Herring

Herring are forage fish, mostly belonging to the family Clupeidae.

This article is about the species of fish. For their use as food, see Herring as food. For other uses, see Herring (disambiguation).
Herring
The Atlantic herring, Clupea harengus
Global commercial capture of herrings
in million tonnes reported by the FAO 1950–2010[1]

Herring often move in large schools around fishing banks and near the coast, found particularly in shallow, temperate waters of the North Pacific and North Atlantic Oceans, including the Baltic Sea, as well as off the west coast of South America. Three species of Clupea are recognised, and provide about 90% of all herrings captured in fisheries. Most abundant of all is the Atlantic herring, providing over half of all herring capture. Fish called herring are also found in the Arabian Sea, Indian Ocean, and Bay of Bengal.

Herring played a pivotal role in the history of marine fisheries in Europe,[2] and early in the 20th century, their study was fundamental to the evolution of fisheries science.[3][4] These oily fish[5] also have a long history as an important food fish, and are often salted, smoked, or pickled.

Also known as "silver darlings".[6]

Species
This article is part of a series on
Commercial fish
Large pelagic
Forage
Demersal
Mixed

A number of different species, most belonging to the family Clupeidae, are commonly referred to as herrings. The origins of the term "herring" is somewhat unclear, though it may derive from the Old High German heri meaning a "host, multitude", in reference to the large schools they form.[7]

The type genus of the herring family Clupeidae is Clupea.[4] Clupea contains three species: the Atlantic herring (the type species) found in the north Atlantic, the Pacific herring found in the north Pacific, and the Araucanian herring found off the coast of Chile. Subspecific divisions have been suggested for both the Atlantic and Pacific herrings, but their biological basis remains unclear.

Herrings in the genus Clupea
Common name Scientific name Maximum
length		 Common
length		 Maximum
weight		 Maximum
age		 Trophic
level		 Fish
Base		 FAO ITIS IUCN status
Araucanian herring Clupea bentincki Norman, 1936 28.4 cm cm kg years 2.69 [8] [9] [10] Not assessed
Atlantic herring Clupea harengus Linnaeus, 1758 45.0 cm 30.0 cm 1.05 kg 22 years 3.23 [11] [12] [13] Least concern[14]
Pacific herring Clupea pallasii Valenciennes, 1847 46.0 cm 25.0 cm 19 years 3.15 [11] [15] [16] Not assessed

In addition, a number of related species, all in the Clupeidae, are commonly referred to as herrings. The table immediately below includes those members of the family Clupeidae referred to by FishBase as herrings which have been assessed by the International Union for Conservation of Nature.

Other herrings in the family Clupeidae
Group Common name Scientific name Maximum
length		 Common
length		 Maximum
weight		 Maximum
age		 Trophic
level		 Fish
Base		 FAO ITIS IUCN status
Freshwater herrings Toothed river herring Clupeoides papuensis (Ramsay & Ogilby, 1886) cm cm kg years [17] [18] Data deficient[19]
Round herrings Day's round herring Dayella malabarica (Day, 1873) cm cm kg years [20] [21] Least concern[22]
Dwarf round herring Jenkinsia lamprotaenia (Gosse, 1851) cm cm kg years [23] [24] Least concern[25]
Gilchrist's round herring Gilchristella aestuaria (Gilchrist, 1913 cm cm kg years [26] [27] Least concern[28]
Little-eye round herring Jenkinsia majua Whitehead, 1963 cm cm kg years [29] [30] Least concern[31]
Red-eye round herring Etrumeus teres (De Kay, 1842) 33 cm 25 cm kg years [32] [33] [34] Not assessed
Two-finned round herring Spratellomorpha bianalis (Bertin, 1940) 4.5 cm cm kg years 3.11 [35] [36] Data deficient[37]
Whitehead's round herring Etrumeus whiteheadi (Wongratana, 1983) 20 cm cm kg years 3.4 [38] [39] [40] Least concern[41]
Venezuelan herring Jenkinsia parvula Cervigón and Velasquez, 1978

cm cm kg years [42] [43] Vulnerable[44]
Thread herrings Galapagos thread herring Opisthonema berlangai (Günther, 1867) 26 cm 18 cm kg years 3.27 [45] [46] Vulnerable[47]
Middling thread herring Opisthonema medirastre Berry & Barrett, 1963 cm cm kg years [48] [49] Least concern[50]
Pacific thread herring Opisthonema libertate (Günther, 1867) 30 cm 22 cm kg years [51] [52] [46] Least concern[53]
Slender thread herring Opisthonema bulleri (Regan, 1904) cm cm kg years [54] [55] Least concern[56]
Other Blackstripe herring Lile nigrofasciata Castro-Aguirre Ruiz-Campos and Balart, 2002 cm cm kg years [57] [58] Least concern[59]
Denticle herring Denticeps clupeoides Clausen, 1959 cm cm kg years [60] [61] Vulnerable[62]
Dogtooth herring Chirocentrodon bleekerianus (Poey, 1867) cm cm kg years [63] [64] Least concern[65]
Graceful herring Lile gracilis Castro-Aguirre and Vivero, 1990 cm cm kg years [66] [67] Least concern[68]
Pacific Flatiron herring Harengula thrissina (Jordan and Gilbert, 1882) cm cm kg years [69] [70] Least concern[71]
Sanaga pygmy herring Thrattidion noctivagus Roberts, 1972 cm cm kg years [72] [73] Least concern[74]
Silver-stripe round herring Spratelloides gracilis (Temminck & Schlegel, 1846) 10.5 cm cm kg years 3.0 [75] [76] Not assessed
Striped herring Lile stolifera (Jordan & Gilbert, 1882) cm cm kg years [77] [78] Least concern[79]
West African pygmy herring Sierrathrissa leonensis Thys van den Audenaerde, 1969 cm cm kg years [80] [81] Least concern[82]

Also, a number of other species are called herrings, which may be related to clupeids or just share some characteristics of herrings (such as the lake herring, which is a salmonid). Just which of these species are called herrings can vary with locality, so what might be called a herring in one locality might be called something else in another locality. Some examples:

Other fishes called herring
Common name Scientific name Maximum
length		 Common
length		 Maximum
weight		 Maximum
age		 Trophic
level		 Fish
Base		 FAO ITIS IUCN status
Longfin herring Bigeyed longfin herring Opisthopterus macrops (Günther, 1867) cm cm kg years [83] [84] Least concern[85]
Dove's longfin herring Opisthopterus dovii (Günther 1868) cm cm kg years [86] [87] Least concern[88]
Hatchet herring Ilisha fuerthii (Steindachner, 1875) cm cm kg years [89] [90] Least concern[91]
Panama longfin herring Odontognathus panamensis (Steindachner, 1876) cm cm kg years [92] [93] Least concern[94]
Tropical longfin herring Neoopisthopterus tropicus (Hildebrand 1946) cm cm kg years [95] [96] Least concern[97]
Vaqueira longfin herring Opisthopterus effulgens (Regan 1903) cm cm kg years [98] [99] Vulnerable[100]
Equatorial longfin herring Opisthopterus equatorialis Hildebrand, 1946 cm cm kg years [101] [102] Least concern[103]
Wolf herring Dorab wolf-herring Chirocentrus dorab (Forsskål, 1775) 100 cm 60 cm kg years 4.50 [104] [105] [106] Not assessed
Whitefin wolf-herring Chirocentrus nudus Swainson, 1839 100 cm cm 0.41 kg years 4.19 [107] [108] Not assessed
Freshwater whitefish Lake herring (cisco) Coregonus artedi Lesueur, 1818 cm cm kg years [109] [110] Not assessed

Characteristics

The species of Clupea belong to the larger family Clupeidae (herrings, shads, sardines, menhadens), which comprises some 200 species that share similar features. These silvery-coloured fish have a single dorsal fin, which is soft, without spines. They have no lateral line and have a protruding lower jaw. Their size varies between subspecies: the Baltic herring (Clupea harengus membras) is small, 14 to 18 cm; the proper Atlantic herring (C. h. harengus) can grow to about 46 cm (18 in) and weigh up 700 g (1.5 lb); and Pacific herring grow to about 38 cm (15 in).

Lifecycle
Herring spawn

At least one stock of Atlantic herring spawns in every month of the year. Each spawns at a different time and place (spring, summer, autumn, and winter herrings). Greenland populations spawn in 0–5 metres (0–16 feet) of water, while North Sea (bank) herrings spawn at down to 200 m (660 ft) in autumn. Eggs are laid on the sea bed, on rock, stones, gravel, sand or beds of algae. Females may deposit from 20,000 to 40,000 eggs, according to age and size, averaging about 30,000. In sexually mature herring, the genital organs grow before spawning, reaching about one-fifth of its total weight.

The eggs sink to the bottom, where they stick in layers or clumps to gravel, seaweed, or stones, by means of their mucous coating, or to any other objects on which they chance to settle.

If the egg layers are too thick they suffer from oxygen depletion and often die, entangled in a maze of mucus. They need substantial water microturbulence, generally provided by wave action or coastal currents. Survival is highest in crevices and behind solid structures, because predators feast on openly exposed eggs. The individual eggs are 1 to 1.4 mm (3⁄64 to 1⁄16 in) in diameter, depending on the size of the parent fish and also on the local race. Incubation time is about 40 days at 3 °C (37 °F), 15 days at 7 °C (45 °F), or 11 days at 10 °C (50 °F). Eggs die at temperatures above 19 °C (66 °F).

The larvae are 5 to 6 mm (3⁄16 to 1⁄4 in) long at hatching, with a small yolk sac that is absorbed by the time the larvae reach 10 mm (13⁄32 in). Only the eyes are well pigmented. The rest of the body is nearly transparent, virtually invisible under water and in natural lighting conditions.

The dorsal fin forms at 15 to 17 mm (19⁄32 to 21⁄32 in), the anal fin at about 30 mm (1 3⁄16 in)—the ventral fins are visible and the tail becomes well forked at 30 to 35 mm (1 3⁄8 in)— at about 40 mm (1 9⁄16 in), the larva begins to look like a herring.

Herring larvae are very slender and can easily be distinguished from all other young fish of their range by the location of the vent, which lies close to the base of the tail; however, distinguishing clupeoids one from another in their early stages requires critical examination, especially telling herring from sprats.

At one year, they are about 10 cm (4 in) long, and they first spawn at three years.

Egg to juvenile
Transparent eggs with the yolk and eyes visible and one larva hatched.
Freshly hatched larva in a drop of water beside a match to demonstrate how tiny it is: The black eyes and the yolk are visible.
Young larva in typical oblique swimming position, with remaining yolk still attached: Another larva at the upper right is in the classical S-shape of the beginning phase of attacking a copepod.
Still transparent juvenile herring, about 38 mm long and 3 months old: Visible are the otoliths, the gut, the silvery swimbladder, and the heart.

Ecology

Prey
See also: Hunting copepods

Herrings consume copepods, arrow worms, pelagic amphipods, mysids, and krill in the pelagic zone. Conversely, they are a central prey item or forage fish for higher trophic levels. The reasons for this success is still enigmatic; one speculation attributes their dominance to the huge, extremely fast cruising schools they inhabit.

Herring feed on phytoplankton, and as they mature, they start to consume larger organisms. They also feed on zooplankton, tiny animals found in oceanic surface waters, and small fish and fish larvae. Copepods and other tiny crustaceans are the most common zooplankton eaten by herring. During daylight, herring stay in the safety of deep water, feeding at the surface only at night when the chance of being seen by predators is less. They swim along with their mouths open, filtering the plankton from the water as it passes through their gills. Young herring mostly hunt copepods individually, by means of "particulate feeding" or "raptorial feeding",[111] a feeding method also used by adult herring on larger prey items like krill. If prey concentrations reach very high levels, as in microlayers, at fronts, or directly below the surface, herring become filter feeders, driving several meters forward with wide open mouth and far expanded opercula, then closing and cleaning the gill rakers for a few milliseconds.

Copepods, the primary zooplankton, are a major item on the forage fish menu. Copepods are typically 1–2 mm (1⁄32–3⁄32 in) long, with a teardrop-shaped body. Some scientists say they form the largest animal biomass on the planet.[112] Copepods are very alert and evasive. They have large antennae (see photo below left). When they spread their antennae, they can sense the pressure wave from an approaching fish and jump with great speed over a few centimetres. If copepod concentrations reach high levels, schooling herrings adopt a method called ram feeding. In the photo below, herring ram feed on a school of copepods. They swim with their mouths wide open and their perculae fully expanded.

Hunting copepods
This copepod has its antennae spread. The antennae detect the pressure wave of an approaching fish.
School of herrings ram feeding on a school of copepods with opercula and mouth expanded: The fish swim in a grid with a distance of the jump length of their prey, as indicated by the animation at the right.
Animation showing how herrings hunt in a synchronised way to capture an alert and evasive copepod

The fish swim in a grid where the distance between them is the same as the jump length of their prey, as indicated in the animation above right. In the animation, juvenile herring hunt the copepods in this synchronised way. The copepods sense with their antennae the pressure wave of an approaching herring and react with a fast escape jump. The length of the jump is fairly constant. The fish align themselves in a grid with this characteristic jump length. A copepod can dart about 80 times before it tires. After a jump, it takes it 60 milliseconds to spread its antennae again, and this time delay becomes its undoing, as the almost endless stream of herring allows a herring to eventually snap up the copepod. A single juvenile herring could never catch a large copepod.[111]

Other pelagic prey eaten by herring includes fish eggs, larval snails, diatoms by herring larvae below 20 mm (13⁄16 in), tintinnids by larvae below 45 mm (1 3⁄4 in), molluscan larvae, menhaden larvae, krill, mysids, smaller fishes, pteropods, annelids, Calanus spp., Centropagidae, and Meganyctiphanes norvegica.

Herrings, along with Atlantic cod and sprat, are the most important commercial species to humans in the Baltic Sea.[113] The analysis of the stomach contents of these fish indicate Atlantic cod is the top predator, preying on the herring and sprat.[113][114] Sprat are competitive with herring for the same food resources. This is evident in the two species' vertical migration in the Baltic Sea, where they compete for the limited zooplankton available and necessary for their survival.[115] Sprat are highly selective in their diet and eat only zooplankton, while herring are more eclectic, adjusting their diet as they grow in size.[115] In the Baltic, copepods of the genus Acartia can be present in large numbers. However, they are small in size with a high escape response, so herring and sprat avoid trying to catch them. These copepods also tend to dwell more in surface waters, whereas herring and sprat, especially during the day, tend to dwell in deeper waters.[115]

Predators
Seabirds, like this European herring gull, attack herring schools from above.
Humpback whales attack herring schools by lunging from below.
See also: Predator avoidance in schooling fish, Bait ball

Predators of herring include seabirds, marine mammals such as dolphins, porpoises, whales, seals, and sea lions, predatory fish such as sharks, billfish, tuna, salmon, striped bass, cod, and halibut. Fishermen also catch and eat herring.

The predators often cooperate in groups, using different techniques to panic or herd a school of herring into a tight bait ball. Different predatory species then use different techniques to pick the fish off in the bait ball. The sailfish raises its sail to make it appear much larger. Swordfish charge at high speed through the bait balls, slashing with their swords to kill or stun prey. They then turn and return to consume their "catch". Thresher sharks use their long tails to stun the shoaling fish. These sharks compact their prey school by swimming around them and splashing the water with their tails, often in pairs or small groups. They then strike them sharply with the upper lobe of their tails to stun them.[116] Spinner sharks charge vertically through the school, spinning on their axes with their mouths open and snapping all around. The sharks' momentum at the end of these spiraling runs often carries them into the air.[117][118]

Some whales lunge feed on bait balls.[119] Lunge feeding is an extreme feeding method, where the whale accelerates from below the bait ball to a high velocity and then opens its mouth to a large gape angle. This generates the water pressure required to expand its mouth and engulf and filter a huge amount of water and fish. Lunge feeding by rorquals, a family of huge baleen whales that includes the blue whale, is said to be the largest biomechanical event on Earth.[120]

Fisheries
↑  All herrings 2010 [1]
Green = Clupea herrings

Adult herring are harvested for their flesh and eggs, and they are often used as baitfish. The trade in herring is an important sector of many national economies. In Europe, the fish has been called the "silver of the sea", and its trade has been so significant to many countries that it has been regarded as the most commercially important fishery in history.[121]

Purse seining for herring in southeast Alaska

Environmental Defense have suggested that the Atlantic herring (Clupea harengus) fishery is an environmentally responsible fishery.[122]

As food
A kipper or split smoked herring
Main article: Herring as food

Herring has been a staple food source since at least 3000 BC. The fish is served numerous ways, and many regional recipes are used: eaten raw, fermented, pickled, or cured by other techniques, such as being smoked as kippers.

Herring are very high in the long-chain omega-3 fatty acids EPA and DHA.[123] They are a source of vitamin D.[124]

Water pollution influences the amount of herring that may be safely consumed. For example, large Baltic herring slightly exceeds recommended limits with respect to PCB and dioxin, although some sources point out that the cancer-reducing effect of omega-3 fatty acids is statistically stronger than the cancer-causing effect of PCBs and dioxins.[125] The contaminant levels depend on the age of the fish which can be inferred from their size. Baltic herrings larger than 17 cm may be eaten twice a month, while herrings smaller than 17 cm can be eaten freely.[126] Mercury in fish also influences the amount of fish that women who are pregnant or planning to be pregnant within the next one or two years may safely eat.

History

The herring has played an enormous role in history both socially and economically. During the Middle Ages, herring prompted the founding of Great Yarmouth, Amsterdam, and Copenhagen.[127]

See also

References

Citations
  1. Based on data sourced from the relevant FAO Species Fact Sheets Archived 2009-05-08 at the Wayback Machine
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  4. Pauly, Daniel (2004) Darwin's Fishes: An Encyclopedia of Ichthyology, Ecology, and Evolution Archived 2016-05-29 at the Wayback Machine Page 109, Cambridge University Press. ISBN 978-0-521-82777-5.
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  6. "Here be herrings: the return of the silver darlings". The Guardian. 2014-11-12.
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  23. Froese, Rainer and Pauly, Daniel, eds. (2012). "Jenkinsia lamprotaenia" in FishBase. April 2012 version.
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  25. Cotto A, Medina E, Bernal O (2010). "Jenkinsia lamprotaenia". IUCN Red List of Threatened Species. 2010. Retrieved April 2012. Check date values in: |access-date= (help)
  26. Froese, Rainer and Pauly, Daniel, eds. (2012). "Gilchristella aestuaria" in FishBase. April 2012 version.
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  28. Bills R (2007). "Gilchristella aestuaria". IUCN Red List of Threatened Species. 2007. Retrieved April 2012. Check date values in: |access-date= (help)
  29. Froese, Rainer and Pauly, Daniel, eds. (2012). "Jenkinsia majua" in FishBase. April 2012 version.
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  31. Munroe TA, Priede IG (2010). "Jenkinsia majua". IUCN Red List of Threatened Species. 2010. Retrieved April 2012. Check date values in: |access-date= (help)
  32. Froese, Rainer and Pauly, Daniel, eds. (2012). "Etrumeus teres" in FishBase. April 2012 version.
  33. Etrumeus teres (Norman, 1936) Archived 2012-11-09 at the Wayback Machine FAO, Species Fact Sheet. Retrieved April 2012.
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  35. Froese, Rainer and Pauly, Daniel, eds. (2012). "Spratellomorpha bianalis" in FishBase. April 2012 version.
  36. "Spratellomorpha bianalis". Integrated Taxonomic Information System. Retrieved April 2012. Check date values in: |access-date= (help)
  37. Loiselle, P; et al. (2011). "Spratellomorpha bianalis". IUCN Red List of Threatened Species. 2011. Retrieved April 2012. Check date values in: |access-date= (help)
  38. Froese, Rainer and Pauly, Daniel, eds. (2012). "Etrumeus whiteheadi" in FishBase. April 2012 version.
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  41. Heemstra PC, Munroe TA, Priede IG (2011). "Etrumeus whiteheadi". IUCN Red List of Threatened Species. 2011. Retrieved April 2012. Check date values in: |access-date= (help)
  42. Froese, Rainer and Pauly, Daniel, eds. (2012). "Jenkinsia parvula" in FishBase. April 2012 version.
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  44. Cotto A, Medina E, Bernal O (2010). "Jenkinsia parvula". IUCN Red List of Threatened Species. 2010. Retrieved April 2012. Check date values in: |access-date= (help)
  45. Froese, Rainer and Pauly, Daniel, eds. (2012). "Opisthonema berlangai" in FishBase. April 2012 version.
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  47. Iwamoto T, Eschmeyer W (2010). "Opisthonema berlangai". IUCN Red List of Threatened Species. 2010. Retrieved April 2012. Check date values in: |access-date= (help)
  48. Froese, Rainer and Pauly, Daniel, eds. (2012). "Opisthonema medirastre" in FishBase. April 2012 version.
  49. "Opisthonema medirastre". Integrated Taxonomic Information System. Retrieved April 2012. Check date values in: |access-date= (help)
  50. Cotto A, Medina E, Bernal O (2010). "Opisthonema medirastre". IUCN Red List of Threatened Species. 2010. Retrieved April 2012. Check date values in: |access-date= (help)
  51. Froese, Rainer and Pauly, Daniel, eds. (2012). "Opisthonema libertate" in FishBase. April 2012 version.
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  54. Froese, Rainer and Pauly, Daniel, eds. (2012). "Opisthonema bulleri" in FishBase. April 2012 version.
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  56. Cotto A, Medina E, Bernal O (2010). "Opisthonema bulleri". IUCN Red List of Threatened Species. 2010. Retrieved April 2012. Check date values in: |access-date= (help)
  57. Froese, Rainer and Pauly, Daniel, eds. (2012). "Lile nigrofasciata" in FishBase. April 2012 version.
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  59. Iwamoto T, Eschmeyer W (2010). "Lile nigrofasciata". IUCN Red List of Threatened Species. 2010. Retrieved April 2012. Check date values in: |access-date= (help)
  60. Froese, Rainer and Pauly, Daniel, eds. (2012). "Denticeps clupeoides" in FishBase. April 2012 version.
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  62. Lalèyè P, Moelants T, Olaosebikan BD (2010). "Denticeps clupeoides". IUCN Red List of Threatened Species. 2010. Retrieved April 2012. Check date values in: |access-date= (help)
  63. Froese, Rainer and Pauly, Daniel, eds. (2012). "Chirocentrodon bleekerianus" in FishBase. April 2012 version.
  64. "Chirocentrodon bleekerianus". Integrated Taxonomic Information System. Retrieved April 2012. Check date values in: |access-date= (help)
  65. Priede IG (2010). "Chirocentrodon bleekerianus". IUCN Red List of Threatened Species. 2010. Retrieved April 2012. Check date values in: |access-date= (help)
  66. Froese, Rainer and Pauly, Daniel, eds. (2012). "Lile gracilis" in FishBase. April 2012 version.
  67. "Lile gracilis". Integrated Taxonomic Information System. Retrieved April 2012. Check date values in: |access-date= (help)
  68. Iwamoto T, Eschmeyer W, Smith-Vaniz B (2010). "Lile gracilis". IUCN Red List of Threatened Species. 2010. Retrieved April 2012. Check date values in: |access-date= (help)
  69. Froese, Rainer and Pauly, Daniel, eds. (2012). "Harengula thrissina" in FishBase. April 2012 version.
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