Genetic assessment of connectivity among marine populations

By M. Hellberg, R. Burton, J. Neigel, Stephen R. Palumbi. 2002

532 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/a605dfc297153844188ae5cc0029b989fed3dbeb

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Citations in the corpus

• Footprints on water: the genetic wake of dispersal among reefs (2007, background): “There have been recent reviews concerning the genetic inferences that can be made about population isolation (Hellberg et al. 2002), and demography (Hellberg 2006a) in marine animals.”
• Genetic discontinuity among regional populations of Lophelia pertusa in the North Atlantic Ocean (2011, unknown): “A positive correlation between genetic and geographic distance (IBD) may provide a means of estimating dispersal in marine systems (Hellberg et al. 2002; Palumbi 2004; Bradbury and Bentzen 2007).”
• Connectivity and stability of mesophotic coral reefs (2011, unknown): “protected areas (Cowen and Sponaugle, 2009; Hedgecock et al., 2007; Hellberg et al., 2002).”
• Seascape Genetics: Populations, Individuals, and Genes Marooned and Adrift (2013, background): “For the many marine species that disperse extensively, population genetic theory predicts high genetic variability and low differentiation across large spatial scales (Waples 1998; Hellberg et al. 2002; Faurby & Barber 2012).”
• Molecular genetic structure suggests limited larval dispersal in grass rockfish, Sebastes rastrelliger (2003, background): “Detection of non-equilibrium patterns at large spatial scales is not uncommon in marine fish and invertebrates (Slatkin 1993; Hellberg 1995; Johnson and Black 1998; Hellberg et al. 2002 ).”
• Biodiversity and phylogeography of Arctic marine fauna: insights from molecular tools (2011, background): “…modes often show varying degrees of genetic isolation from neighboring populations due to variations in dispersal potential, because low dispersal ability constitutes a form of reproductive isolation leading to sympatric speciation in some taxa (Palumbi 1994; Hellberg et al. 2002; Foltz 2003).”
• Genetic structure of natural populations of California red abalone (Haliotis rufescens) using multiple genetic markers (2007, background): “Understanding the genetic structure of a long-lived species with population admixture can be facilitated by sampling speciWc recruitment events or size/age cohorts (Flowers et al. 2002; Hellberg et al. 2002).”
• Larval dispersal and marine population connectivity. (2009, background): “The latter approach is broader taxonomically, but both have the advantage that every individual within the population is marked (see Thorrold et al. 2002, 2007; Hellberg et al. 2002; Planes 2002; Palumbi 2003; Hellberg 2007; Hedgecock et al. 2007).”
• Small effective number of parents (Nb) inferred for a naturally spawned cohort of juvenile European flat oysters Ostrea edulis (2007, unknown): “The actual extent of larval dispersal and its demographic and evolutionary consequences, however, continue to be much debated (Bonhomme and Planes 2000; Hellberg et al. 2002; Taylor and Hellberg 2003), particularly with respect to the design of marine reserves (Palumbi 2003).”
• Effects of brooding and broadcasting reproductive modes on the population genetic structure of two Antarctic gastropod molluscs (2011, background): “Hellberg et al. 2002; Kinlan and Gaines 2003; Palumbi 2003).”
• The relationship between population genetic structure and pelagic larval duration in coral reef fishes on the Great Barrier Reef (2006, background): “Studies using genetic markers have become vital in this context due to the difficulties associated with directly observing the movement among populations in the marine environment (e.g., Hedgecock 1986; Bohonak 1999; Hellberg et al. 2002 ).”
• The ecology of rafting in the marine environment. III. Biogeographical and evolutionary consequences (2006, methodology): “There is a diversity of molecular markers, among which proteins, mitochondrial DNA (mtDNA), microsatellites and fingerprinting methods (e.g., RFLP, RAPDS) are preferred for studies on the population level (Parker et al. 1998, Sunnucks 2000, Hellberg et al. 2002, Féral et al. 2003).”
• Geographical patterns of genetic structure in marine species with contrasting life histories (2009, background): “As barriers shift, species with low dispersal will continue to reflect historical patterns over long time-scales, because low levels of gene flow allow the signal of historical separation to persist for many generations (Hellberg et al., 2002).”
• Implications of life history for genetic structure and migration rates of southern African coastal invertebrates: planktonic, abbreviated and direct development (2007, background): “The greatest inXuence of life history strategies on genetic structure tends to be at intermediate scales of »100 km (Hellberg et al. 2002; Palumbi 2003), while on larger scales of »1000 km, the eVect of currents and environmental discontinuities may result in diversifying selection that aVects all…”