Distribution and Characteristics of Herring Spawning Grounds and Description of Spawning Behavior

1985 ◽  
Vol 42 (S1) ◽  
pp. s39-s55 ◽  
Author(s):  
C. W. Haegele ◽  
J. F. Schweigert

Pacific herring (Clupea harengus pallasi) are winter–spring spawners which exhibit a south to north latitudinal dine in spawning time. In the eastern Pacific, major spawning populations are concentrated near San Francisco, in Puget Sound, and along the coasts of British Columbia and southeastern Alaska. In the Bering Sea, herring spawn in Alaska and along the Kamchatka Peninsula. In the western Pacific, herring spawn in the Sea of Okhotsk and the Japan Sea. Atlantic herring (Clupea harengus harengus) consist of both winter–spring and summer–autumn spawning groups characterized in the northeast Atlantic by oceanic, shelf, and coastal populations. The oceanic group are large migratory fish spawning off the coasts of Norway and Iceland. The shelf group includes the various locally migratory North Sea populations adjacent to the British Isles. The coastal groups consist of smaller fish restricted to the Baltic and White seas. In the northwest Atlantic, spawning occurs from northern Labrador to Virginia with spring spawners predominating in the north and fall spawners in the south. Herring typically congregate near their spawning grounds for several weeks to months prior to spawning. Temperature is one of the factors that determine when spawning occurs. The Atlantic herring exhibits sexual dimorphism in the spawning act with only the female interacting with the spawning substrate. Both sexes of the Pacific herring make physical contact with the substrate on which the adhesive eggs are deposited. Spawning grounds are located in high-energy environments, either nearshore for spring spawners or in tidally active areas for fall spawners. Spawn is deposited on marine vegetation or on bottom substrate, such as gravel, which is free from silting. The eggs are tolerant to temperatures in the range of 5–14 °C and salinities in the range of 3–33‰. Egg mortality results mostly from suffocation due to high egg densities and silting, predation, and, in intertidal spawn, from stresses imposed by exposure to air and from egg loss by wave action.

Author(s):  
Thassya C. dos Santos Schmidt ◽  
Doug E. Hay ◽  
Svein Sundby ◽  
Jennifer A. Devine ◽  
Guðmundur J. Óskarsson ◽  
...  

AbstractLife-history traits of Pacific (Clupea pallasii) and Atlantic (Clupea harengus) herring, comprising both local and oceanic stocks subdivided into summer-autumn and spring spawners, were extensively reviewed. The main parameters investigated were body growth, condition, and reproductive investment. Body size of Pacific herring increased with increasing latitude. This pattern was inconsistent for Atlantic herring. Pacific and local Norwegian herring showed comparable body conditions, whereas oceanic Atlantic herring generally appeared stouter. Among Atlantic herring, summer and autumn spawners produced many small eggs compared to spring spawners, which had fewer but larger eggs—findings agreeing with statements given several decades ago. The 26 herring stocks we analysed, when combined across distant waters, showed clear evidence of a trade-off between fecundity and egg size. The size-specific individual variation, often ignored, was substantial. Additional information on biometrics clarified that oceanic stocks were generally larger and had longer life spans than local herring stocks, probably related to their longer feeding migrations. Body condition was only weakly, positively related to assumingly in situ annual temperatures (0–30 m depth). Contrarily, body growth (cm × y−1), taken as an integrator of ambient environmental conditions, closely reflected the extent of investment in reproduction. Overall, Pacific and local Norwegian herring tended to cluster based on morphometric and reproductive features, whereas oceanic Atlantic herring clustered separately. Our work underlines that herring stocks are uniquely adapted to their habitats in terms of trade-offs between fecundity and egg size whereas reproductive investment mimics the productivity of the water in question.


1987 ◽  
Vol 44 (7) ◽  
pp. 1379-1385 ◽  
Author(s):  
Sharon E. McGladdery

Prevalence of Eimeria sardinae oocysts was closely correlated with the maturity stage of the testes of Atlantic herring (Clupea harengus harengus). Prevalence was low in testes of immature fish, increased in ripe and spawning fish, and decreased in postspawning fish. No correlation was found between prevalence and age of spawning herring. The uniformly high prevalences in mature fish indicated the efficiency of transmission on the spawning grounds, where infective oocysts are released. Infection of first-spawning herring (approximately age 3) indicated that the oocysts may be dispersed to surrounding areas or immature fish may associate with spawning aggregations. Therefore, this parasite could not be used to distinguish first from repeat spawners. Prevalence oF E. sardinae peaked in May and September, and possibly in June and early July, thereby distinguishing two, and possibly three, spawning groups. A previous study indicated no correlation between maturity stage and infections by E. sardinae in northeastern Atlantic herring. The difference between the two sides of the Atlantic is attributed to greater mixing of immature and adult herring around spawning grounds and/or greater dispersal of infective oocysts from spawning grounds in the northeastern Atlantic, compared with those in the northwest.


1975 ◽  
Vol 32 (1) ◽  
pp. 66-68 ◽  
Author(s):  
S. N. Messieh

Analysis of maturity stages of herring samples taken from the southern Gulf of St. Lawrence shows two maturation cycles for spring and autumn spawning herring. The spring population has a spawning peak in May and the summer–autumn population extends spawning from July through September. Spawning grounds of spring and autumn herring populations and their nursery areas are mapped.


<em>Abstract.</em>—San Francisco Bay provides spawning and rearing habitat for California’s largest population of Pacific herring <em>Clupea pallasi</em>. This population provides a food source for other species and supports a valuable fishery for Pacific herring roe. Since the inception of the roe fishery in 1973, the California Department of Fish and Game has conducted annual surveys of spawning in San Francisco Bay as part of an ongoing assessment of population status and management of the fishery. The purpose of this paper is to document (1) regions of San Francisco Bay used by Pacific herring as spawning grounds over time, and (2) time periods in which spawning took place. Spawn data were analyzed by geographic region in the bay and by month for the period 1973–2000. During this period, we documented 269 spawning events from Point San Pablo south to Redwood City. Estimates of spawning adult biomass (fish that were not harvested by the fishery) ranged from 80,813 metric tons in 1981–1982 to 3,199 metric tons in 1997– 1998 (mean = 34,688 ± 19,325 SD). January was the peak spawning month, followed by December and February; small variations in this pattern occurred during some years. Overall, the majority of spawning took place in the north-central bay region (Point Bonita to Richmond-San Rafael Bridge, Angel Island, Point San Pablo, Berkeley flats; 55%) and the San Francisco region (Golden Gate Bridge to Candlestick Point; 34%), although it alternated between these two regions over time. In some years, considerable spawning took place in the Oakland–Alameda region (San Francisco–Oakland Bay Bridge to Bay Farm Island). The largest spawns and peak periods of spawning may not contribute most toward the next generation of Pacific herring, due to differential mortality within the season. For this reason, all regions documented in this study are important spawning grounds for Pacific herring from November through March each year. A number of recent studies have furthered our understanding of Pacific herring early life history and the forces that drive year-class formation in San Francisco Bay. However, studies are especially needed that will improve our ability to adequately address the potential impacts of human activities on Pacific herring in this highly urbanized estuary.


1994 ◽  
Vol 51 (S1) ◽  
pp. 233-239 ◽  
Author(s):  
K. E. Jørstad ◽  
G. Dahle ◽  
O. I. Paulsen

Genetic studies on populations of Atlantic herring (Clupea harengus L.) in Norwegian seawaters have revealed a number of genetically distinct fjord populations. One population in Balsfjord in northern Norway was nearly fixed for several alleles that were very rare in the Atlanto-Scandian herring stock. A comparison with a sample of Pacific herring (Clupea pallasi) from British Columbia demonstrated that these alleles were identical to the more common alleles in this species. Genetic distance estimates based on six polymorphic loci demonstrated that Balsfjord herring were more similar to Pacific herring. Balsfjord and Pacific herring were also similar in vertebrae number and spawning behaviour. Restriction fragment analyses of mitochondrial DNA using five restriction enzymes revealed distinct clones that separated different herring groups. Nucleotide sequence divergence among groups was small.


Author(s):  
D. R. Clarke ◽  
P. E. King

Information regarding spawning grounds of the Atlantic herring Clupea harengus Linnaeus has been based mainly on the collection of spawning fish, newly hatched larvae, or the presence of eggs within the stomachs of predators (Postuma, Saville & Wood, 1977). This type of evidence indicates general areas of spawning, rather than accurately delineating the spawning grounds. Though samples of spawn have been obtained from several localities in the North-East Atlantic (Ewart, 1884; Runnström, 1941; Fridriksson & Timmerman, 1951; Bolster & Bridger, 1957; Parrish et al. 1959; Hemmings, 1965; Bowers, 1969; Anthony, Sauskan & Sigaer, 1970), few quantitative studies of individual grounds have been made. In consequence, little is known of the factors influencing the selection of grounds by Atlantic herring, the shape of these grounds and egg distribution within spawning areas.


1979 ◽  
Vol 36 (9) ◽  
pp. 1097-1101 ◽  
Author(s):  
John R. MacMillan ◽  
Dan Mulcahy

In Puget Sound, Wash., the incidence of viral erythrocytic necrosis (VEN) varied geographically from 0 to 17% in chum salmon (Oncorhynchus keta) and from 4 to 59% in Pacific herring (Clupea harengus pallasi). The disease was experimentally transmitted by intraperitoneal injection to chum, pink (O. gorbuscha), coho (O. kisutch), chinook (O. tshawytscha), sockeye (O. nerka), and Atlantic (Salmo salar) salmon, and rainbow (S. gairdneri), brown (S. trutta), and brook (Salvelinus fontinalis) trout. The disease was transmitted to chum salmon and brook trout by waterborne virus. Virus obtained from herring was experimentally transmitted into chum salmon by intraperitoneal injection. Key words: viral erythrocytic necrosis, fish disease, transmission


1971 ◽  
Vol 28 (9) ◽  
pp. 1269-1273 ◽  
Author(s):  
Richard E. Thorne

An echo integrator, working in combination with an echo sounder, measures the total voltage of the fish echoes received from a given depth interval and sums these voltages over time. Investigations were made on the relation between integrated echo voltage and fish density for juvenile sockeye salmon (Oncorhynchus nerka) in Lake Washington and Pacific hake (Merluccius productus) and Pacific herring (Clupea harengus pallasi) in Puget Sound. When fish were distributed at densities at which they could be acoustically resolved as individual targets, the relation between net catch and integrated voltage was linear. At higher densities when the fish echoes were multiple targets, the net catch was related to the square of the integrated voltage.


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