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A. a. Vila-Gispert, R. Moreno-Amich (1998)
Periodic abundance and depth distribution of Blennius fluviatilis and introduced Lepomis gibbosusHydrobiologia, 386
R. Lewontin, H. Baker, G. Stebbins (1965)
Selection for colonizing abilitty.
D. Venable, Joel Brown (1988)
The Selective Interactions of Dispersal, Dormancy, and Seed Size as Adaptations for Reducing Risk in Variable EnvironmentsThe American Naturalist, 131
R. Mahon (1984)
Divergent structure in fish taxocenes of north temperate streamsCanadian Journal of Fisheries and Aquatic Sciences, 41
A. Vila-Gispert, R. Moreno‐Amich (2002)
Life-history Patterns of 25 species from European Freshwater Fish CommunitiesEnvironmental Biology of Fishes, 65
D. Reznick (1982)
THE IMPACT OF PREDATION ON LIFE HISTORY EVOLUTION IN TRINIDADIAN GUPPIES: GENETIC BASIS OF OBSERVED LIFE HISTORY PATTERNSEvolution, 36
B. Tabachnick, L. Fidell (2000)
Computer-Assisted Research Design and Analysis
(1995)
Recruitment of marine fish : the relative roles of density - dependent and density - independent mortality in the egg , larval , and juvenile stages
M. Armstrong, P. Shelton (1990)
Clupeoid life-history styles in variable environmentsEnvironmental Biology of Fishes, 28
(1987)
Comparison of recruitment variability and life history data among marine and anadromous fishes
M. Paine (1990)
Life history tactics of darters (Percidae: Etheostomatiini) and their relationship with body size, reproductive behaviour, latitude and rarityJournal of Fish Biology, 37
S. Stearns (1976)
Life-History Tactics: A Review of the IdeasThe Quarterly Review of Biology, 51
G. Murphy (1968)
Pattern in Life History and the EnvironmentThe American Naturalist, 102
T. Kawasaki (1980)
Fundamental relations among the selections of life history in the marine teleostsBull. Japan. Soc. Sci. Fish, 46
E. Pianka (1970)
On r- and K-SelectionThe American Naturalist, 104
Daniel Cohen (1967)
Optimizing reproduction in a randomly varying environment when a correlation may exist between the conditions at the time a choice has to be made and the subsequent outcome.Journal of theoretical biology, 16 1
K.O. Winemiller (1995)
Aspects structurels et fonctionnels de la biodiversité des peuplements de poissonsBull. Fr. Pêche Piscic., 337/338/339
G. Potts, R. Wootton, Tactics (1984)
Fish Reproduction: Strategies and Tactics
Kirk Winemiller (1995)
ASPECTS STRUCTURELS ET FONCTIONNELS DE LA BIODIVERSITÉ DES PEUPLEMENTS DE POISSONS.Bulletin Francais De La Peche Et De La Pisciculture, 68
K. Winemiller, K. Rose (1992)
Patterns of Life-History Diversification in North American Fishes: implications for Population RegulationCanadian Journal of Fisheries and Aquatic Sciences, 49
K. Winemiller (1992)
Life-history strategies and the effectiveness of sexual selectionOikos, 63
K. Winemiller (1989)
Patterns of variation in life history among South American fishes in seasonal environmentsOecologia, 81
Hi Browman, D. Cushing, E. DeBlois, B. Ellertsen, P. Fossum, W. Leggett, Ransom Myers, P. Solemdal, S. Sundby (1995)
Commentaries on current research trends in recruitment studiesMarine Ecology Progress Series, 128
Anna Gispert (1996)
Estratègies reproductives de les espècies íctiques de les famílies Centrarchidae i Cyprinidae a l'Estany de Banyoles
R.C. Lewontin (1965)
The Genetics of Colonizing Species
R. Warner, P. Chesson (1985)
Coexistence Mediated by Recruitment Fluctuations: A Field Guide to the Storage EffectThe American Naturalist, 125
K. Rose, J. Cowan, K. Winemiller, R. Myers, R. Hilborn (2001)
Compensatory density dependence in fish populations: importance, controversy, understanding and prognosisFish and Fisheries, 2
M. Boyce (1979)
Seasonality and Patterns of Natural Selection for Life HistoriesThe American Naturalist, 114
T. Kawasaki (1980)
Fundamental Relations among the Selections of Life History in the Marine TeleostsNippon Suisan Gakkaishi, 46
E. García‐Berthou, R. Moreno‐Amich (1993)
Multivariate analysis of covariance in morphometric studies of the reproductive cycleCanadian Journal of Fisheries and Aquatic Sciences, 50
D. Baltz (1984)
Life history variation among female surfperches (Perciformes: Embiotocidae)Environmental Biology of Fishes, 10
A. Vila-Gispert, R. Moreno‐Amich (1998)
Seasonal abundance and depth distribution of Blennius fluviatilis and introduced Lepomis gibbosus, in Lake Banyoles (Catalonia, Spain)Hydrobiologia, 386
A. Vila-Gispert, R. Moreno‐Amich (2000)
Fecundity and spawning mode of three introduced fish species in Lake Banyoles (Catalunya, Spain) in comparison with other localitiesAquatic Sciences, 62
T. Kawasaki (1983)
Why do some pelagic fishes have wide fluctuations in their numbers? Biological basis of fluctuation from the viewpoint of evolutionary ecology
Multivariate analysis identified atwo-dimensional continuum of life-historyvariation among 301 fish species from Europe,North America, South America and the Atlanticand Pacific coasts of North America. The firstaxis was associated with larger body size,higher fecundity, delayed maturation, fewerreproductive events, and shorter breedingseason on one end and small size, lowfecundity, early maturity, multiplereproductive events per year, and prolongedbreeding season on the other. The second axiscontrasted fishes having larger eggs and moreparental care against fishes with the oppositesuite of traits.Phylogenetic affiliations of species wereapparent in the general patterns of ordinationof species within orders, indicatingevolutionary divergences in life-historypatterns. In fact, partitioning the variance oflife-history traits showed that taxonomic orderand latitude were the most important factorsand geographic region and habitat the least.Despite phylogenetic constraints, basiclife-history patterns showed consistencybetween distantly geographical regions,latitudinal ranges and basic adult habitats,indicating convergences in life-historypatterns. Although the basic life-historypatterns seemed repeatable among distantlyrelated taxa, geographical and latitudinalaffiliations were apparent. Species from SouthAmerica are skewed toward the opportunisticendpoint, whereas North American marine speciesare skewed toward the periodic endpoint of thetrilateral continuum model. Most of the fishspecies from South American data set came fromfluctuating environments, so an opportunisticstrategy of early maturation and continuousspawning permits efficient recolonization ofhabitats over small spatial scales. Incontrast, most species in the North Americanand European data sets came from seasonalhabitats that are nonetheless more hydrologicalstable, so a periodic strategy of delayingmaturation to attain large clutches enhancesadult survivorship during suboptimalenvironmental conditions and recruitment whenearly life stages encounter suitableenvironmental conditions. Similarly,latitudinal affiliations were also observed:opportunistic strategists more common intropical latitudes and periodic strategistsmore common in temperate and Arctic latitudes.
Reviews in Fish Biology and Fisheries – Springer Journals
Published: Oct 13, 2004
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