Search

In science, standardization of terminology is crucial to make information accessible and allow proper comparison of studies' results. Climbing plants and the climbing habit have been described in numerous ways, frequently with imprecise and dubious terms. We propose a standardization of terms regarding the climbing habit, with special attention to climbing mechanisms. We abide by previous suggestions that the terms 'primary' and 'secondary' hemiepiphyte be substituted by 'hemiepiphyte' and 'nomadic climber' respectively, thus emphasizing the relationship of the latter to the climbing habit. We also suggest that 'climbing plant' or 'climber' be used to describe plants displaying the climbing habit, and 'liana' and 'vine' be left for describing woody and herbaceous climbers respectively. As for climbing mechanisms, we propose an eight-category classification comprised of two major categories: passive climbing, containing scrambling, hooks or grapnels, and adhesive roots; and active climbing, containing twining, tendrils, prehensile branches, twining petioles, and twining inflorescences. Keywords climbing plants * lianas * vines * climbing mechanisms * standardization * terminology Portuguese Na ciencia, a padronizacao de terminologia e crucial para tomar informacoes acessiveis e possibilitar a comparacao adequada dos resultados de estudos. Trepadeiras e o habito trepador vem sendo descritos de diversas maneiras, frequentemente com termos imprecisos e dubios. Nos propomos urna padronizacao da terminologia relativa ao habito trepador, corn atencao especial aos mecanismos de escalada. Nos acatamos sugestoes anteriores de que os termos 'hemiepifita primaria' e 'secundaria' sejam substituidos por 'hemiepifita' e 'trepadeira nomade' respectivamente, enfatizando assim a relacao desta ultima com o habito trepador. Nos tambem sugerimos que 'trepadeira' seja utilizado para descrever plantas apresentando o habito trepador, e 'liana' e 'trepadeira herbacea' sejam utilizados somente para descrever trepadeiras lenhosas e herbaceas respectivamente. Quanto aos mecanismos de escalada, nos propomos urna classificacao com oito categorias compreendidas em duas grandes categorias: trepadeiras passivas, contendo os mecanismos apoiante, ganchos e raizes grampiformes; e trepadeiras ativas, contendo os mecanismos voluvel, gavinhas, ramos preensores, peciolos voluveis e inflorescencias voluveis. Palavras-chave trepadeiras * lianas * mecanismos de escalada * padronizacao * terminologia, Introduction In an ideal scenario of any biological study, the ternis of scientific language and the concepts they express should be clear and precise to avoid ambiguities, which are a [...]

The monocot family Cyclanthaceae (Pandanales) comprises ca. 230 known species in 12 genera restricted to the Neotropics. The family has not been the subject of a species‐level molecular phylogenetic study to date, with multiple evolutionary and biogeographic questions about Cyclanthaceae still unanswered. In this study, we address genus‐ and species‐level relationships and the historical biogeography of Cyclanthaceae based on a broadly sampled molecular phylogeny. Two low‐copy nuclear genes (phyC, rpb2) and five plastid regions (atpB‐rbcL, psbA‐trnH, trnL‐trnF, trnQ‐rps16, matK) representing 99 species and all genera of Cyclanthaceae were sampled, spanning the taxonomic and biogeographic diversity of the family. Our results strongly support the monophyly of all Cyclanthaceae genera and confirm previously proposed hypotheses of intergeneric relationships. Infrageneric relationships are generally well supported, with some exceptions in the genus Asplundia that may require a broader sampling to clarify. The early diversification of Cyclanthaceae is estimated to date back to the Paleocene‐Eocene period in South America, where the family possibly arrived through a boreotropical route. The origin of most genera is inferred from the Paleocene of the Tumbes‐Chocó‐Magdalena region, possibly indicating an earlier origin for this biodiversity hotspot. The current distribution of Cyclanthaceae is likely to have been strongly influenced by major biogeographical events in the Neotropics, such as the uplift of the Andes and the opening of the South America dry diagonal. Further studies that include a broader sample of the large Asplundia‐Dicranopygium clade and Sphaeradenia group are required. [ABSTRACT FROM AUTHOR]

• A novel multilocus and highly supported phylogeny clarify several previously uncertain relationships in Myrcia. • Our results provide a solid backbone for further evolutionary and taxonomic work. • Previously unplaced Myrcia species formed a new circumscribed clade. • The first phylogenetic relationships for Myrcia sect. Gomidesia are shown with a morphological trait evolution and geographic range distribution approaches. • The inclusion of previously available molecular data with novel sequences of Myrcia and relatives significantly improved our phylogenetic estimates. Myrcia is the largest exclusively Neotropical genus of the plant family Myrtaceae with c. 770 species. Although several studies have elucidated the relationships within particular sections of the genus, to date no phylogeny has been produced that includes a broad taxonomic and geographic representation. Here we present a phylogenetic hypothesis of Myrcia and close relatives comprising 253 species and based on two nuclear and seven plastid markers. We combine previously available sequence data with 234 new sequences of the genus Myrcia for this study. We use this phylogeny to investigate the evolution of selected morphological traits and to infer the biogeographic history of the genus. Our results yield a highly supported phylogenetic tree where the Myrceugenia group is sister to the Myrcia and Plinia groups. Five Myrcia species previously considered unplaced emerge in a newly circumscribed clade. The monophyly of two Myrcia sections previously considered uncertain, Aulomyrcia and Gomidesia, are confirmed with strong support. Flowers with free calyx lobes, 2-locular ovaries, and anthers with symmetrical thecae are ancestral features of Myrcia. The Myrcia sect. Gomidesia is highly supported and recovered as monophyletic, with asymmetric anthers that retain their curvature after dehiscence as a morphological synapomorphy. The Atlantic Forest is the most likely ancestral area of the genus and most of its internal clades, from where multiple lineages colonized different regions of South and Central America, in particular the Brazilian Cerrado through multiple unidirectional range expansions. The southern Atlantic Forest is the ancestral area for Myrcia sect. Gomidesia , with lineages reaching the northern Atlantic Forest, Cerrado, Yungas, and other savanna vegetation of South America. Our results provide a solid backbone for further evolutionary and taxonomic work and clarify several previously uncertain relationships in this mega-diverse plant group, and shed light on its geographical range evolution. [ABSTRACT FROM AUTHOR]

Myrteae (c. 2500 species; 51 genera) is the largest tribe of Myrtaceae and an ecologically important groups of angiosperms in the Neotropics. Systematic relationships in Myrteae are complex, hindering conservation initiatives and jeopardizing evolutionary modelling. A well-supported and robust phylogenetic hypothesis was here targeted towards a comprehensive understanding of the relationships within the tribe. The resultant topology was used as a base for key evolutionary analyses such as age estimation, historical biogeography and diversification rate patterns. One nuclear ( ITS ) and seven chloroplast ( psbA-trnH , matK , ndhF , trnl - trnF , trnQ - rps16 , rpl16 and rpl32 - trnL ) DNA regions for 115 taxa representing 46 out of the 51 genera in the tribe were accessed and analysed using maximum likelihood and Bayesian inference tools for phylogenetic reconstruction. Dates of diversification events were estimated and contrasted using two distinct fossil sets (macro and pollen) in BEAST. The subsequent dated phylogenies were compared and analysed for biogeographical patterns using BioGeoBEARS and diversification rates using BAMM. Myrteae phylogeny presents strong statistical support for three major clades within the tribe: Australasian group, Myrtus group and Main Neotropical Lineage. Dating results from calibration using macrofossil are an average of 20 million years older and show an early Paleocene origin of Myrteae, against a mid-Eocene one from the pollen fossil calibration. Biogeographic analysis shows the origin of Myrteae in Zealandia in both calibration approaches, followed by a widespread distribution throughout the still-linked Gondwana continents and diversification of Neotropical endemic lineages by later vicariance. Best configuration shift indicates three points of acceleration in diversification rates, all of them occurring in the Main Neotropical Lineage. Based on the reconstructed topology, several new taxonomic placements were recovered, including: the relative position of Myrtus communis , the placement of the Blepharocalyx group, the absence of generic endemism in the Caribbean, and the paraphyletism of the former Pimenta group. Distinct calibration approaches affect biogeography interpretation, increasing the number of necessary long distance dispersal events in the topology with older nodes. It is hypothesised that biological intrinsic factors such as modifications of embryo type and polyploidy might have played a role in accelerating shifts of diversification rates in Neotropical lineages. Future perspectives include formal subtribal classification, standardization of fossil calibration approaches and better links between diversification shifts and trait evolution. [ABSTRACT FROM AUTHOR]

• Abiotic dispersal is the ancestral state for Melastomataceae. • Bulk of changes to biotic dispersal were detected early in the history of the family. • Species richness distribution is very similar across dispersal modes. • Range sizes across dispersal modes are not significantly different. • Increased diversification is not dependent on dispersal mode in the family. Species of plants with different life history strategies may differ in their seed dispersal mechanisms, impacting their distribution and diversification patterns. Shorter or longer distance dispersal is favored by different dispersal modes, facilitating (or constraining) population isolation, which can, in turn, impact speciation and species range sizes. While these associations are intuitive, few studies have explicitly tested these hypotheses for large clades of angiosperms. The plant family Melastomataceae is found on disparate habitats with different dispersal modes, representing a good model to address these questions. In this study, we reconstruct the phylogeny of Melastomataceae and gather data on their dispersal mode and range size to test the impact of dispersal mode on diversification and range size evolution. We found that abiotic dispersal is ancestral in the family, while biotic dispersal evolved multiple times. Species richness distribution is very similar across dispersal modes, although abiotically dispersed species tend to be relatively more diverse in seasonal environments. Range sizes across dispersal modes are not significantly different, although biotically dispersed species have slightly wider distributions. Model comparisons indicate that factors other than dispersal mode might have driven diversification heterogeneity. We did not find evidence for the role of dispersal mode driving diversification rates or range size in the Melastomataceae, suggesting a complex macroevolutionary scenario for this diverse angiosperm family. The bulk of changes to biotic dispersal coinciding with an increase in passerine diversification suggests a possible "past" key innovation in Melastomataceae. Future studies should investigate the role of other diversification drivers in the family and the relatively higher diversity of abiotically dispersed species in open habitats. [ABSTRACT FROM AUTHOR]

• Eugenia is monophyletic including related genera previously segregated. • Calyx fused species evolved several times in the evolution of Eugenia. • Deep morphological assessment revealed five development patterns of calyx fusion. • Apparently six-petal species are the result of modification of two petaloid sepals. • Eugenia feijoi group can be recognized by the membranisepalous pattern. Eugenia has a pantropical distribution and comprises ca. 1000 species found mostly in the Neotropics. Recent DNA based phylogenies show that unusual flower morphology of 'eugenioid' collections, e.g. fused calices that open by tearing, consistently emerged within Eugenia. These results emphasize a demand to revaluate flower morphology in a phylogenetic context within the genus. A reassessment of calyx fusion in Eugenia and traditionally related genera is here focused on clarification of the systematic relevance of this apparently recurrent characteristic. Twenty-four Eugenia species with some level of calyx fusion in the bud were newly used (one nuclear and four plastid markers) in conjunction with a representative sample of previously sequenced species to recover a time-calibrated Eugenia phylogeny of 86 accessions. Development of the fused calyx was analysed using scanning electron microscopy, differing patterns were re-coded and subsequently phylogenetic character reconstruction was performed. Eugenia was recovered as monophyletic including the traditionally segregated genera Calycorectes and Catinga. Ancestral character reconstruction uncovered free calyx lobes as the ancestral condition. Five development patterns leading to calyx fusion are reported in Eugenia including species with apparently six petals, which contrast with the standard tetramerous flowers. This condition is interpreted as the petaloid pattern, where two external fused calyx lobes cover the bud while two internal calyx lobes are free and petaloid. The fused calyx condition is homoplastic and evolved independently, several times in Eugenia, as did the different development patterns. Data presented here show that systematic incongruence resulting from multiple, independent origins of the fused calyx in Eugenia is further aggravated by an inability to distinguish parallelism and convergence within the recovered patterns. [ABSTRACT FROM AUTHOR]

• Tapinotaspidini broad phylogeny indicates monophyly of most genera. • Tapinotaspidini bees originated in Cerrado-like savannas in the Paleocene. • Transitions to forested areas slightly increase speciation rates. • Malpighiaceae is the ancestral host for floral oils. • Shifts to other oil plant families are possibly linked to habitat shifts. Worldwide distributed tropical savannas were established only in the Miocene, with climatic cooling and rise of C4 grasses. However, there is evidence for an earlier presence of savanna-like vegetation in southern parts of South America. Here we investigated the biogeographic history of a clade of solitary bees which have endemic groups in areas covered by savannas and other types of open vegetation as well as forested areas. We hypothesized that these bees originated in savanna-like biomes and that shifts to forested areas and floral host shifts increased species diversification along their evolutionary history. We reconstructed a comprehensive phylogeny for Tapinotaspidini bees based majorly on original DNA sequences. We then used macroevolutionary tools to estimate ancestral range area and reconstructed ancestral habitat (open versus forested) and host plant association to analyze the effects of shifts in vegetation type and flower hosts on their diversification. Tapinotaspidini bees originated in the Paleocene and in a savanna-type, Cerrado-like, which is reinforced by reconstruction of open vegetation as the most probable ancestral area, thus bringing additional evidence to a much earlier origin of this vegetation type in South America. Shifts to forested areas occurred at least three times in a period of 30 Ma and were responsible for slight increases in diversification rates. Malpighiaceae is the ancestral floral host; host broadening occurred only in the Miocene and at least in three occasions. Host shifts, i.e. from Malpighiaceae to other oil families, occurred in the Eocene and Miocene. Both host broadening and host shifts did not significantly alter diversification rates, however exploitation of other oil sources were important in occupying new habitats. The link between biomes and host plant shifts and changes in diversification rate brings us additional insights into the evolution of bees and associated flora in South America. [ABSTRACT FROM AUTHOR]