Comparison of early life history between New Zealand temperate eels and Pacific tropical eels revealed by otolith microstructure and microchemistry
By Miho Marui, T. Arai, Michael J. Miller, D. Jellyman, K. Tsukamoto. 2001
87 citations recorded by the source corpus.
Subfields: Aquatic Science, Global and Planetary Change, Physiology
View Paper: https://www.semanticscholar.org/paper/5167baa38c56295cae963323d5002f282bd87c27
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Citations in the corpus
- Contrasting patterns of growth and migration of tropical anguillid leptocephali in the western Pacific and Indonesian Seas (2006, background): “Similarly wide ranges of hatching dates have been obtained from otolith analyses of glass eels of A. marmorata, A. bicolor pacifica and A. celebesensis in the region (e.g. Arai et al. 2001b, Marui et al. 2001).”
- Effect of El Niño on migration and larval transport of the Japanese eel (Anguilla japonica) (2007, background): “Estimates of the spawning season of Japanese eels has usually been based on age determination using otoliths, because increments in otoliths deposited daily have been noted at both early larva and juvenile stages (Tabeta et al., 1987; Tzeng and Tsai, 1992; Arai et al., 2000; Marui et al., 2001).”
- Phenotypic plasticity of habitat use by three temperate eel species, Anguilla anguilla, A. japonica and A. rostrata (2006, unknown): “Tropical species have shorter migrations (Marui et al. 2001).”
- Recruitment mechanisms of tropical eels Anguilla spp. and implications for the evolution of oceanic migration in the genus Anguilla (2001, background): “…A. anguilla (Lecomte-Finiger 1992, Arai et al. 2000b), A. rostrata (Wang & Tzeng 1998, Arai et al. 2000b), A. australis (Arai et al. 1999d), A. bicolor pacifica (Arai et al. 1999c), A. celebesensis, A. marmorata and A. bicolor bicolor (Arai et al. 1999b) and A. dieffenbachi (Marui et al. 2001).”
- Evaluation of the larval distribution and migration of the Japanese eel in the western North Pacific (2011, background): “Due to the spawning area of A. japonica being located so far offshore, its larval phase is long compared to most other types of fishes and is also long compared that of some tropical anguillid eels (Marui et al. 2001) that have shorter spawning migrations (Aoyama et al. 2003).”
- Evidence of different habitat use by New Zealand freshwater eels Anguilla australis and A. dieffenbachii, as revealed by otolith microchemistry (2004, methodology): “Mean annual growth rates were calculated by dividing the TL of individuals minus 59.3 mm in Anguilla australis (Arai et al. 1999) and 66.8 mm in A. dieffenbachii (Marui et al. 2001), which are the mean sizes of the glass eels of these 2 species when they recruit to the New Zealand coasts.”
- Ecology of Anguilliform Leptocephali: Remarkable Transparent Fish Larvae of the Ocean Surface Layer (2009, methodology): “marmorata and other anguillid species, the increment widths decrease even further by the time they recruit to coastal areas and are collected (Marui et al. 2001; Kuroki et al. 2005).”