Energetics and morphology of sockeye salmon: effects of upriver migratory distance and elevation

By G. Crossin, S. Hinch, A. Farrell, D. Higgs, A. Lotto, J. Oakes, M. Healey. 2004

263 citations recorded by the source corpus.

Subfields: Ecology, Global and Planetary Change, Nature and Landscape Conservation

View Paper: https://www.semanticscholar.org/paper/e09526c344673662596a0aa6d9a8ca10487a6e6b

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Ecology

1. S. Cooke
2. S. Hinch
3. M. Baguette
4. A. Farrell
5. D. Patterson
6. H. Van Dyck
7. D. Bonte
8. N. Schtickzelle

In Global and Planetary Change

1. S. Cooke
2. S. Hinch
3. D. Patterson
4. A. Farrell
5. G. Crossin
6. A. Lotto
7. K. English
8. G. Kraak

In Nature and Landscape Conservation

1. S. Cooke
2. S. Hinch
3. D. Patterson
4. A. Farrell
5. G. Crossin
6. A. Lotto
7. M. Baguette
8. K. English

Citations in the corpus

• There and back again: migration in freshwater fishes (2014, background): “Furthermore, Crossin et al. (2004) compared fuel loads in migrating populations of sockeye salmon and found that populations which undertake long-distance migrations or home to natal rivers at high altitude initiated upriver migration with more somatic energy and fewer eggs.”
• Using invasive species to study evolution. Case studies with Drosophila and salmon (2005, background): “One predictable result was the genetically smaller hump size for the population migrating the longer distance (see also Crossin et al. 2004).”
• Physiological and energetic correlates of en route mortality for abnormally early migrating adult sockeye salmon (Oncorhynchus nerka) in the Thompson River, British Columbia (2006, background): “…the Thompson River) begin the freshwater migration with about 8 MJ·kg–1 of somatic energy and complete the migration with about 5 MJ·kg–1, approximately 4 MJ·kg–1 of which is required to sustain their life throughout spawning; thus, they have only a 1 MJ·kg–1 energy buffer (Crossin et al. 2004a).”
• Exposure to high temperature influences the behaviour, physiology, and survival of sockeye salmon during spawning migration (2008, background): “# 2008 NRC Canada are investing significantly more energy in reproductive development during upriver migration (nearly 50% of their GSE stores vs. just 4% for males; Crossin et al. 2004), the metabolic stress imposed by high temperature may put females at greater risk of mortality.”
• Physiology of individual late-run Fraser River sockeye salmon (Oncorhynchus nerka) sampled in the ocean correlates with fate during spawning migration (2006, background): “H fish make a 161 km river migration and gain ~10 m in vertical elevation; Adams fish make a 485 km river migration and gain ~ 366 m vertical elevation; Crossin et al. 2004).”
• Costs of dispersal (2012, background): “Field experimental approaches have also found a reduction in fecundity with increased displacement distances (Crossin et al., 2004; Jonsson & Jonsson, 2006; Kinnison et al., 2001).”
• Ecological and Evolutionary Consequences of Environmental Change and Management Actions for Migrating Fish (2019, background): “, swimming capacity, acceleration, endurance, and ability to sustain high water velocities), and of behavioral (boldness, and latency to pass obstacles) traits (Webb, 1975; Swain, 1992; McDowall et al., 1994; Fleming, 1996; McDowall, 2003; Crossin et al., 2004; Haugen et al., 2008; Long et al., 2011”
• Fishway passage and post‐passage mortality of up‐river migrating sockeye salmon in the Seton River, British Columbia (2011, background): “In our study, all individuals had GSE levels at the time of release that were at least 25%greater than proposed threshold energy level required to sustain life (4MJ kg (1); Crossin et al., 2004).”
• Effects of river temperature and climate warming on stock‐specific survival of adult migrating Fraser River sockeye salmon (Oncorhynchus nerka) (2011, background): “energy density (Crossin et al., 2004), optimum temperature for aerobic scope (Lee et al.”
• Monitoring the spawning behaviour of chum salmon with an acceleration data logger (2006, background): “In general, the energy reserves of salmon stock match the cost of upriver migration and reproduction (Crossin et al. 2004).”
• Fish cardiorespiratory physiology in an era of climate change (2009, background): “…temperatures than coastal salmon, they correspondingly have a greater aerobic scope, critical swimming speed and Topt (Tsuyuki and Williscroft 1977; Lee et al. 2003a, 2003b), as well as a smaller body size, a more fusiform shape and a proportionally smaller total egg mass (Crossin et al. 2004).”
• Slow dam passage in adult columbia river salmonids associated with unsuccessful migration : delayed negative effects of passage obstacles or condition-dependent mortality? (2007, background): “Poor initial condition (Crossin et al. 2004a) and (or) environmental conditions (Rand and Hinch 1998) during migration could further increase the probability of a fish entering this cycle.”
• A Nonlethal, Rapid Method for Assessing the Somatic Energy Content of Migrating Adult Pacific Salmon (2005, methodology): “Such low levels of energy are typical of spawning Pacific salmon (Hendry and Berg 1999; Crossin et al. 2004), thus caution needs to be exercised when using this type of meter to estimate lipid levels in spawning salmon.”
• Effect of water temperature, timing, physiological condition, and lake thermal refugia on migrating adult Weaver Creek sockeye salmon (Oncorhynchus nerka) (2010, background): “15 October is near the historical peak spawning time for Weaver sockeye (Crossin et al. 2004).”