Rafael Felipe de Almeida

Dr. Rafael Felipe de Almeida

APES, University of the Witwatersrand, Johannesburg, Gauteng, South Africa
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Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2015 in Rodriguésia
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DZDaniela Cristina Zappi
Daniela Cristina Zappi
FFFabiana L. Ranzato Filardi
Fabiana L. Ranzato Filardi
PLPaula Leitman
Paula Leitman
VSVinícius C. Souza
Vinícius C. Souza
BWBruno M.T. Walter
Bruno M.T. Walter
CZCarmem S Zickel
Carmem S Zickel
An updated inventory of Brazilian seed plants is presented and offers important insights into the country's biodiversity. This work started in 2010, with the publication of the Plants and Fungi Catalogue, and has been updated since by more than 430 specialists working online. Brazil is home to 32,086 native Angiosperms and 23 native Gymnosperms, showing an increase of 3% in its species richness in relation to 2010. The Amazon Rainforest is the richest Brazilian biome for Gymnosperms, while the Atlantic Rainforest is the richest one for Angiosperms. There was a considerable increment in the number of species and endemism rates for biomes, except for the Amazon that showed a decrease of 2.5% of recorded endemics. However, well over half of Brazillian seed plant species (57.4%) is endemic to this territory. The proportion of life-forms varies among different biomes: trees are more expressive in the Amazon and Atlantic Rainforest biomes while herbs predominate in the Pampa, and lianas are more expressive in the Amazon, Atlantic Rainforest, and Pantanal. This compilation serves not only to quantify Brazilian biodiversity, but also to highlight areas where there information is lacking and to provide a framework for the challenge faced in conserving Brazil's unique and diverse flora.

14 January 2021 in Nordic Journal of Botany
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Rafael Felipe de AlmeidaRafael Felipe de Almeida
Rafael Felipe de Almeida
Cássio van den BergCássio van den Berg
Cássio van den Berg

29 August 2018 in PhytoKeys
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Marco O. O. PellegriniMarco O. O. Pellegrini
Marco O. O. Pellegrini
CHCharles N. Horn
Charles N. Horn
Rafael Felipe de AlmeidaRafael Felipe de Almeida
Rafael Felipe de Almeida
A total evidence phylogeny for Pontederiaceae is herein presented based on new morphological and previously published molecular data. Our results led us to re-circumscribePontederiato includeMonochoria,Pontederias.s.and the polyphyleticEichhornia. We provide the needed ten new combinations and 16 typifications, arrange a total of 25 accepted species (six representing re-established names) in 5 new subgenera. Furthermore, we provide an identification key for the two genera accepted by us in Pontederiaceae, an identification key to the subgenera, identification keys to the species of each subgenus and commentaries onPontederias.l., as well as for each subgenus and each species.

18 July 2017 in Phytotaxa
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Rafael Felipe de AlmeidaRafael Felipe de Almeida
Rafael Felipe de Almeida
AAAndré Márcio Amorim
André Márcio Amorim
ACAngela Maria DA Silva Corrêa
Angela Maria DA Silva Corrêa
Cássio van den BergCássio van den Berg
Cássio van den Berg
Phylogenetic relationships for 14 of the 15 species of Amorimia (Malpighiaceae) were inferred based on ndhF plastid DNA and ETS nuclear ribosomal DNA using both parsimony and Bayesian methods. Our results show that: (1) the monophyly of the genus is corroborated with the new circumscription of the A. rigida complex; (2) several morphological and phytochemical characters support Amorimia and its two main clades; and (3) these clades can be proposed as new subgenera in Amorimia.

19 April 2023 in Plant Ecology and Evolution
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Journal Article
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Rafael Felipe de AlmeidaRafael Felipe de Almeida
Rafael Felipe de Almeida
Marco O. O. PellegriniMarco O. O. Pellegrini
Marco O. O. Pellegrini
IMIsa L. de Morais
Isa L. de Morais
RSRosangela Simão-Bianchini
Rosangela Simão-Bianchini
PRPantamith Rattanakrajang
Pantamith Rattanakrajang
ASAna Rita G. Simões
Ana Rita G. Simões
Background and aims – Keraunea is a Brazilian endemic genus that has sat uncomfortably in Convolvulaceae where it was placed due to an enlarged and adnate fruit bract typical of Neuropeltis. A recent molecular phylogeny suggested that two of its five morphologically almost identical species actually belong to two different families, Malpighiaceae (superrosids) and Ehretiaceae (superasterids). Later studies have demonstrated that Keraunea effectively belongs to Ehretiaceae, but the proposal of one species belonging to Malpighiaceae has remained problematic. In this study, we re-assess this hypothesis, discuss the issues that have led to this assumption, and offer insights on the importance of carefully using herbarium collections and incorporating morphological evidence in systematic studies. Material and methods – Sequences of matK, rbcL, and ITS for all 77 currently accepted genera of Malpighiaceae, K. brasiliensis and Elatinaceae (outgroup) were compiled from GenBank and analysed with Maximum Likelihood and Bayesian Inference criteria for nuclear, plastid and combined datasets. Additional database and herbarium studies were performed to locate and analyse all duplicates of the holotype of K. brasiliensis to check for misidentified or contaminated material. Key results – Our examination of expanded DNA datasets and herbarium sheets of all K. brasiliensis isotypes revealed that a mistake in tissue sampling was, in fact, what led to this species being proposed to belong in Malpighiaceae. Kew’s isotype had a leaf of Malpighiaceae (likely Mascagnia cordifolia) stored in the fragment capsule, which was sampled and sequenced instead of the actual leaves of K. brasiliensis. Recently published studies have settled the placement of Keraunea in Ehretiaceae (Boraginales) and proposed three additional species. Conclusions – DNA sequences can be helpful in classifying taxa when morphology is conflicting or of a doubtful interpretation, with molecular phylogenetic placement being established as a popular tool accelerating the discovery of systematic relationships. Nonetheless, molecular techniques are also susceptible to methodological mistakes, which necessitates building a solid foundation of plant morphology and taxonomy to avoid artefacts in phylogenetic studies.

13 November 2020 in Plants
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Rafael Felipe de AlmeidaRafael Felipe de Almeida
Rafael Felipe de Almeida
Cássio van den BergCássio van den Berg
Cássio van den Berg
We investigated the biogeography of Stigmaphyllon, the second-largest lianescent genus of Malpighiaceae, as a model genus to reconstruct the age and biogeographic history of the Brazilian Atlantic Rainforest (BAF). Few studies to date have focused on the tertiary diversification of plant lineages in the BAFs, especially on Stigmaphyllon. Phylogenetic relationships for 24 species of Stigmaphyllon (18 ssp. From the Atlantic forest (out of 31 spp.), three spp. from the Amazon Rainforest, two spp. from the Caatinga biome, and a single species from the Cerrado biome) were inferred based on one nuclear DNA (PHYC) and two ribosomal DNA (ETS, ITS) regions using parsimony and Bayesian methods. A time-calibrated phylogenetic tree for ancestral area reconstructions was additionally generated, coupled with a meta-analysis of vascular plant lineages diversified in the BAFs. Our results show that: (1) Stigmaphyllon is monophyletic, but its subgenera are paraphyletic; (2) the most recent common ancestor of Stigmaphyllon originated in the Brazilian Atlantic Rainforest/Caatinga region in Northeastern Brazil ca. 26.0 Mya; (3) the genus colonized the Amazon Rainforest at two different times (ca. 22.0 and 6.0 Mya), the Caatinga biome at least four other times (ca. 14.0, 9.0, 7.0, and 1.0 Mya), the Cerrado biome a single time (ca. 15.0 Mya), and the Southern Atlantic Rainforests five times (from 26.0 to 9.0 Mya); (4) a history of at least seven expansion events connecting the Brazilian Atlantic Rainforest to other biomes from 26.0 to 9.0 Mya, and (5) a single dispersion event from South America to Southeastern Asia and Oceania at 22.0 Mya via Antarctica was proposed. Compared to a meta-analysis of time-calibrated phylogenies for 64 lineages of vascular plants diversified in the Brazilian Atlantic Rainforests, our results point to a late Eocene origin for this megadiverse biome.