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Deprea is the genus with the second highest species richness in tribe Physalideae (Solanaceae) and comprises 50 species that are mainly distributed in the Andes of South America. The taxonomy of Deprea has been unstable after controversial hypotheses about its position and circumscription. Additionally, biogeographical inferences are only based on observations of the restricted area of distribution of some species and no ancestral area estimation have been performed. Here, we present a phylogenetic analysis and an ancestral area reconstruction of Deprea in order to establish its circumscription, resolve its position within Physalideae, and reconstruct its biogeographical history. Phylogenetic analyses were conducted using Maximum Likelihood and Bayesian approaches. Forty-three Deprea species and 26 related taxa were sampled for three DNA markers ( psbA-trnH , ITS, and waxy ). A Bayesian binary MCMC model was applied in order to infer ancestral areas. Deprea is resolved as a strongly supported monophyletic group according to its current circumscription and is placed within subtribe Withaninae of Physalideae. The phylogenetic relationships enabled us to solve taxonomic problems including the rejection and acceptance of previous synonyms. The most probable ancestral area for Deprea is the Northern Andes of South America and the Amotape-Huancabamba zone. Our phylogeny provides increased resolution and support for the current position and circumscription of Deprea . Better resolution of interspecific relationships was also obtained, although some affinities remain unclear. The phylogenetic and ancestral area reconstructions provide a framework for addressing taxonomic problems and investigating new evolutionary questions. [ABSTRACT FROM AUTHOR]

Background and Aims Capsicum (Solanaceae), native to the tropical and temperate Americas, comprises the well-known sweet and hot chili peppers and several wild species. So far, only partial taxonomic and phylogenetic analyses have been done for the genus. Here, the phylogenetic relationships between nearly all taxa of Capsicum were explored to test the monophyly of the genus and to obtain a better knowledge of species relationships, diversification and expansion. Methods Thirty-four of approximately 35 Capsicum species were sampled. Maximum parsimony and Bayesian inference analyses were performed using two plastid markers (matK and psbA-trnH) and one single-copy nuclear gene (waxy). The evolutionary changes of nine key features were reconstructed following the parsimony ancestral states method. Ancestral areas were reconstructed through a Bayesian Markov chain Monte Carlo analysis. Key Results Capsicum forms a monophyletic clade, with Lycianthes as a sister group, following both phylogenetic approaches. Eleven well-supported clades (four of them monotypic) can be recognized within Capsicum, although some interspecific relationships need further analysis. A few features are useful to characterize different clades (e.g. fruit anatomy, chromosome base number), whereas some others are highly homoplastic (e.g. seed colour). The origin of Capsicum is postulated in an area along the Andes of western to north-western South America. The expansion of the genus has followed a clockwise direction around the Amazon basin, towards central and south-eastern Brazil, then back to western South America, and finally northwards to Central America. Conclusions New insights are provided regarding interspecific relationships, character evolution, and geographical origin and expansion of Capsicum. A clearly distinct early-diverging clade can be distinguished, centred in western-north-western South America. Subsequent rapid speciation has led to the origin of the remaining clades. The diversification of Capsicum has culminated in the origin of the main cultivated species in several regions of South to Central America. [ABSTRACT FROM AUTHOR]

The Morelloid clade of Solanum, also known as the black nightshades or Maurella (Morelia), is one of the 10 major clades within Solanum. The pantropical clade consists of ca. 76 non-spiny herbaceous and suffrutescent species with simple or branched hairs with or without glandular tips, with a centre of distribution in the tropical Andes. Although the core members of the clade have long been recognised, complete circumscription of the Morelloid clade has remained elusive. Here we provide the first detailed molecular study of the clade. Plastid (trnT-F intergenic spacers), nuclear ribosomal ITS, and low-copy nuclear (waxy) data show three of the four previously unplaced taxa loosely associated with the Morelloids to be placed outside (S. anomalostemon, S. valdiviense, S. reductum), whilst S. salicifolium, a species previously associated with the Dulcamaroid clade, is found to be nested within the group. Four monophyletic groups within the Morelloids can be recognised: (1) Black nightshade clade, including all members of 5. sect. Solanum, S. sect. Campanulisolanum, branched-haired taxa, S. salicifolium, and S. triflorum; (2) Episarcophyllum clade, including most members of S. sect. Episarcophyllum; (3) Chamaesarachidium clade, including members of S. sect. Chamaesarachidium; and (4) Radicans clade, including four species from S. sect. Parasolanum. Incongruence between nuclear and plastid gene trees is discussed in relation to known ploidy level variation across the Morelloid clade, especially the African species often referred to as the S. nigrum complex. A new, revised circumscription of the Morelloid clade is provided together with morphological characterisations of the monophyletic clades recovered within it. A preliminary checklist of accepted names for Morelloids is also presented. [ABSTRACT FROM AUTHOR]

We review the 68 names of plants treated in genera treated or now recognised as Solanaceae from J.M. da C. Vellozo's Flora Fluminensis in the context of current floristic knowledge of the region around Rio de Janeiro in southern Brazil. Most of Vellozo's names are synonyms of names previously published or are illegitimate later homonyms, but several are accepted and in widespread use. Two names do not belong to solanaceaeous taxa, but to species in Apocynaceae and Violaceae respectively. We provide lectotypifications for all names, including those previously lectotypified using the published plates that do not qualify as original material. Type localities, previous lectotypifications and current accepted names are provided for all taxa. [ABSTRACT FROM AUTHOR]