Cladistic analysis and revision of Billardiera (Pittosporaceae)

2004 ◽  
Vol 17 (1) ◽  
pp. 83 ◽  
Author(s):  
L. W. Cayzer ◽  
M. D. Crisp ◽  
I. R. H. Telford
Keyword(s):  
New Taxa ◽  
Cladistic Analysis ◽  
Species Level ◽  
Morphological Data ◽  
New Combinations ◽  
The Family ◽  
Cladistic Analyses ◽  
Definition Of ◽  
First Time

Cladistic analyses of morphological data were used to clarify the definition of Billardiera in the context of other genera of the family Pittosporaceae. These analyses indicate that Billardiera s.str. is monophyletic including the small genera Sollya and Pronaya, but excluding Marianthus and Rhytidosporum, which have been previously included in a broader concept of Billardiera. The re-circumscribed Billardiera is revised, incorporating these changes. Five taxa are reinstated at species level (B. fusiformis, B. mutabilis, B. macrantha, B. speciosa and B.�venusta). Three are new combinations (B. fraseri, B. heterophylla, B. drummondii replacing Sollya drummondii) and three new taxa are described for the first time: B. nesophila, B. rubens and B. viridiflora.

Phylogeny and re-definition of the genus Melanophora (Diptera: Rhinophoridae), with description of a new species from Sardinia

Zootaxa ◽  
2009 ◽  
Vol 2318 (1) ◽  
pp. 552-565 ◽  
Author(s):  
PIERFILIPPO CERRETTI ◽  
THOMAS PAPE
Keyword(s):  
New Species ◽  
Type Species ◽  
Cladistic Analysis ◽  
The Other ◽  
New Combinations ◽  
Generic Delimitation ◽  
Definition Of ◽  
First Time ◽  
A New Species

A cladistic analysis of the genus Melanophora Meigen, 1803 (type-species: Musca grossificationis Linnaeus, 1758 [= Musca roralis Linnaeus, 1758]) is presented and the generic delimitation is critically redefined. The nominal genus-group taxon Bequaertiana Curran, 1929 (type-species: Bequaertiana argyriventris Curran, 1929) is synonymised with Melanophora Meigen syn. nov. The following new combinations are proposed: Melanophora argyriventris (Curran, 1929) comb. nov. and Melanophora basilewskyi (Peris, 1957) comb. nov. Melanophora chia sp. nov. from SW Sardinia is described, illustrated and compared with the other known species of the genus. The male of Melanophora asetosa Kugler, 1978 is described for the first time. Melanophora basilewskyi (Peris, 1957) is recorded from Kenya for the first time.

Auranticarpa, a new genus of Pittosporaceae from northern Australia

2000 ◽  
Vol 13 (6) ◽  
pp. 903 ◽  
Author(s):  
Lindy W. Cayzer ◽  
Michael D. Crisp ◽  
Ian R. H. Telford
Keyword(s):  
New Genus ◽  
Monophyletic Group ◽  
New Combinations ◽  
Northern Australia ◽  
The Family ◽  
Cladistic Analyses ◽  
First Time

Following the revision of the family Pittosporaceae in Australia, a new genus, Auranticarpa, is described and monographed here to accommodate a monophyletic group excluded from Pittosporum in cladistic analyses. Auranticarpa occurs mostly in monsoonal northern Australia, and has six species. New combinations are provided for three taxa previously placed in Pittosporum: A. melanosperma, A. resinosa (reinstated this analysis) and A. rhombifolia; and three are described for the first time: A. edentata, A. ilicifolia and A. papyracea.

scholarly journals Systematic revision of the pantropical whip spider family Charinidae Quintero, 1986 (Arachnida, Amblypygi)

2021 ◽  
Vol 772 ◽  
pp. 1-409
Author(s):  
Gustavo Silva de Miranda ◽  
Alessandro P.L. Giupponi ◽  
Lorenzo Prendini ◽  
Nikolaj Scharff
Keyword(s):  
New Species ◽  
Eastern Mediterranean ◽  
Species Level ◽  
New Combinations ◽  
Present Contribution ◽  
Systematic Revision ◽  
C Elegans ◽  
The Family ◽  
Nomina Dubia ◽  
First Time

The whip spider family Charinidae Quintero, 1986 is the most speciose and widely distributed in the arachnid order Amblypygi Thorell, 1883. It comprises three genera and 95 species distributed across all tropical continents and the eastern Mediterranean. Despite recent advances in the taxonomy of the family, a global revision of all its species, necessary to advance understanding of its systematics, biogeography and evolution, has never been conducted. In the present contribution, the family is revised in its entirety for the first time, including all previous names and 33 new species, 24 in the genus Charinus Simon, 1892: C. alagoanus sp. nov., C. apiaca sp. nov., C. carinae sp. nov., C. carioca sp. nov., C. carvalhoi sp. nov., C. cearensis sp. nov., C. diamantinus sp. nov., C. euclidesi sp. nov., C. goitaca sp. nov., C. guayaquil sp. nov., C. imperialis sp. nov., C. loko sp. nov., C. magalhaesi sp. nov., C. miskito sp. nov., C. mocoa sp. nov., C. monasticus sp. nov., C. palikur sp. nov., C. perquerens sp. nov., C. puri sp. nov., C. renneri sp. nov., C. sooretama sp. nov., C. souzai sp. nov., C. susuwa sp. nov., C. una sp. nov.; eight in the genus Sarax Simon, 1892: S. bilua sp. nov., S. dunni sp. nov., S. gravelyi sp. nov., S. indochinensis sp. nov., S. lembeh sp. nov., S. palau sp. nov., S. rahmadii sp. nov., S. tiomanensis sp. nov.; and one in the genus Weygoldtia Miranda et al., 2018: W. consonensis sp. nov. Taxonomic keys to the 132 species (excluding four nomina dubia) are presented and several taxonomic rearrangements implemented. Four subspecies are elevated to species level: Charinus cavernicolus Weygoldt, 2006, C. elegans Weygoldt, 2006, C. longipes Weygoldt, 2006, and Sarax bispinosus (Nair, 1934). Sarax batuensis Roewer, 1962 is removed from synonymy with Sarax buxtoni (Gravely, 1915) and S. buxtoni newly synonymized with Sarax rimosus (Simon, 1901). Stygophrynus moultoni Gravely, 1915 is transferred to Sarax, resulting in Sarax moultoni (Gravely, 1915) comb. nov. Ten species are transferred from Charinus to Sarax, resulting in new combinations: S. abbatei (Delle Cave, 1986) comb. nov., S. bengalensis (Gravely, 1911) comb. nov., S. dhofarensis (Weygoldt, Pohl & Polak, 2002) comb. nov., S. ioanniticus (Kritscher, 1959) comb. nov., S. israelensis (Miranda et al., 2016) comb. nov., S. omanensis (Delle Cave, Gardner & Weygoldt, 2009) comb. nov., S. pakistanus (Weygoldt, 2005) comb. nov., S. seychellarum (Kraepelin, 1898) comb. nov., S. socotranus (Weygoldt, Pohl & Polak, 2002) comb. nov. and S. stygochthobius (Weygoldt & Van Damme, 2004) comb. nov.

Revision of Rhytidosporum (Pittosporaceae)

1999 ◽  
Vol 12 (5) ◽  
pp. 689 ◽  
Author(s):  
L. W. Cayzer ◽  
M. D. Crisp ◽  
I. R. H. Telford
Keyword(s):  
New South ◽  
New South Wales ◽  
Cladistic Analysis ◽  
Taxonomic Status ◽  
Species Level ◽  
Separate Genus ◽  
South Wales ◽  
The Family ◽  
First Time ◽  
Small Genus

As part of a revision of the family Pittosporaceae in Australia, a cladistic analysis was undertaken to resolve the phylogeny of Rhytidosporum and thereby clarify the taxonomic status of this small genus. Rhytidosporum is confirmed as a separate genus, and five species are now recognised: R. alpinum, R. diosmoides, R. inconspicuum, R. procumbens and R. prostratum. Rhytidosporum inconspicuum, found in subalpine areas mainly in Victoria and Tasmania, is described for the first time. Rhytidosporum diosmoides, which ranges from central New South Wales to southern Queensland, is reinstated at species level.

Larval Sphindidae (Coleoptera : Cucujoidea): phylogenetic implications and new descriptions

2000 ◽  
Vol 14 (6) ◽  
pp. 807 ◽  
Author(s):  
Erica Chiao ◽  
Joseph V. McHugh
Keyword(s):  
Cladistic Analysis ◽  
Sister Group ◽  
Sister Group Relationship ◽  
Data Sets ◽  
Strong Impact ◽  
Length Difference ◽  
Phylogenetic Implications ◽  
The Family ◽  
Cladistic Analyses ◽  
First Time

A new phylogenetic hypothesis of Sphindidae (Coleoptera: Cucujoidea) ispresented, based on a cladistic analysis of 15 larval morphology characters inaddition to 39 adult morphology characters modified from a previous study by McHugh (1993). Results from the combined cladistic analyses show larval characters supporting several previously established relationships and resolving the placement of Notosphindus McHugh & Wheeler. The sister-group relationship betweenCarinisphindus McHugh and SphindusMegerle in Dejean is not supported by the combined analyses. Larval charactersdid not show a disproportionately strong impact on the more basal nodes.Incongruence length difference analysis found an insignificant level ofdiscordance (P = 0.197) between the adult andlarval based data sets. Larval Notosphindus slateriMcHugh & Wheeler, Genisphindus minor McHugh andCarinisphindus purpuricephalus McHugh & Lewis aredescribed for the first time, representing the first larval descriptions forthese genera. A literature review of immature stages of sphindid beetles and ageneric level key to larvae of the family are provided.

First record of the family Caliscelidae (Hemiptera: Fulgoroidea) from Madagascar, with description of new taxa from the Afrotropical Region and biogeographical notes

Zootaxa ◽  
2009 ◽  
Vol 2020 (1) ◽  
pp. 1-36 ◽  
Author(s):  
VLADIMIR M. GNEZDILOV ◽  
THIERRY BOURGOIN
Keyword(s):  
South Africa ◽  
New Taxa ◽  
First Record ◽  
Species Level ◽  
The Family ◽  
Afrotropical Region ◽  
First Time

The family Caliscelidae is revised and listed in the Afrotropical Region and is recorded from Madagascar for the first time. Signoreta victorina gen. et sp. n., Calampocus sphaeroides gen. et sp. n., Patamadaga pauliani gen. et sp. n., Sphenax cuneus gen. et sp. n., Afronaso gryphus sp. n. and A. malagasicus sp. n. are described from Madagascar. Rhinoploeus iwa gen. et sp. n. is described from Zambia and Caliscelis swazi sp. n. from Republic of South Africa and Swaziland. Nubianus gen. n. is erected for Issopulex nasutus Linnavuori, 1973. Issopulex chloe Linnavuori, 1973 is transfered to the genus Savanopulex Dlabola and Caliscelis eximia Stål, 1859 to the genus Chirodisca Emeljanov. Afronaso rhinarius cuneiceps Fennah, 1957 is upgraded to species level. Populonia curculioforma Dlabola, 1987 is placed in synonymy under A. rhinarius cuneiceps, Populonia hammersteini Schmidt, 1932 under Homaloplasis curvata Melichar, 1908, Ugandana fennahi Dlabola, 1987 under Afronaso bayoni Schmidt, 1911, and Caliscelis dreyfus Fernando, 1957 under Caliscelis eximia Stål, 1859. New faunistic records are proposed. The possible Gondwanan origin and monophyly of the Caliscelidae are briefly discussed.

scholarly journals Systematic revision of the pantropical whip spider family Charinidae Quintero, 1986 (Arachnida, Amblypygi)

2021 ◽  
Vol 772 ◽  
pp. 1-409
Author(s):  
Gustavo Silva de Miranda ◽  
Alessandro P.L. Giupponi ◽  
Lorenzo Prendini ◽  
Nikolaj Scharff
Keyword(s):  
New Species ◽  
Eastern Mediterranean ◽  
Species Level ◽  
New Combinations ◽  
Present Contribution ◽  
Systematic Revision ◽  
C Elegans ◽  
The Family ◽  
Nomina Dubia ◽  
First Time

The whip spider family Charinidae Quintero, 1986 is the most speciose and widely distributed in the arachnid order Amblypygi Thorell, 1883. It comprises three genera and 95 species distributed across all tropical continents and the eastern Mediterranean. Despite recent advances in the taxonomy of the family, a global revision of all its species, necessary to advance understanding of its systematics, biogeography and evolution, has never been conducted. In the present contribution, the family is revised in its entirety for the first time, including all previous names and 33 new species, 24 in the genus Charinus Simon, 1892: C. alagoanus sp. nov., C. apiaca sp. nov., C. carinae sp. nov., C. carioca sp. nov., C. carvalhoi sp. nov., C. cearensis sp. nov., C. diamantinus sp. nov., C. euclidesi sp. nov., C. goitaca sp. nov., C. guayaquil sp. nov., C. imperialis sp. nov., C. loko sp. nov., C. magalhaesi sp. nov., C. miskito sp. nov., C. mocoa sp. nov., C. monasticus sp. nov., C. palikur sp. nov., C. perquerens sp. nov., C. puri sp. nov., C. renneri sp. nov., C. sooretama sp. nov., C. souzai sp. nov., C. susuwa sp. nov., C. una sp. nov.; eight in the genus Sarax Simon, 1892: S. bilua sp. nov., S. dunni sp. nov., S. gravelyi sp. nov., S. indochinensis sp. nov., S. lembeh sp. nov., S. palau sp. nov., S. rahmadii sp. nov., S. tiomanensis sp. nov.; and one in the genus Weygoldtia Miranda et al., 2018: W. consonensis sp. nov. Taxonomic keys to the 132 species (excluding four nomina dubia) are presented and several taxonomic rearrangements implemented. Four subspecies are elevated to species level: Charinus cavernicolus Weygoldt, 2006, C. elegans Weygoldt, 2006, C. longipes Weygoldt, 2006, and Sarax bispinosus (Nair, 1934). Sarax batuensis Roewer, 1962 is removed from synonymy with Sarax buxtoni (Gravely, 1915) and S. buxtoni newly synonymized with Sarax rimosus (Simon, 1901). Stygophrynus moultoni Gravely, 1915 is transferred to Sarax, resulting in Sarax moultoni (Gravely, 1915) comb. nov. Ten species are transferred from Charinus to Sarax, resulting in new combinations: S. abbatei (Delle Cave, 1986) comb. nov., S. bengalensis (Gravely, 1911) comb. nov., S. dhofarensis (Weygoldt, Pohl & Polak, 2002) comb. nov., S. ioanniticus (Kritscher, 1959) comb. nov., S. israelensis (Miranda et al., 2016) comb. nov., S. omanensis (Delle Cave, Gardner & Weygoldt, 2009) comb. nov., S. pakistanus (Weygoldt, 2005) comb. nov., S. seychellarum (Kraepelin, 1898) comb. nov., S. socotranus (Weygoldt, Pohl & Polak, 2002) comb. nov. and S. stygochthobius (Weygoldt & Van Damme, 2004) comb. nov.

The limits of the family Evaniidae (Insecta: Hymenoptera) and a new genus from Lebanese Amberamber

2002 ◽  
Vol 33 (1) ◽  
pp. 23-34 ◽  
Author(s):  
Hasan H. Basibuyuk ◽  
Mike G. Fitton ◽  
Alexandr P. Rasnitsyn ◽  
Donald L.J. Quicke
Keyword(s):  
Fore Wing ◽  
New Genus ◽  
Cladistic Analysis ◽  
Wing Venation ◽  
New Genus And Species ◽  
Ground Plan ◽  
The Family ◽  
Definition Of

AbstractThe definition of the family Evaniidae is revised and Cretevaniidae are synonymised with Evaniidae based on evidence derived from recently described Mesozoic taxa and a new genus and species, Lebanevania azari, described here from Lebanese amber. A fore leg with a long trochanter and a 12-segmented antenna are autapomorphies of the new genus. A large, high and wide head and a high and short mesosoma are derived characters shared with other Evaniidae. The new genus also has complete fore wing venation and lacks a tubular petiole, which are ground plan features of the Evanioidea. A cladistic analysis of fossil and extant members of the superfamily Evanioidea and notes on fossil taxa are presented.

New taxa and new records of butterflies from Vietnam (Lepidoptera, Papilionoidea) 

Zootaxa ◽  
2021 ◽  
Vol 5048 (4) ◽  
pp. 486-510
Author(s):  
ALEXANDER L. MONASTYRSKII ◽  
VU VAN LIEN
Keyword(s):  
New Species ◽  
New Taxa ◽  
New Records ◽  
Species Level ◽  
New Subspecies ◽  
The Status ◽  
First Time ◽  
A New Species

A new species and eight new subspecies of Papilionoidea discovered in Vietnam between 2002 and 2020 are described and illustrated. The status of two taxa are revised. New taxa include Pieridae: Delias sanaca bidoupa Monastyrskii & Vu subspec. nov. and Talbotia naganum aurelia Monastyrskii & Vu subspec. nov.; Nymphalidae: Abrota ganga pulcheria Monastyrskii & Vu, subspec. nov.; Bassarona recta consonensis Monastyrskii & Vu, subspec. nov.; Pantoporia bieti aurantina Monastyrskii & To subspec. nov.; Ragadia latifasciata cristata Monastyrskii & Vu, subspec. nov.; Ragadia latifasciata crystallina Monastyrskii & Vu, subspec. nov.; Faunis indistincta luctus Monastyrskii & Vu subspec. nov. & Aemona gialaica Monastyrskii, K. Saito & Vu, spec. nov. The taxon infuscata Devyatkin & Monastyrskii, previously described as the subspecies Aemona tonkinensis infuscata, was elevated to the species level, while the taxon critias (Ragadia critias Riley & Godfrey) was reduced to a subspecies. Three Satyrinae species were recorded from Vietnam for the first time: Palaeonympha opalina Butler, 1871; Ypthima motschulskyi Bremer & Grey, 1853; and Ragadia latifasciata Leech, 1891.  

Contributions to Molecular Phylogeny of Lichen-Forming Fungi 2. Review of Current Monophyletic Branches of the Family Physciaceae

2021 ◽  
Vol 63 (3-4) ◽  
pp. 351-390
Author(s):  
S. Y. Kondratyuk ◽  
L. Lőkös ◽  
I. Kärnefelt ◽  
A. Thell ◽  
M.-H. Jeong ◽  
...  
Keyword(s):  
Costa Rica ◽  
Molecular Phylogeny ◽  
Type Species ◽  
Lichen Species ◽  
New Combinations ◽  
Phylogeny Analysis ◽  
The Family ◽  
Crustose Lichens ◽  
First Time ◽  
Combined Matrix

Seven genera new to science, i.e.: Helmutiopsis, Huriopsis, Johnsheardia, Klauskalbia, Kudratovia, Kurokawia and Poeltonia of the Physciaceae are proposed for the ‘Rinodina’ atrocinerea, the ‘Rinodina’ xanthophaea, the ‘Rinodina’ cinnamomea, the ‘Heterodermia’ obscurata, the ‘Rinodina’ straussii, the ‘Anaptychia’ isidiata and the ‘Physconia’ grisea groups consequently that all form strongly supported monophyletic branches in a phylogeny analysis based on a combined matrix of nrITS and mtSSU sequences. Phylogenetic positions of species belonging to the genera Kashiwadia s. l., Leucodermia, Mischoblastia,Oxnerella, Phaeorrhiza s. l., Polyblastidium and Rinodinella s. l. are discussed. Oxnerella afghanica which for the first time recorded as parasitic lichen species from both epiphytic and saxicolous crustose lichens is designated as type species for the genus Oxnerella. Sequences of the recently described Physcia orientostellaris as well as Huriopsis xanthophaea and additional sequences of Kashiwadia aff. orientalis and Mischoblastia aff. oxydata are submitted to the GenBank. The positions of Polyblastidium casaterrinum from Costa Rica, ‘Rinodina’ efflorescens from Białowieża, Poland, and ‘Mischoblastia’ confragosula from Cambodia in the Physciaceae are confirmed in a phylogeny analysis based on the nrITS sequences. The presence of ‘extraneous mycobiont DNA’ in lichen associations is exemplified with earlier incorrect identifications of Heterodermia, Kashiwadia, Kurokawia,Oxnerella and Poeltonia specimens. Fifty-six new combinations are presented: Helmutiopsis alba (for Rinodina alba Metzler ex Arn.), Helmutiopsis aspersa (for Lecanora aspersa Borrer), Helmutiopsis atrocinerea (for Parmelia atrocinerea Fr.), Huriopsis chrysidiata (for Rinodina chrysidiata Sheard), Huriopsis chrysomelaena (for Rinodina chrysomelaena Tuck.), Huriopsis lepida (for Lecanora lepida Nyl.), Huriopsis luteonigra (for Rinodina luteonigra Zahlbr.), Huriopsis plana (for Rinodina plana H. Magn.), Huriopsis thiomela (for Lecanora thiomela Nyl.), Huriopsis xanthomelana (for Rinodina xanthomelana Müll. Arg.), Huriopsis xanthophaea (for Lecanora xanthophaea Nyl.), Johnsheardia cinnamomea (for Rinodina mniaroea var. cinnamomea Th. Fr.), Johnsheardia herteliana (for Rinodina herteliana Kaschik), Johnsheardia jamesii (for Rinodina jamesii H. Mayrhofer), Johnsheardia reagens (for Rinodina reagens Matzer et H. Mayrhofer), Johnsheardia zwackhiana (for Lecanora zwackhiana Kremp.), Kashiwadia austrostellaris (for Physcia austrostellaris Elix), Kashiwadia jackii (for Physcia jackii Moberg), Kashiwadia littoralis for Physcia littoralis Elix), Kashiwadia nubila (for Physcia nubila Moberg), and Kashiwadia tropica (for Physcia tropica Elix), Klauskalbia crocea (for Heterodermia crocea R. C. Harris), Klauskalbia flabellata (for Parmelia flabellata Fée), Klauskalbia obscurata (for Physcia speciosa (Wulfen) Nyl. *obscurata Nyl.), Klauskalbia paradoxa (for Heterodermia paradoxa Schumm et Schäfer-Verwimp), Kudratovia bohlinii (for Rinodina bohlinii H. Magn.), Kudratovia candidogrisea (for Rinodina candidogrisea Hafellner, Muggia et Obermayer), Kudratovia luridata (for Buellia luridata Körb.), Kudratovia metaboliza (for Rinodina metaboliza Vain.), Kudratovia pycnocarpa (for Rinodina pycnocarpa H. Magn.), Kudratovia roscida (for Lecanora roscida Sommerf.), Kudratovia straussii (for Rinodina straussii J. Steiner), Kudratovia terrestris (for Rinodina terrestris Tomin), Kurokawia bryorum (for Anaptychia bryorum Poelt), Kurokawia isidiata (for Anaptychia isidiata Tomin), Kurokawia mereschkowskii (for Physcia mereschkowskii Tomin), Kurokawia palmulata (for Psoroma palmulatum Michx.), Kurokawia runcinata (for Lichen runcinatus With.), Kurokawia stippea (for Parmelia aquila var. stippea Ach.), Lecania safavidiorum (for Oxnerella safavidiorum S. Y. Kondr., Zarei-Darki, Lőkös et Hur), Leucodermia erinacea (for Lichen erinaceus Ach.), Mischoblastia confragosula (for Lecanora confragosula Nyl.), Mischoblastia destituta (for Lecidea destituta Nyl.), Mischoblastia moziana (for Lecanora moziana Nyl.), Mischoblastia moziana subsp. parasitica (comb. et stat. nova for Rinodina moziana var. parasitica Kaschik et H. Mayrhofer), Mischoblastia ramboldii (for Rinodina ramboldii Kaschik), Mischoblastia vezdae (for Rinodina vezdae H. Mayrhofer), Oxnerella afghanica (for Rinodina afghanica M. Steiner et Poelt), Oxnerella castanomelodes (for Rinodina castanomelodes H. Mayrhofer et Poelt), Physciella nigricans (for Lecanora nigricans Flörke), Poeltonia elegantula (for Physconia elegantula Essl.), Poeltonia grisea (for Lichen griseus Lam.), Poeltonia isidiomuscigena (for Physconia isidiomuscigena Essl.), Poeltonia perisidiosa (for Physcia perisidiosa Erichsen), Poeltonia venusta (for Parmelia venusta Ach.), and Polyblastidium albicans (for Parmelia albicans Pers.) are proposed.

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