89 research outputs found
At Least 23 Genera Instead of One: The Case of Iris L. s.l. (Iridaceae)
Background: Iris L. s.l. is one of the most diverse and well-known genera in the Asparagales, with approximately 250–300 circumscribed species and significant economic impact. The taxonomy of the genus has suffered dramatic changes in the last century, particularly in the last decades after the application of molecular techniques. As a result several contrasting systematic arrangements are currently available to taxonomists. Many genera that were split from Iris s.str. in the past, on the basis of morphology (e.g., Hermodactylus, Iridodictyum, Juno, Pardanthopsis, and Xiphion, among others), are now a priori re-included in a very widely circumscribed Iris s.l. (incl. Belamcanda). This resulted in a more heterogeneous genus that is more difficult to define on morphological grounds. Testing congruence between taxonomic treatments and the results of recent molecular studies of Iris has never been performed, mostly due to the lack of proper taxonomic context. Results: We generated several conventional phylogenies for Iris & outgroups using extensive sampling of taxa (187) and characters (10 plastid loci). We demonstrate that the natural history of Iris, written either as conventional molecular phylogenies or, if viewing in the context of the comparative approach, as a nested most parsimonious hierarchy of patterns, appear to be fully congruent with the narrow taxonomical treatment of the genus, restricted to the rhizomatous "bearded" taxa. The resulting topologies place Belamcanda, Pardanthopsis, and Gattenhofia as sisters to Iris s.str. and genus Siphonostylis as sister to Iris s.l. Conclusion: The present study clearly justifies the splitting of Iris s.l. into at least 23 genera, 18 of which have already been accepted in the past by numerous authorities. These genera are characterized by unique combinations of partly overlapping morphological characters and biogeography. Moreover, nearly the same entities, which we here recognize at a generic rank, were for centuries frequently referred to by horticulturists as "working-name" groups
Crespo, M.B., Martínez-Azorín, M. & Mavrodiev, E.V. (2015) Can a rainbow consist of a single colour? A new comprehensive generic arrangement of the ‘Iris sensu latissimo’ clade (Iridaceae), congruent with morphology and molecular data. Phytotaxa 232: 1–78. [Erratum]
Akhania, a new genus for Salsola daghestanica, Caroxylon canescens and C. carpathum (Salsoloideae, Chenopodiaceae, Amaranthaceae)
Genus Salsola s.l. was recently split into several genera of different phylogenetic placements within Salsoloideae, but both taxonomic and phylogenetic relationships of some parts of the former broadly defined Salsola still need to be clarified. A remarkable example is Salsola canescens nom. illegit. ≡ Salsola boissieri, a taxon with tricky taxonomic history that was only recently transferred to the genus Caroxylon (tribe Caroxyleae). Salsola daghestanica, a narrow endemic of Central Dagestan (Russian Federation), was not even included in previous molecular studies of Salsoloideae and therefore still lacks an appropriate estimation of its relationships. Molecular phylogeny constructed here using nuclear and plastid DNA sequence data clearly placed Salsola daghestanica and Caroxylon carpathum as sister taxa and the clade S. daghestanica, Caroxylon canescens (Salsola boissieri), C. carpathum (Salsola carpatha) as a sister of the monophyletic Caroxylon. All three species are distinct from Caroxylon from a morphological standpoint. In conclusion, a new genus, Akhania, was established for these taxa. The detailed distribution of Akhania daghestanica is presented for the first time
Multiple origins and chromosomal novelty in the allotetraploid Tragopogon castellanus (Asteraceae)
TAXON version 1.1: A simple way to generate uniform and fractionally weighted three-item matrices from various kinds of biological data
An open-access program allowing three-item statement matrices to be generated
from data such as molecular sequences does not exist so far. The recently
developed LisBeth package (ver. 1.0) allows representing hypotheses of homology
among taxa or areas directly as rooted trees or as hierarchies; however, this
is not a standard matrix-based platform. Here we present "TAXON version 1.1"
(TAXON), a program designed for building three-item statement-matrices from
binary, additive (ordered) and non-additive (unordered) multistate characters,
with both fractional and uniform weighting of the resulted statements.Comment: 4 pages, 1 figure, 1 Supplement, 3 Supplemental example
10KP: A phylodiverse genome sequencing plan.
Understanding plant evolution and diversity in a phylogenomic context is an enormous challenge due, in part, to limited availability of genome-scale data across phylodiverse species. The 10KP (10,000 Plants) Genome Sequencing Project will sequence and characterize representative genomes from every major clade of embryophytes, green algae, and protists (excluding fungi) within the next 5 years. By implementing and continuously improving leading-edge sequencing technologies and bioinformatics tools, 10KP will catalogue the genome content of plant and protist diversity and make these data freely available as an enduring foundation for future scientific discoveries and applications. 10KP is structured as an international consortium, open to the global community, including botanical gardens, plant research institutes, universities, and private industry. Our immediate goal is to establish a policy framework for this endeavor, the principles of which are outlined here
Phylogenomic Mining of the Mints Reveals Multiple Mechanisms Contributing to the Evolution of Chemical Diversity in Lamiaceae
The evolution of chemical complexity has been a major driver of plant diversification, with novel compounds serving as key innovations. The species-rich mint family (Lamiaceae) produces an enormous variety of compounds that act as attractants and defense molecules in nature and are used widely by humans as flavor additives, fragrances, and anti-herbivory agents. To elucidate the mechanisms by which such diversity evolved, we combined leaf transcriptome data from 48 Lamiaceae species and four outgroups with a robust phylogeny and chemical analyses of three terpenoid classes (monoterpenes, sesquiterpenes, and iridoids) that share and compete for precursors. Our integrated chemical–genomic–phylogenetic approach revealed that: (1) gene family expansion rather than increased enzyme promiscuity of terpene synthases is correlated with mono- and sesquiterpene diversity; (2) differential expression of core genes within the iridoid biosynthetic pathway is associated with iridoid presence/absence; (3) generally, production of iridoids and canonical monoterpenes appears to be inversely correlated; and (4) iridoid biosynthesis is significantly associated with expression of geraniol synthase, which diverts metabolic flux away from canonical monoterpenes, suggesting that competition for common precursors can be a central control point in specialized metabolism. These results suggest that multiple mechanisms contributed to the evolution of chemodiversity in this economically important family. The mint family (Lamiaceae) includes many culturally and economically important species and collectively exhibits an exceptionally high degree of chemical diversity. Using an integrated chemical-genomic-phylogenetic approach, gene family expansion, altered gene expression of key biosynthetic pathway genes, and flux of precursors were shown to underlie the evolution of chemodiversity observed in this chemically rich clade
Classical Morphology of Plants as an Elementary Instance of Classical Invariant Theory
It has long been known that structural chemistry shows an intriguing correspondence with Classical Invariant Theory (CIT). Under this view, an algebraic binary form of the degree n corresponds to a chemical atom with valence n and each physical molecule or ion has an invariant-theoretic counterpart. This theory was developed using the Aronhold symbolical approach and the symbolical processes of convolution/transvection in CIT was characterized as a potential “accurate morphological method”. However, CIT has not been applied to the formal morphology of living organisms. Based on the morphological interpretation of binary form, as well as the process of convolution/transvection, the First and Second Fundamental Theorems of CIT and the Nullforms of CIT, we show how CIT can be applied to the structure of plants, especially when conceptualized as a series of plant metamers (phytomers). We also show that the weight of the covariant/invariant that describes a morphological structure is a criterion of simplicity and, therefore, we argue that this allows us to formulate a parsimonious method of formal morphology. We demonstrate that the “theory of axilar bud” is the simplest treatment of the grass seedling/embryo. Our interpretations also represent Troll's bauplan of the angiosperms, the principle of variable proportions, morphological misfits, the basic types of stem segmentation, and Goethe's principle of metamorphosis in terms of CIT. Binary forms of different degrees might describe any repeated module of plant organisms. As bacteria, invertebrates, and higher vertebrates are all generally shared a metameric morphology, wider implications of the proposed symmetry between CIT and formal morphology of plants are apparent
A description of the repeated unit of <i>Orontium aquaticum</i> L. (Araceae) containing five phytomers.
<p>A Schematic image of <i>O. aquaticum </i><a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0006969#pone.0006969-Ray1" target="_blank">[30]</a>. B, Diagram of the repeated unit containing five phytomers <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0006969#pone.0006969-Ray1" target="_blank">[30]</a>. C, A description of B by the covariant of five binary cubics. D, Reducible covariant of five binary cubics corresponded to B. P – prophyll; E – mesophyll; M – monopodial leaf; S – sympodial leaf; X – first phytomer of inflorescence; e – foliage leaf, c – cataphyll, s – sylleptic growth <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0006969#pone.0006969-Ray1" target="_blank">[30]</a>. All morphological terminology and images are from <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0006969#pone.0006969-Ray1" target="_blank">[30]</a>.</p
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