Detection of population trends in threatened coho salmon (Oncorhynchus kisutch)

2001 ◽  
Vol 58 (2) ◽  
pp. 375-385 ◽  
Author(s):  
Katriona Shea ◽  
Marc Mangel

Populations of coho salmon (Oncorhynchus kisutch) in California are listed as threatened under the U.S. Endangered Species Act. Such listings refer to adult populations, but often, juvenile life history stages are censused, so it is important to understand what affects the relationship between true adult and observed juvenile numbers. We present models to address how observational uncertainty, census length, and autocorrelation in vital rates affect our ability to observe trends. We ask two questions about our ability to detect declines in one life history stage from censuses of another. First, given an observed decline in parr numbers, what is the chance that this reflects a decline in adults? Second, given that adult numbers are declining, what is the chance that we see that decline in parr? Our results indicate that statistical power decreases with increasing observational uncertainty and decreasing census lengths and demonstrate how these two parameters interact. Power increases as the level of autocorrelation in mortality rates increases. Management recommendations include obtaining more accurate estimates of autocorrelation in mortality and of observational uncertainty.

2020 ◽  
Vol 119 (10) ◽  
pp. 3401-3413
Author(s):  
Peter A. Seeber ◽  
Tetiana A. Kuzmina ◽  
Alex D. Greenwood ◽  
Marion L. East

Abstract In wildlife, endoparasite burden can be affected by host life history stage, environmental conditions, host abundance, and parasite co-infections. We tested the effects of these factors on gastrointestinal parasite infection in plains zebras (Equus quagga) in the Serengeti ecosystem, Tanzania, using fecal egg counts of two nematode families (Strongylidae and Ascarididae) and the presence/absence of cestode (Anoplocephalidae) eggs. We predicted higher egg counts of Strongylidae and Ascarididae, and increased likelihood of Anoplocephalidae infection in individuals (1) during energetically costly life history stages when resource allocation to immune processes may decrease and in young zebras after weaning because of increased uptake of infective stages with forage, (2) when climatic conditions facilitate survival of infective stages, (3) when large zebra aggregations increase forage contamination with infective stages, and (4) in individuals co-infected with more than one parasite group as this may indicate reduced immune competence. Strongylidae egg counts were higher, and the occurrence of Anoplocephalidae eggs was more likely in bachelors than in band stallions, whereas Ascarididae egg counts were higher in band stallions. Strongylidae and Ascarididae egg counts were not increased in lactating females. Strongylidae egg counts were higher in subadults than in foals. Regardless of sex and age, Ascarididae infections were more likely under wet conditions. Co-infections did not affect Strongylidae egg counts. Ascarididae egg counts in adult females were higher when individuals were co-infected with Anoplocephalidae. We present evidence that parasite burdens in plains zebras are affected by life history stage, environmental conditions, and co-infection.


2010 ◽  
Vol 67 (3) ◽  
pp. 486-497 ◽  
Author(s):  
Véronique Thériault ◽  
Gregory R. Moyer ◽  
Michael A. Banks

Survival and life history characteristics were evaluated for a coho salmon ( Oncorhynchus kisutch ) integrated hatchery program using two stocking strategies. Fish were released as unfed fry or smolts and returned as adults, and then molecular analysis was employed to pedigree the entire population. We showed that mean adult survival of individuals released as unfed fry was less than that of individuals released as smolts (0.03% vs. 2.39%). The relative reproductive success (RRS) of the fry release strategy to wild spawning was significantly greater for one of two cohorts, whereas the smolt release strategy to wild RRS was significantly greater for both cohorts. Fish released as smolts were significantly smaller upon returning as adults than either those released as unfed fry or wild returns. Mean run timing was also significantly biased towards an earlier run time for hatchery-released fish when compared with the wild component. The incidence of jacking (males maturing at age 2) was greater among fish stocked as smolts than for fish stocked as fry. Differences in survival, RRS, and life history appeared to be the result of hatchery practices and indicated that a fry stocking strategy produced fish more similar to the wild component of the population than to that of fish released as smolts.


2015 ◽  
Vol 66 (5) ◽  
pp. 399 ◽  
Author(s):  
Peter M. Yates ◽  
Michelle R. Heupel ◽  
Andrew J. Tobin ◽  
Stephen K. Moore ◽  
Colin A. Simpfendorfer

Effective conservation and management of shark populations is complicated by our limited understanding of their spatial ecology. For example, there are scarce data on diversity in community structure and nursery function across broader geographic scales (e.g. across multiple inshore systems) and the implications of this diversity for shark populations. Accordingly, fishery-independent surveys were undertaken to investigate shark communities along ~400km of the tropical eastern coast of Australia (18.1–20.6°S, 146.0–148.8°E). A variety of shark species were encountered, with 19 species of Carcharhiniformes contributing 99.2% of the total shark catch. Of the 1806 sharks captured, 567 were immature, including 336 young-of-the-year individuals. Immature sharks from 18 species were present; however, interspecific variation in the proportions of life-history stages was apparent. Multivariate analyses identified significant spatial heterogeneity in immature-shark communities. Results also highlighted the importance of tropical coastal habitats for numerous shark species, and indicated community-wide spatial structuring of sharks on the basis of body size rather than life-history stage. In addition to building on traditional shark-nursery paradigms, these results demonstrated that data on nursery function from restricted areas may not accurately portray patterns occurring over broader geographic scales, and this diversity may provide population-level benefits for sharks.


<em>Abstract.</em>—Pacific salmon <em>Oncorhynchus </em>spp. are important components of numerous food webs throughout their life history, yet we know very little about the historic and current abundance of these life history stages. We used past cannery records, recent harvest and hatchery records, and salmon life history information drawn from the literature to construct a simple bioregional model of historic and recent salmon abundance at egg, fry, smolt, ocean adult, and spawning stages for five species of Pacific salmon from Alaska to California. We found a historic-to-recent bioregional decline in salmon biomass in all life history stages. Recent salmon egg, fry, smolt, ocean-going adult, and escapement biomass estimates for northwestern North America are 74%, 55%, 59%, 86%, and 35%, respectively, of historic levels. Recent high productivity in Alaskan waters, however, masks a precipitous decline south of Alaska, where recent egg, fry, smolt, ocean-going adult, and escapement biomass levels are 34%, 23%, 50%, 40%, and 15% that of historic levels. Adult production and harvest levels are no longer sufficient measures of salmon management success. Researchers need to quantify and elucidate the ecosystem effects of historic biomass changes in life history stages of Pacific salmon on a watershed basis. Fisheries managers must set and meet specific targets for salmon life history stage abundance—from egg to spawning adult—to restore and maintain ecosystem function.


1989 ◽  
Vol 15 (2) ◽  
pp. 109-125 ◽  
Author(s):  
Gary K. Ostrander ◽  
Marsha L. Landolt ◽  
Richard M. Kocan

2007 ◽  
Vol 363 (1490) ◽  
pp. 425-441 ◽  
Author(s):  
John C Wingfield

The majority of vertebrates have a life span of greater than one year. Therefore individuals must be able to adapt to the annual cycle of changing conditions by adjusting morphology, physiology and behaviour. Phenotypic flexibility, in which an individual switches from one life history stage to another, is one way to maximize fitness in a changing environment. When environmental variation is low, few life history stages are needed. If environmental variation is large, there are more life history stages. Each life history stage has a characteristic set of sub-stages that can be expressed in various combinations and patterns to determine state at any point in the life of the individual. Thus individuals have a finite number of states that can be expressed over the spectrum of environmental conditions in their life spans. Life history stages have three phases–development, mature capability (when characteristic sub-stages can be expressed) and termination. Expression of a stage is time dependent (probably a minimum of one month), and termination of one stage overlaps development of the next stage. It follows that the more life history stages an individual expresses, the less flexibility it will have in timing those stages. Having fewer life history stages increases flexibility in timing, but less tolerance of variation in environmental conditions. To varying degrees it is possible to overlap mature capability of some life history stages to effectively reduce ‘finite stage diversity’ and maximize flexibility in timing. Theoretical ways by which this can be done, and the implications for neuroendocrine and endocrine control mechanisms are discussed. Twelve testable hypotheses are posed that relate directly to control mechanisms.


2021 ◽  
Author(s):  
◽  
Melissa Marquez

<p>Over the last few decades, much effort has been devoted towards evaluating and reducing bycatch in marine fisheries. There has been a particular focus on quantifying the risk to chondrichthyans, primarily because of their relatively high vulnerability to overfishing. A key part of risk assessment is evaluating the distributional overlap of the fish with the fisheries, where fish distribution is influenced by habitat use. I synthesised published observations of habitat use for different life history stages of chondrichthyans and hypothesised the associated catch composition in terms of fish sex, size, and maturity. I then searched for these catch compositions, and thereby locations, using New Zealand research vessel catch data. Results show that some life history stages and habitats for certain species can be identified, whereas others could not. Pupping ground criteria were met for Callorhynchus milii (ELE), Hydrolagus novaezealandiae (GSH), and Hydrolagus bemisi (GSP); nursery ground criteria were met for Callorhynchus milii (ELE), mating ground criteria were met for Callorhynchus milii (ELE), Hydrolagus novaezealandiae (GSH), Hydrolagus bemisi (GSP), and Harriotta raleighana (LCH); lek-like mating criteria were met for Hydrolagus novaezealandiae (GSH). For those life-history stage habitats not found, this may be because these are outside of the coverage of the data set (and likely also commercial fisheries), or because they do not actually exist for some chondrichthyans. On the basis of results, I propose to change the order of species in the New Zealand qualitative (Level 1) risk assessment, and rise the relative risk for Hydrolagus bemisi (GSP), given the species vulnerability of pupping grounds.</p>


1975 ◽  
Vol 32 (12) ◽  
pp. 2542-2547 ◽  
Author(s):  
John C. Mason

Following emergence, more than 51,000 coho salmon (Oncorhynchus kisutch) fry moved seaward from Lymn Creek. Peaks in movement occurred coincident with the new moon and progressively declined through four lunar cycles although 75% of the outmovement took place between early April and the middle of June. Coho smolt migration occurred simultaneously, the run peaking in late May during a period of maximum low tides between sunrise and sunset when the moon was full. Sticklebacks (Gasterosteus) moved seaward sporadically throughout the trapping period from April to September but their numbers increased markedly in August due to the appearance of underyearlings. The seaward movement of coho fry and smolts and of sticklebacks showed no apparent relationship to either stream discharge or temperature.Lunar rhythmicity in movement of coho fry and probable fate of fry are discussed within a framework of behavioral and ecologic concepts pertinent to the species’ life history in the juvenile stage and relevant to concern for enhancing coho salmon production.


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