A synopsis of American Salix

1976 ◽  
Vol 54 (24) ◽  
pp. 2769-2789 ◽  
Author(s):  
Robert D. Dorn

The classification of American Salix (willows) is updated to account for nomenclatural changes, new species and sections, and new data. Evolutionary relationships, biology, and nomenclatural difficulties in the genus are briefly discussed. A preliminary, simplified key to sections is presented along with a synopsis of subgenera, sections, and subsections. One new section and two new subsections are described. Six new combinations are also made. The important literature is cited.

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.


Bothalia ◽  
2010 ◽  
Vol 40 (1) ◽  
pp. 1-36 ◽  
Author(s):  
H. P. Linder ◽  
C. R. Hardy

We propose a new generic classification of the African Restionaceae, tribe Restioneae (subfamily Restionoideae), based on the phylogeny and on extensive morphological data. The phylogeny is based on both plastid sequence data and morphological data. We delimit the genera to be monophyletic, to minimize the nomenclatural changes, and to maximize the ability to diagnose the genera. We recognize eight genera, one of which with nine subgenera, in the tribe. Of the currently accepted genera, only three need changes. We provide descriptions for all genera and subgenera, and include a key to them. In this paper we erect one new genus, Soroveta. redelimit Platycaulos and Restio, and reduce Calopsis and Ischyrolepis to synonomy under Restio. We list the species which we recognize under each genus, make 37 new combinations, propose eight new names, and also describe eight new species that belong in these genera.


Zootaxa ◽  
2016 ◽  
Vol 4202 (1) ◽  
pp. 1 ◽  
Author(s):  
MAXIM NABOZHENKO ◽  
BEKIR KESKIN

A revision of the genus Odocnemis of Turkey, the Caucasus and Iran is presented. Thirty species and four subspecies are distributed in this territory. The following 20 new species and subspecies are described: O. dichroa sp. n., O. allardi sp. n., O. merkli sp. n., O. seducta sp. n., O. aegaeica sp. n., O. euritopica sp. n., O. subtuberculigera sp. n., O. subtuberculigera thracica subsp. n., O. erseni sp. n., O. molecularica sp. n., O. shokhini sp. n., O. inornata sp. n., O. altimontana sp. n., O. amanosica sp. n., O. cordiformis sp. n., O. kakunini sp. n. O. evestigata sp. n., O. torosica sp. n., O. torosica subangulata subsp. n., Odocnemis hakkariensis sp. n. The name of the genus is feminine, therefore all species names are transformed from masculine to feminine. Almost all new taxa are described from Turkey; O. amanosica sp. n. is additionally recorded from Syria, O. allardi sp. n.—from Armenia, Azerbaijan (Nakhchivan) and Iran, O. kakunini sp. n. from Iran. New synonymies are established: Odocnemis anatolica (Pic, 1899) = Stenomax korbi Reitter 1902: 219, syn.n.; Odocnemis recticollis (Allard, 1877) = Stenomax kurdistanus Reitter, 1902: 221, syn.n.; Odocnemis punctata Allard, 1876 = Cylindronotus (Odocnemis) pseudoclarus Reitter, 1922, syn.n. The following lectotypes are designated: Helops (Odocnemis) anatolicus Pic, 1899, Helops (Stenomax) seriegranatus Seidlitz, 1896, Cylindronotus (Odocnemis) opertus Reitter, 1922, Stenomax recticollis Allard, 1876, Odocnemis punctata Allard, 1876, Helops (Odocnemis) protinus Reitter in Bodemeyer, 1900. Holotypes and paratypes of all other Turkish species of Odocnemis are studied. Two new combinations are established: Odocnemis gloriosa (Faldermann, 1837), comb. n. (from Nalassus Mulsant, 1854) and Odocnemis terminasianae (Nabozhenko, 2011), comb. n. (from Armenohelops Nabozhenko, 2002). Five species O. bosphoranus (Allard, 1876), O. amasiae (Seidlitz, 1896), O. scutellatus (Reitter, 1902), O. fundator (Reitter, 1908), O. strangulatus (Reitter, 1922)) are not revised in this work and will be included in the genus Armenohelops in a future revision. Three species which were previously recorded from Turkey erroneously (O. exarata (Germar, 1817), O. crenatostriata (Allard, 1877), O. caudata Allard, 1876) should be removed from the Turkish list. Eight species-groups are characterized in the paper. The following aspects are considered and discussed: classification of the genus, morphology and main evolutionary tendencies, distribution and bionomics. A key to the Turkish, Caucasian and Iranian species of    Odocnemis is given. 


Zootaxa ◽  
2016 ◽  
Vol 4206 (1) ◽  
pp. 1 ◽  
Author(s):  
MUSTAFA ÜNAL

The very rich material of Palaearctic Pamphagidae preserved in the collections including the type specimens of all taxa, the historical unidentified specimens and newly collected material have been studied. 58 genera and 295 species and subspecies are listed. The higher classification of the family is reviewed mainly based on the male phallic complex as well as the traditional and some new external characters. The tribe Haplotropiidini is transferred to the subfamily Thrinchinae. Previously synonymized subfamily Tropidaucheninae is validated as an independent tribe of Pamphaginae. The tribe Nocarodeini is taxonomically reviewed except the genus Bufonocarodes Mistshenko. The male phallic complex is also used as one of the main characters in decisions of the genus group taxa. The following 10 genera are synonymized: Pseudotmethis Bey-Bienko, 1948 and Paratmethis Zheng & He, 1996 (with Filchnerella Karny, 1908), Sinotmethis Bey-Bienko, 1959 and Kanotmethis Yin, 1994 (with Beybienkia Tsyplenkov, 1956), Paktia Pfadt, 1970 (with Mistshenkoella Cejchan, 1969), Pseudosavalania Demirsoy, 1973 (with Paranocarodes I. Bolívar, 1912), Nocaropsis Ramme, 1951 (with Paranothrotes Mistshenko, 1951), Paranocaracris Mistshenko, 1951 and Oronothrotes Mistshenko, 1951 (with Nocaracris Uvarov, 1928) and Savalania Mistshenko, 1951 (with Nocarodes Fischer von Waldheim, 1846). The genera Mistshenkoella Cejchan and Cryptonothrotes La Greca are proposed as subgenera of Saxetania Mistshenko. The following genera are divided: Eremocharis Saussure into 4 species groups, Paranocarodes I. Bolívar into 2 species groups, Paranothrotes Mistshenko into 4 species groups, Nocaracris Uvarov into 7 species groups and Nocarodes Fischer von Waldheim into 4 species groups. The following 24 species and subspecies are synonymized: Tmethis cinerascus cyanipes Werner, 1939 [with Eremopeza angusta (Uvarov, 1934)], Iranotmethis cyanipennis cyanipes Bey-Bienko, 1951 [with Iranotmethis cyanipennis iranicus (Werner, 1939)], Eremocharis granulosa roseipes Uvarov, 1943 [with Eremocharis granulosa granulosa (Walker, 1871)], Eremocharis subsulcata minor Cejchan, 1969 (with Eremocharis maior Ramme, 1952), Asiotmethis limbatus motasi Ramme, 1951 [with Asiotmethis limbatus (Charpentier, 1845)], Tropidauchen marginatum Bolívar, 1912 (with Tropidauchen escalerai Bolívar, 1912), Paranocarodes straubei serratus Uvarov, 1949, Paranocarodes straubei insularis Ramme, 1951 and Paranocarodes fieberi mytilenensis Ramme, 1951 [with Paranocarodes fieberi (Brunner von Wattenwyl, 1882)], Paranocarodes atympanicus Ramme, 1951 (with Paranocarodes tolunayi tolunayi Ramme, 1949), Paranocarodes cilicicus Ramme, 1951 (with Paranocarodes lubricus Mistshenko, 1951), Paranothrotes opacus hakkariana Demirsoy, 1973 [with Paranothrotes opacus opacus (Brunner von Wattenwyl, 1882)], Paranothrotes tenuicornis sordidus Mistshenko, 1951 and Paranothrotes iranicus (Ramme, 1951) (with Paranothrotes tenuicornis Mistshenko, 1951), Paranothrotes elbursianus (Ramme, 1951) [with Paranothrotes demawendi (Ramme, 1951)], Paranocarodes aserbeidshanicus Ramme, 1951 [with Paranothrotes margaritae (Miram, 1938)], Nocaracris burri obscurata Ramme, 1951 [with Nocaracris furvus furvus (Mistshenko, 1951)], Paranocaracris rimansonae ventosus Mistshenko, 1951 [with Nocaracris rimansonae (Uvarov, 1918)], Paranocaracris rigidus Mistshenko, 1951 (with Nocaracris tauricolus Ramme, 1951), Nocaracris cyanipes tristis Ramme, 1951 [with Nocaracris cyanipes (Motschulsky, 1846)], Nocarodes armenus Ramme, 1951 (with Nocarodes serricollis Fischer von Waldheim, 1846), Nocarodes specialis Mistshenko, 1951 [with Nocarodes iranicus (Werner, 1939)], Nocarodes gibbosus Mistshenko, 1951 (with Nocarodes humerosus Mistshenko, 1951), Nocarodes urmianus carinatus Mistshenko, 1951 (with Nocarodes urmianus Ramme, 1939). One new genus in the tribe Nocarodeini, Turkanocaracris Ünal gen. nov., and the following 29 new species and subspecies in four tribes are described: Eremopeza soltanii Ünal, sp. nov., Eremopeza kashmirensis Ünal, sp. nov., Eremocharis subsulcata beccalonii Ünal, ssp. nov., Orchamus massai Ünal, sp. nov., Paracinipe suezensis Ünal & Massa, sp. nov., Saxetania (Mistshenkoella) gorochovi Ünal, sp. nov., Paranocarodes anatoliensis anamas Ünal, ssp. nov., Paranothrotes buzuldagi Ünal, sp. nov., Paranothrotes dentatus Ünal, sp. nov., Paranothrotes eximius bitlis Ünal, ssp. nov., Paranothrotes siirt Ünal, sp. nov., Nocaracris furvus kazdagi Ünal, ssp. nov., Nocaracris istanbul Ünal, sp. nov., Nocaracris tunceli Ünal, sp. nov., Nocaracris tardus Ünal, Bugrov & Jetybayev, sp. nov., Nocaracris emirdagi Ünal, sp. nov., Nocaracris cejchani Ünal, sp. nov., Nocaracris judithae Ünal, sp. nov., Nocaracris minutus Ünal, sp. nov., Nocaracris karadagi Ünal, sp. nov., Nocaracris palandoken Ünal, sp. nov., Nocaracris monticolus Ünal, sp. nov., Nocaracris van Ünal, sp. nov., Nocaracris dilekensis Ünal, sp. nov., Nocaracris karshitoros Ünal, sp. nov., Nocaracris goektepe Ünal, sp. nov., Nocaracris crassipes Ünal, sp. nov., Turkanocaracris levigatus Ünal, sp. nov., Turkanocaracris davisi Ünal, sp. nov. Lectotypes are designated for the following 12 species: Strumiger desertorum desertorum Zubovski, 1896, Ocnerosthenus brunnerianus (Saussure, 1887), Orchamus gracilis (Brunner von Wattenwyl, 1882), Saxetania iranicum (Werner, 1939) [syn. of Saxetania (s.str.) cultricolle (Saussure, 1887)], Paranocarodes straubei (Fieber, 1853), Paranocarodes fieberi (Brunner von Wattenwyl, 1882), Paranothrotes shelkovnikovi (Uvarov, 1918), Paranothrotes nigripes (Stshelkanovtzev, 1916), Eunothrotes derjugini Adelung, 1907, Nocaracris rimansonae (Uvarov, 1918), Nocaracris tridentatus (Stshelkanovtzev, 1916) and Araxiana woronowi (Uvarov, 1918). Many species are given in new combinations and new statuses. Some taxa are proposed as reverted combinations, reverted statuses, reverted genera, species and subspecies. Nomenclatural problems are discussed under the relevant taxa. The authorship of 4 species are discussed and changed as follow: Eremopeza festiva (I. Bolívar, 1884), Paranocarodes tolunayi tolunayi Ramme, 1949, Nocaracris rubripes (Motschulsky, 1846), Nocaracris cyanipes (Motschulsky, 1846). Identification keys for subfamilies, tribes and genera (except the N. African and European genera of Pamphagini) and for each level of the tribe Nocarodeini are prepared. This study is also a review of the Pamphagidae species of Turkey. Therefore all Turkish species are studied in detail except the two genera recently revised by the author, Glyphotmethis Bey-Bienko and Asiotmethis Uvarov. Geographically this paper includes all Pamphagidae species of the following countries and regions: Bulgaria, Turkey, Cyprus, Syria, Israel, Palestine, Jordan, Iraq, Armenia, Georgia, Nakhichevan, Azerbaijan, Pakistan, Greece (except one species), Lebanon (except two species), Arabian Peninsula (except one species), Afghanistan (except some Saxetania) and Iran (except some Saxetania and Tropidauchen). In addition, 848 original figures including 10 distributional maps are provided. 


1954 ◽  
Vol 1 (3) ◽  
pp. 227-248 ◽  
Author(s):  
C. E. van Rooyen

Holmes's classification of the animal viruses, Suborder III, Zoophagineae, has been revised and extended. Four new families, eight new genera, thirty-one new species, sixteen new combinations, and nine new subspecies have been added. A list of these is contained in the summary of proposals. The International Bacteriological Code of Nomenclature provides guidance for the use of the Linnaean system of binomial nomenclature in the orderly naming of a wide range of microbial species. Like the bacteria, the viruses are amenable to orderly arrangement and classification, and the several types may be satisfactorily named.


1997 ◽  
Vol 10 (3) ◽  
pp. 381 ◽  
Author(s):  
M. Lazarides

On the basis of morphological data presented herein, Plectrachne Henr. is included in Triodia R.Br. This congeneric change requires 15 new combinations and three new nominations. In Triodia R.Br. sens. lat., 11 new species are proposed, one subspecies is raised to specific rank, while three species and six varieties are reduced to synonyms. For the first time, Triodia melvillei and T. schinzii are recorded for South Australia, T. bunicola for Victoria, T. mollis for Queensland and T. marginata for New South Wales. Although probably monophyletic, Triodia as here interpreted is widely variable. Thus, a classification of nine informal infrageneric groups is proposed.


Phytotaxa ◽  
2019 ◽  
Vol 398 (1) ◽  
pp. 1 ◽  
Author(s):  
BENOÎT LOEUILLE ◽  
JOÃO SEMIR ◽  
JOSÉ R. PIRANI

A new classification of the subtribe Lychnophorinae is proposed based on the results of phylogenetic analyses. The subtribes Centratherinae and Sipolisiinae are synonyms of Lychnophorinae and three genera (Albertinia, Blanchetia, Gorceixia) are transferred to the subtribe. As now circumscribed, Lychnophorinae comprises 19 genera and 117 species distributed mostly in the Cerrado domain of the Brazilian Central Plateau. Oiospermum is synonymized under Centratherum, and Irwinia under Blanchetia. Because Lychnophora as currently circumscribed is paraphyletic, the genus is dismantled into three monophyletic genera: Lychnophora s.s., Lychnocephalus and a new genus described herein, Lychnophorella. Seven new species are described (Chronopappus lanatus, Lychnophora grisea, L. haplopappa, Lychnophorella jacobinensis, Piptolepis riparia, Prestelia espeletoidea and Proteopsis hermogenesii), 16 new combinations are proposed (Eremanthus reticulatus, E. syncephalus, Lychnocephalus humillimus, L. mellobarretoi, L. sellowii, Lychnophora hatschbachii, Lychnophorella blanchetii, L. bishopii, L. leucodendron, L. morii, L. regis, L. santosii, L. sericea, L. triflora, Piptolepis pabstii, Prestelia purpurascens) as well as eight new synonyms. We also propose a neotype for Ampherephis pulchella, an epitype for Crantzia ovata and lectotypes for 31 names including six second-step lectotypifications (Albertinia brasiliensis, A. polycephala, Ampherephis intermedia, Centratherum fruticosum, Eremanthus leucodendron, E. purpurascens, Gorceixia decurrens, Lychnophora albertinioides, L. brunioides, L. microphylla, L. pohlii, L. reticulata, L. rosmarinus var. affinis, L. rosmarinus var. normalis, L. sellowii, Piptolepis gardneri, Proteopsis sellowii, Symblomeria baldwiniana, Vanillosmopsis albertinioides, V. glomerata, V. pohlii, V. syncephala, Vernonia burchelliana, V. ericoides, V. imbricata, V. involucrata, V. leptospermoides, V. martiana, V. platycephala, V. pseudomyrtus and V. trichocarpha).


Phytotaxa ◽  
2013 ◽  
Vol 110 (1) ◽  
pp. 1 ◽  
Author(s):  
DOMINGOS CARDOSO ◽  
HAROLDO CAVALCANTE DE LIMA ◽  
LUCIANO PAGANUCCI DE QUEIROZ

Morphological and molecular phylogenetic evidence strongly demonstrated the paraphyly of the Genistoid legume genus Diplotropis with respect to the recently described monospecific Guianodendron (a segregate of Acosmium sensu lato). In order to achieve a phylogenetically based classification of the group, the new Amazonian genus Staminodianthus D.B.O.S. Cardoso, H.C. Lima & L.P. Queiroz is described and illustrated to accommodate three species previously placed in Diplotropis sect. Racemosae. We present a synopsis for Staminodianthus, including geographical distribution, lectotypification, and new species circumscriptions of the following three new combinations: Staminodianthus duckei (Yakovlev) D.B.O.S. Cardoso & H.C. Lima, Staminodianthus racemosus (Hoehne) D.B.O.S. Cardoso & H.C. Lima, and Staminodianthus rosae (H.C. Lima) D.B.O.S. Cardoso & H.C. Lima. Staminodianthus differs most notably from its sister genus Guianodendron by having bilaterally symmetrical flowers, calyces with a curved hypanthium, a well-differentiated standard petal, lateral and lower petals without auricles, and the androecium with a combination of five fertile stamens and five short staminodes, a unique feature within the Genistoid legumes.


2020 ◽  
Vol 45 (4) ◽  
pp. 794-801
Author(s):  
Caroline Oliveira Andrino ◽  
Marcelo Fragomeni Simon ◽  
Jair Eustáquio Quintino Faria ◽  
André Luiz da Costa Moreira ◽  
Paulo Takeo Sano

Abstract—We describe and illustrate Paepalanthus fabianeae, a new species of Eriocaulaceae from the central portion of the Espinhaço Range in Minas Gerais, Brazil. Previous phylogenetic evidence based on analyses of nuclear (ITS and ETS) and plastid (trnL-trnF and psba-trnH) sequences revealed P. fabianeae as belonging to a strongly supported and morphologically coherent clade containing five other species, all of them microendemic, restricted to the Espinhaço range. Due to the infrageneric classification of Paepalanthus being highly artificial, we preferred not assigning P. fabianeae to any infrageneric group. Paepalanthus fabianeae is known from two populations growing in campos rupestres (highland rocky fields) in the meridional Espinhaço Range. The species is characterized by pseudodichotomously branched stems, small, linear, recurved, and reflexed leaves, urceolate capitula, and bifid stigmas. Illustrations, photos, the phylogenetic position, and a detailed description, as well as comments on habitat, morphology, and affinities with similar species are provided. The restricted area of occurrence allied with threats to the quality of the habitat, mainly due to quartzite mining, justifies the preliminary classification of the new species in the Critically Endangered (CR) category using the guidelines and criteria of the IUCN Red List.


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