Reproductive Biology of Pacific Herring (Clupea harengus pallasi)

1985 ◽  
Vol 42 (S1) ◽  
pp. s111-s126 ◽  
Author(s):  
D. E. Hay

Most British Columbia herring begin sexual maturation in the late summer and become sexually mature in the subsequent March or April. As they mature, most stocks migrate from summer feeding grounds to overwintering areas and then to shallow nearshore spawning areas. Also, newly recruited, sexually maturing fish join the adult spawning stocks, either on the summer or winter grounds. These events occur in an unpredictable environment. Consequently, reproduction in Pacific herring (Clupea harengus pallasi) may be viewed as a biological problem of maintaining synchrony and precision: specifically the synchronous maturation of (1) males and females and (2) the recruit spawners with the adult fish that have spawned in previous years. Biological precision is required to ensure that gametes are released at the correct place at the correct time. Further precision is required to achieve an appropriate balance between egg number and egg size, and then to control the density of eggs deposited on the bottom. The annual temperature regime is a vital regulator of these processes. Generally, the warmer the temperature, or lower the latitude, the earlier the maturation and spawning time. There are some notable exceptions that indicate local adaptation to other environmental cues. Also, experimental work indicates that food supply can affect the maturation rate. Intensities of egg depositions are generally similar among Pacific North American stocks, and indeed for many documented herring spawnings from Asian and European stocks. It has been shown that eggs in the middle of very thick spawns have lower survival so there is a selective advantage for biological mechanisms that ensure more even and lighter egg densities. This paper suggests that egg density in Pacific herring is controlled by a biological feedback mechanism involving milt concentration and hydrographic factors. Earlier spawners tend to be larger and there is a positive relationship between female size and egg size, a tendency consistent with other herring stocks and species. Size-adjusted fecundity, when compared among different regions and years, is strikingly uniform within British Columbia. On a broad geographic scale (California to Alaska), size-specific fecundity declines with latitude. Recent experimental work reveals that total egg number is higher at early stages of maturation and decreases as spawning time approaches. Presumably, this decrease reflects selective resorption of some developing oocytes, and probably occurs in response to available body energy. The duration and geographical variation in spawning time is relevant to questions concerning the evolutionary and taxonomic relationships between Pacific herring and Atlantic herring (Clupea harengus harengus). Other aspects of reproductive biology have important management implications, particularly for (1) predicting recruitment, (2) deriving stock estimates from spawn surveys, and (3) managing fisheries.


1984 ◽  
Vol 41 (3) ◽  
pp. 414-422 ◽  
Author(s):  
Hans Jürg Meng ◽  
Max Stocker

We conducted an analysis to determine if Pacific herring (Clupea harengus pallasi) stocks occurring in different localities in British Columbia waters could be separated using morphometric and meristic characters. Discriminant function analysis was applied to morphometric and meristic characters taken from food herring samples. Herring found in northern British Columbia waters were detectably different from those found in the Strait of Georgia. We recommend using meristic characters for separation on a broad geographic scale and using "best" morphometric characters for finer resolution within the established broader groups. We defined a set of 12 best morphometric characters for further large-scale studies.



1988 ◽  
Vol 45 (3) ◽  
pp. 399-406 ◽  
Author(s):  
D. E. Hay ◽  
J. R. Brett

Approximately 3 mo before spawning, Pacific herring (Clupea harengus pallasi) were captured and transferred to experimental netpens varying in fish density, cover, and feeding regimes. Fecundity decreased as the fish ripened. Concurrently, ovary weight and egg weight increased and somatic weight decreased. Length-specific fecundities of fed and unfed fish were similar, but the unfed fish had higher weight-specific fecundities, corresponding to a greater loss of somatic tissue during impoundment. Feeding accelerated the rate of maturity, and fed fish spawned earlier with heavier eggs than unfed fish. Relative fecundity (eggs per gram) was highest among the unfed fish. Reduction in preovulatory egg number probably was a consequence of follicular atresia (observed but not quantified here). Age-, length-, and weight-specific fecundity of impounded herring varied within the range observed for naturally maturing populations (1974 and 1980). Fecundity in impounded fish varied no more than observed in nature: there was a greater difference in age-, length-, and weight-specific fecundity between years than there was between experimental treatments. We suggest that reduction in the number of maturing oocytes occurs naturally and reflects a mechanism that allows herring to adjust their egg size and egg number according to energetic resources and environmental conditions.



1982 ◽  
Vol 39 (11) ◽  
pp. 1537-1540 ◽  
Author(s):  
Mary Needler Arai ◽  
Douglas E. Hay

In laboratory tests young Pacific herring (Clupea harengus pallasi) larvae were eaten by several species of hydromedusae common in coastal waters off British Columbia, including the previously controversial Sarsia tubulosa and by the scyphomedusa Aurelia aurita. Field collections and observations confirmed that the distributions of medusae and larvae overlap and that some medusae feed on herring larvae in nature. In coastal waters and bays of British Columbia, the hydromedusae Sarsia tubulosa or Aequorea victoria may be most abundant during the time of peak herring larvae abundance.Key words: herring, larvae, Clupea, Sarsia, Aequorea, predation, medusae



1971 ◽  
Vol 28 (12) ◽  
pp. 1921-1921 ◽  
Author(s):  
Jun Ito ◽  
R. R. Parker

An occurrence of Pacific herring (Clupea harengus pallasi) predation on juvenile chinook salmon (Oncorhynchus tshawytscha) is described. This is the first recorded incidence of this particular predator–prey relation.



1981 ◽  
Vol 38 (4) ◽  
pp. 381-386 ◽  
Author(s):  
C. W. Haegele ◽  
R. D. Humphreys ◽  
A. S. Hourston

Pacific herring (Clupea harengus pallasi) spawn in southern British Columbia was surveyed by divers in 1976 and 1978. These surveys showed that the distribution of eggs is dependent on the type of vegetation on which the eggs are laid and on the slope of the beach. Most of the spawn on pure sea grass beds was deposited in the littoral zone. Spawn on mixtures of vegetation types was mostly sublittoral and the areal extent of these spawnings has been underestimated by surface surveys. To obtain a good estimate of egg deposition, diver surveys are required. Red algae were the major vegetation type for the study area, followed by sea grass, rockweed, kelp, and other brown algae. Eggs were deposited deeper as the beach slope became steeper. A small fraction of the total egg complement becomes exposed to air as a result of normal tidal cycles during the incubation period, and egg loss from predation and storms was estimated at 10%.Key words: Pacific herring, spawn, egg distribution, vegetation, depth, beach slope



1988 ◽  
Vol 45 (3) ◽  
pp. 388-398 ◽  
Author(s):  
D. E. Hay ◽  
J. R. Brett ◽  
E. Bilinski ◽  
D. T. Smith ◽  
E. M. Donaldson ◽  
...  

Approximately 3 mo before spawning, Pacific herring (Clupea harengus pallasi) were captured and transferred to experimental netpens and subjected to different holding conditions: high, medium, and low densities; with and without covers; and fed and not fed. Mortality during impoundment was low. There were no detectable effects of density or cover, but feeding accelerated spawning time and promoted gonadal growth. Fed fish had significantly higher somatic weights, gonad weights, and condition factors and significantly lower gonosomale indices than unfed fish. Water content increased in all fish from about 70%, at the beginning, to about 75% when the fish were ripe. Consequently, total body weight increased in all females, and somatic weight decreased, but the decrease was feast in the fed fish. No significant differences in the percentages of total protein and ash in the carcass were found during impoundment, but the levels of fat and free fatty acids showed a progressive decrease. Glycogen levels in the muscle and liver were higher in fed herring. Oocyte maturation was normal. Preovulatory atresia of vitellogenic oocytes was observed in all groups. Egg diameters of fed females were slightly larger than those of unfed fish. The evidence for winter feeding in Pacific herring is evaluated.



1985 ◽  
Vol 42 (S1) ◽  
pp. s56-s68 ◽  
Author(s):  
D. F. Alderdice ◽  
A. S. Hourston

The euryplastic Pacific herring (Clupea harengus pallasi) generally encounters temperatures ranging between 0 and 10 °C throughout its distribution during the maturation and spawning of adults, incubation of eggs, and hatching of larvae. For many Asian stocks these events occur in the lower half of the temperature range; with North American stocks they tend to occur in the upper half of the range. In British Columbia waters, salinities associated with these events (range, optimum) are spawning (2.6–28.7‰, 27–28.7‰), [Formula: see text] fertilization of eggs (4.5–42‰, 12–15‰), and maximum total hatch and hatch of viable larvae (4.5–42‰, 12–17‰). A low/low–high/high interaction between salinity and temperature also influences total hatch, hatch of viable larvae, and salinity tolerance of larvae. In addition, the following implications arise regarding aspects of the Pacific herring reproductive cycle, based on previously published and new data, and on speculative inference. The response of Pacific herring to salinity and temperature appears to have a commanding influence on the reproductive cycle and, thereby, on distribution of the species. Survival of eggs on substrate, related to respiratory activity, appears to be influenced by the transport and perfusion velocity of interstitial water in an egg mass. Such transport may involve perivitelline fluid colloid osmotic pressure; natural convection; the surge associated with wave action, beach slope, and depth; and possibly differences in resistance to convective flow of deoxygenated water from an egg mass based on orientation of the substrate. These relations would be modified by variations in deposition intensity (number of egg layers) and packing density (eggs per unit volume), and both factors may affect survival of occluded eggs in an egg mass differentially, depending on the substrate used. A review of data on salinity tolerance of herring larvae indicates that a variety of dosage-mortality techiques has been used, leading to noncomparable estimates of response. An assessment of upper incipient lethal salinities will require standardization of such techniques. Recent studies show that salinity tolerance of larvae is influenced significantly by salinity–temperature conditions during egg incubation. At usual incubation conditions in British Columbia waters, the upper boundary of larval tolerance is estimated as 27.5–31.7‰ S (72-h LC10). depending on incubation history. The fate of Pacific herring larvae carried into the higher salinities of offshore waters has been controversial. In the Strait of Georgia, British Columbia, substantial offshore dispersion of larvae occurs where surface conditions generally are 27–28.6‰ and 9–10 °C in the early larval period. Although these salinities are near the upper boundary of salinity tolerance, larvae sampled in offshore waters (1981) had an apparent mean age of 15 d and were actively feeding and growing. From rates of disappearance of larvae in the offshore waters (9% wk) and inshore waters (45% wk) we conclude that usual surface salinities and food supply in the open waters of the Strait were not a dominant influence on larval survival. Assuming the larvae remain in the upper 10 m, we suspect their disappearance, at least offshore, to be largely the result of predation.



1989 ◽  
Vol 46 (10) ◽  
pp. 1776-1784 ◽  
Author(s):  
D. M. Ware ◽  
R. W. Tanasichuk

Maturation rates (measured as the change in the gonosomatic index (GSI) with time) over the last month of the annual maturation cycle were estimated for male and female herring in British Columbia, between 1982–87. The data were analyzed to determine interannual and interregional differences in the maturation rate and its influence on spawning time. The data also indicated that in some areas herring spawned in discrete waves — the largest fish tended to spawn first and the smaller fish in subsequent waves. Each spawning wave lasted about 5–6 d and the interwave interval varied from 8–26 d in the Strait of Georgia. General equations were developed to describe gonadal growth over the entire maturation cycle. These equations accounted for the observed differences in: (1) the maturation rates between the sexes (males initially mature faster), (2) the interregional and interannual variation in the timing of spawning (herring tend to spawn later at higher latitudes, and earlier than normal when its warmer), and (3) provide an explanation for spawning waves. All of these phenomena derive from the fact that the instantaneous rate at which the gonad grows during the maturation cycle in both sexes depends on the weight of the fish, and the daily sea temperature.



1987 ◽  
Vol 44 (8) ◽  
pp. 1485-1495 ◽  
Author(s):  
R. W. Tanasichuk ◽  
D. M. Ware

Data for 2937 fish, collected from seven locations over five years, were analysed to evaluate the effects of sea temperature and stock biomass on size-specific ovary weight and fecundity at spawning. Ovary weight did not vary significantly between years or locations. Size-specific fecundity was higher in 1983, when coastal waters were abnormally warm because of a strong El Niño – Southern Oscillation event. The effect of location was equivocal: one stock that overwintered in warm water tended to have a higher fecundity. Mean sea temperature between 60 and 90 d before spawning (in spring) best accounted for variations in size-specific fecundity. Temperature may influence fecundity by regulating gonadotropin concentration and consequently pre-ovulatory atresia. We hypothesize that the trade-off between fecundity and egg size is adaptive. A theoretical analysis of the early life history of Pacific herring suggests that, to maximize survival to metamorphosis, egg size should decrease and fecundity increase with temperature when the larval growth rate Q10 is less than the mortality rate Q10. Our model seems to explain the differences in egg size between recruit and repeat spawners, and between stocks of Atlantic herring that spawn in different seasons.



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