Skipped spawning in female iteroparous fishes
By R. Rideout, G. Rose, M. Burton. 2005
388 citations recorded by the source corpus.
Subfields: Aquatic Science, Nature and Landscape Conservation, Physiology
View Paper: https://www.semanticscholar.org/paper/c4a539eedb28c3748b5aa017e793d3a05e6a845a
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Aquatic Science
- M. Morgan
- J. Tomkiewicz
- S. Lowerre‐Barbieri
- K. Ganias
- Francisco Saborido-Rey
- C. Jørgensen
- R. Rideout
- R. Haedrich
In Nature and Landscape Conservation
- M. Morgan
- S. Lowerre‐Barbieri
- J. Tomkiewicz
- Francisco Saborido-Rey
- C. Jørgensen
- R. Rideout
- Ulf Dieckmann
- B. Block
In Physiology
- J. Tomkiewicz
- R. Rideout
- M. Morgan
- Francisco Saborido-Rey
- S. Lowerre‐Barbieri
- N. Brown‐Peterson
- A. Alonso‐Fernández
- H. Murua
Citations in the corpus
- The logic of skipped spawning in fish (2006, background): “331 Phenotypic plasticity and the physiology of skipped spawning 332 For fish, the physiology and histology of skipped spawning were recently reviewed by 333 Rideout et al. (2005).”
- A Standardized Terminology for Describing Reproductive Development in Fishes (2011, neutral): “Another variation in the reproductive cycle occurs in spawn-skipping individuals—fish that have reached sexual maturity but do not enter the spawning capable phase during the current reproductive cycle (Rideout et al. 2005).”
- Emerging Issues and Methodological Advances in Fisheries Reproductive Biology (2011, background): “Nevertheless, coldwater species exhibit slower oocyte developmental rates (Rideout et al. 2005) and often have short spawning seasons, resulting in discontinuous recruitment from PG to secondary growth and determinate fecundity, as observed in the Atlantic cod (Kjesbu 2009; Pavlov et al.”
- A review of early life history dynamics of Barents Sea cod (Gadus morhua) (2014, background): “They state that methodological problems in identifying the post-mature non-reproductive state, especially related to the time of sampling, have led fisheries science to underestimate the frequency of skipped spawning and thus also its importance for recruitment (Rideout et al., 2005).”
- Reproductive Timing in Marine Fishes: Variability, Temporal Scales, and Methods (2011, background): “Spawning seasonality typically occurs at the annual scale as most fish exhibit seasonality in peak spawning activity and annual reproductive cycles (Bye 1984; Rideout et al. 2005).”
- A continuum of life histories in deep-sea demersal fishes (2012, background): “, 1998) and in the field between fish in good versus poor nutritional condition (Rideout and Morgan, 2007; Rideout et al., 2005).”
- Influence of diet on growth, condition and reproductive capacity in Newfoundland and Labrador cod (Gadus morhua) : Insights from stable carbon isotopes (δ13C) (2007, methodology): “Females were classified as immature (‘nonspawners’) if ovaries were small and pink, ripening (‘potential spawners’) if opaque eggs were visible, and ‘Spent L’ (‘non-spawners’) if ovaries were small and red with no opaque eggs (Templeman et al., 1978; Rideout et al., 2005).”
- Skipped Spawning in Fishes: More Common than You Might Think (2011, methodology): “Although skipped spawning is almost certainly a rarer means of regulating individual fish reproductive investment than is the downregulation of fecundity via atresia, it has nevertheless been demonstrated to be widespread among fishes (Rideout et al. 2005).”
- Physiological Basis of Climate Change Impacts on North American Inland Fishes (2016, background): “Reproduction Are temperature-driven changes in climate contributing to the adoption of “skipped spawning” strategies (Rideout et al. 2005)? Does climate change differentially influence species according to their spawning strategy and level of parental care? Will early-life survival increase in a cha”
- Life History and Stock Structure of Atlantic Bluefin Tuna (Thunnus thynnus) (2007, background): “The last hypothesis regarding skipped spawning has not received intense scrutiny and may have some merit since reproductive schedules can exhibit large phenotypic plasticity in marine fishes (Rjinsdorp, 1989; Roff, 1991; Rideout et al., 2005).”
- Integrating Reproductive Biology into Scientific Advice for Fisheries Management (2008, background): “Egg size may also vary over the spawning season in fish that spawn multiple batches (Chambers and Waiwood, 1996; DeMartini, 1991; Kjesbu et al., 1996; Marteinsdottir and Steinarsson, 1998; Rideout et al., 2005b).”
- Advances in herring biology: from simple to complex, coping with plasticity and adaptability (2009, background): “The energetic costs of migration and spawning may lead individual fish to skip spawning, especially in their second year of maturity (Rideout et al., 2005).”
- Complex migration routes of Atlantic bluefin tuna (Thunnus thynnus) question current population structure paradigm (2010, neutral): “Skipped spawning has been presented as a survival strategy in iteroparous fishes (Rideout et al. 2005), and although previous tagging studies have suggested the possibility in western Atlantic ABFT, definitive conclusions from tagging studies have been complicated by sampling a mixture of age classe”
- Energy acquisition and allocation to egg production in relation to fish reproductive strategies (2014, background): “Many species do not spawn annually (Rideout et al. 2005; Secor 2008; Rideout and Tomkiewicz 2011).”