Three synergistic growth-related mechanisms in the short-term survival of larval Japanese anchovy Engraulis japonicus in Sagami Bay

By A. Takasuka, Ichiro Aoki, I. Mitani. 2004

99 citations recorded by the source corpus.

Subfields: Global and Planetary Change, Oceanography

View Paper: https://www.semanticscholar.org/paper/1cf763462629b4499fb624985bec14ca959265f8

How researchers see this paper

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

In Global and Planetary Change

1. Yoshioki Oozeki
2. C. Möllmann
3. F. Köster
4. A. Takasuka
5. H. Kubota
6. E. Houde
7. Ichiro Aoki
8. H. Hinrichsen

In Oceanography

1. F. Köster
2. Yoshioki Oozeki
3. C. Möllmann
4. A. Takasuka
5. E. Houde
6. H. Kubota
7. S. Lluch‐Cota
8. Ichiro Aoki

Citations in the corpus

• Multi-species regime shifts reflected in spawning temperature optima of small pelagic fish in the western North Pacific (2008, background): “Growth rates represent survival potential during the early life stages (Takasuka et al. 2003, 2004), and growth variability could cause over 100-fold fluctuations in survival probabilities in theory (Houde 1987, Takasuka et al. 2007a).”
• Optimal growth temperature hypothesis: Why do anchovy flourish and sardine collapse or vice versa under the same ocean regime? (2007, background): “The growth–survival paradigm includes three functional mechanisms in its theoretical framework (Takasuka et al. 2004a).”
• Recruitment variability in Baltic Sea sprat (Sprattus sprattus) is tightly coupled to temperature and transport patterns affecting the larval and early juvenile stages (2006, background): “Temperature-enhanced growth rates certainly appear to reduce cumulative predatory losses in early larval populations (Pepin 1991; Heath 1992), as formulated by the “bigger-isbetter”, the “stage-duration”, or “growth-selective predation” hypotheses (Takasuka et al. 2004).”
• Contrasting spawning temperature optima: Why are anchovy and sardine regime shifts synchronous across the North Pacific? (2008, background): “Growth rates regulate survival potential of larvae through three growth-related mechanisms ( Takasuka et al., 2004a ): the ‘‘bigger is better” (Miller et al., 1988; Hare and Cowen, 1997), ‘‘stage duration” (Houde, 1987; Hare and Cowen, 1997), and ‘‘growth-selective predation” (Takasuka et al., 2003;”
• Emerging from Hjort's Shadow (2008, background): “Size-selective and/or growth-rate-selective predation often is hypothesized or observed to drive this process (Meekan and Fortier, 1996; Vigliola and Meekan, 2002; Takasuka et al., 2003, 2004; Vigliola et al., 2007).”
• When is bigger better? Early marine residence of middle and upper Columbia River spring Chinook salmon (2012, methodology): “The stage-duration hypo - thesis posits that faster growing fish remain suscep - tible to predation for a shorter period (Houde 1987, 2008, Takasuka et al. 2004).”
• Predator-specific growth-selective predation on larval Japanese anchovy Engraulis japonicus (2007, methodology): “This hypothesis was also supported by the characteristics of the survivors (Takasuka et al. 2004a).”
• Early growth and recruitment in Atlantic mackerel Scomber scombrus : discriminating the effects of fast growth and selection for fast growth (2007, background): “…(e.g. Miller et al. 1988), (2) longer exposure to intense predation during plankton life — the ‘stage-duration’ mechanism (e.g. Chambers & Leggett 1987), and/or (3) higher energy gain for predators preying on slow growers — the ‘growth-selective predation’ mechanism (Takasuka et al. 2003, 2004).”