| Year | Pelagic Trawl Num. stations | Pelagic Trawl Num. samples | Pelagic Trawl Num. otoliths | Purse Seine Num. stations | Purse Seine Num. samples | Purse Seine Num. otoliths |
|---|---|---|---|---|---|---|
| 1981 | 0 | 0 | 0 | 32 | 4 237 | 1 813 |
| 1982 | 0 | 0 | 0 | 43 | 4 875 | 2 461 |
| 1983 | 3 | 562 | 278 | 54 | 11 124 | 3 280 |
| 1984 | 1 | 100 | 100 | 37 | 3 562 | 2 799 |
| 1985 | 1 | 100 | 100 | 35 | 5 366 | 2 182 |
| 1986 | 0 | 0 | 0 | 40 | 4 452 | 3 226 |
| 1987 | 0 | 0 | 0 | 55 | 5 743 | 4 295 |
| 1988 | 0 | 0 | 0 | 46 | 4 626 | 4 318 |
| 1989 | 0 | 0 | 0 | 67 | 8 159 | 5 485 |
| 1990 | 2 | 166 | 23 | 55 | 5 404 | 4 450 |
| 1991 | 0 | 0 | 0 | 95 | 12 139 | 5 689 |
| 1992 | 0 | 0 | 0 | 113 | 19 456 | 4 528 |
| 1993 | 92 | 23 489 | 76 | 101 | 18 772 | 3 501 |
| 1994 | 3 | 505 | 23 | 57 | 9 812 | 2 450 |
| 1995 | 0 | 0 | 0 | 66 | 8 577 | 4 042 |
| 1996 | 5 | 668 | 183 | 50 | 5 828 | 3 463 |
| 1997 | 27 | 5 398 | 834 | 39 | 3 928 | 2 883 |
| 1998 | 11 | 2 031 | 148 | 39 | 6 156 | 1 443 |
| 1999 | 41 | 2 101 | 952 | 152 | 15 691 | 5 710 |
| 2000 | 55 | 7 943 | 1 569 | 129 | 9 362 | 5 536 |
| 2001 | 80 | 9 238 | 2 702 | 82 | 9 565 | 2 457 |
| 2002 | 83 | 12 230 | 1 481 | 134 | 22 220 | 1 834 |
| 2003 | 171 | 28 389 | 916 | 205 | 37 084 | 1 841 |
| 2004 | 74 | 4 093 | 1 770 | 291 | 76 214 | 3 960 |
| 2005 | 110 | 7 565 | 1 853 | 157 | 21 847 | 4 080 |
| 2006 | 44 | 4 983 | 1 393 | 118 | 20 152 | 2 217 |
| 2007 | 19 | 2 211 | 658 | 107 | 14 000 | 3 219 |
| 2008 | 17 | 2 724 | 43 | 170 | 18 053 | 5 252 |
| 2009 | 60 | 7 043 | 1 551 | 123 | 10 406 | 8 390 |
| 2010 | 39 | 4 130 | 1 539 | 60 | 7 471 | 6 291 |
| 2011 | 148 | 17 410 | 1 488 | 57 | 4 033 | 3 067 |
| 2012 | 32 | 3 887 | 193 | 76 | 6 513 | 3 519 |
| 2013 | 76 | 5 466 | 1 103 | 67 | 8 032 | 1 480 |
| 2014 | 113 | 10 434 | 2 432 | 2 | 256 | 200 |
| 2015 | 98 | 9 165 | 2 519 | 4 | 364 | 150 |
| 2016 | 133 | 11 729 | 3 369 | 1 | 50 | 50 |
| 2017 | 63 | 4 907 | 1 585 | 1 | 30 | 25 |
| 2018 | 62 | 5 334 | 1 139 | 0 | 0 | 0 |
| 2019 | 87 | 7 558 | 1 665 | 0 | 0 | 0 |
| 2020 | 73 | 7 409 | 1 400 | 0 | 0 | 0 |
| 2021 | 59 | 5 773 | 1 833 | 0 | 0 | 0 |
| 2022 | 79 | 7 464 | 2 194 | 0 | 0 | 0 |
| 2023 | 69 | 4 547 | 2 215 | 0 | 0 | 0 |
| 2024 | 55 | 3 340 | 2 234 | 0 | 0 | 0 |
| 2025 | 108 | 5 819 | 4 309 | 0 | 0 | 0 |
Key signals
The spawning-stock biomass (SSB) was high around 2007, but declined steadily until 2017 due to additional mortality from the Ichthyophonus infection and a series of below-average year classes recruiting to the stock.
The strong 2017–2020 year classes contributed to an increase in SSB after recruiting to the fishable stock. Since 2023, SSB has declined again as these cohorts have become older and subsequent recruitment has been weaker.
The total acoustic biomass index from the 2025/2026 surveys was 597 kt, corresponding to 2.2 billion individuals. This is lower than the record-high estimate in 2024/2025 and closer to the long-term average.
The juvenile survey was reinstated in 2025 after several years without a survey. The resulting age-1 index was above average and is used in the assessment, reducing uncertainty around recent recruitment.
Fishing pressure has been variable over the time series, with high values in the late 1980s followed by a general decline. The current harvest rate is within the range expected under the management plan.
Retrospective patterns are moderate in the current assessment, and Mohn’s rho values do not indicate major concern. However, recent peels for SSB and Fbar(5–10) should continue to be monitored.
General information
The Icelandic summer-spawning herring (Clupea harengus) is a pelagic fish that can be found all around Iceland. It lives in a wide range of depths from the surface down to a depth of 400m and at temperatures from 1-15°C (Jakobsson 2000). Its main wintering grounds have been either shallow or deep east or west of Iceland or shallow in the south (Jakobsson 1980, Óskarsson et al 2009). Herring spawns in July, and its spawning grounds can be found along the south and southwest coast of Iceland (Óskarsson and Taggart 2009, Jakobsson et al. 1969). After hatching of eggs at the bottom, larvae reach the north of the country by currents and the main nursery areas are found in fjords northwest and north of the country (Guðmundsdóttir et al. 2007).
Fishery
The total catch in the 2025/2026 season was 104 591 tonnes (Table 4, Figure 2). This also includes the by-catch of herring in the mackerel and Norwegian spring-spawning herring fisheries in June - November 2025. The recommended TAC for 2025 and the TAC (Regulation No. 672, 2 July 2020) was 103 367. Traditional catches in wintering grounds west of the country in September-December amounted to 73 644 tonnes while 30 776 tonnes were caught as bycatch in the mackerel and Norwegian spring-spawning herring fishery in the east in June-November (Figure 1).
Landing trends
Spatial and temporal patterns
The herring fishing season has changed slightly in the last three decades as detailed in the stock annex. All catches in the year 2025/2026 were caught in pelagic trawls (Figure 2). In the seasons 2007/2008 to 2012/2013, most of the catch (~90%) was caught in Breiðafjörður (Figure 3), but before that it was mainly caught off the south, southeast and east coasts. During the 2013/2014 fishing season, this pattern began to change, with a smaller proportion of catch in Breiðafjörður; and since 2014/2015, most of the fishing has taken place in the west of the country. To protect juvenile herring (27 cm and smaller) in the fishery, area closures are enforced based on a regulation on herring fishing issued by the Ministry of Fisheries (No. 376, 8 October 1992). No closure was enforced in this herring fishery in 2025/2026. Normally, the age of first recruitment to the fishery is age-3, which corresponds to lengths of approximately 26–29 cm.
Data and sampling
The assessment of the age composition of the catch is based on samples from the catch of fishing vessels collected at sea by fishermen and catch information. An overview of the sampled otoliths is shown in Table 1. The geographical location of the catch and sampling in 2025/2026 is shown in Figure 4. This year, the calculations were accomplished by dividing the total catch into two cells confined by season and area. Weight-at-length relationships derived from the length and weight measurements of the catch samples were split using the same structure. Based on differences in length-at-age between the summer and winter months, two length-age keys were applied. Catch at age and total landings are available from the 1940s, but only those from 1980 are used in the assessment (Table 1). From trends in the catch at age, it is evident that the older age classes have been contributing to the catches in larger numbers since 2008 (Figure 5). The large 2017–2019 year classes entered the catch as 4- and 5-year-olds (Table 2).
| Age group | ||||||||||||||
| Year | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | 14 | 15 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1980 | 3,147 | 14,347 | 20,761 | 60,727 | 65,328 | 11,541 | 9,285 | 19,442 | 1,796 | 1,464 | 698 | — | 110 | 79 |
| 1981 | 2,283 | 4,629 | 16,771 | 12,126 | 36,871 | 41,917 | 7,299 | 4,863 | 13,416 | 1,032 | 884 | 760 | 101 | 62 |
| 1982 | 454 | 19,187 | 28,109 | 38,280 | 16,623 | 38,308 | 43,770 | 6,813 | 6,633 | 10,457 | 2,354 | 594 | 75 | 211 |
| 1983 | 1,475 | 22,499 | 151,718 | 30,285 | 21,599 | 8,667 | 14,065 | 13,713 | 3,728 | 2,381 | 3,436 | 554 | 100 | — |
| 1984 | 421 | 18,015 | 32,244 | 141,354 | 17,043 | 7,113 | 3,916 | 4,113 | 4,517 | 1,828 | 202 | 255 | 260 | — |
| 1985 | 112 | 12,872 | 24,659 | 21,656 | 85,210 | 11,903 | 5,740 | 2,336 | 4,363 | 4,053 | 2,773 | 975 | 480 | 581 |
| 1986 | 100 | 8,172 | 33,938 | 23,452 | 20,681 | 77,629 | 18,252 | 10,986 | 8,594 | 9,675 | 7,183 | 3,682 | 2,918 | 1,788 |
| 1987 | 29 | 3,144 | 44,590 | 60,285 | 20,622 | 19,751 | 46,240 | 15,232 | 13,963 | 10,179 | 13,216 | 6,224 | 4,723 | 2,280 |
| 1988 | 879 | 4,757 | 41,331 | 99,366 | 69,331 | 22,955 | 20,131 | 32,201 | 12,349 | 10,250 | 7,378 | 7,284 | 4,807 | 1,957 |
| 1989 | 3,974 | 22,628 | 26,649 | 77,824 | 188,654 | 43,114 | 8,116 | 5,897 | 7,292 | 4,780 | 3,449 | 1,410 | 844 | 348 |
| 1990 | 12,567 | 14,884 | 56,995 | 35,593 | 79,757 | 157,225 | 30,248 | 8,187 | 4,372 | 3,379 | 1,786 | 715 | 446 | 565 |
| 1991 | 37,085 | 88,683 | 49,081 | 86,292 | 34,793 | 55,228 | 110,132 | 10,079 | 4,155 | 2,735 | 2,003 | 519 | 339 | 416 |
| 1992 | 16,144 | 94,860 | 122,626 | 38,381 | 58,605 | 27,921 | 38,420 | 53,114 | 11,592 | 1,727 | 1,757 | 153 | 376 | — |
| 1993 | 2,467 | 51,153 | 177,780 | 92,680 | 20,791 | 28,560 | 13,313 | 19,617 | 15,266 | 4,254 | 797 | 254 | — | — |
| 1994 | 5,738 | 134,616 | 113,290 | 142,876 | 87,207 | 24,913 | 20,303 | 16,301 | 15,695 | 14,680 | 2,936 | 1,435 | 244 | 195 |
| 1995 | 4,555 | 20,991 | 137,232 | 86,864 | 109,140 | 76,780 | 21,361 | 15,225 | 8,541 | 9,617 | 7,034 | 2,291 | 621 | 235 |
| 1996 | 717 | 15,969 | 40,311 | 86,187 | 68,927 | 84,660 | 39,664 | 14,746 | 8,419 | 5,836 | 3,152 | 5,180 | 1,996 | 574 |
| 1997 | 2,008 | 39,240 | 30,141 | 26,307 | 36,738 | 33,705 | 31,022 | 22,277 | 8,531 | 3,383 | 1,141 | 10,296 | 947 | 2,524 |
| 1998 | 23,655 | 45,390 | 175,529 | 22,691 | 8,613 | 40,898 | 25,944 | 32,046 | 14,647 | 2,122 | 2,754 | 2,150 | 1,070 | 1,011 |
| 1999 | 5,306 | 56,315 | 54,779 | 140,913 | 16,093 | 13,506 | 31,467 | 19,845 | 22,031 | 12,609 | 2,673 | 2,746 | 1,416 | 2,514 |
| 2000 | 17,286 | 57,282 | 136,278 | 49,289 | 76,614 | 11,546 | 8,294 | 16,367 | 9,874 | 11,332 | 6,744 | 2,975 | 1,539 | 1,104 |
| 2001 | 27,486 | 42,304 | 86,422 | 93,597 | 30,336 | 54,491 | 10,375 | 8,762 | 12,244 | 9,907 | 8,259 | 6,088 | 1,491 | 1,259 |
| 2002 | 11,698 | 80,863 | 70,801 | 45,607 | 54,202 | 21,211 | 42,199 | 9,888 | 4,707 | 6,520 | 9,108 | 9,355 | 3,994 | 5,697 |
| 2003 | 24,477 | 211,495 | 286,017 | 58,120 | 27,979 | 25,592 | 14,203 | 10,944 | 2,230 | 3,424 | 4,225 | 2,562 | 1,575 | 1,370 |
| 2004 | 23,144 | 63,355 | 139,543 | 182,450 | 40,489 | 13,727 | 9,342 | 5,769 | 7,021 | 3,136 | 1,861 | 3,871 | 994 | 1,855 |
| 2005 | 6,088 | 26,091 | 42,116 | 117,910 | 133,437 | 27,565 | 12,074 | 9,203 | 5,172 | 5,116 | 1,045 | 1,706 | 2,110 | 757 |
| 2006 | 52,567 | 118,526 | 217,672 | 54,800 | 48,312 | 57,241 | 13,603 | 5,994 | 4,299 | 898 | 1,626 | 1,213 | 849 | 933 |
| 2007 | 10,817 | 94,250 | 83,631 | 163,294 | 61,207 | 87,541 | 92,126 | 23,238 | 11,728 | 7,319 | 2,593 | 4,961 | 2,302 | 1,420 |
| 2008 | 10,427 | 38,830 | 90,932 | 79,745 | 107,644 | 59,656 | 62,194 | 54,345 | 18,130 | 8,240 | 5,157 | 2,680 | 2,630 | 1,178 |
| 2009 | 5,431 | 21,856 | 35,221 | 31,914 | 18,826 | 22,725 | 10,425 | 9,213 | 9,549 | 2,238 | 1,033 | 768 | 406 | 298 |
| 2010 | 1,476 | 8,843 | 22,674 | 29,492 | 24,293 | 14,419 | 17,407 | 10,045 | 7,576 | 8,896 | 1,764 | 1,105 | 672 | 556 |
| 2011 | 521 | 9,357 | 24,621 | 20,046 | 22,869 | 23,706 | 13,749 | 16,967 | 10,039 | 7,623 | 7,745 | 1,441 | 618 | 785 |
| 2012 | 403 | 17,827 | 89,432 | 51,257 | 43,079 | 51,224 | 41,846 | 34,653 | 27,215 | 24,946 | 15,473 | 13,631 | 2,556 | 236 |
| 2013 | 6,888 | 46,848 | 24,833 | 35,070 | 17,250 | 18,550 | 19,032 | 21,821 | 15,952 | 15,804 | 10,081 | 9,775 | 6,722 | 2,486 |
| 2014 | — | 3,537 | 53,241 | 50,609 | 70,044 | 34,393 | 22,084 | 22,138 | 13,298 | 17,761 | 7,974 | 4,461 | 2,862 | 1,746 |
| 2015 | 89 | 6,024 | 29,890 | 53,573 | 43,501 | 43,015 | 15,533 | 10,760 | 8,664 | 8,161 | 6,981 | 2,726 | 2,467 | 1,586 |
| 2016 | 72 | 10,740 | 25,575 | 29,908 | 41,952 | 25,823 | 24,925 | 9,516 | 7,734 | 6,088 | 4,284 | 7,154 | 3,108 | 826 |
| 2017 | 1,262 | 5,236 | 31,855 | 18,113 | 10,239 | 15,506 | 10,223 | 8,830 | 5,676 | 3,399 | 1,616 | 2,220 | 1,533 | 1,596 |
| 2018 | — | 8,911 | 19,642 | 34,284 | 16,847 | 12,376 | 17,161 | 6,978 | 7,379 | 3,482 | 1,713 | 1,153 | 2,159 | 489 |
| 2019 | 461 | 4,601 | 15,845 | 12,970 | 16,084 | 12,244 | 6,944 | 9,531 | 6,165 | 4,732 | 2,983 | 2,808 | 2,200 | 1,866 |
| 2020 | 384 | 23,603 | 15,956 | 22,572 | 16,333 | 19,385 | 11,071 | 7,098 | 6,241 | 3,035 | 3,359 | 4,505 | 1,567 | 1,129 |
| 2021 | 12,440 | 21,018 | 88,992 | 37,291 | 37,244 | 17,231 | 21,230 | 13,155 | 11,781 | 7,270 | 5,213 | 3,549 | 2,771 | 1,583 |
| 2022 | — | 23,108 | 90,765 | 86,093 | 26,757 | 25,604 | 11,495 | 14,534 | 6,998 | 6,916 | 4,226 | 3,817 | 2,711 | 1,651 |
| 2023 | — | 8,178 | 75,892 | 90,608 | 56,330 | 26,617 | 29,872 | 11,921 | 16,204 | 9,236 | 8,009 | 4,399 | 3,936 | 2,219 |
| 2024 | — | 1,623 | 23,825 | 55,317 | 70,855 | 62,492 | 16,547 | 16,852 | 13,537 | 7,271 | 7,138 | 4,593 | 5,159 | 4,016 |
| 2025 | — | 26,730 | 28,952 | 67,405 | 86,278 | 72,227 | 53,318 | 18,418 | 14,638 | 7,411 | 7,514 | 4,058 | 2,706 | 1,619 |
Weight at age
Mean weight at age in the stock is shown in Figure 6. As stated in the stock annex, the mean weight-at-age of the stock is derived from catch samples and therefore represents both stock and catch weights. Stock weights of the older year classes have been generally decreasing in recent years.
Proportion mature
Fixed maturity ogives were used in this year’s assessment, as described in detail in the stock annex, where the proportion mature-at-ages 3 and 4 are set to 20% and 85% respectively, while all older fish are considered mature.
Length compositions
Length measurements are taken from the two main commercial fleets, i.e. pelagic trawls and purse seine (Table 1). Length distributions from these two fleets are shown in Figure 7. The sizes caught appear to be fairly stable, primarily catching herring in the size range 27–35 cm. Large cohorts can be seen entering the catches and moving the average length throughout the years.
Surveys data
The scientific data used to assess the Icelandic summer-spawning (ISS) herring stock derives from annual acoustic surveys (IS-Her-Aco-4Q/1Q). The surveys have been operating since 1973, although only data from 1988 is used to produce stock estimates (Table 3). These surveys are conducted from October–January and from March-April. The area surveyed each year is decided by evaluating available information on the distribution of the stock in the previous and current year, including information from the fishery. Thus, the survey area varies spatially between years because it is focused on the adult and incoming year classes, but it is usually considered to cover the whole stock each year.
| Year |
Age Group
|
|||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | 14 | 15 | Total | |
| 1988 | 115.5 | 401.2 | 858.0 | 308.1 | 57.1 | 32.5 | 70.4 | 36.7 | 23.6 | 18.4 | 24.3 | 10.1 | 8.8 | 1,964.8 |
| 1989 | 635.7 | 201.3 | 232.8 | 381.4 | 188.5 | 46.4 | 25.8 | 32.8 | 17.4 | 10.4 | 9.1 | 5.4 | 8.1 | 1,795.2 |
| 1990 | 138.8 | 655.4 | 179.4 | 278.8 | 593.0 | 179.7 | 22.2 | 21.8 | 13.1 | 9.9 | 2.0 | - | - | 2,093.9 |
| 1991 | 403.7 | 132.2 | 258.6 | 94.4 | 191.1 | 514.4 | 79.4 | 37.6 | 9.4 | 12.6 | - | - | - | 1,733.3 |
| 1992 | 598.2 | 1,050.0 | 354.5 | 319.9 | 89.8 | 138.3 | 256.9 | 21.3 | 9.9 | - | 9.3 | - | 1.5 | 2,849.6 |
| 1993 | 267.9 | 830.6 | 729.6 | 158.8 | 130.8 | 54.2 | 96.3 | 96.6 | 24.5 | 1.1 | 1.1 | 3.4 | - | 2,394.9 |
| 1994 | 302.1 | 505.3 | 882.9 | 496.3 | 67.0 | 58.3 | 106.2 | 48.9 | 36.2 | - | 4.2 | 18.1 | - | 2,525.3 |
| 1995 | - | - | - | - | - | - | - | - | - | - | - | - | - | 0.0 |
| 1996 | 217.0 | 133.8 | 761.6 | 277.9 | 385.0 | 176.9 | 98.1 | 48.5 | 16.2 | 29.4 | 47.9 | 4.5 | - | 2,196.9 |
| 1997 | 33.4 | 270.7 | 133.7 | 468.7 | 269.9 | 325.7 | 217.4 | 93.0 | 55.5 | 39.0 | 30.0 | 53.2 | 31.5 | 2,021.6 |
| 1998 | 291.9 | 601.8 | 81.1 | 57.4 | 287.0 | 156.0 | 203.4 | 105.7 | 35.5 | 27.4 | 14.2 | 36.5 | 25.8 | 1,923.6 |
| 1999 | 100.4 | 255.9 | 1,081.5 | 103.3 | 51.8 | 135.2 | 70.5 | 101.6 | 53.9 | 17.4 | 13.6 | 2.6 | 13.0 | 2,001.0 |
| 2000 | 516.2 | 839.5 | 239.1 | 605.9 | 88.2 | 43.4 | 165.7 | 89.9 | 121.3 | 77.6 | 21.5 | 3.7 | 11.1 | 2,823.1 |
| 2001 | 190.3 | 967.0 | 1,316.4 | 191.0 | 482.4 | 34.4 | 15.7 | 37.9 | 14.3 | 15.4 | 14.7 | 1.7 | 3.3 | 3,284.5 |
| 2002 | 1,047.6 | 287.0 | 217.4 | 260.5 | 161.0 | 345.9 | 62.5 | 57.1 | 38.4 | 46.0 | 38.1 | 21.1 | 3.7 | 2,586.3 |
| 2003 | 1,731.8 | 1,919.4 | 553.1 | 205.7 | 262.4 | 153.0 | 276.2 | 99.2 | 47.6 | 55.1 | 18.8 | 24.4 | 25.5 | 5,372.2 |
| 2004 | 1,115.3 | 1,435.0 | 2,058.2 | 330.8 | 109.1 | 100.8 | 38.7 | 45.6 | 7.0 | 6.4 | 7.5 | 10.9 | 2.3 | 5,267.6 |
| 2005 | 2,417.1 | 713.7 | 1,022.3 | 1,046.7 | 171.3 | 62.4 | 44.3 | 10.9 | 23.9 | 12.7 | - | 1.9 | 11.1 | 5,538.5 |
| 2006 | 469.5 | 443.9 | 345.0 | 818.7 | 1,220.9 | 281.4 | 122.2 | 129.6 | 73.3 | 65.3 | 10.1 | 9.2 | 16.0 | 4,005.2 |
| 2007 | 110.0 | 608.2 | 1,059.6 | 410.1 | 424.5 | 693.4 | 96.0 | 123.7 | 48.8 | 1.0 | - | - | 0.5 | 3,575.8 |
| 2008 | 90.2 | 456.8 | 289.3 | 541.6 | 309.4 | 402.9 | 702.7 | 221.6 | 244.8 | 14.0 | 22.1 | 68.1 | 12.9 | 3,376.4 |
| 2009 | 149.5 | 196.1 | 416.9 | 288.2 | 457.7 | 267.0 | 225.7 | 169.0 | 29.9 | 26.3 | 17.8 | 9.9 | 4.2 | 2,258.0 |
| 2010 | 151.1 | 315.9 | 490.7 | 554.8 | 271.4 | 327.3 | 149.1 | 83.9 | 156.9 | 36.7 | 13.6 | 8.5 | 7.0 | 2,567.0 |
| 2011 | 107.6 | 280.6 | 228.9 | 304.9 | 296.3 | 138.7 | 301.3 | 61.0 | 141.3 | 97.4 | 37.0 | - | 4.0 | 1,998.9 |
| 2012 | 705.0 | 978.0 | 436.0 | 290.0 | 281.0 | 246.0 | 149.0 | 175.0 | 83.0 | 104.0 | 94.0 | 21.0 | 5.0 | 3,567.0 |
| 2013 | 178.5 | 781.1 | 631.4 | 166.6 | 127.0 | 142.0 | 110.1 | 97.0 | 74.3 | 69.5 | 43.4 | 38.5 | 8.2 | 2,467.6 |
| 2014 | 16.0 | 314.9 | 218.7 | 345.0 | 151.7 | 132.8 | 120.7 | 118.3 | 89.5 | 74.6 | 48.7 | 44.6 | 42.8 | 1,718.3 |
| 2015 | 152.4 | 90.3 | 330.1 | 260.9 | 259.1 | 187.9 | 112.0 | 91.6 | 37.9 | 76.7 | 30.4 | 10.6 | 32.9 | 1,672.7 |
| 2016 | 381.9 | 164.2 | 174.5 | 312.4 | 225.8 | 215.2 | 93.7 | 62.8 | 75.3 | 42.0 | 15.7 | 26.8 | 25.6 | 1,815.8 |
| 2017 | 97.0 | 220.6 | 137.2 | 151.9 | 262.5 | 136.8 | 241.4 | 61.2 | 55.9 | 62.8 | 11.4 | 20.1 | 14.0 | 1,473.0 |
| 2018 | 32.7 | 22.9 | 95.1 | 171.7 | 201.9 | 319.9 | 209.2 | 255.3 | 75.8 | 34.5 | 83.5 | 54.9 | 53.5 | 1,611.0 |
| 2019 | 306.3 | 137.4 | 67.9 | 201.4 | 101.9 | 110.8 | 167.4 | 163.8 | 73.3 | 30.0 | 30.0 | 38.5 | 16.4 | 1,445.2 |
| 2020 | 1,525.4 | 229.8 | 158.6 | 103.6 | 211.1 | 98.8 | 53.7 | 59.5 | 42.2 | 37.2 | 21.3 | 15.1 | 11.4 | 2,567.8 |
| 2021 | 1,399.8 | 1,114.7 | 424.3 | 138.2 | 82.0 | 127.7 | 66.5 | 102.8 | 82.8 | 63.5 | 57.0 | 22.8 | 32.7 | 3,714.7 |
| 2022 | 629.4 | 655.5 | 400.6 | 153.3 | 237.1 | 179.0 | 174.2 | 81.6 | 83.9 | 82.7 | 32.9 | 46.8 | 21.8 | 2,778.9 |
| 2023 | 136.7 | 823.6 | 994.9 | 574.7 | 244.7 | 159.7 | 109.6 | 72.5 | 87.9 | 38.7 | 57.1 | 34.0 | 31.8 | 3,366.0 |
| 2024 | 482.5 | 242.4 | 296.4 | 294.8 | 273.5 | 194.3 | 99.0 | 90.1 | 47.8 | 10.0 | 48.0 | 27.7 | 23.5 | 2,130.0 |
| 2025 | 30.3 | 158.1 | 406.4 | 826.5 | 946.8 | 776.7 | 229.3 | 272.6 | 188.6 | 142.7 | 97.0 | 90.9 | 54.3 | 4,220.4 |
| 2026 | 316.0 | 159.6 | 314.6 | 462.7 | 330.8 | 264.9 | 141.9 | 68.3 | 16.4 | 81.3 | 25.0 | 11.5 | 3.9 | 2,197.0 |
The acoustic index for the adult component of the Icelandic summer-spawning herring during the winter of 2025/2026 is based on two dedicated surveys conducted onboard RV Þórun Þórðardóttir: (1) A survey in October 2025 (Þ10-2025), targeting ISS herring mixing with Norwegian spring-spawning (NSS) herring in the east, and assessing recruitment (age 3–4) southeast of Iceland; (2) A survey (Þ4-2026) in late March that focused on estimating the fishable stock in the main overwintering area west of Iceland (Figure 8). In addition to obtaining an acoustic estimate of the adult component a juvenile survey for age 1 was conducted in the year 2025, producing a usable index for stock assessment. The survey also aimed to estimate the prevalence of Ichthyophonus infections in the stock. The instruments and methods in the surveys were the same as in previous years. Further details about the surveys can be found in Bjarnason (2026). The biological sampling in the survey is detailed in Table 4.
Survey Results
The fishable component of the Icelandic summer-spawning herring stock was observed in two main areas: west of Iceland in Kolluáll/Snæfellsnes at the end of March 2026, and east and southeast of Iceland in autumn 2025 (Figure 8). The total acoustic estimate from these two surveys was 2.2 billion individuals, with a corresponding total biomass index of 597 kt (Table 3 and Figure 9). When only considering age 3+, the three most numerous year classes were those from 2018 (15,5%), 2019 (21,1%) and 2020 (14.1% Table 3). The annual survey targeting the abundance of herring recruits in the eastern and south-eastern regions was conducted in October 2025. The survey area (Figure 8) was consistent with previous years. Herring distribution was more concentrated in the east, where Icelandic summer-spawning herring overlaps with Norwegian spring-spawning herring. This survey targets the younger portion of the stock on the southern shelf of Iceland; however, limited herring was detected in the southern areas, where only 15% of the surveyed biomass comprised individuals aged three years or younger. In contrast, the western survey focuses on assessing the older segment of the stock. More details on survey results are available in the NWWG working document on survey reports (Bjarnason, 2026)
Number of scales
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N of samples
|
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|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Year | Age 2 | Age 3 | Age 4 | Age 5 | Age 6 | Age 7 | Age 8 | Age 9 | Age 10 | Age 11 | Age 12 | Age 13 | Age 14 | Age 15+ | Total | Total | West | East |
| 1987/88 | 11 | 59 | 246 | 156 | 37 | 28 | 58 | 33 | 22 | 16 | 23 | 10 | 5 | 8 | 712 | 8 | 1 | 7 |
| 1988/89 | 229 | 78 | 181 | 424 | 178 | 69 | 50 | 77 | 42 | 29 | 23 | 13 | 7 | 12 | 1412 | 18 | 5 | 10 |
| 1989/90 | 38 | 245 | 96 | 132 | 225 | 35 | 2 | 2 | 3 | 3 | 2 | 0 | 0 | 0 | 783 | 8 | - | 8 |
| 1990/91 | 418 | 229 | 303 | 90 | 131 | 257 | 28 | 6 | 3 | 8 | 0 | 0 | 0 | 0 | 1473 | 15 | - | 15 |
| 1991/92 | 414 | 439 | 127 | 127 | 33 | 48 | 84 | 5 | 3 | 0 | 2 | 0 | 0 | 1 | 1283 | 15 | - | 15 |
| 1992/93 | 122 | 513 | 289 | 68 | 73 | 28 | 38 | 34 | 6 | 2 | 2 | 6 | 0 | 0 | 1181 | 12 | - | 12 |
| 1993/94 | 63 | 285 | 343 | 129 | 13 | 15 | 7 | 14 | 11 | 0 | 1 | 3 | 0 | 0 | 884 | 9 | - | 9 |
| 1994/95 | - | - | - | - | - | - | - | - | - | - | - | - | - | - | - | - | - | - |
| 1995/96 | 183 | 90 | 471 | 162 | 209 | 107 | 38 | 18 | 8 | 14 | 18 | 2 | 0 | 0 | 1320 | 14 | 9 | 5 |
| 1996/97 | 24 | 150 | 88 | 351 | 141 | 137 | 87 | 32 | 15 | 10 | 7 | 14 | 4 | 2 | 1062 | 11 | 4 | 7 |
| 1997/98 | 101 | 249 | 50 | 36 | 159 | 95 | 122 | 62 | 21 | 13 | 8 | 15 | 8 | 5 | 944 | 14 | 7 | 7 |
| 1998/99 | 130 | 216 | 777 | 72 | 31 | 65 | 59 | 86 | 37 | 22 | 17 | 5 | 6 | 11 | 1534 | 17 | 10 | 7 |
| 1999/00 | 116 | 227 | 72 | 144 | 17 | 13 | 26 | 26 | 27 | 10 | 8 | 2 | 1 | 0 | 689 | 7 | 3 | 4 |
| 2000/01 | 116 | 249 | 332 | 87 | 166 | 10 | 7 | 21 | 8 | 14 | 11 | 3 | 3 | 0 | 1025 | 14 | 10 | 4 |
| 2001/02 | 61 | 56 | 130 | 114 | 62 | 136 | 25 | 24 | 17 | 21 | 17 | 10 | 3 | 0 | 676 | 9 | 4 | 5 |
| 2002/03 | 520 | 705 | 258 | 104 | 130 | 74 | 128 | 46 | 26 | 25 | 13 | 15 | 10 | 1 | 2055 | 22 | 12 | 10 |
| 2003/04 | 126 | 301 | 415 | 88 | 35 | 32 | 15 | 17 | 3 | 4 | 4 | 6 | 1 | 1 | 1048 | 13 | 8 | 5 |
| 2004/05 | 304 | 159 | 284 | 326 | 70 | 29 | 17 | 5 | 8 | 4 | 0 | 3 | 3 | 0 | 1212 | 13 | 4 | 9 |
| 2005/06 | 217 | 312 | 190 | 420 | 501 | 110 | 40 | 38 | 26 | 18 | 5 | 5 | 5 | 7 | 1894 | 22 | 14 | 8 |
| 2006/07 | 19 | 77 | 134 | 64 | 71 | 88 | 22 | 4 | 2 | 2 | 0 | 0 | 0 | 1 | 484 | 6 | 4 | 2 |
| 2007/08 | 58 | 288 | 180 | 264 | 85 | 80 | 104 | 19 | 15 | 2 | 2 | 6 | 1 | 3 | 1107 | 17 | 13 | 4 |
| 2008/09 | 274 | 208 | 213 | 136 | 204 | 123 | 125 | 97 | 18 | 13 | 9 | 7 | 4 | 17 | 1448 | 29 | 19 | 10 |
| 2009/10 | 104 | 100 | 105 | 116 | 60 | 74 | 34 | 19 | 36 | 8 | 3 | 4 | 2 | 2 | 667 | 17 | 10 | 7 |
| 2010/11 | 35 | 74 | 102 | 157 | 139 | 61 | 119 | 22 | 52 | 36 | 13 | 0 | 1 | 0 | 811 | 11 | 8 | 3 |
| 2011/12 | 229 | 330 | 134 | 115 | 100 | 106 | 74 | 87 | 45 | 48 | 51 | 10 | 3 | 3 | 1335 | 15 | 9 | 6 |
| 2012/13 | 42 | 266 | 554 | 273 | 220 | 252 | 198 | 165 | 126 | 114 | 69 | 61 | 12 | 2 | 2370 | 60 | 55 | 5 |
| 2013/14 | 26 | 472 | 275 | 414 | 199 | 200 | 199 | 208 | 163 | 138 | 90 | 85 | 60 | 23 | 2552 | 45 | 37 | 8 |
| 2014/15 | 83 | 50 | 96 | 71 | 72 | 53 | 32 | 26 | 11 | 22 | 8 | 3 | 6 | 4 | 534 | 10 | 8 | 2 |
| 2015/16 | 229 | 112 | 131 | 208 | 148 | 123 | 47 | 32 | 32 | 22 | 13 | 7 | 12 | 4 | 1120 | 14 | 7 | 7 |
| 2016/17 | 66 | 164 | 122 | 137 | 202 | 117 | 169 | 43 | 50 | 44 | 14 | 15 | 9 | 4 | 1162 | 14 | 12 | 2 |
| 2017/18 | 35 | 58 | 82 | 77 | 75 | 101 | 65 | 77 | 29 | 11 | 27 | 18 | 8 | 9 | 672 | 10 | 5 | 5 |
| 2018/19 | 28 | 39 | 31 | 98 | 50 | 53 | 77 | 75 | 36 | 15 | 15 | 21 | 5 | 4 | 547 | 7 | 5 | 2 |
| 2019/20 | 265 | 143 | 94 | 48 | 101 | 60 | 43 | 54 | 45 | 43 | 27 | 26 | 20 | 6 | 975 | 10 | 5 | 5 |
| 2020/21 | 248 | 215 | 116 | 68 | 59 | 104 | 52 | 79 | 55 | 44 | 35 | 13 | 6 | 8 | 1102 | 13 | 5 | 8 |
| 2021/22 | 39 | 89 | 588 | 258 | 254 | 113 | 138 | 87 | 78 | 49 | 34 | 24 | 19 | 8 | 1890 | 12 | 5 | 7 |
| 2022/23 | 214 | 306 | 410 | 388 | 127 | 118 | 120 | 90 | 83 | 83 | 61 | 41 | 37 | 15 | 2093 | 13 | 4 | 9 |
| 2023/24 | 48 | 529 | 652 | 396 | 192 | 208 | 84 | 110 | 65 | 54 | 29 | 25 | 14 | 8 | 2414 | 9 | 6 | 3 |
| 2024/25 | 12 | 173 | 384 | 463 | 412 | 102 | 105 | 94 | 45 | 50 | 28 | 30 | 24 | 3 | 1928 | 10 | 4 | 6 |
| 2025/26 | 78 | 173 | 133 | 207 | 242 | 151 | 136 | 60 | 28 | 18 | 32 | 17 | 4 | 4 | 1283 | 11 | 4 | 7 |
Numbers-at-age from the acoustic surveys since 1988 are shown in Figure 10. The acoustic survey indices show the same prominent year classes as seen in the catch (Figure 5) in recent years, although the 2017 year class was underestimated at age 5 in the surveys. Survey indices from 2025 are high, particularly for older age groups, which may reflect uncertainty in the measurements rather than a true increase in stock size.
A widespread ichthyophoniasis epizootic infection has occurred in the ISS herring stock since late 2008. The infection is caused by the parasite Ichthyophonus sp. Comprehensive analyses for the period 2008–2014 indicated that significant infection-related mortality occurred during the first three years after the outbreak began, 2009–2011, but not in the following years, 2012–2016 [@Oskarsson2018b]. The level of mortality was estimated through a series of runs of the NFT-Adapt assessment model. The best fit to the data was obtained when infection-related mortality was set equivalent to 30% of infected herring dying annually during the first three years of the outbreak.
This assumption is used in the stock assessment by adding infection-related mortality to the fixed natural mortality, \(M_{\text{fixed}} = 0.1\), for each age group and year:
\[ M_{\text{year}, \text{age}} = M_{\text{fixed}} + M_{\text{infected}, \text{year}, \text{age}} \times 0.3 \]
Survey abundance estimates and heart inspection data are used to estimate \(M_{\text{infected}}\).
At the 2024 WKICEHER workshop assessment (ICES 2024), the infection mortality was estimated by the Muppet model using a method similar to Óskarsson et al. (2018b). That model had been used previously also and returned the same multiplier as NFT-Adapt, or 0.3. The multiplier was estimated for the whole time series (2009-2023) on basis of the inter-annual estimates of infection prevalence by the different age groups. Different from the previous estimation, the infection mortality was assumed to have taken place in all years, also in the years 2012-2016. This was considered appropriate because thorough inspection on development of the infection stages and prevalence of the infection has not been done for recent years. The resulting multiplier for the years 2009-2023, and for the coming years until revised again, is 0.22. The revised M for the stock is visualized in Figure 11.
The prevalence of the Ichthyophonus infection in the stock in 2025/26 was estimated in a same way as has been done since the initiation of the infection in the autumn 2008 (Óskarsson and Pálsson, 2018). The prevalence of infection shows a declining trend for all age classes for the past decade. The infection rate for the younger year classes (age 2-5) seems to be low, or <4% in the west (Figure 12). There are still new infections taking place as seen with the younger ages, so infection mortality is assumed to take place in 2026, like in previous years. Thus, in the stock prognosis (Section 11.6), the abundance estimates from the final year of the assessment (1 January 2026) is lowered by this additional M as done in assessments for the past years. The level of M should then follow the results of the WKICEHER workshop (2024), where age specific Minfected (estimated from the catch samples; Figure 12) is multiplied by 0.22 and the fixed M (0.1) added to it. The M for 2025 (Table 11.3.2.1) should be used in the prognosis in 2026 and in the analytical assessment from 2024 and onwards, until better more reliable estimates become available.
Stock assessment
Model and data inputs
In accordance with the recommendation from the 2024 WKICEHER workshop (ICES, 2024), a statistical catch at age model (SAM) was adopted for the 2024 assessment and the reference points were updated. The estimated SAM model parameters are described in the stock annex and illustrated in Figure 13. The catch and survey data used were from 1987/1988–2025/2026. Other input data and model settings consisted of: (i) mean weight at age (Figure 6); (ii) a fixed maturity ogive; (iii) natural mortality (M) was set to 0.1 for all age groups in all years prior to 2009, and from 2009–2025, an additional mortality term was applied because of the Ichthyophonus infection (Figure 11; ICES 2024, Óskarsson et al. 2018a); (iv) the proportion of M before spawning was set to 0.5; and (v) the proportion of F before spawning was set to 0.
Diagnostics and fit
Fits to the catch data and acoustic survey numbers-at-age indices can be found in Figure 14 , Figure 15 and Figure 16. The model follows the catch data reasonably well, but younger age groups (<5) are not as well described by the model as the older age groups. For the herring survey data, the model fit is best for age groups 4-13. In 2025 survey year, the model fit does not reach the relatively high indices of age 6 and older. The model follows the juvenile survey reasonably well.
Observation error residuals (Figure 17) for the herring acoustic survey are generally higher in the period 2000-2010 than other parts of the time series, underlining the inaccuracies in the survey at that time. Positive residuals, where the model estimates are smaller than seen in the survey, can be seen for 1994- and 1999-year classes for almost all age groups and negative residuals for the 2001- and 2003-year classes. Year blocks of positive residuals are apparent for the years ~2000 to 2006 (i.e. referring to 1 January). During these years, the stock was overwintering in offshore areas off the east and west coast, prior to this period the stock was mainly distributed in the east, and from 2006–2012 the stock was overwintering in inshore areas. These positive blocks could therefore reflect changes in catchability of the survey for these years. In 2025, a positive block for all ages, except age 3, can be seen due to a high survey index that year.
Since 2020, a series of positive survey residuals can be seen for recruiting herring, this is due to large year classes entering the stock. The residuals from the catch show no definitive trend other than that they are higher in earlier years of the series. Process residuals showed only a minor trend (Figure 18).
Results
Summary of the assessment is shown in Figure 19. The spawning stock biomass was large around 2007 but steadily declined until 2017 despite small catches. This decrease was due to mortality from the Ichthyophonus infection from 2009–2018, and also due to a number of small year classes entering the stock since 2005, particularly the 2011–2014-year classes. The 2017–2020 year classes are large, and since their recruitment to the fishable stock in 2020, the SSB fallowed an upward trajectory. Since 2023, the SSB has been declining due to lower year class strenght of recruiting herring. The information about recruitment has been poor in recent years which leads to high uncertainty in model estimates. However, the most recent recruitment estimate is based on juvenile survey that shows above average 2024 year class. Fishing mortality of herring in 27.5a has been quite variable since 1980, reaching a peak in late 80‘s and gradually reducing in the following years.
The retrospective analysis indicates a moderate retrospective pattern in the assessment. Mohn’s ρ is positive for fishing mortality, Fbar(5–10), and recruitment, R(age 2), with values of 0.1119 and 0.1364, respectively, while spawning stock biomass has a negative value, ρ = −0.1009. Overall, the peels are generally within, or close to, the confidence intervals of the terminal assessment (Figure 20). The main deviations occur in the two most recent peels for SSB and Fbar(5–10), which fall outside the confidence intervals and indicate some uncertainty in the terminal estimates. Recruitment estimates remain uncertain due to limited information on incoming year classes, but uncertainty is lower than in previous assessments because of the recent juvenile survey.
Short-term projections
The final SAM model, providing number-at-age on 1 January 2026, was used for the prognosis. To account for expected Ichthyophonus-related mortality in spring 2026, SAM outputs were adjusted using the estimated infection ratios, following the additional natural mortality approach from WKICEHER 2024 (ICES 2024). Stock weights were estimated from the previous year’s catch weights (see Stock Annex).
The harvest rate estimated from the assessment for 2025 was 0.21. The spawning-stock biomass in 2026 was estimated at 409 080 tonnes, and recruitment at age 2 in 2026 was estimated at 894 213 thousand individuals. Recruitment at age 2 in 2027 was assumed to be 603 988 thousand individuals, based on the average recruitment over the past 10 years. The reported catch from June 2025 to the end of April 2026 was 104 591 tonnes.
| Quantity | Value | Notes |
|---|---|---|
| Harvest rate, HR (2025) | 0.21 | Harvest rate from the assessment |
| SSB (2026) | 409 080 t | From the assessment |
| Recruitment age 2 (2026) | 894 213 | From the assessment; thousands |
| Recruitment age 2 (2027) | 603 988 | Average of the past 10 years; thousands |
| Total catch (2025) | 104 591 t | Reported catch from June 2025 to the end of April 2026 |
Prognosis results
The management plan harvest rate of 0.19 was applied to the forecast biomass. This gives an advised total catch of 80 307 tonnes for 2026. Under this scenario, the biomass of age 4+ in 2027 is projected to be 439 380 tonnes and the spawning-stock biomass in 2027 is projected to be 423 579 tonnes.
This corresponds to a 4% increase in SSB and a 22% decrease in advice compared with the previous advice.
| Basis | Total catch (2026) | HR (2026) | Biomass age 4+ (2027) | SSB (2027) | % SSB change | % advice change |
|---|---|---|---|---|---|---|
| Management plan | 80 307 t | 0.19 | 439 380 t | 423 579 t | 4 | -22 |
Reference points & advice basis
Precautionary approach reference points
The exploitation rate \(F_{0.1} = F_{\text{MSY}} = 0.22\) proved successful in managing the stock for about 30 years, despite biased assessments. At the 2024 WKICEHER workshop, the precautionary approach (PA) reference points for the stock were verified and revised (ICES 2024).
On the basis of the stock–recruitment relationship derived from a time series spanning 1947–2015, keeping \(B_{\text{lim}} = 200\) kt was considered reasonable at the 2016 NWWG meeting (ICES 2016) and by the Study Group on Precautionary Reference Points for Advice on Fishery Management in February 2003.
Other PA reference points were derived from \(B_{\text{lim}}\) and these data in accordance with the ICES Advice Technical Guidelines:
- \(B_{\text{pa}} = 273\) kt, calculated as \(B_{\text{pa}} = B_{\text{lim}} \times e^{1.645\sigma}\), where \(\sigma = 0.19\).
- \(HR_{\text{lim}} = 0.34\), defined as the harvest rate that leads to \(SSB = B_{\text{lim}}\), given mean recruitment.
- \(HR_{\text{pa}} = 0.248\), defined as the harvest rate leading to \(P(SSB > B_{\text{lim}}) > 95\%\) with \(MSY\ B_{\text{trigger}}\).
MSY based reference points:
At the NWWG meeting in 2011, exploratory work using the HCS program version 10.3 (Skagen, 2012) was used to evaluate possible reference points based on the MSY framework. These reference points could later provide a basis for a management plan and harvest control rule (ICES, 2011b).
A number of runs were carried out with varying settings. The results indicated that the MSY framework was consistent with the currently used precautionary reference points, suggesting that the currently used \(F_{0.1} = 0.22\) could be a valid candidate for \(F_{\text{MSY}}\).
During Management Strategy Evaluations (MSEs) for the stock in April 2017 and again in March 2024 (ICES, 2024, 2017b), simulation results from both evaluations concluded that \(F_{\text{MSY}} = 0.22\) is appropriate.
Management
A Management Strategy Evaluation (MSE) for the stock took place in March 2024 (ICES, 2024). Three different HCRs were tested and all of them were considered precautionary, and, except for the advisory rule applied at that time (FMGT = 0.15), in accordance with the ICES MSY approach. One of the HCRs was later adopted by the Icelandic Government as a Management plan for the stock. This HCR is based on reference biomass of age 4+ in the beginning of the assessment years (Bref, Y), a spawning stock biomass trigger (MGT Btrigger) equal to 273 kt, and the harvest rate (HRMGT) is set as 19% of the reference biomass (age 4+) in the beginning of the assessment year. In the assessment year (Y) the TAC in the next fishing year (1st September of year Y to 31st August of year Y+1) is calculated as follows:
When SSBY is equal or above MGT Btrigger:
TACY = HRMGT*BRef,y
When SSBY is below MGT Btrigger:
TACY = HRMGT* (SSBy/MGT Btrigger) * Bref,y
In the MSE simulation, the ongoing Ichthyophonus epidemic was considered to continue and was accounted for. Consequently, this HCR is independent of the estimated level of Ichthyophonus mortality and requires no further action during such epidemics.
The distribution of the realized harvest rate when the HCR is followed showed that the 90% expected range are within a harvest rate of 0.099–0.22. The recent realized harvest rates are within the above range. In 2025, the Icelandic authorities changed the fishing year for this stock to a calendar year (previously 1 September of year Y to 31 August of year Y+1) (Government of Iceland, 2026).
Management considerations
Uncertainty in the assessment
There are number of factors that could lead to uncertainty in the assessment. Two of them are addressed here. Additional natural mortality caused by the Ichthyophonus infection was set for the whole infection period 2009-2026 (Minfected, age, year multiplied by 0.22 (see Stock Annex). This quantification of the infection mortality is based on Óskarsson et al. (2018b) and was revised at the 2024 WKICEHER workshop (ICES, 2024), and was considered to improve the assessment and reduce its uncertainty. It is worth noting that increasing M has been shown to increase the historical perception of the stock’s size but has minor impacts on the assessment of the final year and the resulting advice. There have been technical issues with the acoustic surveys in 2024-2025 that results in increased uncertainties around the population estimates. Further uncertainty regarding the assessment is the estimate of recruiting year classes. The juvenile survey, which had not been conducted since 2018, was reinstated in autumn 2025 and now provides information on year-class strength at age 1. This reduces uncertainty in the assessment, although recruitment estimates remain uncertain until the year classes are observed at older ages.
Uncertainty in the forecast
It is important to note that the advice for the 2026 fishing season that is derived from the Management plan is independent of the forecast and its uncertainty as it is only based on the reference biomass in the beginning of the assessment year. The uncertainty in the assessment mentioned above related to the apparent new infection in the stock and size of the recruiting year classes, apply also for the forecast.
Assessment quality
For a period in the 2000s, there were concerns regarding the assessment because of retrospective patterns in the results. No assessment was provided in 2005 due to data and model problems, and in the following two years ACFM rejected the assessment because of the retrospective pattern. In the assessments in 2007–2009, an improvement in the pattern from NFT-Adapt was observed, while in 2010–2011 a retrospective pattern appeared again. This was related both to the high natural mortality associated with the Ichthyophonus infection and to new, more optimistic information on incoming year classes to the fishable stock, particularly the 2008 year class, as well as changes in the recent fishing pattern.
In recent years, retrospective patterns have generally remained moderate. In this year’s assessment, Mohn’s rho values indicate some retrospective uncertainty, but they are no longer at a level suggesting major concern. The values are 0.1119 for Fbar(5–10), 0.1364 for recruitment at age 2, and -0.1009 for SSB (Figure 20). Most peels are within, or close to, the confidence intervals of the terminal assessment, with the main deviations occurring in the two most recent peels for SSB and Fbar(5–10). The retrospective pattern is therefore less pronounced than in previous problematic periods and does not indicate a consistent overestimation of stock size together with underestimation of fishing mortality.
Residual patterns should nevertheless continue to be monitored, particularly for recent survey observations and incoming year classes. Overall, the current assessment shows a moderate retrospective pattern, but the Mohn’s rho values do not indicate the same level of concern as previously reported.
Changes in fishing technology and fishing patterns
There are no recent changes in fishing techniques that could lead to different catch compositions. The fishing pattern in the seasons 2014/2015 to 2025/2026 was different from the previous seasons. Instead of fishing only in a small inshore area off the west coast in purse seine, the directed fishery mainly took place in offshore areas west and east of the country. These changes are not considered to affect the selectivity of the fishery because the fishery is still targeting dense schools of overwintering herring in large fishing gears, getting huge catches in each haul and is by no means size selective.
Since around mid-2000s, Icelandic summer-spawning herring has been caught in a mixed (to varying degrees) fishery with the summer fishery for NE-Atlantic mackerel and Norwegian spring-spawning herring. Until that time, no summer fishery on this stock had taken place for decades. Part of this bycatch is on the stock components (e.g. juveniles and herring east of Iceland) that are not fished in the direct fishery on the overwintering grounds in the west. These bycatches are well sampled and normally contribute less than 10% of the total annual catch, but have been unusually high in recent years — accounting for 30% in 2022/2023, 42% in 2023/2024 (approximately 30 kt each year), and again 30% in 2024/2025 (18 kt) and 2025/2026 (30 kt). Easterly distribution of the large incoming year classes from 2017, 2018 and 2019 explains this high level of bycatch, which contributed to 50% of the catches in the east. This is also reflected in the acoustic measurements where measurements in the east have been increasing in recent years (Figure 9; Bjarnason, 2026).
The fishing pattern varies annually as noted in earlier sections and it is related to variation in winter distribution of the different age classes of the stock. This variation can have consequences for the catch composition, but it is impossible to provide a forecast about this variation.
Ecosystem considerations
The reason for the outbreak of Ichthyophonus infection in the herring stock that was first observed in the autumn 2008 is not known but is probably the effect of interaction between environmental factors and distribution of the stock (Óskarsson et al. 2009). It includes that out-break of Ichthyophonus spores in the environment, which infect the herring via oral intake (Jones and Dawe, 2002), could be linked to the observed increased temperature off the southwest coast. Further research on the causes and origins of such an outbreak are ongoing at MFRI. It involves scanning for Ichthyophonus DNA in zooplankton species that the herring feeds on with PCR (Polymerase chain reaction) technique. Results from that work (MS thesis) can be expected in the in the near future, while preliminary results indicate that the source of the infection is widespread and is in various zooplankton groups and species. With respect to the impacts of the outbreak on the herring stock, recent analyses show that significant additional mortality took place over the first three years only (Óskarsson et al., 2018b), despite a high prevalence of infection for the past decade. For how long time this outbreak will last is unknown as this is basically an unprecedented outbreak. The signs of the infection that is found in the stock will most likely remain for some years, even if no new infection will occur, and then decrease and disappear over some years as new year classes replace the older ones. The observed new infection, even if at a relatively low level, will however delay this process.
The Northwestern working group at ICES is not aware of any strong, well-documented ecosystem or environmental signals that consistently influence the dynamics of the Icelandic summer-spawning herring stock, and which could therefore justify incorporating ecosystem drivers into the analytical basis for scientific advice. While some weak positive correlations have been identified—such as between recruitment and the winter North Atlantic Oscillation (NAO) index or sea temperature (Óskarsson and Taggart, 2010)—other potential indicators, like spring zooplankton abundance, have shown no significant effect on recruitment (Óskarsson and Taggart, 2010), nor on the body condition or growth rate of adult herring (Óskarsson, 2008). Based on these historical relationships, combined with relatively warm sea temperatures around Iceland (MRI, 2016) and persistently high NAO values in recent years (NOAA NAO Index), an earlier assessment (ICES, 2021) suggested the likelihood of strong recruitment. This appears to be supported by the emergence of strong year classes in 2017–2019.
However, there are early indications that the NAO index may now be entering a weakening phase. If this trend continues, it could lead to a shift in oceanographic conditions around Iceland potentially cooler waters and altered plankton dynamics which may negatively impact herring recruitment in the coming years. This highlights the need for ongoing monitoring of environmental drivers, even if they are not yet formally included in assessment models, to better anticipate potential changes in stock productivity under shifting climate conditions. All general ecosystem consideration with respect to the stock can be found in the Ecosystem Overview for the Icelandic Ecoregion (ICES, 2017a).
References
Astthorsson, O. S., Valdimarsson H., Gudmundsdóttir, Á., Óskarsson, G.J. 2012. Climate-related variations in the occurrence and distribution of mackerel (Scomber scombrus) in Icelandic waters. ICES Journal of Marine Science. 69: 1289–1297.
Bjarnason, S. 2025. Results of acoustic measurements of Icelandic summer-spawning herring in the winter 2024/2025. ICES North Western Working Group, 26 April - 2 May 2025, Working Document No. 11. 36 pp.
Bjarnason, S. 2026. Results of acoustic measurements of Icelandic summer-spawning herring in the winter 2025/2027. ICES North Western Working Group, 25 - 30 April 2026, Working Document No. 11.
Björnsson, H. 2018. Icelandic herring. ICES Northwestern Working Group, 27 April - 4 May 2018, Working Document No. 20. 2 pp.
Carvalho, F., et al. “A cookbook for using model diagnostics in integrated stock assessments”. In: Fisheries Research 240 (2021), p.105959.
Debes, H., Homrum, E., Jacobsen, J. A., Hátún, H., and Danielsen, J. 2012. The feeding ecology of pelagic fish in the southwestern Norwegian Sea – Inter species food competition between herring (Clupea harengus) and mackerel (Scomber scombrus). ICES CM 2012/M:07. 19 pp.
Fiskistofa, http://www.fiskistofa.is/veidar/aflaupplysingar/heildaraflamarksstada/
Guðmundsdóttir, Á., G.J. Óskarsson, and S. Sveinbjörnsson 2007. Estimating year-class strength of Icelandic summer-spawning herring on the basis of two survey methods. ICES Journal of Marine Science, 64: 1182–1190.
Hafrannsóknastofnun 2016. Þættir úr vistfræði sjávar 2015, https://www.hafogvatn.is/is/midlun/utgafa/haf-og-vatnarannsoknir/thaettir-ur-vistfraedi-sjavar-2015.
ICES. 2011a. Report of the Benchmark Workshop on Roundfish and Pelagic Stocks (WKBENCH 2011), 24–31 January 2011, Lisbon, Portugal. ICES CM 2011/ACOM:38. 418 pp.
ICES. 2011b. Report of the North Western Working Group (NWWG), 26 April - 3 May 2011, ICES Headquarters, Copenhagen. ICES CM 2011/ACOM:7. 975 pp
ICES. 2014. Report of the North Western Working Group (NWWG), 24 April-1 May 2014, ICES HQ, Copenhagen, Denmark. ICES CM 2014/ACOM:07. 902 pp.
ICES. 2016. Report of the North-Western Working Group (NWWG), 27 April–4 May, 2016, ICES Headquarters, Copenhagen. ICES CM 2016/ACOM:08.
ICES. 2017a. Icelandic Waters ecoregion – Ecosystem overview. http://ices.dk/sites/pub/Publication%20Reports/Advice/2017/2017/Ecosystem_overview-Icelandic_Waters_ecoregion.pdf
ICES. 2017b. Report of the Workshop on Evaluation of the Adopted Harvest Control Rules for Icelandic Summer Spawning Herring, Ling and Tusk (WKICEMSE), 21–25 April 2017, Copenhagen, Denmark. ICES CM 2017/ACOM:45. 49 pp.
ICES. 2017c. Report of the North Western Working Group (NWWG), 27 April – 4 May 2017, Copenhagen, Denmark. ICES CM 2017/ACOM:08. 642 pp.
ICES. 2018. Report of the North-Western Working Group (NWWG), 26 April–3 May, 2018, ICES HQ, Copenhagen, Denmark. ICES CM 2018/ACOM:09. 733 pp.
ICES. 2024. Workshop on the assessment and management plan evaluation for Icelandic herring (WKICEHER). ICES Scientific Reports. 6:37. 91 pp. https://doi.org/10.17895/ices.pub.25605135
Jakobsson, Jakob., Vilhjálmsson, Hjálmar & Schopka, Sigfús A. 1969. On the biology of the Icelandic herring stocks. Rit Fiskideildar 4. 1-16.
Jakobsson, Jakob. 1980. Exploitation of the Icelandic spring- and summer spawning herring in relation to fisheries management, 1947-1977. Rapports et Proces-Verbaux des Reunions Conseil International pour l’exploration de la Mer 177. 23-42.
Jakobsson, Jakob. 2000. Lífríki sjávar - Síld. Námsgagnastofnun og Hafrannsóknastofnun. 8 bls.
Jones, S.R.M. and Dawe, S.C., 2002. Ichthyophonus hoferi Plehn & Mulsow in British Columbia stocks of Pacific herring, Clupea pallasi Valenciennes, and its infectivity to chinook salmon, Oncorhynchus tshawytscha (Walbaum). Journal of Fish Diseases 25, 415-421.
Óskarsson, G.J. 2008. Variation in body condition, fat content and growth rate of Icelandic summer-spawning herring (Clupea harengus L.). Journal of Fish Biology 72: 2655–2676.
Óskarsson, G.J. 2019. Estimation on number-at-age of the catch of Icelandic summer-spawning herring in 2018/2019 fishing season and the development of Ichthyophonus sp. infection in the stock. ICES North Western Working Group, 25 April - 1 May 2019, Working Document No. 5. 15 pp.
Óskarsson, G.J., Á. Guðmundsdóttir & Þ. Sigurðsson. 2009. Variation in spatial distribution and migration of Icelandic summer-spawning herring. ICES Journal of Marine Science 66. 1762-1767.
Óskarsson, Guðmundur J. & Taggart, C.T. 2009. Spawning time variation in Icelandic summer-spawning herring (Clupea harengus L.). Canadian Journal of Fisheries and Aquatic Science 66. 1666-1681.
Óskarsson, G.J. and C.T. Taggart 2010. Variation in reproductive potential and influence on Icelandic herring recruitment. Fisheries Oceanography. 19: 412–426.
Óskarsson, G.J. and Pálsson, J. 2018. Estimation on number-at-age of the catch of Icelandic summer-spawning herring in 2017/2018 fishing season and the development of Ichthyophonus sp. infection in the stock. ICES North Western Working Group, 27 April - 4 May 2018, Working Document No. 2. 15 pp.
Óskarsson, G.J., Ólafsdóttir, S.R., Sigurðsson, Þ., and Valdimarsson, H. 2018b. Observation and quantification of two incidents of mass fish kill of Icelandic summer spawning herring (Clupea harengus) in the winter 2012/2013. Fisheries Oceanography. DOI: 10.1111/fog.12253.
Óskarsson, G.J., Pálsson, J., and Gudmundsdottir, A. 2018a. An ichthyophoniasis epizootic in Atlantic herring in marine waters around Iceland. Can. J. Fish. Aquat. Sci. dx.doi.org/10.1139/cjfas-2017-0219.
Skagen, D. 2012. HCS program for simulating harvest control rules. Program description and instructions for users. Version HCS12_2. Available from the author.
Government of Iceland. 2026. Management strategy and harvest control rules. Retrieved May 29, 2026, from https://www.government.is/topics/business-and-industry/fisheries-in-iceland/management-strategy-and-harvest-control-rules/
NOAA 2025: National Oceanic and Atmospheric Administration, National weather service – Climate prediction center http://www.cpc.ncep.noaa.gov/products/precip/CWlink/pna/nao.shtml.
Comments on the assessment
The assessment shows that the stock size was declining 2000–2018 due to a combination of mortality due to Ichthyophonus infection and a series of below average and poor year classes entering the stock. The 2017-2019 year classes which entered the reference biomass in autumn 2021-2023 caused an upward revision of the assessment but a downward revision of spawning biomass estimates and a reduction in the reference biomass is caused by reduced recruitment in recent years.
There is still evidence for new infection by Ichthyophonus in the stock in the winter 2025/26, even if it is less intense than in the years before. This meant applying additional infection mortality in the assessment. If the low levels of new infection in the recent four years, and the resulting low infection rate for the younger age groups, marks a cessation of the outbreak is unclear. This current outbreak adds uncertainty to the assessment and advice.