The Behaviour of Migrating Pink and Chum Salmon Fry

1956 ◽  
Vol 13 (3) ◽  
pp. 309-325 ◽  
Author(s):  
William S. Hoar

Pink salmon fry which have never schooled are negatively phototactic, prefer a cover of stones and do not emerge into bright light. Those which have schooled show a strong cover reaction when exposed to a rapid increase in light intensity but do not seek cover unless the change is abrupt. In general they remain in bright light after they have schooled. This change in behaviour occurs rapidly (15 minutes or less) when the fry school for the first time. Chum salmon fry establish a definite direction of swimming in the quiet water of a circular channel or basin. The established direction is stable and not permanently disturbed by light or darkness, by water currents, by strong avoiding reactions, by changing the location or by excluding direct skylight. The direction may be initially established in relation to water currents.

1957 ◽  
Vol 14 (6) ◽  
pp. 815-830 ◽  
Author(s):  
W. S. Hoar ◽  
M. H. A. Keenleyside ◽  
R. G. Goodall

When given a choice between light and dark areas, schools of chum or pink salmon fry remain in the light, sockeye fry prefer the dark and coho fry show no marked preference for either. Newly emerged sockeye fry are the most strongly photonegative, remaining mostly under stones. Older sockeye fry move more into the light. Sockeye and coho smolts stay in the dark more than sockeye and coho underyearlings. Territorial and "escape" behaviour by fish in the experimental apparatus may obscure these reactions to light. Soon after emerging from the gravel, pink fry swim near the surface under low light intensity and retreat to deeper water in brighter light. Older pink fry seem indifferent to changing light. Recently emerged chum salmon fry do not respond in this way to changing illumination, although older fry tend to swim closer to the surface. This difference between pink and chum salmon fry may be related to differences in schooling behaviour and alarm responses of the two species.


1978 ◽  
Vol 35 (6) ◽  
pp. 797-808 ◽  
Author(s):  
Randall M. Peterman ◽  
Marino Gatto

Several studies have shown that predators can eat large portions (up to 85%) of emerging salmon (Oncorhynchus spp.) fry populations. To understand salmon population dynamics and the effect of salmon enhancement projects, it is necessary to determine how present predation mortality varies with prey density. To predict the shape of this relation outside the range of past observations, we must examine the basic components of the predation process, the functional and numerical responses. A review of past, sparse data on the functional response component shows that predators of salmon fry and smolts were mostly not being saturated (i.e. maximum attack rates were not being achieved) at high prey densities. A method to estimate functional responses from certain types of existing field data is derived and applied to Hooknose Creek pink salmon (O. gorbuscha) and chum salmon (O. keta) information. Results from 7 out of 9 yr corroborate earlier observations that predators are normally operating on the low end of their functional response curves and are therefore capable of causing high mortality on larger prey populations. Also, competition among predators is demonstrated to be significant, resulting in changes in slopes of functional responses. More experimental studies of functional responses are needed, and such research should be carried out in conjunction with perturbations in salmon fry abundance which will result from enhancement projects. Key words: salmon fry, predation, freshwater survival, enhancement, functional response, predator competition


1955 ◽  
Vol 12 (3) ◽  
pp. 369-374 ◽  
Author(s):  
Ferris Neave

The seaward migration of pink and chum salmon fry takes place at night. Strong light is avoided. In pink salmon negative rheotaxis (swimming with a current) is strongly developed and migration is not primarily effected by random swimming and passive displacement. Downstream movement is mainly at or close to the surface. In slack water vertical distribution is more uniform. In the shortest streams examined, each night's migrants appeared to reach the sea before daybreak. In a longer stream, fry were seen to bury themselves at the onset of daylight. After being held in fresh water for an undetermined period, fry show positive rheotaxis and schooling behaviour and no longer avoid light. Behaviour of fry after reaching the sea also differs from that shown during actual migration. Changes in behaviour may coincide with commencement of feeding.


1978 ◽  
Vol 56 (6) ◽  
pp. 1412-1419 ◽  
Author(s):  
Jean-Guy J. Godin ◽  
Cornelis Groot ◽  
M. Connor Armstrong

A photoelectric system, designed to monitor continuously the 'spontaneous' locomotor activity of individual, juvenile pink salmon in the laboratory, is described and evaluated quantitatively. Data on the swimming behaviour of individual fish in the circular channel indicate that the design permitted salmon to swim freely in circuits without physical obstructions impeding or water currents directing their movements. Swimming speeds of individual fish were not influenced by infrared light beams emitted across the activity channel. The photoelectric monitoring system was found to be reliable, equally sensitive in detecting the locomotor movements of small (4.3–5.8 cm) and of large (13.0–19.0 cm) fish, and provided data which closely approximated (on average to within 94.0–102.6%) the total momentary locomotor activity of individual pink salmon.


1950 ◽  
Vol 28d (3) ◽  
pp. 126-136 ◽  
Author(s):  
William S. Hoar ◽  
G. Mary Bell

Histological examination of the thyroid glands from chum salmon fry taken in the river, estuary, or sea shows the organ to be in a quiescent condition at the time of migration. If, however, this species is retained in fresh water for two or three months the gland becomes extremely hyperplastic. The pink salmon thyroid behaves in essentially the same way as that of the chum, but migrating pink fry taken at great distances from the sea have active glands. The thyroids of yearling coho and sockeye moving into the sea display heightened activity. Thyroid activity is apparently greater in coho migrants taken later in the season from the headwaters of rivers. In part, the heightened thyroid activity seen in these migrating Pacific salmon is probably a spring-time seasonal change. It seems, however, to be more particularly related to the increased metabolic work of osmotic regulation and salt balance in a fish physiologically prepared for life in the sea. In general, this study suggests that the increased thyroid activity seen in young migrating salmonoids is largely due to increased demands for thyroid hormone in the metabolism of a fish no longer completely adjusted physiologically to fresh water.


1960 ◽  
Vol 17 (5) ◽  
pp. 655-676 ◽  
Author(s):  
J. McDonald

The downstream migration of sockeye, coho, pink and chum salmon fry is initially nocturnal and appears to be regulated quite precisely by changes in light intensity. Downstream movement is seen to arise from a displacement by the current when firm visual contact with fixed objects in the stream is lost. Once the migration is under way the distribution of the fry varies. The lateral distribution of pink and sockeye, but not chum and coho, was closely and positively related to current speed, above a threshold of 1.3 ft/sec (0.4 m/sec). Pink fry were found to be distributed throughout the total depth of water but greatest catches were made at intermediate depths. The negative response of fry to light appears to change after exposure to it, and pink and chum fry were found to extend their movements into and throughout the daylight hours where the migration route was lengthy. Feeding and schooling activity is probably associated with this change in response to light. Both pink and chum fry were observed to school only near the end of their seaward movement. Pink fry were found to feed to some extent in the natal areas but to a greater extent as the sea was approached.


1965 ◽  
Vol 22 (6) ◽  
pp. 1477-1489 ◽  
Author(s):  
H. T. Bilton ◽  
W. E. Ricker

Among 159 central British Columbia pink salmon that had been marked by removal of two fins as fry and had been recovered in commercial fisheries after one winter in the sea, the scales of about one-third showed a supplementary or "false" check near the centre of the scale, in addition to the single clear-cut annulus. This evidence from fish of known age confirms the prevailing opinion that such extra checks do not represent annuli, hence that the fish bearing them are in their second year of life rather than their third. Unmarked pink salmon from the same area, and some from southern British Columbia, had a generally similar incidence of supplementary checks. In both marked and unmarked fish the supplementary checks varied in distinctness from faint to quite clear. In a sample of scales of 14 double-fin marked chum salmon which were known to be in their 4th year, all fish had the expected 3 annuli, and 12 fish had a supplementary check inside the first annulus.


1967 ◽  
Vol 24 (11) ◽  
pp. 2321-2338 ◽  
Author(s):  
M. C. Healey

During May and June 1966, the migration of pink salmon fry from the Bella Coola River was studied in Burke Channel, British Columbia. The movement of pink fry down Burke Channel was saltatory. Short periods of active migration were interspersed with longer periods when the fry did not migrate and accumulated in bays. Fry were sampled from these accumulations and their ability to orient using celestial cues was examined. During the early morning, fry tended to prefer directions at right angles to their direction of migration, but at other times of the day preferred the direction of migration. The preference for the direction of migration was strongest at midday. Fry were better oriented on clear days than on cloudy days. These data indicate that fry may use celestial cues to find directions during their oceanic migrations.


Trudy VNIRO ◽  
2020 ◽  
Vol 179 ◽  
pp. 90-102
Author(s):  
M. N. Gorokhov ◽  
V. V. Volobuev ◽  
I. S. Golovanov

There are two main areas of pacific salmon fishing in the Magadan region: Shelikhova Gulf and Tauiskaya Bay. The main fishing species is pink salmon in the region. Its share of total salmon catch by odd-year returns reaches 85 %. Data on the dynamics of escapement to the spawning grounds of pink salmon of the Shelikhova Gulf and Tauiskaya Bay are presented. The displacement of the level of spawning returns of pink salmon into the Shelihova Gulf with the simultaneous reduction of its returns to the Tauiskaya Bay is shown. Data on the dynamics of the fishing indicators of pink salmon for the two main fishing areas are provided. The Tauiskaya Bay as the main pink salmon fishery area loses its importance is shown. Graphical data on the escapement of producers pink salmon to the spawning grounds are presented and the optimal values of spawning escapements are estimated. Chum salmon is the second largest and most fishing species. Information on the dynamics of the number of returns, catch and escapement to the spawning grounds of chum salmon is given. The indicators of escapement to the spawning areas and their compliance with the optimal passes of salmon producers are analyzed. The issues of the dynamics of returns number, catch and the escapement to the spawning grounds of coho salmon producers are considered. The level of the escapement to the spawning areas is shown and the ratio of actual to optimal values of passes is estimated. The role of coho salmon as an object of industrial fishing and amateur fishing is shown. The extent of fishing press on individual groups of salmon populations is discussed. It is concluded that it is necessary to remove the main salmon fishery from the Tauiskaya Bay to the Shelikhova Gulf.


Author(s):  
David Fisher

Today we learn at such a young age about the periodic properties of the elements and their atomic structure that it seems as if we grew up with the knowledge, and that everyone must always have known such basic, simple stuff. But till nearly the end of the nineteenth century no one even suspected that such things as the noble gases, with their filled electronic orbits, might exist. Helium was the first one we at Brookhaven looked for in our mass spectrometer, and the first one discovered. This was in 1868, but the discovery was ignored and the discoverer ridiculed. He didn’t care; he had other things on his mind. His name was Pierre Jules César Janssen, and he was a French astronomer who sailed to India that year in order to take advantage of a predicted solar eclipse. With the overwhelming brightness of the sun’s disk blocked by the moon, he hoped to observe the outer layers using the newly discovered technique of absorption spectroscopy. Nobody at the time understood why, but it had been observed that when a bright light shone through a gas, the chemical elements in the gas absorbed the light at specific wavelengths. The resulting dark lines in the emission spectrum of the light were like fingerprints, for it had been found in chemical laboratories that when an element was heated it emitted light at the same wavelengths it would absorb when light from an outside source was shined on it. So the way the technique worked, Janssen reasoned, was that he could measure the wavelengths of the solar absorbed lines and compare them with lines emitted in chemical laboratories where different elements were routinely studied, thus identifying the gases present in the sun. On August 18 of that year the moon moved properly into position, and Janssen’s spectroscope captured the dark absorption lines of the gases surrounding the sun. It was an exciting moment, as for the first time the old riddle could be answered: “Twinkle twinkle, little star, how I wonder what you are.” The answer now was clear: the sun, a typical star, was made overwhelmingly of hydrogen. But to Janssen’s surprise there was one additional and annoying line, with a wavelength of 587.49 nanometers.


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