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Titlebook: Ecology and ethology of fishes; Proceedings of the 2 David L. G. Noakes,Jack A. Ward Conference proceedings 1981 Springer Science+Business

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Synchronized maturation and breeding in natural populations of , (Poeciliidae),ime. This coordinate development has also been seen in the laboratory. We hypothesize that juveniles resembling each other experience fewer aggressive responses from males than do juveniles without ‘look-alikes’, because of habituation of aggression. This would decrease social inhibition and permit
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Maintenance of female mimicry as a reproductive strategy in bluegill sunfish (,),reduction in male reproductive effort, sometimes occur. Female mimicry in bluegill sunfish (.) is an example of an obligate alternative male strategy. Female mimics are small, sexually mature males which mimic the details of female behavior, and gain access to functional females attracted to the nes
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Patterns of parental investment, dispersal and size among coral-reef fishes,een patches. For large species (> 100 mm SL) and widely separated patches, numerous propagules are needed, often with specialized pelagic intervals. Individuals of small species are confined to portions of the reef. They are unable to produce enough eggs for effective long-range dispersal, and so th
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Reproductive tactics of the Asian cichlids of the genus , in Sri Lanka,e for nest construction and maintaining visual contact with offspring. These are the drier premonsoonal and monsoonal seasons when water turbidity decreased and salinity increased. When breeding in isolation orange chromide pairs selected dense vegetation where nests were camouflaged. During the pea
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https://doi.org/10.1007/978-3-7091-9148-4between size of fish and their distance to the center of the school. Furthermore, the tendency to seek cover increased in the presence of Schreckstoff. The greater organization in school structure appears to be an adaptive response to aquatic predators, whereas increased cover seeking may be an adaptive response to aerial predators.
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