While examining herbarium specimens of Trithuria inconspicua Cheeseman, we observed differences in the stigmatic hairs among plants from New Zealand’s North and South Islands. This motivated us to assess genetic and morphological variation within this species and its sister T. filamentosa Rodway from Tasmania. Samples were collected from lakes in the three disjunct geographic areas where the two species occur. Genetic variation in both species was assessed with simple sequence-repeat (SSR, microsatellite) markers and analyses of genetic distances. We also compared the morphology of northern and southern New Zealand T. inconspicua using fresh material. Samples of each species clustered together in a minimum evolution tree built from genetic distances. Trithuria filamentosa had more genetic diversity than did T. inconspicua. Within T. inconspicua, plants from lakes in the North Island and the South Island formed discrete genetic groups diagnosable by subtle morphological differences. Low levels of heterozygosity in both species are consistent with a high level of selfing, as suggested for other co-sexual Trithuria species, but unusual for a putative apomict. On the basis of genetic and morphological variation, we propose recognition of the northern New Zealand and southern New Zealand lineages of T. inconspicua at subspecies rank.

Eucalyptus magnificata L.A.S.Johnson & K.D.Hill is an endangered species endemic to the New England Tablelands Bioregion of eastern Australia, with taxonomic conflict regarding its recognition. Analyses of morphology, phytochemistry and genomic DNA were used to test species limits of E. magnificata. Morphometric and phytochemical phenetic analyses found distinct differences among E. magnificata, E. baueriana and a putative entity recognised during field collection, i.e. E. sp. Dalveen. Another putative entity, E. sp. Oxley, was morphologically and phytochemically intermediate between E. magnificata and E. conica. Phenetic analysis of single-nucleotide polymorphism (SNP) data supported the results from morphological and phytochemical analyses. The original circumscription of E. magnificata, as distinct from E. baueriana, was strongly corroborated. Eucalyptus magnificata was found to be restricted in distribution to the Macleay Gorges area south-east of Armidale. Multiple lines of evidence provided strong support for the recognition of E. sp. Dalveen as a separately evolving entity at a species level, here described as Eucalyptus dalveenica T.L.Collins, R.L.Andrew & J.J.Bruhl. A full description of the new species, a table distinguishing E. dalveenica from closely related taxa, and an identification key are provided. Distribution, habitat and conservation status are discussed.

The eucalypts, which include Eucalyptus, Angophora and Corymbia, are native to Australia and Malesia and include over 800 named species in a mixture of diverse and depauperate lineages. We assessed the fit of the eucalypt taxonomic classification to a phylogeny of 711 species scored for DNA sequences of plastid matK and psbA–trnH, as well as nuclear internal transcribed spacer and external transcribed spacer. Two broadly similar topologies emerge from both maximum likelihood and Bayesian analyses, showing Angophora nested within Corymbia, or Angophora sister to Corymbia. The position of certain species-poor groups on long branches fluctuated relative to the three major Eucalyptus subgenera, and positions of several closely related species within those subgenera were unstable and lacked statistical support. Most sections and series of Eucalyptus were not recovered as monophyletic. We calibrated these phylogenies against time, using penalised likelihood and constraints obtained from fossil ages. On the basis of these trees, most major eucalypt subgenera arose in the Late Eocene and Early Oligocene. All Eucalyptus clades with taxa occurring in south-eastern Australia have crown ages <20 million years. Several eucalypt clades display a strong present-day geographic disjunction, although these clades did not have strong phylogenetic statistical support. In particular, the estimated age of the separation between the eudesmids (Eucalyptus subgenus Eudesmia) and monocalypts (Eucalyptus subgenus Eucalyptus) was consistent with extensive inland water bodies in the Eocene. Bayesian analysis of macroevolutionary mixture rates of net species diversification accelerated in five sections of Eucalyptus subgenus Symphyomyrtus, all beginning 2–3 million years ago and associated with semi-arid habitats dominated by mallee and mallet growth forms, and with open woodlands and forests in eastern Australia. This is the first time that a calibrated molecular study has shown support for the rapid diversification of eucalypts in the recent past, most likely driven by changing climate and diverse soil geochemical conditions.

We investigated the floral anatomy and development of Macarthuria australis Hügel ex Endl., an unusual genus endemic to Australia, in the context of floral evolution of core Caryophyllales. Flower initiation is spiral, with sepals developing quincuncially. The first two petals continue the sequence of sepal initiation, but the remaining petals arise from common stamen–petal primordia. The androecium develops sequentially as three inner antesepalous and five outer antepetalous stamens. The globular ovary is trimerous with a short symplicate zone and two arillate ovules per locule. The rapid emergence of the androecium leads to a partial absorption of the petal primordia within the androecial tissue. The two first-formed petals have more room for development and precede the androecium, supporting the fact that petals are not staminodial in origin. This heterochronic shift correlates with an inversed developmental sequence of the antesepalous stamens. The constraint caused by the spatial occupation of sepals and carpels leads to the loss of two stamens, and the re-arrangement of stamens and petals along the flanks of the carpels. The floral development of Macarthuria anticipates a syndrome of stamen and petal development in other core Caryophyllales and culminating in the Caryophyllaceae.

Ptilotus macrocephalus (R.Br.) Poir. (Amaranthaceae), commonly known as a featherhead, is a widespread and common species in many parts of Australia. In the present study, we assess morphological variation in P. macrocephalus throughout its geographic range and provide evidence for the recognition of two new species, namely, P. psilorhachis T.Hammer & R.W.Davis and P. xerophilus T.Hammer & R.W.Davis. Geospatial analyses indicated that these new species are partitioned ecologically and geographically.

The Hibbertia commutata Steud. species group comprises 27 species in Hibbertia Andr. subgenus Hibbertia, all being endemic in south-western Western Australia; it is the largest species group in that state. Several taxa in the group have been the subject of considerable confusion in the past, with inadequate understanding of species boundaries leading to mixed determinations on specimens. All taxa in the group are treated here, and the following are described as new: Hibbertia acrotoma K.R.Thiele, H. ambita K.R.Thiele, H. barrettiae K.R.Thiele, H. davisii K.R.Thiele, H. elegans K.R.Thiele, H. hortiorum K.R.Thiele, H. improna K.R.Thiele, H. inopinata K.R.Thiele, H. sandifordiae K.R.Thiele, H. semipilosa K.R.Thiele, H. spectabilis K.R.Thiele, H. wheelerae K.R.Thiele.