The relationship between population genetic structure and pelagic larval duration in coral reef fishes on the Great Barrier Reef

By Line K. Bay, Ross H. Crozier, M. Caley. 2006

144 citations recorded by the source corpus.

Subfields: Ecology, Genetics, Nature and Landscape Conservation

View Paper: https://www.semanticscholar.org/paper/7409618419787e309e1c7be0b7260c66659b0876

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Citations in the corpus

Larval retention and connectivity among populations of corals and reef fishes: history, advances and challenges (2009, background): “Similarly, reef fishes range from species with direct development through to species with larval durations in excess of 50 days (Victor 1986; Wellington and Victor 1989; Doherty et al. 1995; Bay et al. 2006), and larvae vary greatly in their swimming ability (Stobutzki and Bellwood 1997; Leis 2006).”
Elevated temperature restricts growth potential of the coral reef fish Acanthochromis polyacanthus (2008, background): “The rearing temperatures were chosen to represent the long-term average, minimum and maximum summer temperatures of the collection location (Orpheus Island, GBR).”
Footprints on water: the genetic wake of dispersal among reefs (2007, background): “And while mtDNA did reveal extensive diVerentiation among populations of some brooding species of reef Wsh (Planes et al. 2001), a more general relationship between pelagic larval duration and degree of subdivision is not evident (Shulman and Bermingham 1995; Bay et al. 2006; Bowen et al. 2006).”
Phylogeography of New Zealand's coastal benthos (2009, background): “2006), but there is no consensus as to how variation in the length of larval duration might determine the scale at which propagules disperse or the genetic structure of populations (Mayr 1954; Ehrlich & Raven 1969; Burton 1983; Scheltema 1986; Bohonak 1999; Bay et al. 2006; Bradbury et al. 2008; Mil”
Climate change and the future for coral reef fishes (2008, background): “There is evidence for strong genetic connectivity among populations of coral reef fishes in some regions, such as the Great Barrier Reef in Australia (Doherty et al. 1995; Messmer et al. 2005; Bay et al. 2006).”
Effects of brooding and broadcasting reproductive modes on the population genetic structure of two Antarctic gastropod molluscs (2011, background): “Ayre and Hughes 2000; Bay et al. 2006; Nishikawa et al. 2003; Underwood et al. 2009).”
Elevated temperature reduces the respiratory scope of coral reef fishes (2009, background): “…able to maintain this reduced aerobic scope when exposed to 32 and 33 1C. A. polyacanthus exhibits significant local genetic structure on the GBR (Bay et al., 2006; Van Herwerden & Doherty, 2006), and a major reason for this is that A. polyacanthus, unlike most other damselfishes, does not have…”
Phylogeography and the conservation of coral reef fishes (2007, background): “…may be strongly correlated to geographic ranges and genetic structure in species that have extreme (very long or very short) pelagic larval stages (Bay et al. 2006; Purcell et al. 2006), but it remains a poor predictor of population structure for coral reef organisms with the common pelagic…”
Phylogeography of two Atlantic squirrelfishes (Family Holocentridae): exploring links between pelagic larval duration and population connectivity (2006, background): “1995) are anchored by species that lack a pelagic dispersive stage, and the significant relationship is weakened without these examples (Bohonak 1999; Bay et al. 2006).”
Endemism and dispersal: comparative phylogeography of three surgeonfishes across the Hawaiian Archipelago (2009, background): “Counter to these Wndings, a similar abundance of direct and indirect tests of the link between PLD and dispersal ability have found the relationship to be negligible at both ecological (Victor and Wellington 2000; Bay et al. 2006; Paulay and Meyer 2006) and evolutionary time scales (Planes et al. ”