Linum flos-carmini (Linaceae), a new species from northern Morocco

Linum bicolor is a problematic North African taxon associated with L. setaceum. A consensus on the taxonomic status of a putative form (L. setaceum var. bicolor f. robusta) has not been achieved yet. We conducted a morphological study based on herbarium and field collections, combined with nuclear (ITS) and plastid (ndhF5-8 and trnL-F) phylogenies to clarify its status. The phylogenetic analysis did not reveal molecular divergence, but a comparative morphological study revealed substantial differences in traits previously used to distinguish the two taxa (stems, leaves, corolla and calyx size). In addition, we found that the indumentum of sepals, petal colour, and the arrangement of anthers and stigmas differed so clearly between the form robusta and L. setaceum s. stricto, that recognizing the former taxon as an independent species was justified. We provide an identification key to the yellow- and white-flowered Linum species in NW Africa. We also revised the unplaced name L. bicolor Schoubs. ex DC. and lectotypified it to avoid nomenclatural problems

Novel microsatellite markers for Dalechampia scandens (Euphorbiaceae) and closely related taxa:application to studying a species complex

We developed novel microsatellite markers for D alechampia scandens L. (Euphorbiaceae). The target plants belong to a distinct, but undescribed, species in the D . scandens species complex, characterized by small resin-producing glands. In total, 110 alleles over 36 novel markers were identified across 39 individuals from three populations. The number of alleles varied from one to seven, with an average of 3.06 ± 0.26 alleles per locus. The developed markers, along with previously developed ones for a large-glanded D . scandens species, were tested for amplification in 11 additional species of the genus D alechampia. Four markers did not produce any detectable allele in 37 individuals from two populations of the large-glanded species. Average expected heterozygosity across all small- and large-glanded specific loci was 0.36 and 0.15, for the small and large glanded populations, respectively. Cross-species amplification showed that 89% of all markers were successfully amplified in at least one of the 11 other D alechampia species. These microsatellite markers may be useful for detecting undescribed species in the D . scandens species complex, and can be used for comparative analyses of genetic structure, mating system and phylogeography of other D alechampia species

Novel microsatellite markers for Dalechampia scandens(Euphorbiaceae) and closely related taxa:application to studying a species complex

We developed novel microsatellite markers for D alechampia scandens L. (Euphorbiaceae). The target plants belong to a distinct, but undescribed, species in the D . scandens species complex, characterized by small resin-producing glands. In total, 110 alleles over 36 novel markers were identified across 39 individuals from three populations. The number of alleles varied from one to seven, with an average of 3.06 ± 0.26 alleles per locus. The developed markers, along with previously developed ones for a large-glanded D . scandens species, were tested for amplification in 11 additional species of the genus D alechampia. Four markers did not produce any detectable allele in 37 individuals from two populations of the large-glanded species. Average expected heterozygosity across all small- and large-glanded specific loci was 0.36 and 0.15, for the small and large glanded populations, respectively. Cross-species amplification showed that 89% of all markers were successfully amplified in at least one of the 11 other D alechampia species. These microsatellite markers may be useful for detecting undescribed species in the D . scandens species complex, and can be used for comparative analyses of genetic structure, mating system and phylogeography of other D alechampia species