Taxonomic revision of five species groups of ebracteate-erect Myosotis (Boraginaceae) endemic to New Zealand, based on morphology, and description of new subspecies

Disentangling relationships among eastern Mediterranean Cymbalaria including description of a novel species from the southern Peloponnese (Greece)

Plant Systematics and Evolution ◽

10.1007/s00606-020-01730-3 ◽

2021 ◽

Vol 307 (2) ◽

Author(s):

Pau Carnicero ◽

Núria Garcia-Jacas ◽

Llorenç Sáez ◽

Theophanis Constantinidis ◽

Mercè Galbany-Casals

Keyword(s):

Eastern Mediterranean ◽

Phylogenetic Analyses ◽

Taxonomic Revision ◽

Distribution Patterns ◽

Morphological Characters ◽

Molecular Data ◽

Morphological Data ◽

Long Distance ◽

Aegean Islands ◽

Molecular Phylogenetic

AbstractThe eastern Mediterranean basin hosts a remarkably high plant diversity. Historical connections between currently isolated areas across the Aegean region and long-distance dispersal events have been invoked to explain current distribution patterns of species. According to most recent treatments, at least two Cymbalaria species occur in this area, Cymbalaria microcalyx and C. longipes. The former comprises several intraspecific taxa, treated at different ranks by different authors based on morphological data, evidencing the need of a taxonomic revision. Additionally, some populations of C. microcalyx show exclusive morphological characters that do not match any described taxon. Here, we aim to shed light on the systematics of eastern Mediterranean Cymbalaria and to propose a classification informed by various sources of evidence. We performed molecular phylogenetic analyses using ITS, 3’ETS, ndhF and rpl32-trnL sequences and estimated the ploidy level of some taxa performing relative genome size measures. Molecular data combined with morphology support the division of traditionally delimited C. microcalyx into C. acutiloba, C. microcalyx and C. minor, corresponding to well-delimited nrDNA lineages. Furthermore, we propose to combine C. microcalyx subsp. paradoxa at the species level. A group of specimens previously thought to belong to Cymbalaria microcalyx constitute a well-defined phylogenetic and morphological entity and are described here as a new species, Cymbalaria spetae. Cymbalaria longipes is non-monophyletic, but characterized by being glabrous and diploid, unlike other eastern species. The nrDNA data suggest at least two dispersals from the mainland to the Aegean Islands, potentially facilitated by marine regressions.

Combined molecular and morphological phylogeny of Ephemerellinae (Ephemerellidae: Ephemeroptera), with remarks about classification

Zootaxa ◽

10.11646/zootaxa.1991.1.2 ◽

2009 ◽

Vol 1991 (1) ◽

pp. 28-42 ◽

Cited By ~ 6

Author(s):

T. HEATH OGDEN ◽

JONATHAN T. OSBORNE ◽

LUKE M. JACOBUS ◽

MICHAEL F. WHITING

Keyword(s):

Morphological Analysis ◽

Sequence Data ◽

Histone H3 ◽

Morphological Characters ◽

Morphological Data ◽

Rdna Genes ◽

Dna Sequence Data ◽

Extant Genus ◽

Species Groups ◽

Combined Data

This study represents the first combined molecular and morphological analysis for the mayfly family Ephemerellidae (Ephemeroptera), with a focus on the relationships of genera and species groups of the subfamily Ephemerellinae. The phylogeny was constructed based on DNA sequence data from 3 nuclear (18S rDNA, 28S rDNA, histone H3) and 2 mitochondrial (12S rDNA, 16S rDNA) genes, and 23 morphological characters. Taxon sampling for Ephemerellidae included exemplars from all 25 extant genus groups and additional representatives from those genera with the highest diversity. Ephemerellidae appears to consist of three major clades. Ephemerella, the largest genus of Ephemerellidae, and Serratella were not supported as monophyletic, and each had representatives in two of the three major clades. However, the genera Drunella and Cincticostella were supported as monophyletic. Lineages strongly supported as monophyletic include a grouping of the Timpanoginae genera Timpanoga, Dannella, Dentatella and Eurylophella, and groupings of the Ephemerellinae genera Torleya, Hyrtanella and Crinitella and the genera Kangella, Uracanthella and Teloganopsis. The placement of the Timpanoginae genus Attenella fell within Ephemerellinae, based on molecular and combined data, but it grouped with other Timpanoginae based on morphological data alone. Further study and analysis of Ephemerellidae morphology is needed, and classification should be revised, if it is to reflect phylogenetic relationships.

A revision of Australian species of Radula subg. Odontoradula

Australian Systematic Botany ◽

10.1071/sb13035 ◽

2013 ◽

Vol 26 (6) ◽

pp. 408 ◽

Cited By ~ 6

Author(s):

Matt A. M. Renner ◽

Nicolas Devos ◽

Elizabeth A. Brown ◽

Matt J. von Konrat

Keyword(s):

New Zealand ◽

Morphological Characters ◽

Molecular Data ◽

Morphological Data ◽

South Eastern ◽

Chloroplast Markers ◽

Molecular Divergence ◽

Wet Tropics ◽

Australian Flora ◽

Morphological Differences

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 south-eastern 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 south-eastern 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.

Taxonomic revision of the “mexicanus” group of the genus Vaejovis C. L. Koch, 1836 (Scorpiones: Vaejovidae)

Zootaxa ◽

10.11646/zootaxa.4596.1.1 ◽

2019 ◽

Vol 4596 (1) ◽

pp. 1 ◽

Cited By ~ 1

Author(s):

CONTRERAS-FÉLIX GERARDO A. ◽

FRANCKE B. OSCAR F.

Keyword(s):

New Species ◽

Natural History ◽

Taxonomic Revision ◽

Morphological Characters ◽

The Other ◽

Species Groups ◽

Males And Females ◽

First Time

Within the scorpion genus Vaejovis C.L. Koch, the “mexicanus” group is composed of species distributed in the mountains of México. This group presents taxonomic problems, because its characterization and the species included in the group have varied through the years. In the present work, we redefine this group based on several morphological characters, and we differentiate it from the other two species groups within the genus: “vorhiesi” and “nit dulus+nigrescens”. Additionally, five new species are described: Vaejovis ceboruco sp. nov., Vaejovis nanchititla sp. nov., Vaejovis santibagnezi sp. nov., Vaejovis talpa sp. nov. and Vaejovis tapalpa sp. nov; the males of three species are described for the first time (V. dugesi, V. nigrofemoratus and V. tesselatus); and the updated diagnosis for all species is included. Keys for the identification of males and females of the 30 species included in this group are given. Lastly, notes on the natural history and distribution of some species are provided, with maps of known distribution for all the species.

The ‘xenosmatoid’ group of Cortinarius (Agaricales) in New Zealand

Phytotaxa ◽

10.11646/phytotaxa.438.4.1 ◽

2020 ◽

Vol 438 (4) ◽

pp. 223-236

Author(s):

BÁLINT DIMA ◽

KARL SOOP

Keyword(s):

New Species ◽

New Zealand ◽

Bayesian Inference ◽

Type Species ◽

Phylogenetic Analyses ◽

Morphological Characters ◽

The Other ◽

Morphological Data ◽

Nrdna Its ◽

One New Species

Cortinarius section Xenosmatae, originally based on solely morphological characters, was subsequently shown to contain phylogenetically distantly related species. The type species C. xenosma is a singleton, and this study aims to revise the other members of the section using combined molecular (nrDNA ITS and LSU) and morphological data. Based on phylogenetic analyses using RAxML, PhyML and Bayesian Inference and additional morphological features one new species (C. paraxenosma) and one new section (sect. Olorinati) are proposed. Furthermore sect. Carbonelli is extended and emended to include two former members of sect. Xenosmatae. A key to the species in New Zealand with xenosmatoid morphology is provided.

Eucalypt phylogeny — molecules and morphology

Australian Systematic Botany ◽

10.1071/sb9950483 ◽

1995 ◽

Vol 8 (4) ◽

pp. 483 ◽

Cited By ~ 32

Author(s):

PY Ladiges ◽

F Udovicic ◽

AN Drinnan

Keyword(s):

Parallel Evolution ◽

5S Rdna ◽

Taxonomic Revision ◽

Morphological Characters ◽

Morphological Data ◽

Separate Analysis ◽

Data Sets ◽

Data Set ◽

Seed Characters ◽

Different Levels

Molecular (5S rDNA spacer and chloroplast DNA RnPs) and morphological data sets are informative at different levels of the eucalypt clade. They allow separate analysis of major subclades, the results of which, when combined, give a single, phylogenetic tree for Angophora Cav. and Eucalyptus L'Hér. For taxonomic revision, the tree supports the recognition of bloodwood eucalypts as monophyletic, but shows that informal subgenus Corymbia Pryor & Johnson is paraphyletic. The tree supports recognition of three major clades within the non-bloodwood eucalypts ('eudesmids', 'symphyomyrts' and 'monocalypts') and suggests relationships for taxa within each of these. Ovule and seed characters proved to be most informative in the morphological data set. The phylogenetic hypothesis suggests interpretations for homoplasious morphological characters, including parallel evolution of sepaline and petaline opercula (and associated stemonophore) and types of conflorescence.

Corrigendum to: Systematics and distribution of world hyptiogastrine wasps (Hymenoptera : Gasteruptiidae)

Invertebrate Systematics ◽

10.1071/it01048_co ◽

2002 ◽

Vol 16 (6) ◽

pp. 957 ◽

Cited By ~ 1

Author(s):

J. T. Jennings ◽

A. D. Austin

Keyword(s):

New Species ◽

New Zealand ◽

South America ◽

New Caledonia ◽

Cladistic Analysis ◽

Taxonomic Revision ◽

Morphological Characters ◽

The Family ◽

New Hebrides ◽

New Britain

This study examines the phylogeny, taxonomy, distribution and biology of the gasteruptiid subfamily Hyptiogastrinae and, at the same time, presents an overview of the family. Following a cladistic analysis of 35 discrete morphological characters, two monophyletic genera are recognised, Hyptiogaster Kieffer and Pseudofoenus s. l. Kieffer. As a consequence, the genera Aulacofoenus Kieffer, Crassifoenus Crosskey, and Eufoenus Szépligeti are synonymised with Pseudofoenus. A total of 88 species are recognised for the subfamily, 10 species of Hyptiogaster, which are restricted to mainland Australia, and 78 species of Pseudofoenus, 40 of which are described as new. Pseudofoenus has a restricted Gondwanan distribution and is found in Australia including Tasmania (65 spp.), New Guinea and New Britain (5 spp.), the south-west Pacific (New Caledonia, New Hebrides and Fiji – 2 spp.), New Zealand (4 spp.) and South America (2 spp.). No new species have been recorded from either New Zealand or South America. For Pseudofoenus, information on the distribution of each species, their biology (if known) and an identification key are presented.Following a taxonomic revision, the following new species are described: P. baileyi, sp. nov., P. baitetaensis, sp. nov., P. beverlyae, sp. nov., P. caperatus, sp. nov., P. cardaleae, sp. nov., P. carrabinensis, sp. nov., P. claireae, sp. nov., P. collessi, sp. nov., P. coorowensis, sp. nov., P. crosskeyi, sp. nov., P. douglasorum, sp. nov., P. eliseae, sp. nov., P. ericae, sp. nov., P. eustonensis, sp. nov., P. feckneri, sp. nov., P. gressitti, sp. nov., P. gullanae, sp. nov., P. hackeri, sp. nov., P. imbricatus, sp. nov., P. iqbali, sp. nov., P. kadowi, sp. nov., P. karimuiensis, sp. nov., P. kelleri, sp. nov., P. leinsterensis, sp. nov., P. macdonaldi, sp. nov., P. malkini, sp. nov., P. marshalli, sp. nov., P. masneri, sp. nov., P. mitchellae, sp. nov., P. morganensis, sp. nov., P. nalbarraensis, sp. nov., P. pumilis, sp. nov., P. schmidti, sp. nov., P. stevensi, sp. nov., P. tasmaniensis, sp. nov., P. taylori, sp. nov., P. umboiensis, sp. nov., P. walkeri, sp. nov. and P. zborowskii, sp. nov. The synonymy of Aulacofoenus, Crassifoenus and Eufoenus with Pseudofoenus result in the following new combinations: from Aulacofoenus: P. bungeyi (Jennings & Austin), comb. nov., P. deletangi (Schletterer), comb. nov., P. fallax (Schletterer), comb. nov., P. fletcheri (Jennings & Austin), comb. nov., P. goonooensis (Jennings & Austin), comb. nov., P. infumatus (Schletterer), comb. nov., P. kurmondi (Jennings & Austin), comb. nov., P. loxleyi (Jennings & Austin), comb. nov., P. marionae (Jennings & Austin), comb. nov., P. perenjorii (Jennings & Austin), comb. nov., P. swani (Jennings & Austin), comb. nov., P. thoracicus (Guérin Menéville), comb. nov., P. whiani (Jennings & Austin), comb. nov. and P. wubinensis (Jennings & Austin), comb. nov.; from Crassifoenus: P. houstoni (Jennings & Austin), comb. nov., P. grossitarsis (Kieffer), comb. nov and P. macronyx (Schletterer), comb. nov.; and from Eufoenus: P. antennalis (Schletterer), comb. nov., P. australis (Westwood), comb. nov., P. crassitarsis (Kieffer), comb. nov., P. darwini (Westwood), comb. nov., P. extraneus (Turner), comb. nov., P. ferrugineus (Crosskey), comb. nov., P. floricolus (Turner), comb. nov., P. inaequalis (Turner), comb. nov., P. melanopleurus (Crosskey), comb. nov., P. minimus (Turner), comb. nov., P. nitidiusculus (Turner), comb. nov., P. patellatus (Westwood), comb. nov., P. pilosus (Kieffer), comb. nov., P. reticulatus (Crosskey), comb. nov., P. rieki (Crosskey), comb. nov., P. ritae (Cheesman), comb. nov. and P. spinitarsis (Westwood), comb. nov. Pseudofoenus microcephalus (Crosskey), comb. nov. is transferred from Hyptiogaster and Eufoenus flavinervis (Kieffer) remains incertae sedis.

Journeys Through Shape and Time: Palaeobiology of Cenozoic New Zealand Spissatella and Eucrassatella (Bivalvia, Crassatellidae)

10.26686/wgtn.17004097 ◽

2021 ◽

Author(s):

◽

Katie Susanna Collins

Keyword(s):

New Zealand ◽

Taxonomic Revision ◽

Integrated Approach ◽

Morphological Data ◽

Shell Shape ◽

Shape Variation ◽

Morphometric Data ◽

Hard Part ◽

Outline Shape ◽

External Shell

A novel, highly-integrated approach combining morphometric, stratocladistic and sclerochronological methods has been applied to two genera of New Zealand Cenozoic crassatellid bivalve (Family Crassatellidae): Spissatella Finlay, 1926 and Eucrassatella Iredale, 1924. This study builds on previous work on Spissatella that demonstrated their amenability to shape analysis and provided a foundation for evolutionary studies of the group. The taxonomy of these crassatellids has been in need of revision; a number of changes to generic placement having been proposed in recent publications without redescription. These bivalves are character-depauperate and known only from fossil material within New Zealand, making them challenging subjects for the phylogenetic analysis that would, ideally, inform taxonomic revision. Geometric morphometric methods have been used to characterise the morphological variation of the study group in terms of shape. Landmarks/semilandmarks that capture internal hard-part morphology and external shell shape, have been compared with internal landmarks only, outline shape semilandmarks only, and outline shape Fourier transform methods, and are shown to best combine comprehensive coverage of total shell form with high correct reassignment of individuals to taxa in multidimensional morphospace. Procrustes-superimposed landmark/semilandmark configurations have been ordinated using Principal Components Analysis (PCA), and PCA plots have been used to compare the shape variation of each species. The independance in morphospace of Spissatella n. sp. C from S. trailli and S. clifdenensis has been established. Covariation of internal morphology and shell-shape has been interpreted as supporting the interdependance of shell and body/mantle proposed by Stasek (1963). PCA scores have been combined with traditional morphological characters and stratigraphic data to produce a phylogenetic tree using stratocladistics, a form of parsimony-based analysis which seeks to minimise combined morphological and stratigraphic debt. This technique also assesses the placement of taxa in ancestral positions on internal nodes of the tree. Combining discretised morphometric data with stratigraphic and morphological data in a single analysis has been shown to produce a more resolved tree than analyses based only on continuous morphometric data. The new analyses demonstrate paraphyly of both Eucrassatella and Spissatella as previously recognised. A taxonomic revision of the studied taxa has been undertaken, incorporating information from both morphometric and phylogenetic studies. Spissatella subobesa and S. maudensis are referred to Eucrassatella. Spissatella discrepans is synonymised with S. acculta. Triplicitella n. gen. and S.maxwelli n. sp. are described. Oxygen isotope analysis has been employed to show that shell-banding in these species is, on average, likely to have been laid down annually. Using this information, the longitudinal dataset of outlines from Crampton & Maxwell (2000) has been recalibrated to use chronological age rather than size to compare shape across taxa, and investigate heterochrony in twelve pairs of species representing either ancestor-descendant, sister-group or lineage-segment relationships. All of the heterochronic processes sensu Gould (1977), namely progenesis, neoteny, acceleration and hypermorphosis, as well as proportioned dwarfism and proportioned gigantism, are identified as having affected evolution within this clade.

Journeys Through Shape and Time: Palaeobiology of Cenozoic New Zealand Spissatella and Eucrassatella (Bivalvia, Crassatellidae)

10.26686/wgtn.17004097.v1 ◽

2021 ◽

Author(s):

◽

Katie Susanna Collins

Keyword(s):

New Zealand ◽

Taxonomic Revision ◽

Integrated Approach ◽

Morphological Data ◽

Shell Shape ◽

Shape Variation ◽

Morphometric Data ◽

Hard Part ◽

Outline Shape ◽

External Shell

A novel, highly-integrated approach combining morphometric, stratocladistic and sclerochronological methods has been applied to two genera of New Zealand Cenozoic crassatellid bivalve (Family Crassatellidae): Spissatella Finlay, 1926 and Eucrassatella Iredale, 1924. This study builds on previous work on Spissatella that demonstrated their amenability to shape analysis and provided a foundation for evolutionary studies of the group. The taxonomy of these crassatellids has been in need of revision; a number of changes to generic placement having been proposed in recent publications without redescription. These bivalves are character-depauperate and known only from fossil material within New Zealand, making them challenging subjects for the phylogenetic analysis that would, ideally, inform taxonomic revision. Geometric morphometric methods have been used to characterise the morphological variation of the study group in terms of shape. Landmarks/semilandmarks that capture internal hard-part morphology and external shell shape, have been compared with internal landmarks only, outline shape semilandmarks only, and outline shape Fourier transform methods, and are shown to best combine comprehensive coverage of total shell form with high correct reassignment of individuals to taxa in multidimensional morphospace. Procrustes-superimposed landmark/semilandmark configurations have been ordinated using Principal Components Analysis (PCA), and PCA plots have been used to compare the shape variation of each species. The independance in morphospace of Spissatella n. sp. C from S. trailli and S. clifdenensis has been established. Covariation of internal morphology and shell-shape has been interpreted as supporting the interdependance of shell and body/mantle proposed by Stasek (1963). PCA scores have been combined with traditional morphological characters and stratigraphic data to produce a phylogenetic tree using stratocladistics, a form of parsimony-based analysis which seeks to minimise combined morphological and stratigraphic debt. This technique also assesses the placement of taxa in ancestral positions on internal nodes of the tree. Combining discretised morphometric data with stratigraphic and morphological data in a single analysis has been shown to produce a more resolved tree than analyses based only on continuous morphometric data. The new analyses demonstrate paraphyly of both Eucrassatella and Spissatella as previously recognised. A taxonomic revision of the studied taxa has been undertaken, incorporating information from both morphometric and phylogenetic studies. Spissatella subobesa and S. maudensis are referred to Eucrassatella. Spissatella discrepans is synonymised with S. acculta. Triplicitella n. gen. and S.maxwelli n. sp. are described. Oxygen isotope analysis has been employed to show that shell-banding in these species is, on average, likely to have been laid down annually. Using this information, the longitudinal dataset of outlines from Crampton & Maxwell (2000) has been recalibrated to use chronological age rather than size to compare shape across taxa, and investigate heterochrony in twelve pairs of species representing either ancestor-descendant, sister-group or lineage-segment relationships. All of the heterochronic processes sensu Gould (1977), namely progenesis, neoteny, acceleration and hypermorphosis, as well as proportioned dwarfism and proportioned gigantism, are identified as having affected evolution within this clade.

The taxonomy, phylogeny and biogeography of the New Zealand Thomisidae (Arachnida: Araneae)

10.26686/wgtn.17142893.v1 ◽

2021 ◽

Author(s):

◽

Phil J. Sirvid

Keyword(s):

New Species ◽

New Zealand ◽

Type Species ◽

Taxonomic Revision ◽

Genetic Data ◽

Junior Synonym ◽

Morphological Data ◽

Distribution Data ◽

Australian Species ◽

Recent Establishment

The New Zealand Thomisidae (crab spiders) are represented in New Zealand by two subfamilies (Stephanopinae and Thomisinae) and were used as a model group to test two competing theories on the origins of the New Zealand spider fauna. The New Zealand thomisids are also given their first full taxonomic revision. The two origin models essentially represent species radiations following recent dispersal or ancient vicariance events. Modern distribution data suggested that the stephanopines are poor dispersers and may provide evidence demonstrating a long period of separation from Australia; while in contrast, thomisines are known to be excellent dispersers. Maximum Likelihood and Bayesian analyses of cytochrome c suboxidase subunit I (COI), 28S ribosomal RNA (28S), histone H3 (H3), NADH dehyrogenase 1 (ND1) data and a combined genetic dataset was undertaken. Results indicate New Zealand stephanopines and thomisines form distinct endemic groups separate from sampled Australian species and appear to have separated from them around 5-6 million years ago. Additionally, genetic data from this study showed i) colour variations are not indicative of cryptic species; ii) previously described species are genetically distinct; iii) several suspected new species are also genetically distinct; iv) the relatively recent establishment of two Australian stephanopines and the occurrence of similar COI haplotypes in disjunct locations suggest that the dispersal ability of stephanopines is greater than previously thought and that radiation following colonization from Australia is a plausible explanation for the current diversity of the New Zealand thomisid biota. The taxonomic revision raises the number of described species from eight to eleven based on a combination of morphological and genetic data. In the stephanopines, Bryantymella Gen. nov. is erected to contain the type species Bryantymella angularis (Urquhart, 1885) comb. nov. as well as B. angulata (Urquhart, 1885) comb. nov., B. thorini sp. nov. and B. brevirostris sp. nov. Two Australian species, Sidymella longipes (Koch, 1874) and S. trapezia (Koch, 1874), are also recorded for New Zealand. Sidymella benhami (Hogg, 1910) is considered to be a junior synonym of Bryantymella angulata (Urquhart, 1885). In the thomisines, all species are now included in the previously monotypic genus Cymbachina Bryant, 1933. The genus now encompasses the type species C. albobrunnea (Urquhart, 1893), C. ambara (Urquhart, 1885) comb. nov., C. albolimbata (L. Koch, 1893) comb. nov., C. sphaeroides (Urquhart, 1885) comb. nov. and D. urquharti sp. nov. Synema suteri Dahl, 1907 is regarded as a junior synonym of C. ambara (L. Koch 1893). All previously described species are redescribed to a modern standard and sexes for some species are described for the first time. Three new species are described. Photographs of adults and diagnostic genitalic characters are included, as are diagnostic keys and updated synonymic, geographic and biological information. Overall, this study indicates that New Zealand thomisids appear to have split from their Australian relatives some 5-6 million years ago and taken in concert with the recent establishment of two Australian stephanopine species, it appears that dispersal to New Zealand by Australian colonists and subsequent radiation into endemic New Zealand forms is a plausible explanation for the current state of the fauna. Genetic and morphological data are mutually supporting and in concert have helped inform the first taxonomic revision ever undertaken for this family in New Zealand.