2010
DOI: 10.1016/b978-0-12-381308-4.00002-9
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Genetics of Northern Krill (Meganyctiphanes norvegica Sars)

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Cited by 7 publications
(4 citation statements)
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“…Evidence for allopatric divergence between populations within species also has been reported for other holoplanktonic copepods (Goetze 2005(Goetze , 2011 and other planktonic, neustonic and pleustonic species in oceanic habitats (e.g. Andersen et al 2000;Patarnello et al 2010;Churchill et al 2014). These examples provide strong evidence that oceanographic barriers both within and between ocean basins are effective at isolating populations for significant time periods even within these oceanic species.…”
Section: Discussionsupporting
confidence: 58%
“…Evidence for allopatric divergence between populations within species also has been reported for other holoplanktonic copepods (Goetze 2005(Goetze , 2011 and other planktonic, neustonic and pleustonic species in oceanic habitats (e.g. Andersen et al 2000;Patarnello et al 2010;Churchill et al 2014). These examples provide strong evidence that oceanographic barriers both within and between ocean basins are effective at isolating populations for significant time periods even within these oceanic species.…”
Section: Discussionsupporting
confidence: 58%
“…Furthermore, dispersal of individuals is key to controlling a population's ability to adapt to changes and colonize suitable areas (Kokko & L opez-Sepulcre 2006). Holozooplankton have shown significant genetic differentiation over a wide range of geographical scales (Cowen et al 2007;Goetze 2005;Hellberg 2009), including within the North Atlantic Ocean Patarnello et al 2010;Peijnenburg et al 2006;Unal & Bucklin 2010;Yebra et al 2011). However, most (if not all) of the findings of significant genetic structuring have involved the presence of hydrographic or geological barriers (e.g.…”
Section: Introductionmentioning
confidence: 99%
“…Rates of divergence and amounts of variation differ among these markers, but many studies have documented significant genetic differentiation of zooplankton populations at large, ocean basin scales using mitochondrial DNA (e.g., Goetze 2005;Goetze and Ohman 2010;Miyamoto et al 2010;Blanco-Bercial et al 2011a;Miller et al 2012;Norton and Goetze 2013;Dawson et al 2015) and microsatellite markers (Bolte et al 2013;Andrews et al 2014). A number of studies have used mitochondrial DNA markers to resolve population structure of zooplankton populations associated with physical barriers to gene flow, including ocean circulation, for copepods (Aarbakke et al 2011;Blanco-Bercial et al 2011b and euphausiids (Bucklin et al 1997;Zane et al 1998Zane and Patarnello 2000;Papetti et al 2005;Patarnello et al 2010). …”
Section: Population Genetic Diversity and Structurementioning
confidence: 99%
“…8) is abundant throughout the North Atlantic and western Mediterranean Sea. The species exhibits clear genetic differentiation among geographic populations based on various mtDNA markers (see review by Patarnello et al 2010). Consistent evidence of local adaptation of the species, including enzyme activities (Saborowski and Buchholz 2002), is now being analyzed using differential gene expression made possible by a reference transcriptome (Maas and Blanco-Bercial 2016).…”
Section: Acartia Tonsa (Copepoda)mentioning
confidence: 99%