scholarly journals Quercus rajushkinae, a new name for Quercus lavrovii Rajushkina (Fagaceae)

Phytotaxa ◽  
2015 ◽  
Vol 221 (1) ◽  
pp. 100 ◽  
Author(s):  
Alexander Borisovitch Doweld

The fossil species Quercus lavrovii Rajushkina (1987: 146) was described on the fossil leaf remains of an oak from the Miocene sediments of Dzhungarian Aktau, Ili depression (Kazakhstan, Central Asia). However, according to Art. 53.1 of ICN (McNeill et al. 2012) this name is illegitimate because of the existence of an overlooked earlier homonym, Quercus lavrovii Budantsev (1955: 93) which was originally described from the earlier Oligocene deposits of Bestau, Turgay (Kazakhstan). The homonymy between these fossil species emerged during the creation of the International Fossil Plant Names Index, which is planned to list all fossil plant species (IFPNI 2014 onwards). Since the preoccupied species P. lavrovii Rajushk. is systematically recognized as a valid species in current use and it does not have any synonym, a nomen novum, Q. rajushkinae, is here formally proposed as a replaced name.

Phytotaxa ◽  
2015 ◽  
Vol 226 (2) ◽  
pp. 199
Author(s):  
Alexander Borisovitch Doweld

The fossil species Chara elliptica Nikolskaja (1984: 1092) was established on the gyrogonite remains from the Holocene sediments of Majkara (Kazakhstan, Central Asia). However, according to Art. 53.1 of ICN (McNeill et al., 2012) this name is illegitimate because of the existence of an overlooked earlier homonym, Chara elliptica Fritzsche (1924: 93) which was originally described from the earlier Cretaceous (Campanian) deposits of Tres Cruces and Negra Muerta, Province Jujuy, North Argentina (South America). Due to the creation of the International Fossil Plant Names Index with listing of all fossil plant and algal species, the fact of the homonymy between fossil species was solidly established (IFPNI, 2014-).


Phytotaxa ◽  
2016 ◽  
Vol 243 (2) ◽  
pp. 190 ◽  
Author(s):  
Alexander Borisovitch Doweld

The International Fossil Plant Names Index (IFPNI, 2014 onwards) lists some fossil plant species names which have precedence over homonymic extant species names. A few cases of the homonymy between extant and fossil species were recently resolved (Turner 2014, Doweld 2015a, 2015b, 2015c, 2015d).


Phytotaxa ◽  
2020 ◽  
Vol 460 (3) ◽  
pp. 235-236
Author(s):  
ALEXANDER B. DOWELD

In revising fossil records of the genus Styrax Linnaeus (1753: 444) for the International Fossil Plant Names Index (IFPNI, 2014 onwards) with the aim of listing all fossil plant species (Doweld 2015, 2016a), it became apparent that a few fossil-species are later illegitimate homonyms of the extant species of Styrax, and their nomenclature was recently resolved by proposing new replacement names for them (Doweld 2016b). However, an additional case of the homonymy of an extant species by a preoccupied name in fossils remained unsettled.


Phytotaxa ◽  
2015 ◽  
Vol 227 (3) ◽  
pp. 299 ◽  
Author(s):  
Alexander Borisovitch Doweld

The creation of the International Fossil Plant Names Index (IFPNI 2014 onwards, Doweld 2015) with listing of all fossil plant, algal and fungal species reveals the homonymy between fossil-species belonging to genus Elaeocarpus Linnaeus (1753: 515). The fossil-species Elaeocarpus microphyllus Budantsev & Sveshnikova (1964: 102) was described based on the leaf remains from the Tertiary (Oligocene) sediments near Svetlogorsk, Kaliningrad region, Russian Federation (former East Prussia). However, Elmer (1911) and independently Warburg (1922), proposed the earlier homonyms Elaeocarpus microphyllus Elmer (1911: 1189) and E. microphyllus Warburg (1922: 328) respectively, which were overlooked. According to Art. 53.1 of the ICN (McNeill et al. 2012), a junior fossil homonym, Elaeocarpus microphyllus Budants. & Sveshn. is illegitimate and hence a new name is proposed here. A new nomenclatural act was registered through a pilot registration version in the International Fossil Plant Names Index (IFPNI 2014 onwards), with unique persistent registration barcode (LSID) listed under each newly proposed fossil plant taxon.


Phytotaxa ◽  
2015 ◽  
Vol 231 (1) ◽  
pp. 99 ◽  
Author(s):  
Alexander Borisovitch 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. The name Cissus spectabilis (Kurz) Planchon (1887: 1092), originally published as Vitis spectabilis Kurz (1874: 196), is an illegitimate later homonym of Cissus spectabilis Heer (1878: 45) (Art. 53.1 of the ICN, McNeill et al., 2012). C. spectabilis Heer is a fossil-species currently accepted (Kirchheimer 1939, Sosnowsky 1949, 1974, Kryshtofovich & Baikovskaja 1960), described from the Upper Cretaceous (Coniacian) deposits of Sakhalin island (Far East, Russian Federation). Since the preoccupied extant species C. spectabilis (Kurz) Planch., a narrow Indian endemic restricted to Sikkim, Siliguri and neighboring localities of West Bengal, is also currently recognized as a valid species (The Plant List 2013 onwards; eFlora of India 2014 onwards) and it does not have any synonym, a nomen novum, C. notabilis, is here formally proposed as a replacement name.


Phytotaxa ◽  
2015 ◽  
Vol 239 (2) ◽  
pp. 199
Author(s):  
Sergei Vasilyevich Vikulin

The fossil species  Oreodaphne obtusifolia Berry (1916: 301) was described, based on the fossil leaf remains of the most abundant laurel from the Early Eocene Wilcox Group sediments of Holly Springs: Marshall Co, Grenada Co., Miss.: Mississippi embayment (Southeastern North America). Nowadays, most systematists consider the extant Oreodaphne to be a member of Ocotea (Mez, 1889: 219; Rohwer, 1986; van der Werff, 2002; Chanderbali et al., 2001). LaMotte (1952) transferred Berry’s (1916: 301) combination to Ocotea, and this transfer was followed by Dilcher (1963), who reinforced attribution of Wilcox leaf megafossils to Ocotea by cuticular analysis of epidermis and stomata (Dilcher & Lott, 2005). However, according to Art. 53.1 of the ICN (McNeill et al.  2012) the name Ocotea obtusifolia (Berry) LaMotte (1952) is illegitimate because of the existence of the earlier overlooked homonym, Ocotea obtusifolia Kunth (1817: 165–166), an extant lauraceous species from Colombia (Muséum National d’Histoire Naturelle, holotype: http://plants.jstor.org/stable/10.5555/al.ap.specimen.P00128771). The homonymy between these fossil and extant American species of Ocotea was revealed during the description of the new fossil Early Oligocene species Ocotea rossica Vikulin from the south of the Middle-Russian upland (Vikulin, 2015: 326). Since Ocotea obtusifolia (Berry) LaMotte has been systematically recognized as a valid species in current use and it does not have any synonym, a nomen novum, O. dilcherii, is formally proposed here as a replaced name. Because a type specimen was not indicated among the validating illustrations of Berry (1916: pl. 80, fig. 1; pl. 83, fig. 2–5, and pl. 84, fig. 1 and 2), a lectotype must be designated here, from the specimens illustrated in the protologue (Berry, 1916: 301–302) amongst those perfect specimens with blunt leaf apex, which are very abundant in the clays at Puryear, Tenn. (Proposed lectotype: paleobotany collection # USNM 35867, Smithsonian National Museum of Natural History (USA), illustrated in Berry, 1916: 301, pl. 83, fig. 5.


Phytotaxa ◽  
2021 ◽  
Vol 490 (3) ◽  
pp. 298-300
Author(s):  
PEDRO LUÍS RODRIGUES DE MORAES

In the present communication, after checking fossil plant names in the International Fossil Plant Names Index (IFPNI 2014–onwards), the homonymy of two fossil and extant species names of Ocotea Aublet (1775: 780) has been detected and resolved. Ocotea alata van der Werff (1991: 416) (extant) is replaced by a new name O. loretensis nom. nov., because of the earlier homonym O. alata Givulescu (1975: 173) (fossil leaves), according to Article 53.1 of the ICN (Turland et al. 2018). Similarly, O. morona-santiagoensis nom. nov. is proposed to replace the later illegitimate homonym O. pilosa van der Werff (2020: 220) (extant) non O. pilosa Givulescu (1975: 172) (fossil leaves). An additional homonym was found in extant Litsea Lamarck (1792: 574) that is preoccupied by a fossil. However, since it is currently recognized as a taxonomic synonym of Litsea tomentosa Blume (1826: 566), there is no need to create a nomen novum for it.


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 297 (1) ◽  
pp. 62 ◽  
Author(s):  
ALEXANDER B. DOWELD

The nomenclature of some fossil and extant homonymic species of Aralia is resolved. Aralia laevis J. Wen (extant) is replaced by a new name A. indonesica nom. nov., because of earlier homonym, A. laevis E.M.Reid (fossil). Aralia debilis J. Wen is rehabilitated as a legitimate substitute to the later homonym, A. elegans Ho, due to the existence of several earlier homonyms, the extant A. elegans Linden ex Koch, A. elegans Cunn. ex W.Hill and A. elegans Hort. ex Saporta, and the fossil A. elegans Velenovský. Additional four new replacement names are proposed for fossil species based on endocarp remains from the Miocene sediments of Siberia: Aralia asiatica nom. nov. for A. rugosa Dorofeev non Blume, A. mammuthica nom. nov. for A. dubia V.P. Nikitin non Sprengel nec Fontaine, A. borealis nom. nov. for A. tertiaria Dorofeev non Pilar, and A. tobolica nom. nov. for A. lucida Dorofeev non Hasskarl. The later homonym A. angustiloba Kolakovsky non Lesquereux, based on the fossil foliage from the Pliocene sediments of Transcaucasus, is transferred into Brassaiopsis as B. kolakovskyana nom. nov. Fossil species A. furcata, described on the basis of leaf remains from the Upper Cretaceous (Cenomanian) of Bohemia, is transferred into Haliserites as H. furcatus comb. nov. The fossil later homonym A. serrata Knowlton non Saporta, described on the basis of leaf remains from the Palaeocene of North America, is transferred into Platanus as P. serrata nom. nov.


Phytotaxa ◽  
2019 ◽  
Vol 388 (2) ◽  
pp. 179
Author(s):  
ALEXANDER B. DOWELD

New names are proposed for the fossil European Tertiary species of Ilex (The Palaeoflora Europaea Project): Ilex angustifolioides nom. nov., Ilex boulayi nom. nov., Ilex friedrichii nom. nov., Ilex latifolioides nom. nov., and Ilex opacina nom. nov. Ilex integrifolia Baikovskaja from Central Asia is renamed Ilex aschutassica nom. nov. (non extant Ilex integrifolia Hort. ex Vilmorin and Ilex integrifolia Chapman ex Knowlton). Ilex mormonica nom. nov. of North America is proposed in place of Ilex acuminata Becker (fossil) non Ilex acuminata Willdenow (extant). Ilex polarica nom. nov. from Greenland is validated in place of Ilex macrophylla Heer (fossil) non Ilex macrophylla Blume (extant). Ilex fortunensis Hahn (extant) is renamed Ilex hahnii nom. nov. (not fossil Ilex fortunensis van der Burgh). Ilex subrotunda sp. nov. is validated instead of the previously invalidly published I. ohashii, lacking holotype designation when published. Fossil-species of Ilex, based on the dispersed pollen, Ilex major, I. colchiciformis, I. hyrcaniformis, I. macroclavata, I. tener, are transferred to the pollen fossil-genus Ilexpollenites. Fossil-species based on leaves, Ilex artocarpidioides and Ilex ovata are segregated into a separate genus Celastrilex gen. nov. Fossil-species Ilex pseudostenophylla, based on leaf remains, is excluded from Ilex and placed into a new fossil-genus Frangulops gen. nov. The following new combinations are proposed: Ilex ulmacea comb. nov., Ilexpollenites: Ilexpollenites major comb. nov., I. colchiciformis comb. nov., I. hyrcaniformis comb. nov., I. macroclavata comb. nov., I. tener comb. nov.; Celastrilex artocarpidioides, C. populifolia; Frangulops pseudostenophylla. Furthermore, Celastrus ulmaceus is neotypified; Ilex acuminata Saporta, I. berberidifolia, I. mougeotii and I. rueminiana are lectotypified.


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