scholarly journals Three new combinations in African Cyperus (Cyperaceae)

2019 ◽  
Vol 152 (3) ◽  
pp. 561-562
Author(s):  
Isabel Larridon ◽  
Marc Reynders

Background – During the past decade several molecular phylogenetic studies tackled the complex relationships within tribe Cypereae. Based on these studies, previously accepted segregate genera such as Pycreus were sunk into the genus Cyperus. Recently, while revising the West African species of Cyperus, three taxa previously placed in Pycreus were identified for which a name in Cyperus is lacking.Methods – The taxonomic changes are performed according to the International Code of Nomenclature for algae, fungi, and plants.Results – Three new combinations in Cyperus are made for names currently placed in Pycreus.

2020 ◽  
Vol 153 (3) ◽  
pp. 446-454
Author(s):  
Luciana Pereira-Silva ◽  
Rafael Trevisan ◽  
Ana Claudia Rodrigues ◽  
Isabel Larridon

Background and aims – Molecular phylogenetic studies have provided a clearer understanding of the complex relationships within the family Cyperaceae. These studies have consistently shown that 12 allied genera are nested in the genus Cyperus. However, early Sanger sequencing-based phylogenies that included the two species of the small South American genus Androtrichum were inconclusive in placing this genus either as sister to Cyperus or as part of its early divergent lineages. A recent phylogenetic analysis however conclusively placed the two species of Androtrichum within the C3 Cyperus Grade. In this study, we investigate if the morphology and anatomy of Androtrichum species provide additional evidence for their placement in the genus Cyperus. In addition, we provide descriptions and distribution data for the species.Material and methods – Herbarium material from FLOR, FURB, GENT, ICN, and K has been studied. Samples of the culm and leaf were studied using histological methods. Taxonomic changes and typifications of names were performed according to the International Code of Nomenclature for algae, fungi, and plants. Key results – The morphology and the non-Kranz anatomy observed in the Androtrichum species confirm their placement among the other C3  Cyperus species. Androtrichum is combined into Cyperus. For one species, a combination in Cyperus is already available: Cyperus trigynus. For the other species, a new name in Cyperus is published: Cyperus byssaceus. Two typifications are established and morphological descriptions and distribution data are provided. Conclusion – By integrating recent molecular phylogenetic data with additional evidence from morphology and anatomy, Androtrichum is combined into Cyperus. As a result of this taxonomic change, a single monophyletic genus Cyperus is now recognised in the Cyperus Clade of tribe Cypereae.


2020 ◽  
Vol 86 (1) ◽  
pp. 1-26
Author(s):  
S T Williams ◽  
Y Kano ◽  
A Warén ◽  
D G Herbert

ABSTRACT The assignment of species to the vetigastropod genus Solariella Wood, 1842, and therefore the family Solariellidae Powell, 1951, is complicated by the fact that the type species (Solariella maculata Wood, 1842) is a fossil described from the Upper Pliocene. Assignment of species to genera has proved difficult in the past, and the type genus has sometimes acted as a ‘wastebasket’ for species that cannot easily be referred to another genus. In the light of a new systematic framework provided by two recent publications presenting the first molecular phylogenetic data for the group, we reassess the shell characters that are most useful for delimiting genera. Shell characters were previously thought to be of limited taxonomic value above the species level, but this is far from the case. Although overall shell shape is not a reliable character, our work shows that shell characters, along with radular and anatomical characters, are useful for assigning species to genera. Sculpture of the early teleoconch (the region immediately following the protoconch) and the columella are particularly useful characters that have not been used regularly in the past to distinguish genera. However, even with the combination of all morphological characters used in this study (shell, radular and eye), a few species are still difficult to assign to genera and in such cases molecular systematic data are essential. In the present study, we discuss 13 genera—12 of which were recovered as well-supported clades in recent molecular systematic studies—and provide morphological characters to distinguish them. We describe several new taxa: Chonospeira n. gen. (referred to as ‘clade B’ in previous molecular systematic studies), Phragmomphalina n. gen. (Bathymophila in part in molecular systematic studies) and Phragmomphalina vilvensi n. sp. (type species of Phragmomphalina n. gen.). We synonymize Hazuregyra Shikama, 1962 with Minolia A. Adams, 1860, Minolia subangulata Kuroda & Habe, 1952 with Minolia punctata A. Adams, 1860 and M. gemmulata Kuroda & Habe, 1971 with M. shimajiriensis (MacNeil, 1960). We also present the following new combinations: Bathymophila bairdii (Dall, 1889), B. dawsoni (Marshall, 1979), B. regalis (Marshall, 1999), B. wanganellica (Marshall, 1999), B. ziczac (Kuroda & Habe in Kuroda, Habe & Oyama, 1971), Chonospeira nuda (Dall, 1896), C. iridescens (Habe, 1961), C. ostreion (Vilvens, 2009), C. strobilos (Vilvens, 2009), Elaphriella corona (Lee & Wu, 2001), E. diplax (Marshall, 1999), E. meridiana (Marshall, 1999), E. olivaceostrigata (Schepman, 1908), E. opalina (Shikama & Hayashi, 1977), Ilanga norfolkensis (Marshall, 1999), I. ptykte (Vilvens, 2009), I. zaccaloides (Vilvens, 2009), Minolia shimajiriensis (MacNeil, 1960), M. watanabei (Shikama, 1962), Phragmomphalina alabida (Marshall, 1979), P. diadema (Marshall, 1999), P. tenuiseptum (Marshall, 1999), Spectamen euteium (Vilvens, 2009), S. basilicum (Marshall, 1999), S. exiguum (Marshall, 1999) and S. flavidum (Marshall, 1999).


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.


2021 ◽  
Vol 77 (1) ◽  
pp. 166-186
Author(s):  
Christopher J. Cleal ◽  
Barry A. Thomas

Fossil plants are extinct plants whose remains (referred to as plant fossils) are found preserved in sedimentary deposits. Plant fossils are classified using fossil-taxa as defined in the International Code of Nomenclature. Fossil-taxa differ conceptually from taxa of living plants in that they often do not refer to whole organisms, but to the remains of one or more parts of the parent organism, in one or more preservational states. There can be complications when two parts of a plant are shown to be connected, or when two preservational states are correlated, and to avoid disrupting the wider palaeobotanical taxonomy it is often best to keep the fossil-taxa separate. Extinct fossil plants reconstructed by piecing together the plant fossils are best not given formal Linnean taxonomic names. There can also be problems using living plant taxa for fossils, even when there is a close morphological similarity of particular plant parts. Fossil-taxa for different plant parts can reflect different taxonomic ranks of the parent plants so care must be taken when using such taxa in floristic or phylogenetic studies. Because of taphonomic factors, a number of “artificial” fossil-taxa have proved useful, despite that they do not fully reflect the systematic positions of the parent plants.


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.


2018 ◽  
Vol 16 (2) ◽  
Author(s):  
Renata Rúbia Ota ◽  
Gabriel de Carvalho Deprá ◽  
Weferson Júnio da Graça ◽  
Carla Simone Pavanelli

ABSTRACT The book “Peixes da planície de inundação do alto rio Paraná e áreas adjacentes” represents the most cohesive data compilation for the rio Paraná floodplain. However, considering the dynamicity of the taxonomy of freshwater fishes, several new records and taxonomic changes occurred along the past years. Therefore, the results of that publication were revisited, providing an update of the species list, their taxonomic status, records and geographic distribution, and also new keys for genera and species. The species included were those recorded in the rio Paraná basin, from the mouth of the rio Paranapanema to the Itaipu Reservoir, following the general methodology presented in the book. A total of 10 orders, 41 families, 126 genera, and 211 species were registered, with an increase of one order, six families, 14 genera, and 29 species when compared to the book. Additionally, four new genera recently described, five synonymization proposals, 14 new identifications, four new combinations, 12 new species recently described, 34 new records, and nine misidentified species were recorded. These results are associated with the redirection of human and financial resources to that area, which enabled monitoring and intensive exploration of its watercourses; as well as training of taxonomists, and new taxonomic resolutions.


2015 ◽  
Vol 65 (Pt_7) ◽  
pp. 2342-2342 ◽  
Author(s):  
Aharon Oren ◽  
and George M. Garrity

We propose emendation of Rule 27(2)(b) of the International Code of Nomenclature of Prokaryotes so that for new combinations the basonym and its reference must be given. We also propose minor changes to Note 1 and Note 2 of Rule 27.


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 ◽  
2016 ◽  
Vol 252 (3) ◽  
pp. 228 ◽  
Author(s):  
ALEXANDER B. DOWELD

The creation of the International Fossil Plant Names Index (IFPNI, 2014 onwards) with the aim of listing of all fossil plant species reveals a few new cases of homonymy between fossil and extant species. In the present paper there are proposed two new combinations in Hemitrapa Miki (1941: 289) and four replacing names for later homonyms of Trapa Linnaeus (1753: 120) that are illegitimate (Art. 53.1 of the International Code of Nomenclature for Algae, Fungi and Plants—ICN, McNeill et al., 2012).


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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