2002
DOI: 10.1016/s1055-7903(02)00281-6
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Phylogenetic relationships of the southern African freshwater crab fauna (Decapoda: Potamonautidae: Potamonautes) derived from multiple data sets reveal biogeographic patterning

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Cited by 78 publications
(65 citation statements)
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“…The sequence data were sufficiently long (592 bp) and could resolve the phylogeny at the species level with high divergence between species. There are reports of sequence divergence for 12SrRNA in the range of 0.65-43.4% in freshwater crabs of Potamonautidae (Daniels et al, 2002). A low divergence rate for nuclear 18SrRNA was observed in concordance with the moderate value among species (5.8-7.2%) in decapod suborder Pleocyemata (Toon et al, 2009).…”
Section: Sequence Divergence For Various Markersmentioning
confidence: 62%
“…The sequence data were sufficiently long (592 bp) and could resolve the phylogeny at the species level with high divergence between species. There are reports of sequence divergence for 12SrRNA in the range of 0.65-43.4% in freshwater crabs of Potamonautidae (Daniels et al, 2002). A low divergence rate for nuclear 18SrRNA was observed in concordance with the moderate value among species (5.8-7.2%) in decapod suborder Pleocyemata (Toon et al, 2009).…”
Section: Sequence Divergence For Various Markersmentioning
confidence: 62%
“…Phylogenetic trees were rooted using Potamonautes warreni and Potamonautes unispinus as outgroups (Daniels et al, 2002(Daniels et al, , 2006a. Daniels et al (2002) demonstrated that these two species formed a well-supported monophyletic group with other large-bodied freshwater crab species, including P. perlatus s.l.…”
Section: Phylogenetic Analysesmentioning
confidence: 99%
“…These three genes provided independent datasets, with different rates of evolution, with which to infer relationships at various taxonomic levels (Crandall et al, 2000;Daniels et al, 2002;Pérez-Losada et al, 2002;Øines & Schram, 2008). Two microlitres of the diluted DNA solution were added to a 50 μl PCR reaction containing the following: 5 μl 10X Taq buffer, 5-8 μl 25 mM MgCl, 8 μl 10 mM dNTPs, 5 μl each of two 10 mM primers, and 0.3 μl of 1.25 units of Taq polymerase (Promega) and ddH 2 O.…”
Section: Dna Extractionmentioning
confidence: 99%