scholarly journals Conservation physiology in practice: how physiological knowledge has improved our ability to sustainably manage Pacific salmon during up-river migration

2012 ◽  
Vol 367 (1596) ◽  
pp. 1757-1769 ◽  
Author(s):  
Steven J. Cooke ◽  
Scott G. Hinch ◽  
Michael R. Donaldson ◽  
Timothy D. Clark ◽  
Erika J. Eliason ◽  
...  

Despite growing interest in conservation physiology, practical examples of how physiology has helped to understand or to solve conservation problems remain scarce. Over the past decade, an interdisciplinary research team has used a conservation physiology approach to address topical conservation concerns for Pacific salmon. Here, we review how novel applications of tools such as physiological telemetry, functional genomics and laboratory experiments on cardiorespiratory physiology have shed light on the effect of fisheries capture and release, disease and individual condition, and stock-specific consequences of warming river temperatures, respectively, and discuss how these findings have or have not benefited Pacific salmon management. Overall, physiological tools have provided remarkable insights into the effects of fisheries capture and have helped to enhance techniques for facilitating recovery from fisheries capture. Stock-specific cardiorespiratory thresholds for thermal tolerances have been identified for sockeye salmon and can be used by managers to better predict migration success, representing a rare example that links a physiological scope to fitness in the wild population. Functional genomics approaches have identified physiological signatures predictive of individual migration mortality. Although fisheries managers are primarily concerned with population-level processes, understanding the causes of en route mortality provides a mechanistic explanation and can be used to refine management models. We discuss the challenges that we have overcome, as well as those that we continue to face, in making conservation physiology relevant to managers of Pacific salmon.

1965 ◽  
Vol 22 (3) ◽  
pp. 775-782 ◽  
Author(s):  
J. R. McBride ◽  
U. H. M. Fagerlund ◽  
M. Smith ◽  
N. Tomlinson

It has been shown that sockeye salmon, Oncorhynchus nerka, will start to eat soon after capture during their freshwater spawning migration. Some will continue to eat up to, during, and after spawning, while others stop eating shortly before spawning. The effect of feeding has been investigated histologically in a number of tissues by comparison of feeding fish, unfed controls, and fish spawned in the wild. Atrophy, and often degeneration of the liver, stomach, and intestine in post-spawned unfed controls and fish spawned in the wild was equally marked, but was absent or much less pronounced in fed fish.


2014 ◽  
Vol 496 ◽  
pp. 71-84 ◽  
Author(s):  
SM Wilson ◽  
SG Hinch ◽  
SM Drenner ◽  
EG Martins ◽  
NB Furey ◽  
...  

2021 ◽  
Author(s):  
QinQin Yu ◽  
Matti Gralka ◽  
Marie-Cécilia Duvernoy ◽  
Megan Sousa ◽  
Arbel Harpak ◽  
...  

AbstractDemographic noise, the change in the composition of a population due to random birth and death events, is an important driving force in evolution because it reduces the efficacy of natural selection. Demographic noise is typically thought to be set by the population size and the environment, but recent experiments with microbial range expansions have revealed substantial strain-level differences in demographic noise under the same growth conditions. Many genetic and phenotypic differences exist between strains; to what extent do single mutations change the strength of demographic noise? To investigate this question, we developed a high-throughput method for measuring demographic noise in colonies without the need for genetic manipulation. By applying this method to 191 randomly-selected single gene deletion strains from the E. coli Keio collection, we find that a typical single gene deletion mutation decreases demographic noise by 8% (maximal decrease: 81%). We find that the strength of demographic noise is an emergent trait at the population level that can be predicted by colony-level traits but not cell-level traits. The observed differences in demographic noise from single gene deletions can increase the establishment probability of beneficial mutations by almost an order of magnitude (compared to in the wild type). Our results show that single mutations can substantially alter adaptation through their effects on demographic noise and suggest that demographic noise can be an evolvable trait of a population.


2013 ◽  
Vol 59 (4) ◽  
pp. 485-505 ◽  
Author(s):  
Jon E. Brommer

Abstract Individual-based studies allow quantification of phenotypic plasticity in behavioural, life-history and other labile traits. The study of phenotypic plasticity in the wild can shed new light on the ultimate objectives (1) whether plasticity itself can evolve or is constrained by its genetic architecture, and (2) whether plasticity is associated to other traits, including fitness (selection). I describe the main statistical approach for how repeated records of individuals and a description of the environment (E) allow quantification of variation in plasticity across individuals (IxE) and genotypes (GxE) in wild populations. Based on a literature review of life-history and behavioural studies on plasticity in the wild, I discuss the present state of the two objectives listed above. Few studies have quantified GxE of labile traits in wild populations, and it is likely that power to detect statistically significant GxE is lacking. Apart from the issue of whether it is heritable, plasticity tends to correlate with average trait expression (not fully supported by the few genetic estimates available) and may thus be evolutionary constrained in this way. Individual-specific estimates of plasticity tend to be related to other traits of the individual (including fitness), but these analyses may be anti-conservative because they predominantly concern stats-on-stats. Despite the increased interest in plasticity in wild populations, the putative lack of power to detect GxE in such populations hinders achieving general insights. I discuss possible steps to invigorate the field by moving away from simply testing for presence of GxE to analyses that ‘scale up’ to population level processes and by the development of new behavioural theory to identify quantitative genetic parameters which can be estimated.


1960 ◽  
Vol 38 (1) ◽  
pp. 553-558 ◽  
Author(s):  
Violet M. Chang ◽  
D. R. Idler

Liver glycogen levels were determined for a pure stock of sockeye salmon (Oncorhynchus nerka) taken at three locations during spawning migration. The liver glycogen content of the male was found to be consistently greater than that of the female throughout the entire river migration. In both sexes liver glycogen decreased during the earlier phase of migration, but increased during the later stage so that the levels at the spawning grounds were approximately twice those at the mouth of the river. The changes which occur are discussed in relation to sex differences, energy expenditures, and plasma steroid hormone levels.


1962 ◽  
Vol 40 (7) ◽  
pp. 919-927 ◽  
Author(s):  
H. Tsuyuki ◽  
E. Roberts ◽  
R. E. A. Gadd

The muscle myogens and other components of the spring salmon (O. tshawytscha), chum salmon (O. keta), coho salmon (O. kisutch), and sockeye salmon (O. nerka), as well as the lingcod (Ophiodon elongatus), were separated by the use of diethylaminoethyl (DEAE) cellulose columns. Significant amounts of slowly dialyzable inosine and inosinic acid which may lead to spurious peaks in moving-boundary electrophoretic separations have been shown to be present in the muscle myogen preparations. The basic differences in the muscle myogen components of the Pacific salmon and the lingcod are compared.


2011 ◽  
Vol 112 (1-2) ◽  
pp. 85-95 ◽  
Author(s):  
Marika Kirstin Gale ◽  
Scott G. Hinch ◽  
Erika J. Eliason ◽  
Steven J. Cooke ◽  
David A. Patterson

2011 ◽  
Vol 68 (6) ◽  
pp. 1122-1130 ◽  
Author(s):  
James R. Irvine ◽  
Masa-aki Fukuwaka

Abstract Irvine, J. R., and Fukuwaka, M. 2011. Pacific salmon abundance trends and climate change. – ICES Journal of Marine Science, 68: 1122–1130. Understanding reasons for historical patterns in salmon abundance could help anticipate future climate-related changes. Recent salmon abundance in the northern North Pacific Ocean, as indexed by commercial catches, has been among the highest on record, with no indication of decline; the 2009 catch was the highest to date. Although the North Pacific Ocean continues to produce large quantities of Pacific salmon, temporal abundance patterns vary among species and areas. Currently, pink and chum salmon are very abundant overall and Chinook and coho salmon are less abundant than they were previously, whereas sockeye salmon abundance varies among areas. Analyses confirm climate-related shifts in abundance, associated with reported ecosystem regime shifts in approximately 1947, 1977, and 1989. We found little evidence to support a major shift after 1989. From 1990, generally favourable climate-related marine conditions in the western North Pacific Ocean, as well as expanding hatchery operations and improving hatchery technologies, are increasing abundances of chum and pink salmon. In the eastern North Pacific Ocean, climate-related changes are apparently playing a role in increasing chum and pink salmon abundances and declining numbers of coho and Chinook salmon.


Abstract.—Upon entering marine waters, juvenile Pacific salmon <em>Oncorhynchus </em>spp. depend on feeding at high and sustained levels to achieve growth necessary for survival. In the last decade, several concurrent studies have been examining the food habits and feeding intensity of juvenile Pacific salmon in the shelf regions from California to the northern Gulf of Alaska. In this paper, we compared results from feeding studies for all five species of juvenile salmon (Chinook salmon <em>O. tshawytscha</em>, coho salmon <em>O. kisutch</em>, chum salmon <em>O. keta, </em>sockeye salmon <em>O. nerka</em>, and pink salmon <em>O. gorbuscha</em>) between 2000 and 2002, years when these regions were sampled extensively. Within these years, we temporally stratified our samples to include early (May–July) and late (August–October) periods of ocean migration. Coho and Chinook salmon diets were most similar due to a high consumption of fish prey, whereas pink, chum, and sockeye salmon diets were more variable with no consistently dominant prey taxa. Salmon diets varied more spatially (by oceanographic and regional factors) than temporally (by season or year) in terms of percentage weight or volume of major prey categories. We also examined regional variations in feeding intensity based on stomach fullness (expressed as percent body weight) and percent of empty or overly full stomachs. Stomach fullness tended to be greater off Alaska than off the west coast of the United States, but the data were highly variable. Results from these comparisons provide a large-scale picture of juvenile salmon feeding in coastal waters throughout much of their range, allowing for comparison with available prey resources, growth, and survival patterns associated with the different regions.


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