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The genus Hydrangea s.l. (Hydrangeaceae), a favorite among gardeners, comprises more than 80 species that are important understory plants in natural temperate and subtropical forests of the Northern Hemisphere. These species are hypervariable in morphology, especially in indumentum and floral characters, warranting a thorough exploration of the complex evolutionary history of morphological characters of the genus. Ideally, this is done within a robust phylogenetic framework with extensive taxon sampling. In this study, we propose a comprehensive taxonomic reassessment of Hydrangea based on a reconstruction of its molecular phylogeny based mainly on the chloroplast genome (plastome) and the most representative taxon sampling reported to date. Phylogenomic reconstruction yielded five well‐resolved major clades and three newly recognized subclades. Inspection of the 28 characters employed in traditional taxonomic revisions revealed homoplasy in many of these traits. Our results show that characters such as growth habit, woody stem type, number of enlarged marginal sepals, style and stamen number, fruit shape, and ovary position are useful for circumscribing infrageneric divisions. Unique synapomorphies are limited. For example, herb and subshrub growth habits are associated with all the species in H. sect. Deinanthe and sect. Cardiandra, respectively. Character state combinations are proposed for distinguishing infrageneric taxa. Based on a robust phylogenetic framework, our findings suggest a complex evolutionary history of Hydrangea morphological characters. Following the criterion of monophyly and considering the morphological consistency and synapomorphy of single and combined characters to diagnose relevant lineages, we update the classification of Hydrangea into 5 subgenera and 19 sections. Our proposed taxonomic scheme, based on a robust phylogenetic framework and in‐depth character study, provides an updated perspective on the infrageneric subdivision of Hydrangea s.l. [ABSTRACT FROM AUTHOR]

The floral morphological and developmental patterns in three species of Impatiens (Balsaminaceae), namely I. columbaria, I. hawkeri, and I. niamniamensis, were studied to contribute to a better understanding of floral evolution in the genus. Strangely enough, the highly diverse floral morphology and ontogeny of this horticulturally important genus have never been studied thoroughly (e.g., using scanning electron microscopic techniques). We discuss the position and the developmental sequence of the different perianth members. We hypothesized that in the course of evolution, the anterolateral sepals become reduced and that a morphocline can be recognized going from species with five sepals, over species with rudimentary sepals that fuse postgenitally with the anterior petal, to species where congenital fusion between these sepals and the anterior petal has taken place. Ovules generally are in one or two vertical rows per locule, but there are several vertical rows per locule in I. columbaria. The outer parts of the septa disintegrate to enable the explosive dehiscence of the capsules. Key words: Balsaminaceae; Ericales: floral development; floral evolution; floral morphology; Impatiens; scanning electron microscopy.

China is known for its abundant plant resources, but biodiversity conservation faces unprecedented challenges. To provide feasible suggestions for sustainable conservation, we used the species richness algorithm and complementary algorithm to study distribution patterns of 34,082 seed plants based on 1,007,196 county-level distribution records. We reconstructed a phylogenetic tree for 95.35% of species and estimated the spatial phylogenetics, followed by correlation analyses between different distribution patterns. We identified 264 counties concentrated in southern and southwestern mountainous areas as hotspots which covered 10% of the land area of China and harbored 85.22% of the Chinese seed plant species. The biodiversity conservation priorities we identified were highly representative as we have considered multiple conservation indicators. We evaluated the conservation effectiveness and gaps in the network of nature reserves and identified 31.44, 32.95, and 9.47%, respectively, of the hotspot counties as gaps in the national nature reserves, provincial nature reserves and both together, with respectively 55.77, 61.53, and 28.94% of the species. Analysis of the species composition showed there were a large number of threatened and endemic species occurring in the nature reserves' gaps. The conservation gaps need to be filled by establishing new nature reserves or national parks, especially in south-western China, and more attentions should be paid to strengthen the conservation of specific plant taxa due to the apparent mismatches between different distribution patterns. [ABSTRACT FROM AUTHOR]

Abstract Background Myco-heterotrophy evolved independently several times during angiosperm evolution. Although many species of myco-heterotrophic plants are highly endemic and long-distance dispersal seems unlikely, some genera are widely dispersed and have pantropical distributions, often with large disjunctions. Traditionally this has been interpreted as evidence for an old age of these taxa. However, due to their scarcity and highly reduced plastid genomes our understanding about the evolutionary histories of the angiosperm myco-heterotrophic groups is poor. Results We provide a hypothesis for the diversification of the myco-heterotrophic family Burmanniaceae. Phylogenetic inference, combined with biogeographical analyses, molecular divergence time estimates, and diversification analyses suggest that Burmanniaceae originated in West Gondwana and started to diversify during the Late Cretaceous. Diversification and migration of the species-rich pantropical genera Burmannia and Gymnosiphon display congruent patterns. Diversification began during the Eocene, when global temperatures peaked and tropical forests occurred at low latitudes. Simultaneous migration from the New to the Old World in Burmannia and Gymnosiphon occurred via boreotropical migration routes. Subsequent Oligocene cooling and breakup of boreotropical flora ended New-Old World migration and caused a gradual decrease in diversification rate in Burmanniaceae. Conclusion Our results indicate that extant diversity and pantropical distribution of myco-heterotrophic Burmanniaceae is the result of diversification and boreotropical migration during the Eocene when tropical rain forest expanded dramatically.

Background and Aims Floral diversity as a result of plant–pollinator interactions can evolve by two distinct processes: shifts between pollination systems or divergent use of the same pollinator. Although both are pollinator driven, the mode, relative importance and interdependence of these different processes are rarely studied simultaneously. Here we apply a phylogenetic approach using the Balsaminaceae (including the species-rich genus Impatiens) to simultaneously quantify shifts in pollination syndromes (as inferred from the shape and colour of the perianth), as well as divergent use of the same pollinator (inferred from corolla symmetry). Methods For 282 species we coded pollination syndromes based on associations between floral traits and known pollination systems, and assessed corolla symmetry. The evolution of these traits was reconstructed using parsimony- and model-based approaches, using phylogenetic trees derived from phylogenetic analyses of nuclear ribosomal and plastid DNA sequence data. Key Results A total of 71 % of studied species have a bee pollination syndrome, 22 % a bimodal syndrome (Lepidoptera and bees), 3 % a bird pollination syndrome and 5 % a syndrome of autogamy, while 19 % of species have an asymmetrical corolla. Although floral symmetry and pollination syndromes are both evolutionarily labile, the latter shifts more frequently. Shifts in floral symmetry occurred mainly in the direction towards asymmetry, but there was considerable uncertainty in the pattern of shift direction for pollination syndrome. Shifts towards asymmetrical flowers were associated with a bee pollination syndrome. Conclusion Floral evolution in Impatiens has occurred through both pollination syndrome shifts and divergent use of the same pollinator. Although the former appears more frequent, the latter is likely to be underestimated. Shifts in floral symmetry and pollination syndromes depend on each other but also partly on the region in which these shifts take place, suggesting that the occurrence of pollinator-driven evolution may be determined by the availability of pollinator species at large geographical scales. [ABSTRACT FROM AUTHOR]

The systematic position of Montiniaceae remains uncertain: a relationship with Cornales has been suggested on phytochemical and embryological evidence, while molecular data point to a relationship with Solanales. We investigated the floral development and anatomy of the South African Montinia caryophyllacea to add a new set of characters for clarifying the systematic position of the family Montiniaceae. Pistillate inflorescences show a higher degree of reduction than staminate, with flowers set terminally on short lateral branches. Flowers have an irregular initiation sequence, with frequent abortions of organs. In Montinia, petals grow rapidly, and no zonal growth takes place. The gynoecium develops as a pit surrounded by a girdle. Placentation is basically parietal and becomes axillary by the postgenital fusion of placental lobes; unitegmic ovules are arranged in two parallel rows with adjacent ovules partly overlapping each other. Unisexuality is respectively attained at the stage of anther development and carpel initiation. The floral anatomy of pistillate and staminate flowers is illustrated and discussed. Observations on Montinia are compared with data of taxa from Saxifragaceae sensu stricto, Cornales, and Solanales. The absence of sympetaly in Montinia is discussed. Morphological and anatomical evidence points to a high similarity with Escalloniaceae. Although a position in the asterids is most probable, there is little support for the relationship with Solanales indicated by molecular data. Key words: Cornales; Escalloniaceae; floral anatomy; floral ontogeny; Montiniaceae; placentation; Saxifragaceae; Solanales; sympetaly.