Literature DB >> 21562025

How Nemo finds home: the neuroecology of dispersal and of population connectivity in larvae of marine fishes.

Jeffrey M Leis1, Ulrike Siebeck, Danielle L Dixson.   

Abstract

Nearly all demersal teleost marine fishes have pelagic larval stages lasting from several days to several weeks, during which time they are subject to dispersal. Fish larvae have considerable swimming abilities, and swim in an oriented manner in the sea. Thus, they can influence their dispersal and thereby, the connectivity of their populations. However, the sensory cues marine fish larvae use for orientation in the pelagic environment remain unclear. We review current understanding of these cues and how sensory abilities of larvae develop and are used to achieve orientation with particular emphasis on coral-reef fishes. The use of sound is best understood; it travels well underwater with little attenuation, and is current-independent but location-dependent, so species that primarily utilize sound for orientation will have location-dependent orientation. Larvae of many species and families can hear over a range of ~100-1000 Hz, and can distinguish among sounds. They can localize sources of sounds, but the means by which they do so is unclear. Larvae can hear during much of their pelagic larval phase, and ontogenetically, hearing sensitivity, and frequency range improve dramatically. Species differ in sensitivity to sound and in the rate of improvement in hearing during ontogeny. Due to large differences among-species within families, no significant differences in hearing sensitivity among families have been identified. Thus, distances over which larvae can detect a given sound vary among species and greatly increase ontogenetically. Olfactory cues are current-dependent and location-dependent, so species that primarily utilize olfactory cues will have location-dependent orientation, but must be able to swim upstream to locate sources of odor. Larvae can detect odors (e.g., predators, conspecifics), during most of their pelagic phase, and at least on small scales, can localize sources of odors in shallow water, although whether they can do this in pelagic environments is unknown. Little is known of the ontogeny of olfactory ability or the range over which larvae can localize sources of odors. Imprinting on an odor has been shown in one species of reef-fish. Celestial cues are current- and location-independent, so species that primarily utilize them will have location-independent orientation that can apply over broad scales. Use of sun compass or polarized light for orientation by fish larvae is implied by some behaviors, but has not been proven. Use of neither magnetic fields nor direction of waves for orientation has been shown in marine fish larvae. We highlight research priorities in this area.
© The Author 2011. Published by Oxford University Press on behalf of the Society for Integrative and Comparative Biology. All rights reserved.

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Year:  2011        PMID: 21562025     DOI: 10.1093/icb/icr004

Source DB:  PubMed          Journal:  Integr Comp Biol        ISSN: 1540-7063            Impact factor:   3.326


  32 in total

1.  Patterns, causes, and consequences of marine larval dispersal.

Authors:  Cassidy C D'Aloia; Steven M Bogdanowicz; Robin K Francis; John E Majoris; Richard G Harrison; Peter M Buston
Journal:  Proc Natl Acad Sci U S A       Date:  2015-10-27       Impact factor: 11.205

2.  Experimental evaluation of imprinting and the role innate preference plays in habitat selection in a coral reef fish.

Authors:  Danielle L Dixson; Geoffrey P Jones; Philip L Munday; Serge Planes; Morgan S Pratchett; Simon R Thorrold
Journal:  Oecologia       Date:  2013-08-31       Impact factor: 3.225

3.  The nose knows: linking sensory cue use, settlement decisions, and post-settlement survival in a temperate reef fish.

Authors:  E K Fobert; S E Swearer
Journal:  Oecologia       Date:  2017-02-23       Impact factor: 3.225

Review 4.  Does fish larval dispersal differ between high and low latitudes?

Authors:  Jeffrey M Leis; Jennifer E Caselle; Ian R Bradbury; Trond Kristiansen; Joel K Llopiz; Michael J Miller; Mary I O'Connor; Claire B Paris; Alan L Shanks; Susan M Sogard; Stephen E Swearer; Eric A Treml; Russell D Vetter; Robert R Warner
Journal:  Proc Biol Sci       Date:  2013-03-20       Impact factor: 5.349

5.  Effect of elevated CO2 and small boat noise on the kinematics of predator-prey interactions.

Authors:  Mark I McCormick; Sue-Ann Watson; Stephen D Simpson; Bridie J M Allan
Journal:  Proc Biol Sci       Date:  2018-03-28       Impact factor: 5.349

6.  Ocean acidification alters temperature and salinity preferences in larval fish.

Authors:  Jennifer C A Pistevos; Ivan Nagelkerken; Tullio Rossi; Sean D Connell
Journal:  Oecologia       Date:  2016-11-25       Impact factor: 3.225

7.  First evidence of fish larvae producing sounds.

Authors:  Erica Staaterman; Claire B Paris; Andrew S Kough
Journal:  Biol Lett       Date:  2014-10       Impact factor: 3.703

8.  Ocean acidification boosts larval fish development but reduces the window of opportunity for successful settlement.

Authors:  Tullio Rossi; Ivan Nagelkerken; Stephen D Simpson; Jennifer C A Pistevos; Sue-Ann Watson; Laurene Merillet; Peter Fraser; Philip L Munday; Sean D Connell
Journal:  Proc Biol Sci       Date:  2015-12-22       Impact factor: 5.349

9.  Using insights from animal behaviour and behavioural ecology to inform marine conservation initiatives.

Authors:  Rohan M Brooker; William E Feeney; James R White; Rachel P Manassa; Jacob L Johansen; Danielle L Dixson
Journal:  Anim Behav       Date:  2016-04-29       Impact factor: 2.844

10.  An integrative investigation of sensory organ development and orientation behavior throughout the larval phase of a coral reef fish.

Authors:  John E Majoris; Matthew A Foretich; Yinan Hu; Katie R Nickles; Camilla L Di Persia; Romain Chaput; E Schlatter; Jacqueline F Webb; Claire B Paris; Peter M Buston
Journal:  Sci Rep       Date:  2021-06-11       Impact factor: 4.379

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