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Setchellanthus caeruleus, which has disjunct populations in the north of the Chihuahuan Desert and in the Tehuacán-Cuicatlán valley, was selected to understand the evolutionary history of plants in this desert and its southerly relicts. This species constitutes the monotypic family Setchellanthaceae, which forms part of a group of plants that produce mustard-oil glucosides or glucosinolates. Molecular phylogenetic analyses based on DNA plastid sequences of plants of S. caeruleus from both areas, including representative taxa of the order Brassicales, were carried out to estimate the time of origin of the family (based on matK + rcbL) and divergence of populations (based on psbI-K, trnh-psbA, trnL-trnF). In addition, comparative ecological niche modelling was performed to detect if climate variables vary significantly in northern and southern populations. Analyses revealed that Setchellanthaceae is an ancient lineage that originated between 78 and 112 Mya during the mid-late Cretaceous—much earlier than the formation of the Chihuahuan Desert. The molecular data matrix displayed a few indel events as the only differences of plastid DNA sequences between northern and southern populations. It is suggested that due to climate changes in this desert in the Pliocene, populations of Setchellanthus remained in the Sierra de Jimulco and in Cuicatlán, in climatically stable locations. Ecological niche models of northern populations predict niches of southern populations and identity niche tests indicate that there are no differences in their ecological niches. [ABSTRACT FROM AUTHOR]

Phyllonoma, a small tree genus of four species distributed from Mexico to Peru, has been placed in various families (mainly in Saxifragaceae), but now, based on molecular evidence, is placed in a distinct family Phyllonomaceae in Aquifoliales. To better understand the morphological relationships of the genus and family, I studied its floral morphology, anatomy, and vasculature using P. tenuidens. Most of the external and internal floral characteristics were described more than 120 years ago. Although some of them were confirmed, some were substantially revised, mainly those concerning the gynoecial structure. Flowers are small and basically pentamerous, consisting of five sepals, five petals, five stamens, and a gynoecium composed of two carpels usually in transversal position. Comparisons with other Aquifoliales show that Phyllonomaceae share the inferior ovary, epiphyllous inflorescence and epigynous disc nectary with East-Asian Helwingiaceae ( Helwingia only), but clearly differ from Helwingiaceae in having glandular trichomes on the sepal margins and a bicarpellate, unilocular gynoecium bearing many ovules on the parietal placentae. Evidence from floral morphology and structure supports the distinctness of Phyllonomaceae and its sister-group relationship with Helwingiaceae. Its floral characteristics suggest that Phyllonomaceae have evolved by adapting to distinct biological habitats in relation to pollination and seed dispersal. [ABSTRACT FROM AUTHOR]

There are many non-mutually exclusive mechanisms for exotic invasions but few studies have concurrently tested more than one hypothesis for the same species., Here, we tested the evolution of increased competitive ability ( EICA) hypothesis in two common garden experiments in which Chromolaena odorata plants originating from native and nonnative ranges were grown in competition with natives from each range, and the novel weapons hypothesis in laboratory experiments with leachates from C. odorata., Compared with conspecifics originating from the native range, C. odorata plants from the nonnative range were stronger competitors at high nutrient concentrations in the nonnative range in China and experienced far more herbivore damage in the native range in Mexico. In both China and Mexico, C. odorata was more suppressed by species native to Mexico than by species native to China. Species native to China were much more inhibited by leaf extracts from C. odorata than species from Mexico, and this difference in allelopathic effects may provide a possible explanation for the biogeographic differences in competitive ability., Our results indicate that EICA, innate competitive advantages, and novel biochemical weapons may act in concert to promote invasion by C. odorata, and emphasize the importance of exploring multiple, non-mutually exclusive mechanisms for invasions. [ABSTRACT FROM AUTHOR]

We analyzed the geographical and elevational distributions of two Polypodium complexes from Mexico and Central America. Distribution data of nine species of the Polypodium colpodes complex and the Polypodium plesiosorum complex were obtained from almost 1500 herbarium specimens, field collections in Mexico and Costa Rica, and literature studies. The presence of each species was recorded for each Mesoamerican country, in 1° × 1° grid-cells and biogeographical provinces. The rarity of species was also evaluated. Although the two complexes show extensive overlap, the P. colpodes complex is distributed mainly along the Pacific versant of Mexico and Central America, whereas the P. plesiosorum complex occurs mainly along the Atlantic versant. Those biogeographical provinces with maximum species diversity are Chiapas (seven species), Sierra Madre del Sur (six species), and the Trans-Mexican Volcanic belt (six species). Grid-cells with more species are located mainly in the mountains of central-southern Mexico and northern Central America. Richness does not decrease or increase with latitude. Elevation distributions showed that most Polypodium species are concentrated in the montane interval and three species groups were recognized based on elevational preferences. Polypodium colpodes and P. plesiosorum are the most widely distributed species, whereas Polypodium castaneum and Polypodium flagellare are the only two species that possess the three attributes of rarity (narrow geographical distribution, high habitat specificity, and scarce local populations). Polypodium species of both complexes are present mainly in the montane regions of the study area and show some degree of geographical sympatry, especially in southern Mexico and northern Central America. This overlapping is explained by the elevation tolerance within montane systems and because most species inhabit three or more vegetation types. The distributional patterns of these complexes coincided with the three regional highlands of Mesoamerica, which are separated from each other by the Isthmus of Tehuantepec and by the lowlands of Nicaragua. © 2012 The Linnean Society of London, Biological Journal of the Linnean Society, 2012, ••, ••-••. [ABSTRACT FROM AUTHOR]

Animals frequently evolve unique suites of traits on islands, but whether plants evolve comparable island syndromes remains unresolved. Here, we test the prediction on the basis of natural history observations that insect-pollinated plants evolve smaller flowers on islands than on mainland communities. We examined 556 plant species representing 136 phylogenetically independent contrasts between island and mainland sister taxa. We focused on endemic taxa originating from the Americas associated with seven tropical and subtropical islands of the Pacific Ocean. Contrary to conventional wisdom, flowers were not on average smaller on islands than on the mainland. On specific archipelagos (the Galápagos Islands and Revillagigedo Islands), however, island taxa did evolve smaller flowers. Divergence in flower size between island and mainland taxa also varied among taxonomic families, such that some plant families evolved smaller flowers on islands, other families evolved larger flowers on islands, and some families exhibited no divergence in flower size between island and mainland taxa. Overall, our results show that there is no general island syndrome for flower size, but instead that the evolution of floral morphology is complex and context dependent, depending on variation among islands and plant families. Our results also suggest that if island floras are typically dominated by small flowered species, as suggested by natural history observations, then ecological filtering is a more likely explanation of this pattern than evolutionary divergence postcolonization. We propose future studies that could disentangle the relative roles of ecological filtering and evolution in the distribution of floral traits on islands.

The article presents a response to a commentary on a study that designates the oldest eight-row cobs from Roller Skate and Tornillo Shelters in New Mexico as Proto-Maiz de Ocho. It argues that the designation was not intended to imply that they were different from the eight-rowed race from numerous older sites from Tehuacan, Mexico to Ayacucho, Peru. The author believes that Harinoso de Ocho of the Southwest may have affinities with Kcello from Ecuador.