Re-evaluation of the genus Babingtonia (Myrtaceae) in eastern Australia and New Caledonia

2007 ◽  
Vol 20 (4) ◽  
pp. 302 ◽  
Author(s):  
Peter G. Wilson ◽  
Margaret M. Heslewood ◽  
Christopher J. Quinn

The validity of the generic concept of Babingtonia Lindl. adopted by Bean (1997a) is tested in the light of molecular and morphological data. Molecular analyses support recognition of segregate genera, none of which is closely related to the type of the genus, Babingtonia camphorosmae, a western Australian species. Two genera, Sannantha and Kardomia, are described as new and a third genus, Harmogia, resurrected from synonymy; new combinations are provided in the new genera. A fourth group, consisting of ‘Babingtonia’ behrii and its allies, appears distinct but, as a predominantly southern group, with numerous western Australian representatives, is not treated further.

Zootaxa ◽  
2021 ◽  
Vol 4951 (1) ◽  
pp. 130-136
Author(s):  
PAWEŁ JAŁOSZYŃSKI

Horaeomorphus Schaufuss is an easily identifiable genus of Stenichnini, predominantly distributed in the Australasian realm. Many scydmaenines occurring in other regions, however, have been misplaced in Horaeomorphus, and therefore the true distribution of this genus remains unclear. In previous studies several new genera were established for Australian species misplaced in Horaeomorphus, and a few species misplaced in Euconnus Thomson, Stenichnus Thomson, and Syndicus Motschulsky were transferred to Horaeomorphus. Three species that inhabit New Caledonia were placed in this genus: Horaeomorphus australis Franz, H. baloghi Franz, and H. novaecaledoniae Franz. Examination of these taxa revealed that none of them was conspecific with the SE Asian type species of Horaeomorphus. Three new combinations are proposed: Heterotetramelus (s. str.) australis (Franz) comb. n., Heterotetramelus (s. str.) baloghi (Franz) comb. n., and Heterotetramelus (s. str.) novaecaledoniae (Franz) comb. n.; each species is redescribed. 


Zootaxa ◽  
2016 ◽  
Vol 4198 (1) ◽  
pp. 1 ◽  
Author(s):  
JOHN F. LAWRENCE

The Australian ciid fauna is revised based on 75 described species (56 of them new) and three undescribed species, placed in 22 genera (nine of them new and nine newly recorded from Australia). The revision is considered preliminary, since about 50 other undescribed Australian species have been seen (usually as uniques or in short series), and it is likely that more will be found with increased intensive collecting. One additional New Caledonian species is also described, and one Cis species is considered to be based on a mislabelled Hawaiian specimen. The subfamily Ciinae, to which all species belong, is described based on adults and larvae, and keys are included to all known Australian genera and described species. Where material has been available, male and female genitalia have been described and many of those illustrated. The following new genera are described: Amphibolocis Lawrence gen. nov., Australocis Lawrence gen. nov., Ctenocis Lawrence gen. nov., Echinocis Lawrence gen. nov., Ditrichocis Lawrence gen. nov., Glyphidope Lawrence gen. nov., Malleecis Lawrence gen. nov., Notapterocis Lawrence gen. nov., Pseudeuxestocis Lawrence gen. nov. The following genera are recorded for the first time from Australia: Acanthocis Miyatake, Ceracis Mellié, Dichodontocis Kawanabe, Ennearthron Mellié, Hadreule Thomson, Neoennearthron Miyatake, Paratrichapus Scott, Scolytocis Blair and Xylographella Miyatake (the last three without described Australian species). The following new species are described (all native to Australia or its territories, unless otherwise indicated): Amphibolocis glabratus Lawrence, sp. nov., Australocis ruber Lawrence, sp. nov., Ceracis christmasensis Lawrence, sp. nov., Cer. communis Lawrence, sp. nov., Cer. divergens Lawrence sp. nov., Cer. fictus Lawrence sp. nov., Cis biconcavus Lawrence & Paviour-Smith, sp. nov., C. bisericeus Lawrence sp. nov., C. blackburni Lawrence & Paviour-Smith sp. nov., C. canberrae Lawrence sp. nov., C. capillatus Lawrence sp. nov., C. clypeodentes Lawrence & Paviour-Smith sp. nov., C. convexiformis Lawrence sp. nov., C. crassus Lawrence sp. nov., C. deficiens Lawrence sp. nov., C. denticulatus Lawrence sp. nov., C. deserticolus Lawrence sp. nov., C. dissidens Lawrence sp. nov., C. echidnoides Lawrence & Paviour-Smith sp. nov., C. eremicus Lawrence sp. nov., C. guangxiensis Lawrence sp. nov. (introduced from China), C. inflatus Lawrence, sp. nov., C. microcerus Lawrence  sp. nov., C. minutipunctatus Lawrence sp. nov., C. nitidonotum Lawrence sp. nov., C. obscuronotum Lawrence sp. nov., C. parviniger Lawrence sp. nov., C. planomarginatus Lawrence & Paviour-Smith sp. nov., C. simillimus Lawrence sp. nov., C. sordidus Lawrence & Paviour-Smith, sp. nov., C. subglaber Lawrence & Paviour-Smith sp. nov., C. subparallelus Lawrence sp. nov., C. tasmanorae Lawrence sp. nov., C. tricolor Lawrence sp. nov., C. victoriae Lawrence sp. nov., C. yorkensis Lawrence sp. nov., Ctenocis caledonicus Lawrence sp. nov. (New Caledonia), Ctenocis pectinipes Lawrence & Paviour-Smith sp. nov., Dichodontocis queenslandicus Lawrence sp. nov., Echinocis phellinophilus Lawrence sp. nov., Ennearthron alienindicus Lawrence sp. nov. (introduced from India), Glyphidope simplex Lawrence sp. nov., G. variabilis Lawrence sp. nov., Hadreule australiense Lawrence sp. nov., Malleecis flavus Lawrence sp. nov., Neoennearthron meridionale sp. nov., Notapterocis ellipticus Lawrence sp. nov., Notapterocis globulus Lawrence sp. nov., Notapterocis grossulus Lawrence sp. nov., Notapterocis hirsutulus Lawrence sp. nov., Notapterocis sannio Lawrence sp. nov., Octotemnus ambiguus Lawrence sp. nov., Octotemnus exilis Lawrence sp. nov., Orthocis latemarginatus Lawrence sp. nov., Orthocis quadrimaculatus Lawrence sp. nov., Pseudeuxestocis burwelli Lawrence sp. nov. The following new combinations are proposed: Acanthocis armiger (Blair, 1940) (Cis), comb. nov., Ctenocis zeelandicus (Reitter, 1880) (Cis), comb. nov., Ditrichocis pulchellus (Scott, 1926) (Ennearthron), comb. nov., Ditrichocis bifasciatus (Reitter, 1877) (Cis), comb. nov. and Paratrichapus lobipes (Broun, 1895) (Cis), comb. nov. The following synonymies are proposed: Cis recurvatus Broun, 1883 (= Cis victoriensis Blackburn, 1891 syn. nov., = Cis tasmanicus Blair, 1940 syn. n.). The following 13 genera are redescribed: Acanthocis Miyatake, 1955; Ceracis Mellié, 1849; Cis Latreille, 1796; Dichodontocis Kawanabe, 1994; Ennearthron Mellié, 1847; Hadreule Thomson, 1859; Neoennearthron Miyatake, 1954; Octotemnus Mellié, 1847; Orthocis Casey, 1898; Paratrichapus Scott, 1926; Scolytocis Blair, 1928; Xylographella Miyatake, 1985; Xylographus Mellié, 1847. The following 20 species are redescribed: Acanthocis armiger (Blair, 1940); Cis australis Blackburn, 1888; Cis bilamellatus Wood, 1884; Cis cavifrons Blair, 1940; Cis cervus Blair, 1940; Cis chinensis Lawrence, 1991; Cis clarki Blair, 1940; Cis fuscipes Mellié, 1849; Cis laminicollis Blair, 1940; Cis recurvatus Broun, 1883; Cis sellatus Blair, 1940; Cis setiferus Blackburn, 1888; Cis walkeri Blair, 1940; Ditrichocis pulchellus (Scott, 1926); Octotemnus dilutipes (Blackburn, 1891); Octotemnus walkeri Blair, 1940; Orthocis aequalis (Blackburn, 1888); Orthocis auriculariae Lawrence, 1991; Orthocis leanus (Blackburn, 1907); Xylographus bynoei Blair, 1940. The introduced species Cis chinensis Lawrence, 1991, and Orthocis auriculariae Lawrence, 1991, are recorded for the first time from Australia. The species Cis adelaidae Blackburn, 1888, is considered to be based on a mislabelled Hawaiian species near Cis setarius Sharp in Blackburn & Sharp, 1885. The name Cis sharpi Lawrence nom. nov. is proposed as a replacement name for another species in this Hawaiian group: Cis bimaculatus Sharp in Blackburn & Sharp, 1885, not Germain, 1855. Lectotypes are designated for Acanthocis armiger (Blair, 1940), Cis cavifrons Blair, 1940, Cis clarki Blair, 1940, Cis laminicollis Blair, 1940, Cis recurvatus Broun, 1883, Octotemnus walkeri Blair, 1940 and Orthocis leanus (Blackburn, 1907). 


Brunonia ◽  
1982 ◽  
Vol 5 (1) ◽  
pp. 1 ◽  
Author(s):  
NT Burbidge

It is reported that Gaudichaud was correct in describing, under Brachycome Cass., three species, B. triloba, B. dentata and B. spathulata. Reference is made to the nomenclatural status of these species in accordance with the results of a revision of Brachycome by Davis (1948). De Candolle erred in transferring the species to Vittadinia A. Rich, for which the New Zealand V. australis is the type. Reasons are given for regarding V. triloba (Gaudich.) DC. as synonymous with V. australis var. dissecta Benth., and the variety is raised to specific rank. Included with V. australis and V. dissecta in Vittadinia s. str. (i.e. in Vittadinia subgenus Vittadinia) are V. cuneata DC. (a name which can be applied to a complex group of taxa widespread in southern and eastern Australia) and a further 17 species of which the following are new: V. cervicularis (with four varieties), V. constricta, V. condyloides, V. decora, V. eremaea, V. humerata, V. nullarborensis, V. pustulata, V. simulans and V. sulcata, while V. gracilis (J. D. Hook.) N. Burbidge and V. australasica (Turcz.) N. Burbidge are new combinations. V. scabra DC. and a group of taxa which have been referred to it or, incorrectly, to V. macrorhiza (DC.) A. Gray have been placed in a new subgenus of Vittadinia under the name Peripleura. Within this subgenus nine species are recognized: V. scabra DC., V, hispidula F. Muell. ex A. Gray (with two varieties), and the new species V. arida, V. bicolor, V. diffusa, V. obovata, V. sericea, V. spechtii (with two varieties) and V. virgata. With the exception of V. australis which is endemic to New Zealand and V. simulans, a New Caledonian species, all are endemic to Australia; however, V. hispidula has been reported for New Caledonia where it is deemed to be an alien and V. gracilis and possibly V. muelleri appear to have become naturalized in New Zealand. V. brachycomoides (F. Muell.) Benth. becomes the type of a new genus, Camptacra, with two species, both distributed in northern and north-eastern Australia. Eurybiopsis DC. is reinstated, with its single species, E. macrorhiza DC., found only in northern Australia.


2016 ◽  
Vol 85 (4) ◽  
pp. 387-422 ◽  
Author(s):  
Roberto Arrigoni ◽  
Francesca Benzoni ◽  
Danwei Huang ◽  
Hironobu Fukami ◽  
Chaolun Allen Chen ◽  
...  

The scleractinian family Lobophylliidae is undergoing a major taxonomic revision thanks to the combination of molecular and morphological data. In this study, we investigate the evolutionary relationships and the macro- and micromorphology of six nominal coral species belonging to two of the nine molecular clades of the Lobophylliidae, clades A and B, and of Symphyllia wilsoni, a lobophylliid species analyzed from a molecular point of view for the first time. Sequence data from mitochondrial DNA (COI and the intergenic spacer between COI and l-rRNA), and nuclear DNA (histone H3 and ITS region) are used to generate robust molecular phylogenies and a median-joining haplotype network. Molecular results are strongly in agreement with detailed observations of gross- and fine-scale morphology of skeletons, leading to the formal revision of the genera Micromussa and Homophyllia and the description of two newly discovered zooxanthellate shallow-water species, Micromussa pacifica sp. nov. Benzoni & Arrigoni and Micromussa indiana sp. nov. Benzoni & Arrigoni, and a new genus, Australophyllia gen. nov. Benzoni & Arrigoni. In particular, Acanthastrea lordhowensis and Montastraea multipunctata are moved into Micromussa, A. hillae is synonymized with A. bowerbanki and is transferred to Homophyllia, and a revised diagnosis for both genera is provided. Micromussa pacifica sp. nov. is described from the Gambier Islands with its distribution spanning New Caledonia and eastern Australia. Despite a superficial resemblance with Homophyllia australis, it has distinctive macroand micromorphological septal features. Micromussa indiana sp. nov., previously identified as M. amakusensis, is here described from the Gulf of Aden and the southern Red Sea as a distinct species that is genetically separated from M. amakusensis and is morphologically distinct from the latter due to its smaller corallite size and lower number of septa. Finally, molecular trees show that S. wilsoni is closely related, but molecularly separated from clades A and B, and, also based on a unique combination of corallite and sub-corallite characters, the species is moved into Australophyllia gen. nov. These findings confirm the need for using both genetic and morphological datasets for the ongoing taxonomic revision of scleractinian corals.


Zootaxa ◽  
2009 ◽  
Vol 2293 (1) ◽  
pp. 35-52 ◽  
Author(s):  
RACHAEL A. KING

Amphipods within the family Chiltoniidae are an abundant yet taxonomically poorly known member of Australian freshwater habitats. With only four species known from Australia, the group is inadequately defined and marked by taxonomists as difficult to identify. Recent molecular analyses of chiltoniids from mound springs in South Australia detected several distinct species, prompting a morphological revision of material from the central and southern Lake Eyre region. Clear groups defined by unique combinations of morphological characters (focusing on uropodal, coxal, male gnathopod 2, and antennal morphology) were found that closely correlated with clades found in the molecular analyses. Arabunnachiltonia n. gen. is established for A. murphyi n. sp. from Strangways Springs in South Australia. Wangiannachiltonia n. gen. is established for W. guzikae n. sp. from Davenport Springs in South Australia. The chiltoniid genera are discussed and a key is presented to the known Australian species.


ZooKeys ◽  
2020 ◽  
Vol 985 ◽  
pp. 71-126
Author(s):  
Jose I. Martinez

The endemic Neotropical genus Gaujonia Dognin is revised. Morphological characters and a phylogenetic analysis demonstrate paraphyletic relationships among the species. Four different groups are interpreted to represent four different genera. The G. arbosi group is the only remaining clade in the genus Gaujonia, and the other groups have been arranged into three new genera: Milleranagen. nov., Oculicattusgen. nov., and Cicadoformagen. nov. Additionally, two other genera Cicadomorphusgen. nov., and Gaujopteragen. nov. were found using morphological and molecular analyses based on some specimens that were misidentified as Gaujonia spp. A total of five new genera, three new combinations (Cicadoforma vau-nigrum Hampson, comb. nov., Oculicattus renifera Hampson, comb. nov., and Millerana arbosioides Dognin, comb. nov.) and 21 new species (Cicadoforma ocelotussp. nov., Cicadomorphus chicharrasp. nov., Cicadomorphus chuyasp. nov., Cicadomorphus falkasiskasp. nov., Cicadomorphus lilianaesp. nov., Gaujonia bichusp. nov., Gaujonia chiqyaqsp. nov., Gaujonia kanakusikasp. nov., Gaujonia sourakovisp. nov., Gaujoptera amsasp. nov., Millerana austinisp. nov., Millerana cajassp. nov., Millerana cundinamarquensissp. nov., Millerana matthewsaesp. nov., Millerana tigrinasp. nov., Oculicattus bolivianasp. nov., Oculicattus brehmisp. nov., Oculicattus incasp. nov., Oculicattus raizaesp. nov., Oculicattus schmidtisp. nov., and Oculicattus uturunkusp. nov.) are established.


2018 ◽  
Vol 31 (2) ◽  
pp. 166
Author(s):  
Gareth D. Holmes ◽  
Peter H. Weston ◽  
Daniel J. Murphy ◽  
Carolyn Connelly ◽  
David J. Cantrill

Proteaceae subfamily Persoonioideae, as presently circumscribed, consists of the monogeneric tribe Placospermeae (Placospermum) and the tribe Persoonieae. The latter comprises the diverse genus Persoonia and monospecific genera found in New Zealand (Toronia), New Caledonia (Garnieria) and south-western Western Australia (Acidonia). Persoonia has 101 species distributed across Australia and has been classified into 11 informal groups. Using data derived from plastid DNA (trnL–trnF region), nuclear rDNA (ITS) and morphological characters, we constructed a phylogeny of Persoonioideae and compared the results to the existing classification. Bayesian and parsimony analyses indicated that Persoonia, as currently defined, is non-monophyletic. The molecular data and combined molecular and morphological data place Toronia in a moderately well supported clade with the monophyletic Rufiflora group of Persoonia from Western Australia. This clade is sister to Acidonia, Garnieria and the remaining Persoonia species. Of the other informal groups in Persoonia, the Teretifolia, Quinquenervis, Laurina, Arborea, Graminea and Chapmaniana groups are supported as monophyletic. The Lanceolata group can be re-circumscribed to be monophyletic by the addition of P. elliptica R.Br. (Longifolia group) and the Dillwynioides group. Relationships within this large, geographically widespread clade are largely unresolved and low DNA-sequence variation within it suggests a recent radiation followed by isolation in south-western and eastern Australia. All endemic Tasmanian Persoonia (Gunnii group taxa) are unresolved at the second-most basal node of the Persoonieae. Our results suggest that the Rufiflora group should be treated as a new genus and that the infrageneric taxonomy of Persoonia requires minor amendment.


1985 ◽  
Vol 33 (1) ◽  
pp. 27 ◽  
Author(s):  
TG Hartley

The genus Medicosma Hooker f., which has traditionally been considered to be monotypic and endemic to Australia, consists of 22 species. Six of these are endemic to eastern Australia, one is endemic to southern New Guinea and 15 are endemic to New Caledonia. The genus is described and its taxonomic history and relationships to other genera are discussed. The species are described, keyed and their relationships are outlined and discussed. Seventeen species are described as new, namely M. elliptica, M. obovata, M, glandulosa, M, diversifolia, M. articulata, M. parvifolia, M. obliqua, M. tahafeana, M. emarginata, M. verticillata, M. congests, M. latifolia, M. subsessilis, M. suberosa, M. petiolaris, M. exigua and M. gracilis, and new combinations are made for M. fareana (F. Mueller) T. Hartley, M. sessiliflora (C. T. White) T. Hartley, M. riparia (van Royen) T. Hartley and M. leratii (Guillaumin) T. Hartley.


1987 ◽  
Vol 1 (5) ◽  
pp. 473
Author(s):  
G Daniels

Neoaratus Ricardo is redefined and considered as monotypic. Six new genera, Abrophila, Colepia, Dolopus, Mauropteron, Reburrus and Zosteria, are erected to accommodate 19 species previously placed in Neoaratus as well as 39 new species described below. The following are proposed as new synonyms: Asilus grandis Macquart, 1848 = A. rufiventris Macquart, 1838; Asilus leon Walker, 1849 = A. rubrithorax Macquart, 1838; Mochtherus lautus van der Wulp, 1872 = A. biligata Walker, 1864; Asilus ferrugineiventris Macquart, 1850 = A. fulvipubescens Macquart, 1850. Asilus grandis Macquart is removed from synonymy with Neoaratus hercules (Wiedemann) and proposed as a synonym of A. rufiventris Macquart, 1838. Abrophila whitei is proposed as a replacement name for the preoccupied Asilus aureus White, 1918. The following are new combinations: Colepia abludo (Daniels, 1983), C. ingloria (Macleay, 1826), C. malleola (Walker, 1849), C. rufiventris (Macquart, 1838); Dolopus genitalis (Hardy, 1920), D. rubrithorax (Macquart, 1838); Mauropteron pelago (Walker, 1849); Reburrus bancrofti (Hardy, 1935), R. kochi (de Meijere, 1913), R. macquarti (Bigot, 1860), R. wieneckii (van der Wulp, 1872); Zosteria alcetas (Walker, 1849), Z. biligata (Walker, 1864); Z. fulvipubescens (Macquart, 1850), Z. iflingworthi (Hardy, 1922), Z. murina (Macquart, 1838), Z. rosevillensis (Hardy, 1935), Z. sydneensis (Macquart, 1838). The following new species are described: Colepia chrysochaites, C. comatacauda, C. compernis, C. cultripes, C. flavifacies, C. horrida, C. ignicolor, C. lanata, C. naevia, C. novaeguineae; Dolopus mirus, D. silvestris, D. simulans; Mauropteron farinum; Reburrus aquilonius, R. caledonicae, R. peninsularis; Zosteria affinis, Z. alpina, Z. caesariata, Z. calignea, Z, claudiana, Z. clausum, Z. clivosa, Z. eastwoodi, Z. hispida, Z. lineata, Z. longiceps, Z. montana, Z, nigrifemorata, Z. novazealandica, Z. punicea, Z. queenslandi, Z. rubens, Z. ruspata, Z. suda, Z. varia and Z. venato. All seven genera occur in Australia. Species of three genera, Colepia, Reburrus and Zosteria, also occur elsewhere, as follows: Timor (R. wieneckii], New Guinea (C. novaeguineae, R. kocki, Z. biligata and Z. illingworthi), New Caledonia and New Hebrides (R. caledonicae and R. macquarti], and New Zealand (Z. novazealandica). Z. illingworthi is common to Australia and New Guinea. The female reproductive system and the components of the male terminalia are illustrated and briefly described for most species. Pupal exuviae of C. ingloria, C. malleola, C, rufiventris, N. hercules, Z. fulvipubescens and Z. sydneensis are illustrated and/or described. Keys to the genera of Australian Asilini and the species of the new genera are given. Lectotypes are designated for Antipalus wieneckii, Asilus ferrugineiventris, A. leon, A. murinus, A. pelago, A. rufiventris, Neoaratus bancrofti and N. rosevillensis. Asilus regius Jaennicke and Asilus tasmaniae Macquart, formerly considered as species of Neoaratus, are not treated because their status is uncertain.


Zootaxa ◽  
2007 ◽  
Vol 1570 (1) ◽  
pp. 1-84 ◽  
Author(s):  
PAUL D. BROCK ◽  
JACK HASENPUSCH

The Australian phasmid fauna has been revised prior to publication of a field guide by the same authors. Six new genera are described: Austrosipyloidea Brock & Hasenpusch, Cornicandovia Hasenpusch & Brock, Davidrentzia Brock & Hasenpusch, Micropodacanthus Brock & Hasenpusch, Paratropidoderus Brock & Hasenpusch and Spinosipyloidea Hasenpusch & Brock. Sixteen new species from various parts of Australia are described and figured: Candovia robinsoni Brock & Hasenpusch, Rhamphosipyloidea palumensis Hasenpusch & Brock, Scionecra milledgei Hasenpusch & Brock, Sipyloidea brevicerci Hasenpusch & Brock, Sipyloidea garradungensis Hasenpusch & Brock, Sipyloidea larryi Hasenpusch & Brock, Sipyloidea lewisensis Hasenpusch & Brock, Sipyloidea rentzi Brock & Hasenpusch, Sipyloidea whitei Brock & Hasenpusch, Spinosipyloidea doddi Hasenpusch & Brock [all Necrosciinae], Pachymorpha spinosa Brock & Hasenpusch [Pachymorphinae], Davidrentzia valida Brock & Hasenpusch [Platycraninae], Micropodacanthus mouldsi Brock & Hasenpusch, Micropodacanthus sztrakai Brock & Hasenpusch, Paratropidoderus spinosus Brock & Hasenpusch and Podacanthus keyi Brock & Hasenpusch [Tropidoderinae].        A number of new combinations are proposed, new synonyms and incorrect synonymy corrected following detailed examination of type and other material: 1. (Lonchodinae): Austrocarausius Brock, 2000: Carausius macerrimus Brunner, 1907 is a new synonym of Austrocarausius nigropunctatus (Kirby, 1896). Denhama Werner, 1912: D. austrocarinata (Otte & Brock, 2005), D. longiceps (Brunner, 1907), D. striata (Sjöstedt, 1918) and D. eutrachelia (Westwood, 1859) are transferred from Hyrtacus Stål, 1875, the latter species also removed from synonymy with Hyrtacus coenosa (Gray, 1833). D. gracilis (Sjöstedt, 1918), a former Marcenia species, is also transferred. Hyrtacus Stål, 1875 (= Marcenia Sjöstedt, 1918 syn. n.): H. caurus (Tepper, 1905) comb. n. transferred from Lonchodes Gray, 1835 (three new synonyms also reported for this species: Bacillus peristhenellus Tepper, 1905, Hyrtacus cunctatrix (Sjöstedt, 1918) and Hyrtacus nigrogranulosus Sjöstedt, 1918). Marcenia frenchi (Wood-Mason, 1877) is a new synonym of Hyrtacus tuberculatus Stål, 1875. 2. (Necrosciinae): Austrosipyloidea Brock & Hasenpusch, gen. n.: A. carterus (Westwood, 1859) comb. n., transferred from Sipyloidea Brunner, 1893 (= Sipyloidea filiformis Redtenbacher, 1908 syn. n.). Candovia Stål, 1875 is removed from synonymy with Hyrtacus, along with the type species, C. coenosa. This has resulted in all former Australian species placed in Parasipyloidea Redtenbacher, 1908 being transferred to Candovia i.e. C. aberrata (Brunner, 1907) comb. n., C. annulata (Brunner, 1907) comb. n., C. granulosa (Brunner, 1907) comb. n., C. pallida (Sjöstedt, 1918), comb. n., C. spurcata (Brunner, 1907) comb. n. and C. strumosa (Redtenbacher, 1908) comb. n. In addition, C. evoneobertii (Zompro & Adis, 2001) comb. n. and C. peridromes (Westwood, 1859) comb. n. (including its new synonyms Clitarchus longipes Brunner, 1907, Bacunculus tener Brunner, 1907 and E. cercatus (Redtenbacher, 1908)) are transferred from Echetlus Stål, 1875. Cornicandovia Hasenpusch & Brock gen n.: C. australica (Redtenbacher, 1908) comb. n. Sipyloidea Brunner, 1893: S. bella (Tepper, 1905) comb. n. (new synonym S. ovabdita Rentz & John, 1987) is transferred from Necroscia Serville, 1838, S. caeca Sjöstedt, 1918 rev. stat., is removed from synonymy with Sipyloidea carterus (Westwood, 1859).  Rhamphosipyloidea Redtenbacher, 1908: R. queenslandica (Sjöstedt, 1918) comb. n. is transferred from Sipyloidea, also removed from synonymy with carterus. 3. (Pachymorphinae): Pachymorpha Gray, 1835: P. pasithoe (Westwood, 1859) is a new synonym of P. simplicipes Serville, 1838. 4. (Eurycanthinae). Eurycantha Boisduval, 1835: E. sifia (Westwood, 1859) is a new synonym of E. calcarata Lucas, 1870. 5. (Phasmatinae): Vetilia Stål, 1875 is a new synonym of Acrophylla Gray, 1835, resulting in the transfer of these species to Acrophylla: A. enceladus (Gray, 1835) comb. n. and A. thoon (Stål, 1875) comb. n. Vetilia ligia Redtenbacher, 1908 is a new synonym of Acrophylla wuelfingi Redtenbacher, 1908. A. paula (Tepper, 1905) and A. aliena Redtenbacher, 1908 are new synonyms of A. nubilosa Tepper, 1905. A. caprella (Westwood, 1859) comb. n. is transferred from Ctenomorpha Gray, 1833. Anchiale Stål, 1875 (= Ctenomorphodes Karny, 1923 syn. n.), resulting in the transfer of  A. briareus (Gray, 1834) comb. n. and A. tessulata (Gray, 1835) which is renamed Anchiale austrotessulata name nov., as tessulata Gray is preoccupied by Anchiale tessulata (Goeze, 1778). Austroclonistria Redtenbacher, 1908 is a new synonym of Arphax Stål, 1875, as A. serrulataa Redtenbacher, 1908) is a new synonym of Arphax dolomedes (Westwood, 1859). Ctenomorpha Gray, 1833: Paractenomorpha macrotegmus (Tepper, 1887) is confirmed as a synonym of Ctenomorpha marginipennis Gray, 1833. Hermarchus Stål, 1875: H. polynesicus Redtenbacher, 1908 is a new synonym of H. insignis (Kaup, 1871). Paronchestus Redtenbacher, 1908: P. cornutus (Tepper, 1905) comb. n. is transferred from Acrophylla Gray, 1835 and P. pasimachus (Westwood, 1859) from Onchestus Stål, 1875. 6. (Platycraninae): Megacrania batesii (Kirby, 1896) is removed from synonymy with Megacrania alpheus (Westwood, 1859). 7. (Tropidoderinae): Didymuria Kirby 1904: D. virginea Stål, 1875 is removed from synonymy with D. violescens (Leach, 1814). Lysicles Stål, 1877: L. periphanes (Westwood, 1859) comb. n. is transferred from Echetlus Stål, 1875. Tropidoderus Gray 1835: T. michaelseni Werner, 1912 is removed from synonymy with T. childrenii (Gray, 1833). 8. (Xeroderinae): Cooktownia Sjöstedt, 1918 becomes a new synonym of Xeroderus Gray, 1835, as Cooktownia plana Sjöstedt, 1918 is a new synonym of Xeroderus kirbii Gray, 1835.Lectotypes are designated for Clitarchus longipes Brunner, 1907, Sipyloidea filiformis Redtenbacher, 1908 and Vetilia ligula Redtenbacher, 1908.As a result of this work, there are now 104 Australian species (+ 1 subspecies) and in order to facilitate further research on these insects, an updated checklist is provided, also a detailed bibliography.


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