Plumbaginaceae is characterized by a history of multiple taxonomic rearrangements and lacks a broad molecular phylogenetic framework. Limonium is the most species‐rich genus of the family with ca. 600 species and cosmopolitan distribution. Its center of diversity is the Mediterranean region, where ca. 70% of all Limonium species are endemic. In this study, we sample 201 Limonium species covering all described infrageneric entities and spanning its wide geographic range, along with 64 species of other Plumbaginaceae genera, representing 23 out of 29 genera of the family. Additionally, 20 species of the sister family Polygonaceae were used as outgroup. Sequences of three chloroplast (trnL‐F, matK, and rbcL) and one nuclear (ITS) loci were used to infer the molecular phylogeny employing maximum likelihood and Bayesian analyses. According to our results, within Plumbaginoideae, Plumbago forms a non‐monophyletic assemblage, with Plumbago europaea sister to Plumbagella, while the other Plumbago species form a clade sister to Dyerophytum. Within Limonioideae, Ikonnikovia is nested in Goniolimon, rejecting its former segregation as genus distinct from Goniolimon. Limonium is divided into two major clades: Limonium subg. Pteroclados s.l., including L. sect. Pteroclados and L. anthericoides, and L. subg. Limonium. The latter is divided into three well‐supported subclades: the monospecific L. sect. Limoniodendron sister to a clade comprising a mostly non‐Mediterranean subclade and a Mediterranean subclade. Our results set the foundation for taxonomic proposals on sections and subsections of Limonium, namely: (a) the newly described L. sect. Tenuiramosum, created to assign L. anthericoides at the sectional rank; (b) the more restricted circumscriptions of L. sect. Limonium (= L. sect. Limonium subsect. Genuinae) and L. sect. Sarcophyllum (for the Sudano‐Zambezian/Saharo‐Arabian clade); (c) the more expanded circumscription of L. sect. Nephrophyllum (including species of the L. bellidifolium complex); and (d) the new combinations for L. sect. Pruinosum and L. sect. Pteroclados subsect. Odontolepideae and subsect. Nobiles.

The higher genetic diversity observed in the Azorean population studied suggested a possible refugium in this region from which mainland Europe has been recolonized after the Pleistocene glaciations. High among-population genetic differentiation indicated restricted gene flow (i.e. lack of spore exchange) across the highly fragmented area occupied by D. aemula. The deviations from Hardy-Weinberg equilibrium reflected strong inbreeding in D. aemula, a trait rarely observed in homosporous ferns. The absence of spatial genetic structure indicated effective spore dispersal over short distances. Additionally, the cross-amplification of some D. aemula microsatellites makes them suitable for use in other Dryopteris taxa.

The Sinai primrose (Primula boveana) is one of the most endangered plant species worldwide, with less than 200 wild individuals surviving in the Sinai mountains of Egypt. There has been a decline in both the number and size of its populations in recent times, possibly caused by threats that include habitat aridification and the impact of human activities. Studying the standing genetic variation and extent of inbreeding of P. boveana is necessary for the design of appropriate conservation strategies for this species. In the present work, we used a set of seven, recently developed, polymorphic microsatellite markers to characterize the genetic variation and levels of inbreeding of the extant populations of P. boveana. We found low levels of genetic variation (H T = 0.470), high differentiation between populations (F ST = 0.737, R ST = 0.935), and very elevated levels of inbreeding (F = 0.862) due to recurrent selfing. These results may be the reflection of low levels of genetic variation and high levels of inbreeding over a long evolutionary period, suggesting that the current genetic pool of the species may enable P. boveana to persist in a habitat where water availability and pollinator services are restricted. Nevertheless, in sight of its rapidly dwindling abundance, it seems prudent to adopt swift measures, including habitat restoration and ex-situ conservation, to prevent the impending extinction of this emblematic species.

For many plants, sex is not fixed by genotype but determined by environmental conditions during development. In homosporous pteridophytes, sex is environmentally determined by the presence or absence of antheridiogens, maleness-inducing pheromones. It has been proposed that antheridiogens primarily reduce growth rate, with small gametophyte size responsible for maleness. To test this hypothesis, the effects of antheridiogen and intergametophytic competition on gender expression and gametophyte size were studied in a culture experiment with Woodwardia radicans. We found that (1) antheridiogen inhibited growth of gametophytes; and (2) slow growth favored maleness, whereas fast growth favored femaleness, irrespective of the presence or absence of antheridiogen. Both conclusions are consistent with the hypothesis that, in W. radicans, antheridiogen effect is mediated by size. They also agree with the "size-advantage" hypothesis in which energetic limitations associated with relatively small individual size impose a less severe limitation for male reproductive success than for female reproductive success. The results are also discussed with regard to a genetic sex-determining pathway that has recently been identified.

Environmental sex determination is present in several animal and plant lineages, in which gender depends on diverse factors such as temperature, light and water availability. This study examines effects of water availability and pheromones on the production of female and male organs by three fern species adapted to dry habitats. Isolated individuals become first female and then bisexual, irrespective of the degree of soil moisture, and, consequently, may self-fertilize. However, female individuals release pheromones that induce maleness in nearby individuals, thus favouring cross-fertilization.