scholarly journals Pyramidanthe and Mitrella (Annonaceae, Uvarieae) unified: molecular phylogenetic and morphological congruence, with new combinations in Pyramidanthe

Author(s):  
Rattikarn Bangkomnate ◽  
Anissara Damthongdee ◽  
Abdulromea Baka ◽  
Kithisak Aongyong ◽  
Tanawat Chaowasku
2003 ◽  
Vol 60 (3) ◽  
pp. 533-568 ◽  
Author(s):  
J. C. MANNING ◽  
P. GOLDBLATT ◽  
M. F. FAY

A revised generic synopsis of sub-Saharan Hyacinthaceae is presented, based on a molecular phylogenetic analysis of the family. Generic rank is accorded only to reciprocally monophyletic clades that can be distinguished by recognizable morphological discontinuities, thereby permitting an appropriate generic assignment of species not included in the analysis. Three subfamilies are recognized within the region. Subfamily Ornithogaloideae, characterized by flattened or angular seeds with tightly adhering testa, is considered to include the single genus Ornithogalum, which is expanded to include the genera Albuca, Dipcadi, Galtonia, Neopatersonia and Pseudogaltonia. Recognizing any of these segregates at generic level renders the genus Ornithogalum polyphyletic, while subdivision of Ornithogalum into smaller, morphologically distinguishable segregates in order to preserve the monophyly of each is not possible. Subfamily Urgineoideae, characterized by flattened or winged seeds with brittle, loosely adhering testa, comprises the two mainland African genera Bowiea and Drimia. The latter is well circumscribed by its deciduous, short-lived perianth and includes the previously recognized genera Litanthus, Rhadamanthus, Schizobasis and Tenicroa. The monotypic Madagascan Igidia is provisionally included in the subfamily as a third genus on the basis of its seeds, pending molecular confirmation of its relationships. Subfamily Hyacinthoideae resolves into three clades, distinguished as tribes Hyacintheae (strictly northern hemisphere and not treated further), Massonieae and Pseudoprospereae tribus nov. Full descriptions and a key to their identification are provided for all genera. New combinations reflecting the generic circumscriptions adopted here are made for most African and all Indian and Madagascan species.


Phytotaxa ◽  
2020 ◽  
Vol 468 (3) ◽  
pp. 275-282
Author(s):  
ERIC H. ROALSON ◽  
RAIMUNDO LUCIANO SOARES NETO

Physostemon (Cleomaceae) includes 15 taxa in 10 species distributed from Mexico and the Caribbean south to Brazil and Paraguay. A full nomenclatural synonymy is presented including 7 lectotypes and 5 new combinations. Mitostylis species are moved to Physostemon based on morphological and molecular phylogenetic evidence. A table of characteristics for differentiating species is included.


2013 ◽  
Vol 70 (3) ◽  
pp. 385-404 ◽  
Author(s):  
D. J. Middleton ◽  
A. Weber ◽  
T. L. Yao ◽  
S. Sontag ◽  
M. Möller

Following recent molecular phylogenetic studies in Old World Gesneriaceae the nomenclatural implications for names in Henckelia are examined. New combinations are made in Codonoboea and Loxocarpus to account for species now excluded from Henckelia. A list is presented in which the current position of all species hitherto assigned to Henckelia is given, including the new combination Henckelia rotundata (Barnett) D.J.Middleton & Mich.Möller. A new combination in Oreocharis is made.


2020 ◽  
pp. 515-576
Author(s):  
Frank Bungartz ◽  
Ulrik Søchting ◽  
Ulf Arup

The lichen family Teloschistaceae from the Galapagos is revised. Most of the species belong to the Caloplacoideae, two to Teloschistoideae and a few to Xanthorioideae, three subfamilies not validly published, which is remedied here. Four different datasets were analyzed using Bayesian inference. For the bulk of the species, a combined dataset of nrITS, nrLSU and mrSSU was analyzed. Additionally, three analyses were performed using nrITS to further investigate phylogenetic relationships within and between species in each subfamily, and in the genera Xanthomendoza and Squamulea. Four new genera are described: Lacrima, Oceanoplaca, Phaeoplaca, Sucioplaca. Twenty-four species are reported, of which ten are new to science: Caloplaca nigra, Lacrima galapagoensis, Oceanoplaca chemoisidiosa, O. sideritoides, Phaeoplaca tortuca, Squamulea chelonia, S. humboldtiana, S. osseophila, S. oceanica, and Xanthomendoza leoncita. Several new combinations are proposed and three species of Xanthomendoza are reduced to synonymy. Several new combinations and species placed into synonymy do not occur in the Galapagos, but are treated as a consequence of our taxonomic revision. Morphology, anatomy, secondary chemistry, distribution and molecular phylogenetic affiliation are presented for each species and a key is provided. Eight different chemical patterns are quantitatively described based on HPLC analyses. The new genus Lacrima includes L. galapagoensis, a species without vegetative propagules, and two densely isidiate species, L. epiphora and L. aphanotripta that are morphologically similar to ‘Caloplaca’ wrightii. The only species of Galapagos Teloschistaceae that contains xanthones is placed into Huneckia. Oceanoplaca includes two species with the new anthraquinone isidiosin, O. isidiosa and O. chemoisidiosa, while a third species, O. sideritoides, does not contain this secondary metabolite. Phaeoplaca camptidia has previously been reported from Galapagos, but our phylogenetic analysis suggests that it is a new species, here named P. tortuca. An isolated position is occupied by ‘Caloplaca’ diplacia, which we place in it its own monotypic genus Sucioplaca. Some Galapagos Teloschistaceae can be considered a ‘residue’ of unresolved Caloplaca s.l., i.e. the corticolous C. floridana is possibly related to the saxicolous C. nigra, while C. cupulifera can currently not be placed. Squamulea remains particularly problematic and includes S. phyllidizans, that is nested among otherwise unresolved Squamulea species. Based on molecular data, S. phyllidizans is close to ‘Huriella’. ‘Huriella’ flakusii, described from Peru, is confirmed to occur in the Galapagos and the genus is reduced to synonymy with Squamulea. The Squamulea squamosa/subsoluta group remains largely unresolved, but the new species S. chelonia, S. humboldtiana, S. oceanica, and S. osseophila are phylogenetically distinct. Foliose Teloschistaceae are represented only by one species, described as Xanthomendoza leoncita, while the only fruticose species, Teloschistes chrysophthalmus and T. flavicans, are cosmopolitan.


2021 ◽  
Vol 741 ◽  
pp. 1-168
Author(s):  
Sergey A. Belokobylskij ◽  
Alejandro Zaldívar-Riverón

The classification of the genera belonging to the doryctine tribe Rhaconotini (Braconidae) is updated. The following new taxa are described: Troporhaconotus gen. nov. (with 12 species), Afroipodoryctes subgen. nov. (of Ipodoryctes Granger, 1949) (with three species), Hexarhaconotinus subgen. nov. (of Rhaconotinus Hedqvist, 1965) (with ten species), Bathycentor zimbabwensis sp. nov., Ipodoryctes (Afroipodoryctes) reunionus sp. nov., I. (A.) saintphilippensis sp. nov., Platyspathius (Platyspathius) venezuelicus sp. nov., P. (P.) ranomafanus sp. nov., Rhacontsira haeselbarthi sp. nov., Rh. mozambiquensis sp. nov., Rh. saigonensis sp. nov. and Rh. toamasina sp. nov. The generic status of Euryphrymnus Cameron, 1910 is resurrected. The generic name Aptenobracon Marsh, 1965 is synonymised under Rhaconotus Ruthe, 1854 (syn. nov.); Rhaconotus asiaticus Belokobylskij, 1990 is synonymised under Rh. kerzhneri Belokobylskij, 1985 (syn. nov.). The new name, Rhaconotinus austrochinensis nom. nov., is suggested for the preoccupied name Rhaconotus chinensis Chen & Shi, 2004 (December) not Rhaconotus chinensis Belokobylskij & Chen, 2004 (June). New species contents, in many cases with numerous new combinations, are suggested for the genera Bathycentor Saussure, 1892, Euryphrymnus Cameron, 1910, Ipodoryctes Granger, 1949, Rhaconotinus Hedqvist, 1965 and Rhaconotus. The tribe Leptorhaconotini is synonymised with Rhaconotini based on previously published molecular phylogenetic studies, though we leave this group within the subtribe Leptorhaconotina.


Phytotaxa ◽  
2020 ◽  
Vol 434 (1) ◽  
pp. 13-21 ◽  
Author(s):  
MICHAEL W. FROHLICH ◽  
MATS THULIN ◽  
MARK W. CHASE

Many new combinations are needed in Euploca, previously regarded as Heliotropium section Orthostachys, to correspond with results of our forthcoming, world-wide, molecular phylogenetic analysis. We also need these names for our many δ13C determinations that identify many Euploca species exhibiting C4 photosynthesis and show that other Euploca species are not C4. Here we make the many new combinations required to support these results.


Phytotaxa ◽  
2019 ◽  
Vol 425 (5) ◽  
pp. 279-289
Author(s):  
MICHAEL G. SIMPSON ◽  
MAKENZIE E. MABRY ◽  
KRISTEN HASENSTAB-LEHMAN

Based on a previous molecular phylogenetic analysis, Cryptantha, an herbaceous plant genus of the family Boraginaceae, subtribe Amsinckiinae, was split into five genera: Eremocarya, Greeneocharis, Johnstonella, Oreocarya, and a reduced Cryptantha, the last in two separate clades. As a result of this study, Johnstonella was expanded to 13 species and 15 minimum-rank taxa, these formerly classified in Cryptantha s.l. More recent analyses of this complex, with an increased sample size and high-throughput sequence data, indicate that four additional Cryptantha species not previously sampled—C. albida, C. mexicana, C. texana—plus what was originally identified as C. hispida nest within Johnstonella with strong support. However, the identity of C. hispida used in this analysis is now in doubt. The material used likely represents a new species, in the process of being investigated. Two additional species not sequenced to date—C. geohintonii and C. gypsites—are clearly close relatives of C. albida and C. mexicana, based on morphological similarity. In order to maintain monophyly of genera, we here make new combinations in transferring four of these species from Cryptantha to Johnstonella, with the new combinations Johnstonella albida, J. geohintonii, J. gypsites, and J. mexicana. We delay the transfer of Cryptantha texana to Johnstonella because of its morphological similarity to other species that clearly nest within Cryptantha s.s. These same molecular phylogenetic studies may also support the transfer of two previously recognized Johnstonella species—J. echinosepala and J. micromeres—to Cryptantha, one to each of two separate clades. Additional phylogenetic studies focusing on some of these taxa are needed to confirm the position of these latter three species and the possible recognition of a new genus in the complex.


Phytotaxa ◽  
2015 ◽  
Vol 234 (1) ◽  
pp. 51 ◽  
Author(s):  
Kuan Zhao ◽  
Gang Wu ◽  
Roy Halling ◽  
Zhu L. Yang

Boletus peckii, B. pulchriceps and B. roseopurpureus, which were originally described from North America, are characterized by a yellow tube layer that often bruises blue, a yellow reticulated stipe especially at the apex, firm yellow-tinged flesh that often turns blue when exposed, smooth spores and an interwoven trichodermic pileipellis. The phylogenetic positions of the three species are inferred by molecular phylogenetic analysis based on DNA sequences of four gene markers (ITS, nrLSU, tef1-α and rpb1). Both morphological features and molecular phylogenetic evidence indicate that these three boletes belong to Butyriboletus, and thus, should be transferred to the genus.


Phytotaxa ◽  
2017 ◽  
Vol 298 (2) ◽  
pp. 195
Author(s):  
GANG YAO

Based on results from recent molecular phylogenetic studies, Solitaria ramellata (F.N. Williams) Gang Yao, S. forrestii (Diels) Gang Yao and S. rhodantha (Pax & Hoffmann) Gang Yao, three new combinations of Caryophyllaceae, are proposed. Additionally, the two names S. ramellata and S. rhodantha are lectotypified.


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