Asterolasia beckersii (Rutaceae), a new species from the Northern Tablelands, New South Wales (original) (raw)
Related papers
Disentangling a taxonomic nightmare: a revision of the Australian,
Zootaxa 3918 (4): 503–551, 2015
The genus Altica Geoffroy, 1762, is revised for Australia, the west Pacific region and the Indomalayan Archipelago, with 6 valid species: A. aenea (Olivier, 1808); A. birmanensis (Jacoby, 1896); A. caerulea (Olivier, 1791); A. corrusca (Erichson, 1842); A. cyanea Weber, 1801; A. gravida (Blackburn, 1896). The following new synonymy is recognised, in original combinations, senior synonym first: Galeruca aenea Olivier = Haltica ignea Blackburn, 1889, syn. nov., = Haltica bicolora Jacoby, 1904, syn. nov., = Altica jussiaeae Gressitt, 1955, syn. nov.; Galeruca caerulea Olivier = Haltica elongata Jacoby, 1884, syn. nov., = Altica brevicosta Weise, 1922; Haltica corrusca Erichson = Haltica pagana Blackburn, 1896, syn. nov.; Haltica birmanensis Jacoby = Haltica indica Shukla, 1960, syn. nov. Altica brevicosta and A. birmanensis are removed from synonymy with A. cyanea and A. indica is removed from synonymy with A. caerulea. The Altica caerulea of Maulik and subsequent authors (not Olivier) is a misidentification of two species, correctly named A. cyanea and A. birmanensis. The Altica cyanea of Maulik and subsequent authors (not Weber) is a misidentification, correctly named A. aenea. Altica bicosta Shukla, 1960, is removed from synonymy with A. brevicosta and regarded as a valid species. Altica splendida Olivier, 1808, and Haltica ferruginis Blackburn, 1889, are transferred to Sutrea Baly, 1876, as S. splendida (comb. nov.) and S. ferruginis (comb. nov.). The type species of Sutrea is designated as S. elegans Baly, 1876. Altica albicornis Medvedev, 2004, is transferred to Phygasia Dejean, 1836, as P. albicornis (comb. nov.). Lectotypes are designated for A. australis, A. birmanensis, A. caerulea, A. cyanea, A. elongata, A. ignea and A. pagana. A neotype is designated for A. aenea. Altica caerulea is newly recorded from Australia and A. cyanea is removed from the Australian fauna. Altica corrusca and A. gravida are endemic to Australia; all published records of these species from outside Australia refer to the widespread Asian-Pacific species A. aenea. The single record of the European Altica oleracea (L., 1758) from New Caledonia is regarded as a label error and this species removed from the Pacific fauna. A key, based primarily on genitalic structures, is provided for the six regional species and all are redescribed. Host plant records are reviewed: A. corrusca is a minor agricultural pest; A. aenea, A. caerulea and A. cyanea may be useful for biocontrol of weeds.
A revision of Australian species of Radula subg. Odontoradula
The current paper presents molecular data from three chloroplast markers (atpB–rbcL spacer, trnG G2 intron, trnL–trnF intron and spacer); morphological data, and geographic data to support the recognition of nine species belonging to Radula subg. Odontoradula in Australasia. R. ocellata, the subgeneric type from the Wet Tropics bioregion, is maintained as distinct from its sister species, R. pulchella, from southeastern Australian rainforests; both species are Australian endemics. Reinstatement of R. allisonii from synonymy, under R. retroflexa, is supported by molecular data and morphological characters, including the absence of triradiate trigones on leaf-lobe cell walls, the apex of lobules on primary shoots not being turned outwards, the oblong-elliptic female bracts, and the perianths having a pronounced wing. Reinstatement of R. weymouthiana, from synonymy under R. retroflexa, is also supported by molecular data and morphological characters, including the presence of a single low dome-shaped papilla over each leaf-lobe cell, and the large imbricate lobules on primary shoots. R. weymouthiana occurs in Tasmania and New Zealand, whereas R. allisonii is a New Zealand endemic. Australian R. retroflexa exhibits differentiation into epiphytic and rheophytic morphs, interpreted as ecotypes. Australian individuals, comprising both epiphytic and rheophytic morphs, are monophyletic and nested within a clade containing individuals from other regions. R. novae-hollandiae is newly reported for the New Zealand Botanical Region, from Raoul Island in the Kermadecs. R. novae-hollandiae exhibits decoupling of morphological and molecular divergence, with Australian individuals forming two clades reflecting geography (a Wet Tropics bioregion clade and a southeastern Rainforest clade). These clades exhibit equivalent levels of molecular divergence, as observed in R. pulchella and R. ocellata, but no morphological differences. Similar levels of molecular divergence were observed in trans-Tasman populations of R. tasmanica. The New Zealand endemic, R. plicata, is excluded from the Australian flora, and R. cuspidata replaces R. dentifolia for the New Zealand endemic species formerly known by both names.
Australian Systematic Botany, 2013
Various published hypotheses regarding circumscription and relationships of species within the Radula parvitexta and R. ventricosa species groups were tested using molecular data from three chloroplast markers. The phylogeny resolves five clades within the R. parvitexta species group in Australia, which proves polyphyletic across two subgenera, or three subgenera if R. madagascariensis is included. One clade represents an undescribed species, R. psychosis sp. nov., one corresponds to R. madagascariensis, a new record for Australia, the others to R. ratkowskiana, R. tasmanica and R. robinsonii. R. ratkowskiana is reinstated from synonymy of R. tasmanica, and R. parvitexta is placed into synonymy of R. robinsonii. A second new species belonging to the R. parvitexta species group, R. kilgourii sp. nov., is described; however, it was not included in the phylogeny. Three clades were resolved within the R. ventricosa species group in Australia, which is nested within subg. Metaradula. These clades corresponded to R. jovetiana, R. loriana, which is reinstated from synonymy of R. ventricosa, and two new species, namely, R. myriopoda sp. nov. and R. forficata sp. nov. R. ventricosa is excluded from the Australian flora, because all material is referrable to R. loriana. R. forficata and R. kilgourii had not been collected before the present study. R. myriopoda and R. jovetiana exhibit overlap in morphology of the sterile gametophyte and can be eliably separated only on characters associated with the perianth mouth. They can be considered semicryptic species, and would not have been recognised independent of fieldwork and molecular investigations conducted as part of the present study.