 | 11.4 | 286.5 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 286.5 |
| 2019 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| 2020 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| 2021 | 67.0 | 49.4 | 6.4 | 6.6 | 129.4 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| 2022 | 433.8 | 122.3 | 29.5 | 26.6 | 612.1 | 4.3 | 0.0 | 0.0 | 0.6 | 0.0 | 4.9 | 617.0 |
| 2023 | 325.7 | 50.4 | 22.8 | 46.3 | 445.2 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| 2024 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| 2025 | 5.5 | 0.0 | 0.8 | 3.0 | 9.4 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 9.4 |
| 2026 | 151.8 | 0.0 | 9.0 | 29.3 | 190.1 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
Key signals
The size of the capelin stock and the catches have fluctuated between years and reflect the size of the incoming cohort at any given time. Since changes occurred in the stock’s nursery and feeding grounds around 2000, both stock size and catches have generally been smaller.
Recruitment of the 2024 year class is estimated to be large, with an index of 118.7 billion juvenile capelin in the autumn survey 2025, the 5th largest recruitment on record.
The capelin initial TAC for the 2026/2027 fishing year is advised not to exceed 358 044 tonnes when following the harvest control rule. This advice is based on acoustic measurements of the immature part of the stock in the autumn.
The autumn survey in 2025 was able to cover the main areas of the stock.
General information
The capelin is a small pelagic schooling fish. It is a cold-water species that inhabits arctic and subarctic waters in the North Atlantic and North Pacific. Capelin in the Iceland-East Greenland-Jan Mayen area (IEGJM) is considered to be a single stock, and is denoted hereafter as the IEGJM capelin stock.
Fisheries of capelin began in Iceland in the mid-1960s. Besides being commercially important, capelin is a key species in the marine ecosystem off Iceland. It feeds on small zooplankton, especially copepods but also amphipods and krill. It is also itself an important food for cod, saithe, haddock, halibut and other commercial fish, as well as for whales and seabirds. Thus, capelin is an important link in the transfer of energy and nutrients to the upper levels of the food web. The preferred temperature for capelin is usually 1-3°C during its feeding migration and it is then often at the southern extent of cold Arctic water. When adult capelin migrate from the feeding areas far north of Iceland, east and southeast of Greenland, they are mainly considered to approach the shelf break north of Iceland and then migrate clockwise around the island. Part of the main migration continues all the way towards the coast west of Iceland. Spawning takes place in shallow water in March-April in relatively warm seas along the south and southwest coast of the country. Spawning has also been observed in coastal areas north of Iceland but the extent of that spawning has been considered small compared to the number that spawns in the south. The majority of capelin dies after spawning, usually at the age of 3 years, although mainly females may survive spawning (Christiansen et al., 2008). The migrations of capelin contribute to a huge transfer of energy into the ecosystem of the Icelandic continental shelf. Larvae and juveniles drift clockwise along the continental shelf north and east of Iceland and in variable quantities towards the Denmark Strait and to the shelf of East Greenland. Nursery grounds of capelin are in the waters north of Iceland and increasingly on the continental shelf of East Greenland since the early 2000s (Bardarson et al., 2021; Singh et al., 2023).
Fishery
Landing trends
Landings of capelin in the IEGJM area have fluctuated since the start of the fishery in the mid-1960s, with peaks in the late 1990s and early 2000s, followed by a marked decline in the mid-2000s. The catch from the IEGJM capelin stock in the 2025/2026 fishing season was 190 086 tonnes. The total historical catch of the stock is shown in Figure 1 by season and by country in Figure 2.
Spatial distribution of the catch
The distribution of the catches of the Icelandic fishing fleet by year can be seen in Figure 3.
Historically, most of the catch has been taken with purse seines, but a variable amount has been taken with pelagic trawl throughout the fishing seasons, depending on the size of the TAC and when it is issued. Discards have been considered negligible. The catches in 2025/26 were taken 98% by purse seine and by 2% by pelagic trawls.
Capelin catches with pelagic trawl are concentrated along the northern, northeastern coast, and eastern shelf break of Iceland. Pelagic trawl catches are distributed more broadly in the areas off the shelf break, while purse seine catches are distributed in an narrower strip extending from the offshore southeast onto the shelf and near the coast from southeast to southwest and west of Iceland (Figure 5). In 2026, catches were mostly confined to a narrow shallow coastal strip extending from the southeast and almost continuously into Breiðafjörður, west of Iceland (Figure 3).
Total catches peaked in the late 1990s, reaching over 1200 thous. tonnes, followed by a marked decline from around 2002 to 2010, coinciding with periods of low stock biomass (Figure 6). Catches reported in the logbooks of the Icelandic fleet show a clear spatial pattern in fishing activity. The proportional contribution of catches across spatial areas displayed high interannual variability throughout the period 1990 to 2026, with no single area maintaining consistent dominance until 2005. After 2005, a notable shift was observed with the western area increasingly accounting for a larger proportion of total catches, suggesting a redistribution of fishing activities (Figure 6). During periods of high stock abundance (late 1990s), catches were more widely distributed across regions, whereas during low-biomass periods, catches became increasingly concentrated in fewer core fishing areas in the west and southwest (Figure 6).
Seasonally, most catches occur between January and April (Figure 7). Purse seine has historically dominated the catch, though the relative contribution of pelagic trawl has fluctuated, peaking at 50% in the mid-2000s and again at 65% in the mid-2020s, and the relative contribution has decreased in recent years (Figure 8).
Fleet size and fishing effort
The vessels in the capelin fishery use either purse seine or pelagic trawl. The TAC and when it is used affect the decision on which gear type to deploy; a later date of issue and lower quota reduce the probability of pelagic trawl being used.
The number of vessels accounting for 95% of annual capelin landings declined from around 40 during the 1993-2004 period, despite a notable increase in total catch (Figure 9). Between 2000 and 2009, vessel numbers declined further to below 20, in line with reduced catches. After a temporary increase during 2009- 2014, the number of vessels accounting for 95% of annual capelin landings has since decreased to around 10, reaching a historical low by 2025 (Figure 9).
As noted in the WKCAPELIN benchmark (ICES, 2023), catch per unit effort is not considered a reliable index of abundance for capelin, as catch rates are strongly influenced by capelin’s tendency to form dense schools (which inflates catch efficiency whenever a school is encountered), as well as by the ability of vessels to actively target known aggregations, and by quota constraints and fleet gear types. Acoustic survey indices remain the primary basis for stock assessment and management advice.
Table 2 summarizes the landing of the capelin fishery by gear type and year.
| Year | Other Vessel (number) | Other Vessel Catch (th. t) | Purse seine (number) | Purse seine Catch (th. t) | Pelagic trawl (number) | Pelagic trawl Catch (th. t) | Total Catch (th. t) |
|---|---|---|---|---|---|---|---|
| 2001 | 0 | 68.8 | 165 | 815.1 | 29 | 115.0 | 998.9 |
| 2002 | 2 | 141.9 | 146 | 846.7 | 59 | 239.4 | 1228.0 |
| 2003 | 0 | 210.9 | 107 | 371.4 | 63 | 319.6 | 901.9 |
| 2004 | 0 | 9.9 | 94 | 367.5 | 50 | 157.0 | 534.4 |
| 2005 | 1 | 0.0 | 90 | 414.5 | 57 | 190.0 | 604.5 |
| 2006 | 0 | 0.0 | 50 | 165.1 | 30 | 23.4 | 188.5 |
| 2007 | 1 | 0.0 | 64 | 258.8 | 34 | 50.5 | 309.3 |
| 2008 | 1 | 1.8 | 46 | 122.3 | 19 | 24.9 | 149.0 |
| 2009 | 0 | 0.0 | 15 | 15.1 | 0 | 0.0 | 15.1 |
| 2010 | 0 | 0.0 | 48 | 113.2 | 4 | 3.2 | 116.4 |
| 2011 | 1 | 51.7 | 64 | 250.9 | 22 | 79.5 | 382.1 |
| 2012 | 0 | 86.9 | 65 | 392.3 | 44 | 197.5 | 676.7 |
| 2013 | 1 | 23.7 | 50 | 335.6 | 30 | 121.3 | 480.6 |
| 2014 | 0 | 0.5 | 39 | 91.9 | 18 | 20.3 | 112.7 |
| 2015 | 0 | 0.0 | 55 | 309.7 | 19 | 44.7 | 354.4 |
| 2016 | 0 | 0.0 | 34 | 96.6 | 4 | 5.4 | 102.0 |
| 2017 | 0 | 0.0 | 42 | 197.9 | 0 | 0.0 | 197.9 |
| 2018 | 0 | 0.0 | 37 | 117.3 | 17 | 71.6 | 188.9 |
| 2021 | 0 | 0.0 | 34 | 69.5 | 21 | 77.9 | 147.4 |
| 2022 | 0 | 0.0 | 46 | 202.1 | 49 | 249.2 | 451.3 |
| 2023 | 0 | 325.7 | 46 | 320.6 | 6 | 5.2 | 651.5 |
| 2025 | 0 | 0.0 | 9 | 5.6 | 0 | 0.0 | 5.6 |
| 2026 | 0 | 0.0 | 37 | 150.9 | 2 | 1.0 | 151.9 |
Cohort composition and mean weight at age
Sampling of catches spans cohorts from birth years 1961-2024, reflecting the capelin age composition in the fishery (Figure 10). In recent years, catches appear to consist of a narrower range of cohorts because the fishery is mainly conducted between January and April, and autumn fishery is becoming less common. These analyses reflect the selectivity of the fishery, and may not be representative of the overall population age structure, as the fishery is highly selective for certain age classes, and possibly targeting the larger, older individuals.
The number of fish sampled per year increased from the 1980s, peaking in the mid-1990s, consistent with the period of highest catches (Figure 10). Sampling declined substantially after the 2000s, with further reductions during periods of low stock size. Cohorts vary across years, reflecting high interannual variability in recruitment strength and the small size of some year classes.
Mean weight at age deviates notably from the overall mean across cohorts and ages, indicating considerable variability in individual growth among year classes (Figure 11). Variability increases with age, with some cohorts showing deviations exceeding 5 - 10 g. After the 2000s, the mean weight at older ages (3 to 5) appears to be above the long-term average.
Total catch in numbers (billions) and weight (thous. tonnes) in autumn and winter is given in Table 3 and Table 4, respectively.
| Year | Age 1 | Age 2 | Age 3 | Age 4 | Age 5 | Total number | Total weight |
|---|---|---|---|---|---|---|---|
| 1985 | 0.8 | 25.6 | 15.4 | 0.2 | 0.0 | 42.0 | 919.7 |
| 1986 | 0.0 | 10.0 | 23.3 | 0.5 | 0.0 | 33.8 | 772.9 |
| 1987 | 0.0 | 27.7 | 6.7 | 0.0 | 0.0 | 34.4 | 458.6 |
| 1988 | 0.3 | 13.6 | 5.4 | 0.0 | 0.0 | 19.3 | 371.4 |
| 1989 | 1.7 | 6.0 | 1.5 | 0.0 | 0.0 | 9.2 | 121.0 |
| 1990 | 0.8 | 5.9 | 1.0 | 0.0 | 0.0 | 7.7 | 111.2 |
| 1991 | 0.3 | 2.7 | 0.4 | 0.0 | 0.0 | 3.4 | 56.0 |
| 1992 | 1.7 | 14.0 | 2.1 | 0.0 | 0.0 | 17.8 | 298.1 |
| 1993 | 0.2 | 24.9 | 5.4 | 0.2 | 0.0 | 30.7 | 611.6 |
| 1994 | 0.6 | 15.0 | 2.8 | 0.0 | 0.0 | 18.4 | 324.1 |
| 1995 | 1.5 | 9.7 | 1.1 | 0.0 | 0.0 | 12.3 | 205.7 |
| 1996 | 0.2 | 25.2 | 12.7 | 0.2 | 0.0 | 38.4 | 773.7 |
| 1997 | 1.8 | 33.4 | 10.2 | 0.4 | 0.0 | 45.8 | 763.6 |
| 1998 | 0.9 | 25.1 | 2.9 | 0.0 | 0.0 | 28.9 | 440.5 |
| 1999 | 0.3 | 4.7 | 0.7 | 0.0 | 0.0 | 5.7 | 102.4 |
| 2000 | 0.2 | 12.9 | 3.3 | 0.1 | 0.0 | 16.5 | 265.1 |
| 2001 | 0.0 | 17.6 | 1.2 | 0.0 | 0.0 | 18.8 | 294.0 |
| 2002 | 0.0 | 18.3 | 2.5 | 0.0 | 0.0 | 20.8 | 339.7 |
| 2003 | 0.3 | 11.8 | 1.0 | 0.0 | 0.0 | 14.3 | 199.5 |
| 2004 | 0.0 | 5.3 | 0.5 | 0.0 | 0.0 | 5.8 | 92.0 |
| 2005 | 0.0 | 0.4 | 0.0 | 0.0 | 0.0 | 0.4 | 9.0 |
| 2006 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| 2007 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| 2008 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| 2009 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| 2010 | 0.0 | 0.2 | 0.0 | 0.0 | 0.0 | 0.2 | 5.4 |
| 2011 | 0.0 | 2.5 | 1.6 | 0.0 | 0.1 | 4.1 | 72.1 |
| 2012 | 0.0 | 0.2 | 0.2 | 0.0 | 0.0 | 0.4 | 10.4 |
| 2013 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| 2014 | 0.0 | 2.2 | 0.6 | 0.0 | 0.0 | 2.8 | 45.5 |
| 2015 | 0.0 | 0.1 | 0.0 | 0.0 | 0.0 | 1.4 | 2.5 |
| 2016 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| 2017 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| 2018 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| 2019 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| 2020 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| 2021 | 0.0 | 2.6 | 0.6 | 0.0 | 0.0 | 4.2 | 77.1 |
| 2022 | 0.0 | 0.0 | 0.1 | 0.0 | 0.0 | 0.2 | 4.9 |
| 2023 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| 2024 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| 2025 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| 2026 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| Year | Age 1 | Age 2 | Age 3 | Age 4 | Age 5 | Total number | Total weight |
|---|---|---|---|---|---|---|---|
| 1986 | 0 | 0.1 | 9.8 | 6.9 | 0.2 | 17.0 | 391.8 |
| 1987 | 0 | 0.0 | 6.9 | 15.5 | 0.0 | 22.4 | 560.5 |
| 1988 | 0 | 0.0 | 23.4 | 7.2 | 0.3 | 30.9 | 657.2 |
| 1989 | 0 | 0.1 | 22.9 | 7.8 | 0.0 | 30.8 | 665.1 |
| 1990 | 0 | 1.4 | 24.8 | 9.6 | 0.1 | 35.9 | 686.8 |
| 1991 | 0 | 0.5 | 7.4 | 1.5 | 0.0 | 9.4 | 202.4 |
| 1992 | 0 | 2.7 | 29.4 | 2.8 | 0.0 | 34.9 | 621.1 |
| 1993 | 0 | 0.2 | 20.1 | 2.5 | 0.0 | 22.8 | 489.6 |
| 1994 | 0 | 0.6 | 22.7 | 3.9 | 0.0 | 27.2 | 567.1 |
| 1995 | 0 | 1.3 | 17.6 | 5.9 | 0.0 | 24.8 | 539.8 |
| 1996 | 0 | 0.6 | 27.4 | 7.7 | 0.0 | 35.7 | 723.6 |
| 1997 | 0 | 0.9 | 29.1 | 11.0 | 0.0 | 41.0 | 797.6 |
| 1998 | 0 | 0.3 | 20.4 | 5.4 | 0.0 | 26.1 | 481.3 |
| 1999 | 0 | 0.5 | 31.2 | 7.5 | 0.0 | 39.2 | 658.9 |
| 2000 | 0 | 0.3 | 36.3 | 5.4 | 0.0 | 42.0 | 830.3 |
| 2001 | 0 | 0.4 | 27.9 | 6.7 | 0.0 | 35.0 | 787.2 |
| 2002 | 0 | 0.1 | 33.1 | 4.2 | 0.0 | 37.4 | 955.0 |
| 2003 | 0 | 0.1 | 32.2 | 1.9 | 0.0 | 34.4 | 648.0 |
| 2004 | 0 | 0.6 | 24.6 | 3.0 | 0.0 | 28.3 | 542.9 |
| 2005 | 0 | 0.1 | 31.5 | 3.1 | 0.0 | 34.7 | 692.0 |
| 2006 | 0 | 0.1 | 10.4 | 0.3 | 0.0 | 10.8 | 230.0 |
| 2007 | 0 | 0.3 | 19.5 | 0.5 | 0.0 | 20.3 | 376.8 |
| 2008 | 0 | 0.5 | 10.6 | 0.4 | 0.0 | 11.5 | 202.4 |
| 2009 | 0 | 0.1 | 0.6 | 0.1 | 0.0 | 0.7 | 15.1 |
| 2010 | 0 | 0.7 | 5.3 | 0.9 | 0.0 | 6.9 | 150.7 |
| 2011 | 0 | 0.1 | 16.2 | 0.6 | 0.0 | 17.0 | 385.2 |
| 2012 | 0 | 0.6 | 25.0 | 6.1 | 0.0 | 31.8 | 674.4 |
| 2013 | 0 | 0.3 | 12.1 | 9.7 | 0.2 | 22.3 | 541.0 |
| 2014 | 0 | 0.1 | 4.8 | 1.3 | 0.0 | 6.1 | 141.8 |
| 2015 | 0 | 0.3 | 17.5 | 4.7 | 0.1 | 22.7 | 471.9 |
| 2016 | 0 | 0.4 | 5.5 | 2.0 | 0.0 | 8.0 | 171.1 |
| 2017 | 0 | 0.4 | 5.4 | 4.1 | 0.1 | 10.0 | 299.8 |
| 2018 | 0 | 0.6 | 10.4 | 0.9 | 0.0 | 11.9 | 286.5 |
| 2019 | 0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| 2020 | 0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| 2021 | 0 | 0.0 | 4.8 | 0.3 | 0.0 | 5.2 | 129.4 |
| 2022 | 0 | 0.2 | 22.6 | 1.5 | 0.0 | 24.3 | 612.1 |
| 2023 | 0 | 0.0 | 7.9 | 9.2 | 0.1 | 17.2 | 445.2 |
| 2024 | 0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
| 2025 | 0 | 0.0 | 0.3 | 0.0 | 0.0 | 0.3 | 9.3 |
| 2026 | 0 | 0.1 | 6.8 | 0.7 | 0.0 | 7.6 | 190.0 |
Data and Sampling
Commercial data
The sampling coverage from the commercial catches is generally good (Figure 12), with a long time series of biological samples collected from the catches. The samples are collected from purse seine and pelagic trawl catches, with a focus on ensuring representative sampling across different areas and times of the year. The majority of the age proportion of the catches is of age 3 over the past 10 years.
Biological sampling
At least 50 to 100 individuals per sample are processed from the catches for biological analysis, weight, length measurements and gonad weight and maturation stages. The age of the fish is determined by examining otoliths under a microscope, while length measurements are taken using standard measuring millimeter boards. The biological data collected from these samples are crucial for understanding the age structure, and maturation composition of the capelin stock, which in turn informs stock assessments and management decisions. The sampling strategy aims to ensure that the collected data are representative of the overall fisheries locations, covering different areas and times of the year to capture potential spatial and temporal variations in the stock’s biological characteristics.
Table 5 summarizes the number of biological samples, length measurements, and otolith samples by year and gear type (Pelagic Trawl and Purse Seine).
| Year | Number of samples | Length (Purse Seine) | Length (Pelagic Trawl) | Otolith (Purse Seine) | Otolith (Pelagic Trawl) |
|---|---|---|---|---|---|
| 1993 | 95 | 9304 | 0 | 9292 | 0 |
| 1994 | 63 | 6208 | 0 | 6199 | 0 |
| 1995 | 59 | 5900 | 0 | 5898 | 0 |
| 1996 | 85 | 8438 | 0 | 8400 | 0 |
| 1997 | 115 | 10926 | 500 | 10911 | 500 |
| 1998 | 72 | 7196 | 0 | 7176 | 0 |
| 1999 | 54 | 5388 | 0 | 5385 | 0 |
| 2000 | 91 | 9097 | 0 | 8962 | 0 |
| 2001 | 81 | 8096 | 0 | 8078 | 0 |
| 2002 | 67 | 6322 | 0 | 6006 | 0 |
| 2003 | 32 | 3200 | 0 | 3190 | 0 |
| 2004 | 31 | 3100 | 0 | 3092 | 0 |
| 2005 | 20 | 1950 | 0 | 1943 | 0 |
| 2006 | 14 | 1400 | 0 | 1387 | 0 |
| 2007 | 35 | 3402 | 0 | 3268 | 0 |
| 2008 | 29 | 2899 | 0 | 2889 | 0 |
| 2009 | 9 | 814 | 0 | 796 | 0 |
| 2010 | 44 | 4363 | 0 | 4162 | 0 |
| 2011 | 44 | 4359 | 0 | 4350 | 0 |
| 2012 | 25 | 2465 | 0 | 2426 | 0 |
| 2013 | 26 | 2541 | 0 | 2535 | 0 |
| 2014 | 44 | 3942 | 0 | 3940 | 0 |
| 2015 | 61 | 5538 | 200 | 5528 | 200 |
| 2016 | 17 | 1700 | 0 | 1600 | 0 |
| 2017 | 65 | 6105 | 0 | 5982 | 0 |
| 2018 | 57 | 2295 | 2889 | 2062 | 2888 |
| 2020 | 2 | 0 | 200 | 0 | 200 |
| 2021 | 56 | 4276 | 889 | 4123 | 872 |
| 2022 | 100 | 5048 | 4542 | 4805 | 4519 |
| 2023 | 42 | 1470 | 2376 | 1464 | 2370 |
| 2025 | 16 | 74 | 1274 | 74 | 1273 |
| 2026 | 48 | 1798 | 750 | 1174 | 749 |
Survey data
Capelin acoustic assessment surveys
The IEGJM capelin stock has been assessed by acoustics annually since 1978. The surveys have been conducted in autumn (September-December) and in winter (January-February). An overview of the assessment method is given in the International Council for the Exploration of the Seas Northwestern Working Group report stock annex ICES NWWG .
Autumn survey 2025
Autumn surveys are conducted with the aim of assessing both the immature and the maturing part of the stock (Bardarson et al., 2024). Since 2010, the autumn surveys have started in September (and partly in late August), a month earlier than in the preceding years because of difficulties in covering the stock due to drift ice and bad weather during later months at the more north-westerly feeding grounds of the stock since the early 2000s (Vilhjálmsson, 2007).
The 2025 survey was conducted on behalf of the MFRI by the r/v Arni Fridriksson and r/v Tarajoq on behalf of the GINR (Greenland Institute of Natural Resources) (Figure 13). The survey area was on and along the shelf edge off East Greenland from about 64°30´N towards about 72°15´N, also covering the Denmark Strait and the slope off northwest Iceland. The Iceland Sea and Jan Mayen area were only briefly scouted due to time constraints and for the same reason hydrographic measurements and zooplankton sampling were limited due to bad weather conditions. The initial planned survey tracks had to be changed due to stormy weather.
In general, drift ice only limited the coverage of the survey vessels in a few regions although icebergs and a lack of information on bottom topography occasionally affected routes and limited the extent of transects towards the Greenlandic coast (Figure 13).
Maturing capelin was mainly observed outside the Icelandic continental slope North and Northwest of Iceland (between 68-70°N and 20-22°W, see Figure 14). In the western Denmark Strait maturing capelin was mixed with immature capelin, while mainly mature capelin was found further northeast outside of Scoresby Sound. Similar to last year, the distribution of mature capelin did not spread far east of Denmark Strait, remaining close to its eastern margin. Further, no capelin was found near the western part of the Jan Mayen ridge or further north of 71°N. Juveniles (0-group) of various species, including capelin (although not quantified) were observed along the continental shelf north and northwest of Iceland and along the southwestern portion of the Greenlandic shelf. Immature capelin was found along the Greenlandic shelf, dominating in the southwestern part of the survey area and close to the coast along Denmark Strait (Figure 14).
The total capelin biomass estimate was 1 209 thous. tonnes and thereof 417.5 thous. tonnes of mature capelin. The immature part was 791 thous. tonnes or 118.7 billion in number, the 5th largest juvenile index in the time series and indicating that the year class 2024 (spawned in spring 2024) is large. Table 6 gives information on the age-disaggregated numbers and biomass of the capelin total stock.
| Category | Length | age1 | age2 | age3 | age4 | age5 | Total Number | Total Biomass (tonnes) |
|---|---|---|---|---|---|---|---|---|
| Immature | 8.5 | 1165 | 0 | 0 | 0 | 0 | 1165 | 3337 |
| Immature | 9 | 3680 | 0 | 0 | 0 | 0 | 3680 | 11877 |
| Immature | 9.5 | 2939 | 0 | 0 | 0 | 0 | 2939 | 10583 |
| Immature | 10 | 5293 | 0 | 0 | 0 | 0 | 5293 | 21200 |
| Immature | 10.5 | 10316 | 0 | 0 | 0 | 0 | 10316 | 44837 |
| Immature | 11 | 8386 | 0 | 0 | 0 | 0 | 8386 | 40235 |
| Immature | 11.5 | 12052 | 0 | 0 | 0 | 0 | 12052 | 63357 |
| Immature | 12 | 12267 | 0 | 0 | 0 | 0 | 12267 | 71473 |
| Immature | 12.5 | 11810 | 79 | 0 | 0 | 0 | 11890 | 76413 |
| Immature | 13 | 10220 | 79 | 0 | 0 | 0 | 10300 | 71446 |
| Immature | 13.5 | 10512 | 79 | 0 | 0 | 0 | 10591 | 80606 |
| Immature | 14 | 11482 | 316 | 0 | 0 | 0 | 11798 | 97963 |
| Immature | 14.5 | 5111 | 238 | 79 | 0 | 0 | 5429 | 49484 |
| Immature | 15 | 3791 | 477 | 79 | 0 | 0 | 4347 | 43612 |
| Immature | 15.5 | 2648 | 711 | 0 | 0 | 0 | 3359 | 36974 |
| Immature | 16 | 676 | 412 | 0 | 0 | 0 | 1087 | 12572 |
| Immature | 16.5 | 446 | 1027 | 0 | 0 | 0 | 1474 | 17682 |
| Immature | 17 | 446 | 250 | 79 | 0 | 0 | 776 | 10291 |
| Immature | 17.5 | 96 | 397 | 79 | 0 | 0 | 573 | 8589 |
| Immature | 18 | 16 | 430 | 25 | 0 | 0 | 471 | 6807 |
| Immature | 18.5 | 0 | 128 | 159 | 0 | 0 | 287 | 5059 |
| Immature | 19 | 0 | 159 | 0 | 0 | 0 | 159 | 2941 |
| Immature | 19.5 | 0 | 96 | 0 | 0 | 0 | 96 | 1791 |
| Immature | 20 | 0 | 48 | 79 | 0 | 0 | 128 | 2701 |
| Mature | 8.5 | 25 | 0 | 0 | 0 | 0 | 25 | 141 |
| Mature | 9 | 78 | 0 | 0 | 0 | 0 | 78 | 508 |
| Mature | 9.5 | 25 | 0 | 0 | 0 | 0 | 25 | 185 |
| Mature | 10 | 356 | 0 | 0 | 0 | 0 | 356 | 2741 |
| Mature | 10.5 | 329 | 0 | 0 | 0 | 0 | 329 | 2899 |
| Mature | 11 | 530 | 25 | 0 | 0 | 0 | 555 | 5608 |
| Mature | 11.5 | 491 | 126 | 0 | 0 | 0 | 617 | 6727 |
| Mature | 12 | 343 | 178 | 0 | 0 | 0 | 521 | 5919 |
| Mature | 12.5 | 511 | 434 | 79 | 0 | 0 | 1024 | 12946 |
| Mature | 13 | 187 | 665 | 0 | 79 | 0 | 931 | 13104 |
| Mature | 13.5 | 231 | 1079 | 0 | 0 | 0 | 1310 | 19810 |
| Mature | 14 | 157 | 1946 | 105 | 0 | 0 | 2207 | 37769 |
| Mature | 14.5 | 25 | 1651 | 82 | 0 | 0 | 1758 | 32437 |
| Mature | 15 | 0 | 2304 | 89 | 0 | 0 | 2393 | 47764 |
| Mature | 15.5 | 0 | 1404 | 50 | 0 | 0 | 1455 | 32198 |
| Mature | 16 | 0 | 2058 | 119 | 0 | 0 | 2177 | 52370 |
| Mature | 16.5 | 0 | 1168 | 176 | 0 | 0 | 1344 | 34923 |
| Mature | 17 | 0 | 1218 | 278 | 0 | 0 | 1496 | 42556 |
| Mature | 17.5 | 0 | 718 | 213 | 16 | 0 | 948 | 28345 |
| Mature | 18 | 0 | 379 | 113 | 41 | 0 | 533 | 17403 |
| Mature | 18.5 | 0 | 145 | 147 | 0 | 16 | 308 | 10889 |
| Mature | 19 | 0 | 25 | 64 | 0 | 0 | 89 | 3342 |
| Mature | 19.5 | 0 | 0 | 122 | 0 | 0 | 122 | 4867 |
| Mature | 20 | 0 | 0 | 25 | 0 | 0 | 25 | 1257 |
| Immature | Total | 113351 | 4929 | 582 | 0 | 0 | 118861 | 791828 |
| Mature | Total | 3288 | 15522 | 1663 | 137 | 16 | 20626 | 416708 |
Stock weight at age
The historical trend of mean weight of immature 1 to 3 year old capelin during the autumn survey is shown in Figure 15, as well as the trend of the mean weight of the mature capelin at age 1 to 4 year old in Figure 16. The mean weights have generally increased across all age classes since the 2000s. Estimates for the 4 year old age clas of mature capelin are based on few fish and should be interpreted with caution (Figure 16) and therefore exhibit the most variability in mean weight.
Winter surveys 2025/2026
The main objective of the winter surveys is to assess the mature part of the stock using acoustic stock assessment accompanied by pelagic trawl sampling. These surveys are coordinated by MFRI in collaboration with research vessels and commercial vessels normally chartered by MFRI. Scientists from MFRI are normally on board each vessel during the main surveys in January, overseeing and interpreting the acoustic measurements. All participating vessels have calibrated echo sounders, with calibration generally performed shortly before the surveys.
January 2026: exploratory survey
The first winter survey was conducted from 5 to 12 January on the r/v Árni Friðriksson (Figure 17), and was planned as an exploratory survey. The survey tracks were designed to cover strata centred along the east and northeast of Iceland with the objective of evaluating the progression of the capelin migration and assisting with the planning of the larger expedition. During the survey, the majority of the mature capelin (150 thous. tonnes) were found in the north and northeast of Iceland (Figure 17), indicating that the capelin was still in the north and had not migrated southwards. The survey had a relatively high coefficient of variation (CV=0.25) for the mature stock estimate. Table 7 gives information on the age-disaggregated numbers and biomass of the capelin stock components.
| Category | Length | age2 | age3 | age4 | age5 | Total Number | Total Biomass (tonnes) |
|---|---|---|---|---|---|---|---|
| Immature | 8.5 | 0 | 9 | 0 | 0 | 9 | 52 |
| Immature | 9.5 | 19 | 0 | 0 | 0 | 19 | 136 |
| Immature | 10 | 38 | 0 | 0 | 0 | 38 | 317 |
| Immature | 10.5 | 19 | 0 | 0 | 0 | 19 | 159 |
| Immature | 11 | 28 | 0 | 0 | 0 | 28 | 244 |
| Immature | 11.5 | 47 | 0 | 0 | 0 | 47 | 462 |
| Immature | 12 | 38 | 9 | 0 | 0 | 47 | 524 |
| Immature | 12.5 | 57 | 9 | 0 | 0 | 66 | 722 |
| Immature | 13 | 9 | 0 | 0 | 0 | 9 | 111 |
| Immature | 13.5 | 9 | 38 | 0 | 0 | 47 | 630 |
| Immature | 14 | 38 | 28 | 0 | 0 | 66 | 922 |
| Immature | 14.5 | 9 | 47 | 0 | 0 | 57 | 835 |
| Immature | 15 | 0 | 47 | 0 | 0 | 47 | 817 |
| Immature | 15.5 | 0 | 19 | 0 | 0 | 19 | 322 |
| Immature | 16 | 0 | 38 | 9 | 0 | 47 | 848 |
| Immature | 16.5 | 0 | 38 | 0 | 0 | 38 | 740 |
| Immature | 17 | 0 | 38 | 0 | 0 | 38 | 811 |
| Immature | 17.5 | 0 | 9 | 0 | 0 | 9 | 219 |
| Immature | 18.5 | 0 | 9 | 0 | 0 | 9 | 254 |
| Immature | 19 | 0 | 9 | 0 | 0 | 9 | 294 |
| Immature | 20 | 0 | 9 | 0 | 0 | 9 | 287 |
| Mature | 8.5 | 9 | 9 | 0 | 0 | 19 | 106 |
| Mature | 12 | 57 | 19 | 0 | 0 | 76 | 834 |
| Mature | 12.5 | 57 | 104 | 0 | 0 | 161 | 1910 |
| Mature | 13 | 38 | 104 | 0 | 0 | 142 | 1847 |
| Mature | 13.5 | 28 | 351 | 0 | 0 | 379 | 5413 |
| Mature | 14 | 28 | 398 | 0 | 0 | 427 | 6841 |
| Mature | 14.5 | 9 | 417 | 0 | 0 | 427 | 7178 |
| Mature | 15 | 0 | 967 | 9 | 0 | 976 | 18468 |
| Mature | 15.5 | 9 | 758 | 9 | 0 | 777 | 15773 |
| Mature | 16 | 0 | 777 | 38 | 0 | 815 | 17916 |
| Mature | 16.5 | 9 | 645 | 28 | 0 | 682 | 16152 |
| Mature | 17 | 9 | 720 | 66 | 9 | 806 | 20626 |
| Mature | 17.5 | 0 | 474 | 57 | 0 | 531 | 15153 |
| Mature | 18 | 0 | 332 | 47 | 0 | 379 | 11607 |
| Mature | 18.5 | 0 | 171 | 28 | 9 | 209 | 6738 |
| Mature | 19 | 0 | 38 | 9 | 0 | 47 | 1717 |
| Mature | 19.5 | 0 | 19 | 19 | 0 | 38 | 1386 |
| Mature | 20 | 0 | 0 | 9 | 0 | 9 | 338 |
| Immature | Total | 313 | 360 | 9 | 0 | 682 | 9704 |
| Mature | Total | 256 | 6303 | 322 | 19 | 6900 | 150000 |
January 2026: assessment survey
The second winter survey was conducted from 19 to 26 January 2026 on the research vessels Árni Friðriksson and Þórunn Þórðardóttir, and the fishing vessels Barði, Heimaey, and Polar Ammassak (Figure 18). The survey tracks were designed to cover four strata, centered on the east, northeast, north, and northwest of Iceland. During the survey, the majority of mature capelin were found in the north and east of Iceland (Figure 18). The capelin found furthest northwest of Iceland were immature fish. The mature part of the stock was estimated to be 710 800 t (CV=0.24), where about 55% (382 thous. tonnes) was east of Iceland, following the traditional spawning migration clockwise to the area south and west of the country, and about 45% northwest of Iceland (328 thous. tonnes). It was not clear which direction the mature stock component north of Iceland would migrate, and the third survey was conducted to explore that further (see Section 5.3.3). Table 8 gives information on the age and length disaggregated numbers and biomass of the capelin stock.
The capelin distribution in January 2026 had a similar distribution to that in the winter of 2023 (the parents’ generation). In the 2023 advice on fishing opportunities of the parents’ generation, MFRI proposed that in addition to the total catch limit, precaution should be taken to avoid heavy fishing focused solely on the stock component that followed the traditional spawning route east of the country, where fishing tends to be more efficient. MFRI proposed that two-thirds of the catch limit should focus on capelin offshore from Húnaflói (after the February monitoring survey) to prevent local depletion of diversity in mature stock components. Subsequently, this advice was abandoned when it was considered clear that the capelin to the northwest were returning west for spawning.
| Category | Length | age2 | age3 | age4 | age5 | Total Number | Total Biomass (tonnes) |
|---|---|---|---|---|---|---|---|
| Immature | 8.5 | 30 | 0 | 0 | 0 | 30 | 104 |
| Immature | 9 | 30 | 0 | 0 | 0 | 30 | 104 |
| Immature | 9.5 | 50 | 0 | 0 | 0 | 50 | 208 |
| Immature | 10 | 139 | 0 | 0 | 0 | 139 | 695 |
| Immature | 10.5 | 253 | 0 | 0 | 0 | 253 | 1368 |
| Immature | 11 | 265 | 16 | 0 | 0 | 281 | 1704 |
| Immature | 11.5 | 321 | 16 | 0 | 0 | 337 | 2229 |
| Immature | 12 | 392 | 0 | 0 | 0 | 392 | 2903 |
| Immature | 12.5 | 291 | 0 | 0 | 0 | 291 | 2314 |
| Immature | 13 | 378 | 17 | 0 | 0 | 395 | 3451 |
| Immature | 13.5 | 159 | 22 | 0 | 0 | 181 | 1784 |
| Immature | 14 | 171 | 70 | 0 | 0 | 241 | 2620 |
| Immature | 14.5 | 77 | 61 | 0 | 0 | 139 | 1754 |
| Immature | 15 | 70 | 134 | 0 | 0 | 204 | 2763 |
| Immature | 15.5 | 37 | 97 | 17 | 0 | 151 | 2301 |
| Immature | 16 | 1 | 96 | 0 | 0 | 97 | 1552 |
| Immature | 16.5 | 17 | 204 | 16 | 0 | 237 | 3933 |
| Immature | 17 | 0 | 38 | 0 | 0 | 38 | 716 |
| Immature | 17.5 | 0 | 1 | 0 | 0 | 1 | 21 |
| Immature | 18.5 | 0 | 28 | 0 | 0 | 28 | 580 |
| Immature | 20 | 0 | 0 | 17 | 0 | 17 | 534 |
| Mature | 8.5 | 0 | 28 | 0 | 0 | 28 | 177 |
| Mature | 9 | 28 | 0 | 0 | 0 | 28 | 267 |
| Mature | 10 | 116 | 16 | 0 | 0 | 131 | 1216 |
| Mature | 10.5 | 98 | 18 | 0 | 0 | 117 | 1146 |
| Mature | 11 | 173 | 220 | 0 | 0 | 393 | 4282 |
| Mature | 11.5 | 129 | 238 | 0 | 0 | 367 | 4394 |
| Mature | 12 | 76 | 318 | 0 | 0 | 394 | 5056 |
| Mature | 12.5 | 236 | 1101 | 18 | 0 | 1356 | 19296 |
| Mature | 13 | 108 | 964 | 0 | 0 | 1073 | 16443 |
| Mature | 13.5 | 37 | 1578 | 17 | 0 | 1632 | 26826 |
| Mature | 14 | 69 | 3408 | 70 | 0 | 3546 | 63686 |
| Mature | 14.5 | 26 | 2130 | 53 | 0 | 2209 | 43853 |
| Mature | 15 | 34 | 2674 | 49 | 0 | 2758 | 57472 |
| Mature | 15.5 | 55 | 4229 | 162 | 17 | 4463 | 102783 |
| Mature | 16 | 0 | 2617 | 311 | 0 | 2929 | 72043 |
| Mature | 16.5 | 0 | 2713 | 230 | 0 | 2944 | 76341 |
| Mature | 17 | 0 | 2831 | 600 | 17 | 3448 | 98822 |
| Mature | 17.5 | 0 | 1171 | 234 | 0 | 1405 | 42704 |
| Mature | 18 | 0 | 795 | 191 | 0 | 986 | 31916 |
| Mature | 18.5 | 0 | 373 | 280 | 17 | 671 | 22717 |
| Mature | 19 | 0 | 153 | 28 | 0 | 181 | 6623 |
| Mature | 19.5 | 0 | 0 | 235 | 0 | 235 | 8805 |
| Mature | 20 | 0 | 43 | 16 | 0 | 59 | 2478 |
| Immature | Total | 2680 | 801 | 50 | 0 | 3531 | 33638 |
| Mature | Total | 1186 | 27618 | 2495 | 52 | 31350 | 709344 |
February 2026: research survey
A third winter survey was conducted northwest and north of Iceland from 11 to 18 February (Figure 19) on board the r/v Árni Fríðriksson. The main objective of this survey was to investigate the spawning migration and estimate the stock biomass of capelin in the northwest and north of Iceland (Figure 19); this survey was not used in the stock assessment. The survey coverage began west of Dohrnbank with the vessel tracking northward along the slope off the Westfjords all the way to Skagagrunn (Figure 19). Mature capelin were found near the continental slope off Bardagrunn (145 600 t), while immature capelin were found further offshore near the Westfjords, close to drifting sea ice. Almost no capelin was observed north of Skagagrunn.
Table 9 gives information on the age disaggregated numbers and biomass of the capelin stock components.
| Category | Length | age2 | age3 | age4 | Total Number | Total Biomass (tonnes) |
|---|---|---|---|---|---|---|
| Immature | 8.5 | 101 | 0 | 0 | 101 | 416 |
| Immature | 9 | 605 | 0 | 0 | 605 | 2431 |
| Immature | 9.5 | 605 | 0 | 0 | 605 | 2693 |
| Immature | 10 | 1110 | 0 | 0 | 1110 | 5293 |
| Immature | 10.5 | 706 | 0 | 0 | 706 | 3427 |
| Immature | 11 | 1210 | 0 | 0 | 1210 | 6726 |
| Immature | 11.5 | 1311 | 0 | 0 | 1311 | 7518 |
| Immature | 12 | 1210 | 0 | 0 | 1210 | 7803 |
| Immature | 12.5 | 1110 | 0 | 0 | 1110 | 7583 |
| Immature | 13 | 2118 | 101 | 0 | 2219 | 16510 |
| Immature | 13.5 | 1412 | 101 | 0 | 1513 | 12330 |
| Immature | 14 | 2219 | 605 | 0 | 2824 | 24625 |
| Immature | 14.5 | 706 | 101 | 0 | 807 | 7428 |
| Immature | 15 | 1614 | 101 | 0 | 1715 | 17111 |
| Immature | 15.5 | 1009 | 303 | 0 | 1311 | 14022 |
| Immature | 16 | 908 | 605 | 0 | 1513 | 17230 |
| Immature | 16.5 | 504 | 101 | 0 | 605 | 7424 |
| Immature | 17 | 303 | 807 | 0 | 1110 | 13881 |
| Immature | 17.5 | 0 | 504 | 0 | 504 | 7494 |
| Immature | 18 | 202 | 605 | 0 | 807 | 11959 |
| Immature | 18.5 | 101 | 303 | 0 | 403 | 6266 |
| Immature | 19 | 0 | 202 | 0 | 202 | 3286 |
| Immature | 19.5 | 0 | 605 | 0 | 605 | 10801 |
| Immature | 20 | 0 | 101 | 0 | 101 | 2360 |
| Mature | 8.5 | 303 | 202 | 0 | 504 | 4817 |
| Mature | 9 | 303 | 202 | 0 | 504 | 5558 |
| Mature | 9.5 | 303 | 0 | 0 | 303 | 3353 |
| Mature | 10.5 | 303 | 202 | 0 | 504 | 7145 |
| Mature | 11 | 0 | 634 | 0 | 634 | 9313 |
| Mature | 11.5 | 0 | 115 | 0 | 115 | 1678 |
| Mature | 12 | 29 | 303 | 0 | 332 | 5490 |
| Mature | 12.5 | 101 | 462 | 0 | 563 | 9709 |
| Mature | 13 | 0 | 346 | 0 | 346 | 6259 |
| Mature | 13.5 | 0 | 737 | 0 | 737 | 14087 |
| Mature | 14 | 0 | 403 | 0 | 403 | 8315 |
| Mature | 14.5 | 0 | 678 | 15 | 693 | 15192 |
| Mature | 15 | 0 | 333 | 15 | 348 | 8960 |
| Mature | 15.5 | 0 | 159 | 15 | 174 | 4479 |
| Mature | 16 | 0 | 131 | 15 | 146 | 4009 |
| Mature | 16.5 | 0 | 434 | 29 | 463 | 12439 |
| Mature | 17 | 0 | 161 | 29 | 190 | 5803 |
| Mature | 17.5 | 0 | 188 | 44 | 232 | 7736 |
| Mature | 18 | 0 | 29 | 0 | 29 | 984 |
| Mature | 18.5 | 0 | 174 | 44 | 218 | 7887 |
| Mature | 19.5 | 0 | 29 | 15 | 44 | 1746 |
| Mature | 20 | 0 | 0 | 15 | 15 | 620 |
| Immature | Total | 19064 | 5144 | 0 | 24208 | 216616 |
| Mature | Total | 1340 | 5924 | 234 | 7498 | 145578 |
A one-day second coverage was conducted on the return to Hafnafjörður harbour to investigate the progression of the mature component observed near the continental slope, to assess whether the spawning migration was advancing westward (Figure 20) and to verify consistency between the two coverage estimates. Mature capelin were again found near the continental slope on Bardagrunn (166 500 t), while immature capelin were absent from the second coverage.
Based on these results, approximately 23 % of the mature stock was estimated to have migrated southwest, while the largest portion migrated eastward clockwise around Iceland, to spawn in coastal areas in the south and west. Table 10 gives information on the length disaggregated numbers and biomass of the capelin stock components during the second coverage.
Additionally, the r/v Þórunn Þórðardóttir, conducting a concurrent hydrographic survey around Iceland from 3 to 17 February, also collected acoustic data. Capelin registrations were found mainly along Kögurgrunn and close to drifting sea ice to the northwest; no capelin registrations were found on the Siglunes transect or further north and northeast (figure not shown). Capelin schools were also observed in shallow waters (30-100 m depth) in the south (from Alviðruhamar to Selvogsbanki section).
| Length (cm) | N (millions) | Biomass (tonnes) |
|---|---|---|
| 15 | 124.9 | 1843 |
| 15.5 | 156.2 | 2620 |
| 16 | 468.5 | 8330 |
| 16.5 | 687.2 | 13894 |
| 17 | 812.1 | 18741 |
| 17.5 | 1030.8 | 26353 |
| 18 | 1062.0 | 30490 |
| 18.5 | 1030.8 | 32417 |
| 19 | 655.9 | 22961 |
| 19.5 | 124.9 | 4902 |
| 20 | 93.7 | 3909 |
| Total | 6247.0 | 166460 |
The fishing season 2025/2026
Stock assessment
The initial advice for capelin in the fishing year 2025/2026 was based on measurements of the immature part of the stock in the autumn survey 2024. The measurements resulted in 58.9 billion individuals and initial advice of 46 384 tonnes based on the HCR.
The biomass of the fishable stock (mature part) is estimated based on a combination of autumn (weighted 1/3) and winter measurements (weighted 2/3). The 2025 autumn measurement is based on the survey covering the East Greenland area, resulted in a biomass of 417.5 thous. tonnes (CV=0.20). The January 2026 winter survey measurement for the whole area, northwest to southeast of Iceland yielded a biomass estimate of 710.2 thous. tonnes (CV=0.24). Hence, weighted together, the estimated biomass of the fishable stock (mature) was 612 666 t, which was the starting values of the predation model.
Table 11 give the recruitment index as measured in autumn survey, spawning-stock biomass at the time of spawning at the end of the fishing season, and landings as sum of total landings in the season. Fishing season 1978/79 and 1979/80 are based on historical stock estimates while later values are based on the predation model in current HCR.
| Season (Summer/winter) | Recruitment | Landings | Spawning-stock biomass |
|---|---|---|---|
| 1978/79 | 0.0 | 1195 | 0 |
| 1979/80 | 22.0 | 980 | 0 |
| 1980/81 | 23.5 | 684 | 106 |
| 1981/82 | 21.0 | 626 | 116 |
| 1982/83 | 68.0 | 0 | 206 |
| 1983/84 | 44.1 | 573 | 338 |
| 1984/85 | 73.8 | 896 | 315 |
| 1985/86 | 33.8 | 1312 | 156 |
| 1986/87 | 58.6 | 1334 | 365 |
| 1987/88 | 21.3 | 1116 | 257 |
| 1988/89 | 43.9 | 1036 | 139 |
| 1989/90 | 29.2 | 807 | 91 |
| 1990/91 | 27.2 | 313 | 245 |
| 1991/92 | 60.0 | 677 | 203 |
| 1992/93 | 104.6 | 788 | 294 |
| 1993/94 | 100.4 | 1178 | 307 |
| 1994/95 | 119.0 | 864 | 144 |
| 1995/96 | 165.0 | 930 | 380 |
| 1996/97 | 111.9 | 1570 | 426 |
| 1997/98 | 66.8 | 1246 | 272 |
| 1998/99 | 121.0 | 1100 | 230 |
| 1999/00 | 89.8 | 932 | 120 |
| 2000/01 | 103.7 | 1071 | 233 |
| 2001/02 | 101.8 | 1249 | 242 |
| 2002/03 | 0.0 | 988 | 10 |
| 2003/04 | 4.9 | 742 | 109 |
| 2004/05 | 7.9 | 784 | 226 |
| 2005/06 | 0.0 | 247 | 16 |
| 2006/07 | 44.7 | 377 | 217 |
| 2007/08 | 5.7 | 203 | 65 |
| 2008/09 | 12.6 | 150 | 261 |
| 2009/10 | 15.4 | 151 | 261 |
| 2010/11 | 101.2 | 391 | 204 |
| 2011/12 | 9.6 | 747 | 257 |
| 2012/13 | 19.4 | 551 | 301 |
| 2013/14 | 60.7 | 142 | 289 |
| 2014/15 | 58.0 | 518 | 342 |
| 2015/16 | 5.4 | 174 | 336 |
| 2016/17 | 9.2 | 300 | 356 |
| 2017/18 | 25.9 | 287 | 384 |
| 2018/19 | 11.8 | 0 | 166 |
| 2019/20 | 83.3 | 0 | 142 |
| 2020/21 | 140.6 | 129 | 374 |
| 2021/22 | 85.8 | 689 | 510 |
| 2022/23 | 28.7 | 450 | 356 |
| 2023/24 | 47.7 | 0 | 123 |
| 2024/25 | 58.9 | 9 | 184 |
| 2025/26 | 118.7 | 190 | 457 |
Predation model results
Following the completion of surveys 2025/2026, estimations of stock parameters (input parameters are listed in the 2025/2026 advice sheet) and their uncertainties from 100 thousand bootstrap replicates of the mature part of the stock were used as starting values for predation model runs. Results from the predation model runs are given in Table 12 and shown in Figure 22 and Figure 23.
| mean | 5% | 25% | 50% | 75% | 95% | |
|---|---|---|---|---|---|---|
| SSB | 266410 | 114360 | 189670 | 255490 | 330800 | 457280 |
| Predation | 148230 | 101360 | 125450 | 145240 | 167880 | 205070 |
The predation model (ICES 2023, ICES 2024) is designed to cover predation of cod, haddock and saithe on the main spawning migration of capelin between 15 January and 15 March. A schematic description of the model is shown in Figure 21.
The fishing season 2026/2027
Initial advice
In June 2026, the initial advice for 2026/2027 is above the zero because the index for immature fish from the autumn acoustic survey 2025 was 118.7 billion, and was above the Utrigger value (50 billion). Based on this rule (see Section 10), the initial TAC was 358 044 t for the fishing season starting 15 October 2026 to 15 April 2027 (Figure 24).
State of the stock
The mature part of the stock (or the fishable stock) was estimated at a median of 418 000 tonnes in the autumn 2025 and 710 200 tonnes in January 2026. The predation model (ICES, 2015), accounting for catches and predation by cod, saithe and haddock between surveys and spawning, estimated an SSB of 266 410 tonnes would be left for spawning in spring 2026 if the HCR were followed (Table 12). Given the uncertainty estimates, there was a 95% probability that at least 114 000 tonnes was left for spawning, if the catches taken amounted to 197 474 tonnes. The acoustic estimate of immature capelin in autumn 2025 was 118.7 billion. The estimate is above the long-term average (Figure 25, Figure 26), and the initial advice for the HCR is 358 044 tonnes for the 2026/2027 fishing season issued by ICES and MFRI in June 2026.
The estimated SSB at spawning time (March-April) has been recalculated for 1981-2025 (Figure 27), using the model adopted in 2015 and 2023, i.e. taking into account uncertainty in the acoustic measurements and using the predation model adopted in 2015. Uncertainty in acoustic measurements was recompiled for the years 2002-2006 and 2012-2014 by recalculating the acoustic indices and bootstrapping the results. Since 2015 uncertainty has been available as the advice was given based on the new HCR. For earlier years, the CV in the acoustic measurements was estimated by looking at survey reports as well as text from Vilhjálmsson, (1994). The estimated CV was in the range of 0.15-0.25 and was included as a lognormal multiplier on available average values from the same sources.
Uncertainties in assessment and forecast
The uncertainty of the assessment and forecast depends largely on the quality of the acoustic surveys in terms of coverage, conditions for acoustic measurements and the aggregation of capelin (i.e., high patchiness leads to high variance).
The uncertainty is estimated by bootstrapping (see WKICE 2015). The CV for the immature abundance was estimated to be 0.11 in the 2025 autumn survey. The survey had a relatively high coefficient of variation (CV=0.2) for the mature stock estimate. While the autumn survey was affected by time constraints, the distribution of immature and mature components of the capelin stock seemed to have been covered.
Agreed management plan and HCR
The Coastal States (Iceland, Greenland, and Norway) agreed (Anon. 2015; Anon. 2023) to use the following harvest control rule as the basis for management, following the rule developed and revised by ICES (ICES, 2015; ICES, 2023).
The objective of the Harvest Control Rule is to set a final TAC which ensures, with a 95% probability, that a minimum of 114 000t (Blim) remains for spawning. This is achieved by a series of acoustic surveys from September - February and the TAC is determined in three stages; an initial TAC, an intermediate TAC and a final TAC.
The initial TAC for the next fishing season is set based on estimates of the immature part of the stock following an acoustic survey in autumn (September - October).
Two fixed points are defined:
Utrigger = 50 billion immature capelin.
TACMax = 400,000 tonnes for U > 127 billion immature capelin.
The method for setting the initial/preliminary TAC is:
TAC = 0 if Uimm < 50 billion.
TAC = 5.2 x (Uimm - Utrigger) thous. tonnes for Uimm in the range 50–127 billion.
TAC = 400,000 tonnes if Uimm > 127 billion.
The intermediate TAC for the current fishing season is set following the acoustic survey in autumn. Estimates on capelin spawning stock biomass (SSB) with uncertainty estimate are combined with data on predicted predator stocks size and distribution. The estimates are fed into a predation model run with varying catches until spawning in March. The intermediate TAC is set at 2/3 of the catch giving p(SSB < Blim = 114 000 tonnes) < 0.05.
The final TAC is set following an acoustic survey in winter (January-February). Estimates on capelin spawning stock biomass with uncertainty estimate are combined with data on predicted predator stocks size and distribution. Final TAC is set based on all valid acoustic surveys on the mature part of the stock from autumn to winter. The estimates are fed into a predation model run with varying catches until spawning in March. The final TAC is set at the catch giving p(SSB < Blim = 114 000 tonnes) < 0.05. After ICES (2023), it was decided that the autumn survey is weighted a maximum of 1/3.
Reference points
| Framework | Reference points | Value | Technical basis | Source |
|---|---|---|---|---|
| Maximum sustainable yield (MSY) approach | MSY Bescapement | Not defined* | ||
| Maximum sustainable yield (MSY) approach | FMSY | Not defined | ||
| Precautionary approach | Blim | 114 000 | Blim = Bloss, the average of the three lowest spawning-stock biomass (SSB) estimates which led to average recruitment (in 1981, 1982, and 1990); in tonnes | ICES (2023) |
| Management plan | Bmgt | 114 000 | From the management plan; in tonnes | Anon. (2015) and revised in Framework arrangement… (2023) |
| Management plan | Utrigger | 50 | From the management plan; immature index value; in billions | ICES (2015) |
| Management plan | Cap | 127 | From the management plan; immature index value; in billions | ICES (2015) |
- MSY Bescapement has not been defined, as the escapement strategy uses directly the >95% probability of SSB being above Blim
Management considerations
Over the years, the fishery has been closed during April–late June and the season has started in July/August or later, depending on the state of the stock.
Areas with high abundances of juvenile age 1 and 2 capelin (on the shelf region off NW-, N- and NE-Iceland) have usually been closed to the summer and autumn fishery.
It is permissible to transfer catches from the purse seine of one vessel to another vessel, in order to avoid slippage. However, if the catches are beyond the carrying capacity of the vessel and no other vessel is nearby, slippage is allowed. In recent years, reporting of such slippage has not been frequent. Industrial trawlers do not have the permission to slip capelin in order to harmonize catches to processing.
In Icelandic waters, fishing with pelagic trawl is only allowed in a limited area off the northeast coast (fishing in January) to protect juvenile capelin and to reduce the risk of affecting the spawning migration route.
As a precautionary measure to protect juvenile capelin, the coastal states (Iceland, Greenland and Norway) agreed that fishing shall not start until 15 October (in effect since 2021).
History of management of the stock
Since the early 1980s the stock was managed according to an escapement strategy, leaving 400 000 tonnes for spawning. Uncertainty of the estimates was not considered.
A new HCR and management plan were developed at an ICES benchmark meeting in 2015 and adopted the same year (ICES, 2015). The main changes involved accounting for uncertainty in the measurements and in the predation on the capelin stock up to the spawning period. At the ICES benchmark meeting in 2022 (ICES, 2023), minor adjustments were made, which the coastal states meeting agreed to base the advice on. Among other things, these changes included lowering the Blim from 150 000 tonnes to 114 000 tonnes (Figure 28).
Table 13 shows the TAC and advice history for capelin in the IEGJM area since 1981. The table includes the year, the initial TAC set based on the autumn survey, the intermediate TAC set based on the predation model and autumn survey, and the final TAC set based on all available surveys and the predation model. The table also includes the reported catch for each year.
Fishing year | Initial TAC | Rec. final TAC | Final TAC | Total catch |
|---|---|---|---|---|
1986/1987 | 1 100 000 | 1 333 400 | 1 290 000 | 1 334 000 |
1987/1988 | 500 000 | 1 115 800 | 1 115 000 | 1 117 000 |
1988/1989 | 900 000 | 1 036 500 | 1 065 000 | 1 036 000 |
1989/1990 | 900 000 | 807 800 | 900 000 | 808 000 |
1990/1991 | 600 000 | 313 600 | 250 000 | 313 000 |
1991/1992 | 0 | 677 100 | 740 000 | 677 000 |
1992/1993 | 500 000 | 787 700 | 900 000 | 788 000 |
1993/1994 | 900 000 | 1 178 700 | 1 250 000 | 1 179 000 |
1994/1995 | 950 000 | 863 900 | 850 000 | 864 000 |
1995/1996 | 800 000 | 929 300 | 1 390 000 | 926 000 |
1996/1997 | 1 100 000 | 1 570 900 | 1 600 000 | 1 569 000 |
1997/1998 | 850 000 | 1 244 900 | 1 265 000 | 1 245 000 |
1998/1999 | 950 000 | 1 099 400 | 1 200 000 | 1 100 000 |
1999/2000 | 866 000 | 1 000 000 | 1 000 000 | 931 000 |
2000/2001 | 650 000 | 1 110 000 | 1 090 000 | 1 070 000 |
2001/2002 | 700 000 | 1 300 000 | 1 300 000 | 1 249 000 |
2002/2003 | 690 000 | 1 000 000 | 1 000 000 | 989 000 |
2003/2004 | 555 000 | 875 000 | 900 000 | 743 000 |
2004/2005 | 335 000 | 985 000 | 985 000 | 784 000 |
2005/2006 | 0 | 238 000 | 235 000 | 247 000 |
2006/2007 | 0 | 385 000 | 385 000 | 377 000 |
2007/2008 | 207 000 | 207 000 | 207 000 | 203 000 |
2008/2009 | 0 | 0 | 0 | 15 000 |
2009/2010 | 0 | 150 000 | 150 000 | 151 000 |
2010/2011 | 0 | 390 000 | 390 000 | 391 000 |
2011/2012 | 366 000 | 765 000 | 765 000 | 748 000 |
2012/2013 | 0 | 570 000 | 570 000 | 551 000 |
2013/2014 | 0 | 160 000 | 160 000 | 142 000 |
2014/2015 | 225 000 | 580 000 | 580 000 | 517 000 |
2015/2016 | 53 600 | 173 000 | 173 000 | 173 500 |
2016/2017 | 0 | 299 000 | 299 000 | 297 732 |
2017/2018 | 0 | 285 000 | 285 000 | 287 000 |
2018/2019 | 0 | 0 | 0 | 0 |
2019/2020 | 0 | 0 | 0 | 0 |
2020/2021 | 169 520 | 127 300 | 127 300 | 128 647 |
2021/2022 | 400 000 | 869 600 | 869 600 | 689 200 |
2022/2023 | 400 000 | 459 800 | 459 800 | 330 051 |
2023/2024 | 0 | 0 | 0 | 0 |
2024/2025 | 0 | 8 589 | 8 589 | 9 439 |
2025/2026 | 46 384 | 197 474 | 197 474 | 190 086 |
2026/2027 | 358 044 |
Ecosystem considerations
Capelin is an important forage fish and its dynamics are expected to have implications for the productivity of its predators.
The importance of capelin in the East Greenlandic marine ecosystem is not well documented. However, the research effort has increased considerably during autumn surveys towards evaluation of capelin’s role in the ecosystem e.g. by research on feeding of capelin, estimates of prey availability, predators’ distributions and environmental monitoring (Petursdottir et al., 2026, Sigurðsson et al., 2026, Singh et al., 2026).
In Icelandic waters, capelin is the main item in the diet of Icelandic cod, a key prey for several species of marine mammals and seabirds and also important as food for several other commercial fish species (see e.g. Vilhjálmsson, 2002, Singh et al., 2023). Diet studies of cod from the groundfish survey in March clearly demonstrate the importance of capelin in its diet, while also showing the variability in capelin availability between years (Figure 29). The relative frequency of capelin in cod stomachs showed interannual variability, and in some cases matched the different dynamics of the winter migration as observed in the February 2026 portion of the mature stock, which was migrating westwards (Figure 29).
References
Anon. 2015. Agreed Record of Conclusions of Coastal State consultations on the management of the capelin stock in the Iceland–East Greenland–Jan Mayen area. 2015. Reykjavík, Iceland. 7–8 May 2015. https://www.regjeringen.no/contentassets/37b66bdf33d84e99924bb27553641719/samledokument-lodde-mai-2015---agreed-records---bilateral-avtale.pdf Last accessed: 31 May 2025.
Anon. 2023. Framework arrangement between Greenland and Iceland on the conservation and management of capelin. 2023. Reykjávik, Iceland 3 July 2023. 4 pp. https://www.althingi.is/altext/pdf/154/fylgiskjol/s1655-f_I.pdf Last accessed: 31 May 2025.
Bardarson, B, Heilman, L, Jonsson, SÞ and Jansen, T 2024. Cruise report of acoustic assessment of the Iceland-East Greenland-Jan Mayen capelin stock in the autumn 2024. Kver Hafrannsóknastofnunar. KV2024-10. 18 pp.
Bardarson, B, Gudnason, K, Singh, W, Petursdottir, H, & Jonsson, SÞ (2021). Loðna (Mallotus villosus). Í Guðmundur J. Óskarsson (ritstj.), Staða umhverfis og vistkerfa í hafinu við Ísland og horfur næstu áratuga. Haf- og vatnarannsóknir, HV 2021-14, 31–34.
Christiansen, JS, Præbel, K, Siikavuopio, SI, Carscadden, JE 2008. Facultative semelparity in capelin Mallotus villosus (Osmeridae)-an experimental test of a life history phenomenon in a sub-arctic fish, Journal of Experimental Marine Biology and Ecology, Volume 360, Issue 1, 2008, Pages 47-55, ISSN 0022-0981, https://doi.org/10.1016/j.jembe.2008.04.003.
Engilbertsson, V, Óskarsson, GJ and Marteinsdóttir, G (2012). Inter-annual Variation in Fat Content of the Icelandic Capelin. ICES CM 2013/N:26.
Gjøsæter, H, Bogstad, B, and Tjelmeland, S 2002. Assessment methodology for Barents Sea capelin, Mallotus villosus (Müller). – ICES Journal of Marine Science, 59: 1086–1095.
Gudmundsdottir, A, and Vilhjálmsson, H 2002. Predicting Total Allowable Catches for Icelandic capelin, 1978–2001. ICES Journal of Marine Science, 59: 1105–1115.
Gudmundsdottir, A, and Sigurdsson, Th 2014. Growth of capelin in the Iceland-East Greenland-Jan Mayen area. NWWG 2014/WD:29.
ICES. 2015. Report of the Benchmark Workshop on Icelandic Stocks (WKICE), 26-30 January, 2015. ICES Headquarters. ICES CM 2015/ACOM:31. 335 pp.https://doi.org/10.17895/ices.pub.5295
ICES. 2023. Benchmark workshop on capelin (WKCAPELIN). ICES Scientific Reports. 5:62. 282 pp.https://doi.org/10.17895/ices.pub.23260388
ICES 2024. Capelin (Mallotus villosus) in subareas 5 and 14 and Division 2.a west of 5°W (Iceland and Faroes grounds, East Greenland, Jan Mayen area). ICES Advice: Recurrent Advice. Report. https://doi.org/10.17895/ices.advice.25663980.v1
Jansen, T, Hansen, FT, Bardarson, B 2021. Larval drift dynamics, thermal conditions and the shift in juvenile capelin distribution and recruitment success around Iceland and East Greenland. Fisheries Research, 236.
MFRI. 2024. State of Marine Stocks and Advice 2024, advice on capelin. Marine and Freshwater Research Institute, 11 October 2024.
Petursdottir H, Jansen T, Silva T et al. 2026. Diet composition and feeding behavior of capelin (Mallotus villosus) in the changing Iceland–East Greenland–Jan Mayen ecosystem. Rev Fish Biol Fish, 36(1). https://doi.org/10.1007/s11160-025-10022-3.
Sigurðsson GM, Víkingsson G, Chosson V et al. 2026 Spatiotemporal co-occurrence of whales and capelin on the east Greenland shelf during autumn. Mar Biol, 173(1). https://doi.org/10.1007/s00227-025-04778-2.
Singh, W, Ólafsdóttir, AH, Jónsson, SÞ, Óskarsson, GJ 2023. Capelin in a changing environment. Haf- og vatnarannsóknir, HV 2023-43. https://www.hafogvatn.is/static/research/files/capelin_2023_eng.pdf
Singh W, Giorgi E, Jónsson S et al. 2026. Habitat characterization of capelin along East Greenland: insights from hydrographic conditions and feeding distribution patterns. Rev Fish Biol Fish, 36(1). https://doi.org/10.1007/s11160-025-10019-y.
Vilhjálmsson, H 1994. The Icelandic capelin stock. Capelin, Mallotus villosus (Müller), in the Iceland– Greenland–Jan Mayen area. Rit Fiskideildar, 13: 281 pp.
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Glossary
Abbreviations and indices used in the report:
| Term | Definition |
|---|---|
| Blim | Biomass limit reference point (114 000 tonnes for capelin); the minimum spawning stock biomass that should be maintained with 95% probability |
| CV | Coefficient of Variation; a measure of uncertainty or variability in survey estimates |
| HCR | Harvest Control Rule; the agreed management strategy used by coastal states to set TAC based on stock estimates |
| IEGJM | Iceland–East Greenland–Jan Mayen area; the management area for this capelin stock |
| MFRI | Marine and Freshwater Research Institute (Iceland) |
| MSY | Maximum Sustainable Yield |
| MSY Bescapement | Maximum Sustainable Yield escapement biomass; the spawning stock biomass that would produce the maximum sustainable yield |
| NASC | Nautical Area Scattering Coefficient; acoustic measurement unit used in fish acoustic surveys |
| NWWG | ICES Northwestern Working Group |
| PSE | Purse Seine; a fishing gear type |
| PGT | Pelagic Trawl; a fishing gear type |
| SSB | Spawning Stock Biomass; the estimated total weight of mature fish available for spawning |
| TAC | Total Allowable Catch; the maximum permitted catch for a fishing season |
| TACMax | Maximum TAC cap (400 000 tonnes) applied when immature stock is very high |
| Uimm | Abundance index of immature capelin from acoustic surveys (measured in billions) |
| Utrigger | Trigger point for immature stock (50 billion); threshold used in HCR for setting initial TAC |
| WKCAPELIN | ICES Benchmark Workshop on Capelin in 2022; a scientific meeting to review and update the assessment and management of the capelin stock |