Speciation in coral-reef fishes

By Luiz A. Rocha, Brian W. Bowen. 2008

224 citations recorded by the source corpus.

Subfields: Ecology, Genetics, Paleontology

View Paper: https://www.semanticscholar.org/paper/dd74de7dc2fea69ad9091da0ea10998c3556b4b9

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Citations in the corpus

Shifting seas: the impacts of Pleistocene sea‐level fluctuations on the evolution of tropical marine taxa (2015, background): “Population breaks are also found at other locations bordering the Indo-Pacific, such as the Red Sea where the crown-of-thorns starfish (Vogler et al., 2008) and several fishes (DiBattista et al., 2013) exhibit population breaks.”
Origins of species richness in the Indo‐Malay‐Philippine biodiversity hotspot: evidence for the centre of overlap hypothesis (2013, background): “Others have suggested that increased rates of speciation in the hotspot are driven by intense competition (Briggs, 2005; Bowen et al., 2013) and differing selection pressures in a highly heterogeneous environment (Rocha & Bowen, 2008).”
The historical biogeography of coral reef fishes: global patterns of origination and dispersal (2013, background): “Such studies have been limited in the Indo-Pacific (Rocha & Bowen, 2008) and those that have been undertaken have not found the level of species division seen in the Atlantic.”
Marine shelf habitat: biogeography and evolution (2013, background): “However, a recent review of speciation in reef fishes noted that parapatric speciation is a common (and possibly prevalent) mode of diversification (Rocha & Bowen, 2008).”
Phylogeography unplugged: comparative surveys in the genomic era (2014, background): “—Comparative studies can explore the relative importance of allopatric, parapatric, and sympatric speciation, providing insights into the causes of diversification (Rocha and Bowen 2008, Bird et al. 2011, Dawson et al. 2012).”
Genetic evaluation of marine biogeographical barriers: perspectives from two widespread Indo‐Pacific snappers (Lutjanus kasmira and Lutjanus fulvus) (2009, background): “Unusual local environmental conditions may reinforce the biogeographical isolation of the Marquesan fish fauna (see Rocha & Bowen, 2008).”
Fish biodiversity and conservation in South America. (2016, background): “…and early 1990s back to the classical centre of origin and dispersion scenario of pre-cladistic times, is actually based on a host of empirical and theoretical evidence, and seems to be particularly valid for the highly diversified tropical reef-fish biota (Rocha & Bowen, 2008; Bowen et al., 2013).”
Shore fishes and biogeographic subdivisions of the Tropical Eastern Pacific (2009, background): “Rocha & Bowen (2008) have argued that, given the absence of hard barriers to dispersal in the sea and the great abilities of pelagic larvae of reef fishes to cross habitat barriers, parapatric speciation may be the predominant mode of speciation in coral reef fishes.”
The application of genetics to marine management and conservation: Examples from the Indo-Pacific (2014, background): “Some of the strongest evidence for both cryptic species comes from coral reef fishes (Rocha and Bowen 2008), which display morphological variation that can be used as a baseline for genetic investigations.”
Eurythoe complanata (Polychaeta: Amphinomidae), the ‘cosmopolitan’ fireworm, consists of at least three cryptic species (2010, background): “This scenario would be compatible with an allopatric or, more likely, parapatric speciation (Coyne and Orr 2004; Rocha and Bowen 2008 ) of the two species of Eurythoe, because these species inhabit a fragmented environment (reefs or rocky shores) and include pelagic larvae in their life cycles.”
Paradigm shifts in marine fisheries genetics: ugly hypotheses slain by beautiful facts (2008, background): “The reverse causal pathway is also possible, and adaptive divergence may constrain gene flow by selection against immigrants and hybrids, so-called reinforcement of adaptive divergence (Garant et al. 2007), potentially leading to ecological speciation (Rocha and Bowen 2008).”