1998
DOI: 10.2307/1224017
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Plastid rbcL sequence data indicate a close affinity between Diegodendron and Bixa

Abstract: Summary Fay, M. F., Bayer, C., Alverson, W. S., Bruijn, A. Y. de & Chase, M. W.: Plastid rbcL sequence data indicate a close affinity between Diegodendron and Bixa. ‐ Taxon 47: 43–50. 1998. ‐ ISSN 0040‐0262. Diegodendron humbertii Capuron (Diegodendraceae Capuron) is endemic to Madagascar. The family is monospecific, and whereas various affinities have been suggested, its phylogenetic position has remained unclear. Analysis of rbcL sequence data indicates a close relationship to Bixa. Together these taxa form … Show more

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Cited by 162 publications
(82 citation statements)
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“…For rbcL the primers 1F/724R (Olmstead & al., 1992), 636F/1460R (Fay & al., 1997(Fay & al., , 1998 and 217F, 922F, 536R and 1104R (Pirie & al., 2005) were used. The trnL-trnF region was amplified and sequenced using primers c, d, e and f (Taberlet & al., 1991).…”
Section: Methodsmentioning
confidence: 99%
“…For rbcL the primers 1F/724R (Olmstead & al., 1992), 636F/1460R (Fay & al., 1997(Fay & al., , 1998 and 217F, 922F, 536R and 1104R (Pirie & al., 2005) were used. The trnL-trnF region was amplified and sequenced using primers c, d, e and f (Taberlet & al., 1991).…”
Section: Methodsmentioning
confidence: 99%
“…This analysis narrowed the possible relationships of Rhizophoraceae/Anisophylleaceae to the rosid clades. (2) Accordingly, we next sampled representatives of each family in the rosid clade for which rbcL sequences were available, guided by phylogenetic analyses of groups within this clade (Albert, Williams, and Chase, 1992;Price and Palmer, 1993;Swensen, Mullin, and Chase, 1994;Conti, Litt, and Sytsma, 1996;Swensen, 1996;Fay, Swensen, and Chase, 1997;Savolainen, Spichinger, and Manen, 1997;Alverson et al, 1998;Fay et al, 1998). When sequences for several species of one family were available, we chose one or two representative species.…”
Section: Methodsmentioning
confidence: 99%
“…Herbarium and silica gel-dried material was ground in a dry state before adding extraction buffer, while the frozen material was ground after adding extraction buffer. DNA amplifications were performed in 50 u,L reactions containing 1.25U Taq polymerase (Promega, Madison, Wisconsin, USA), reaction buffer A supplied by Promega, 1.5 mmol/L MgCl 2 , 25 pmol of each primer and 0.2 mmol/L of each dNTR The flanking primer sequences for rbcL (IF and 1460R) were used as in Fay et al (1998); additional internal primers were designed for maximum fit in the Rhizophoraceae (674F: 5 -TTTATAAAGCACA-GGCGGAA-3'; 795R: 5 -CTGTTAAGTAGTCATGCATT-3'). The trnL-trnF spacer region was amplified using primers E and F from Taberlet et al (1991).…”
Section: Methodsmentioning
confidence: 99%
“…The rbcL gene was amplified and sequenced in two overlapping fragments using the primers 1F/724 R (Olmstead et al, 1992) and 636F/1460R (Fay et al, 1997(Fay et al, , 1998. PCR amplifications were performed with the thermocycler PTC-100 TM Programmable Thermal Controller (MJ Research Inc.).…”
Section: Taxon Samplingmentioning
confidence: 99%