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      A new species of Fordiophyton (Sonerileae, Melastomataceae) from Yunnan, China

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          Abstract

          Abstract

          Fordiophyton jinpingense ( Melastomataceae ; Sonerileae), a species occurring in south-eastern Yunnan, China, is described as new, based on morphological and molecular data. Phylogenetic analyses, based on nrITS sequence data, showed that, except F. breviscapum , all species sampled in Fordiophyton formed a strongly supported clade in which two geographical lineages were recovered. The generic placement of F. jinpingense is well supported by phylogenetic analyses and a character combination of 4-merous flowers, distinctly dimorphic stamens and the connectives basally not calcarate. Molecular divergence and morphological evidence indicate that F. jinpingense is well separated from other members of the genus, thus justifying its recognition as a distinct species. Fordiophyton jinpingense is phylogenetically closest to F. repens , but differs markedly from the latter in stem morphology (short, obtusely 4-sided vs. long, 4-angular), habit (erect vs. creeping), leaf size (6–16.5 × 4.5–13 cm vs. 4–7.5 × 4–6.5 cm) and flower number per inflorescence (5–13 vs. 3–6).

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          A rapid DNA isolation procedure for small quantities of fresh leaf tissue

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            Molecular phylogenetics of Melastomataceae and Memecylaceae: implications for character evolution.

            Melastomataceae are among the most abundant and diversified groups of plants throughout the tropics, but their intrafamily relationships and morphological evolution are poorly understood. Here we report the results of parsimony and maximum likelihood (ML) analyses of cpDNA sequences from the rbcL and ndhF genes and the rpl16 intron, generated for eight outgroups (Crypteroniaceae, Alzateaceae, Rhynchocalycaceae, Oliniaceae, Penaeaceae, Myrtaceae, and Onagraceae) and 54 species of melastomes. The sample represents 42 of the family's currently recognized ∼150 genera, the 13 traditional tribes, and the three subfamilies, Astronioideae, Melastomatoideae, and Memecyloideae (= Memecylaceae DC.). Parsimony and ML yield congruent topologies that place Memecylaceae as sister to Melastomataceae. Pternandra, a Southeast Asian genus of 15 species of which five were sampled, is the first- branching Melastomataceae. This placement has low bootstrap support (72%), but agrees with morphological treatments that placed Pternandra in Melastomatacaeae because of its acrodromal leaf venation, usually ranked as a tribe or subfamily. The interxylary phloem islands found in Memecylaceae and Pternandra, but not most other Melastomataceae, likely evolved in parallel because Pternandra resembles Melastomataceae in its other wood characters. A newly discovered plesiomorphic character in Pternandra, also present in Memecylaceae, is a fibrous anther endothecium. Higher Melastomataceae lack an endothecium as do the closest relatives of Melastomataceae and Memecylaceae. The next deepest split is between Astronieae, with anthers opening by slits, and all remaining Melastomataceae, which have anthers opening by pores. Within the latter, several generic groups, corresponding to traditional tribes, receive solid statistical support, but relationships among them, with one exception, are different from anything predicted on the basis of morphological data. Thus, Miconieae and Merianieae are sister groups, and both are sister to a trichotomy of Bertolonieae, Microlicieae + Melastomeae, and Dissochaeteae + Blakeeae. Sonerileae/Oxysporeae are nested within Dissochaeteae, Rhexieae within Melastomeae, and African and Asian Melastomeae within neotropical Melastomeae. These findings have profound implications for our understanding of melastome morphological evolution (and biogeography), implying, for example, that berries evolved from capsules minimally four times, stamen connectives went from dorsally enlarged to basal/ventrally enlarged, and loss of an endothecium preceded poricidal dehiscence.
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              Historical biogeography of Melastomataceae: the roles of Tertiary migration and long-distance dispersal.

              Melastomataceae and Memecylaceae are pantropically distributed sister groups for which an ndhF gene phylogeny for 91 species in 59 genera is here linked with Eurasian and North American fossils in a molecular clock approach to biogeographical reconstruction. Nine species from the eight next-closest families are used to root phylogenetic trees obtained under maximum likelihood criteria. Melastomataceae comprise ∼3000 species in the neotropics, ∼1000 in tropical Asia, 240 in Africa, and 225 in Madagascar in 150-166 genera, and the taxa sampled come from throughout this geographic range. Based on fossils, ranges of closest relatives, tree topology, and calibrated molecular divergences, Melastomataceae initially diversified in Paloecene/Eocene times in tropical forest north of the Tethys. Their earliest (Eocene) fossils are from northeastern North America, and during the Oligocene and Miocene melastomes occurred in North America as well as throughout Eurasia. They also entered South America, with earliest (Oligocene) South American fossils representing Merianieae. One clade (Melastomeae) reached Africa from the neotropics 14-12 million years ago and from there spread to Madagascar, India, and Indochina. Basalmost Melastomataceae (Kibessieae, Astronieae) are species-poor lineages restricted to Southeast Asia. However, a more derived Asian clade (Sonerileae/Dissochaeteae) repeatedly reached Madagascar and Africa during the Miocene and Pliocene. Contradicting earlier hypotheses, the current distribution of Melastomataceae is thus best explained by Neogene long-distance dispersal, not Gondwana fragmentation.
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                Author and article information

                Contributors
                Journal
                PhytoKeys
                PhytoKeys
                3
                urn:lsid:arphahub.com:pub:f7fce910-8e78-573f-9c77-7788555f8aad
                PhytoKeys
                Pensoft Publishers
                1314-2011
                1314-2003
                2019
                28 May 2019
                : 122
                : 15-28
                Affiliations
                [1 ] State Key Laboratory of Biocontrol and Guangdong Key Laboratory of Plant Resources, School of Life Sciences, Sun Yat-sen University, No. 135, Xin-Gang-Xi Road, Guangzhou 510275, China Sun Yat-sen University Guangzhou China
                [2 ] Management Bureau of Fenshuiling National Nature Reserve, Jinping 661500, China Management Bureau of Fenshuiling National Nature Reserve Jinping China
                Author notes
                Corresponding author: Ying Liu ( liliumrosa@ 123456163.com )

                Academic editor: Ricardo Kriebel

                Author information
                https://orcid.org/0000-0003-0613-837X
                Article
                35260
                10.3897/phytokeys.122.35260
                6548766
                bb15a946-af9d-4c35-b158-71bcea398f28
                Jin-Hong Dai, Qiu-Jie Zhou, Zhi-Yong Yu, Ren-Chao Zhou, Ying Liu

                This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 11 April 2019
                : 25 April 2019
                Funding
                The National Natural Science Foundation of China and the Science and Technology Planning Project of Guangdong Province
                Categories
                Research Article
                Melastomataceae
                Phylogeny
                Taxonomy
                Asia

                Plant science & Botany
                fordiophyton , melastomataceae ,taxonomy,phylogeny,plantae,myrtales,melastomataceae

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