The artoriine wolf spiders of Australia: the new genus Kochosa and a key to genera (Araneae: Lycosidae).

A key to the six Australian genera of the wolf spider (Lycosidae Sundevall, 1833) subfamily Artoriinae Framenau, 2007 is provided, now including Artoria Thorell, 1877, Artoriopsis Framenau, 2007, Diahogna Roewer, 1960, Kangarosa Framenau, 2010, Kochosa gen. nov. and Tetralycosa Roewer, 1960. Kochosa gen. nov. is described to include 16 species: K. australia sp. nov. (type species; from New South Wales, Queensland, South Australia, Victoria, Western Australia), K. aero sp. nov. (Western Australia), K. asterix sp. nov. (New South Wales, Queensland, Tasmania and Victoria), K. confusa sp. nov. (Queensland), K. erratum sp. nov. (Queensland), K. fleurae sp. nov. (Victoria), K. mendum sp. nov. (Australian Capital Territory, New South Wales, Queensland), K. nigra sp. nov. (Queensland), K. obelix sp. nov. (Western Australia), K. queenslandica sp. nov. (Queensland), K. sharae sp. nov. (South Australia), K. tanakai sp. nov. (New South Wales, Queensland), K. tasmaniensis sp. nov. (Tasmania), K. timwintoni sp. nov. (Western Australia), K. tongiorgii sp. nov., (Queensland), and K. westralia sp. nov. (Western Australia). Kochosa gen. nov. differs distinctly from all other genera within the Artoriinae by somatic and genitalic morphology. Most conspicuous is a distinct off-white or yellowish-white cardiac mark on an otherwise generally uniformly dark abdomen. The cardiac mark is rendered by thick black setae, which are particularly dense posteriorly. The tegular apophysis of the male pedipalp is heavily reduced, generally forming a semi-transparent small lobe. In turn, the embolic division is often complex with a variety of apophyses. Kochosa gen. nov. generally inhabit mesic habitats such as temperate and tropical shrubs and forests along the eastern and south-eastern coast and in the south-western parts of Australia.

Two new species in the orb-weaving spider genus Larinia Simon, 1874 (Araneae, Araneidae) from Western Australia.

Two new species in the orb-weaving spider genus Larinia Simon, 1874 are described, L. sexta n. sp. and L. tumulus n. sp. This elevates the Australian number of described species in the genus to seven. With the exception of two females of L. sexta n. sp. recorded from mainland Western Australia, both species have so far exclusively been found on Barrow Island, 50 km off the north-western Western Australian coast where a third species, L. montagui Hogg, 1914, also occurs. Both new species appear to favour spinifex (Triodia spp.) grassland, but specimen numbers in collections are too low to accurately characterize life history patterns and habitat preferences.

A taxonomic revision of the tube-web spiders of the genus Ariadna (Araneae: Segestriidae) in Tasmania.

The genus Ariadna Audouin, 1826 is revised for Tasmania to include 13 species, ten of which are described as new: Ariadna abbreviata sp. nov., A. alta sp. nov., A. amabilia sp. nov., A. crypticola sp. nov., A. ferrogrisea sp. nov., A. fragilis sp. nov., A. gonzo sp. nov., A. muscosa Hickman, 1929, A. segmentata Simon, 1893, A. subnubilum sp. nov., A. thylacinus sp. nov. and A. tigrina sp. nov.. The species described in this manuscript exhibit high levels of sympatry.

Revision of the new Australasian orb-weaving spider genus Salsa (Araneae, Araneidae).

A new Australasian genus in the orb-weaving spider family Araneidae Clerck, 1757 is described to include seven species: Salsafuliginata (L. Koch, 1871) comb. nov. (type species; = Epeirarubicundula Keyserling, 1887) syn. nov.) (Australia, introduced to New Zealand); S.brisbanae (L. Koch, 1867) comb. nov. (Australia); S.canalae (Berland, 1924) comb. nov. (New Caledonia); S.neneba sp. nov. (Papua New Guinea); S.recherchensis (Main, 1954) comb. nov. (Australia); S.rueda sp. nov. (Australia); and S.tartara sp. nov. (Australia; Lord Howe Island endemic). Salsa gen. nov. belongs to the Australasian informal backobourkiine clade and differs from other genera of this clade by a distinct abdominal shape (single posterior abdominal tubercle) and ventral colouration (pale lateral spindle-shaped bands), male pedipalp morphology (C-shaped median apophysis that has teeth-like tubercles inside the basal arch) and the shape of the female epigyne scape (partially translucent and generally shorter than the epigyne plate). Based mainly on male pedipalp morphology within the backobourkiines, Salsa gen. nov. has closest morphological affinities with Acroaspis Karsch, 1878 and Socca Framenau, Castanheira & Vink, 2022.

A ghost in the salt: A new species of halotolerant tube-web spider in the genus emAriadna/em (Araneae: Segestriidae).

A new species of halotolerant Ariadna Audouin, 1826 is described from Western Australia, based on morphological features of both the male and female, and elevating the total number of described species of Ariadna in Australia to 14. This is the first record of the tube-web spider family Segestriidae Simon, 1893 inhabiting salt lakes, where they construct burrows in to the lake surface. The species is likely to be of conservation importance, due to its specialised habitat requirements and the many threats posed to the salt lake ecosystem. We provide recommendation for Ariadna phantasma sp. nov. to be considered for inclusion in the IUCN Red List.

A further study on the wolf spider subfamily Artoriinae from China (Araneae: Lycosidae).

The further collection and study of Chinese wolf spiders, family Lycosidae Sundevall, 1833, expand the known distribution of the subfamily Artoriinae Framenau, 2007 from Yunnan to Guangxi, Guizhou, and Sichuan Provinces of South China. Sinartoria gen. nov. is described to include two new species, S. damingshanensis sp. nov. (type species) and S. zhuangius sp. nov. In addition, a new Artoria species, A. hamata sp. nov. is described and new distribution records for A. ligulacea (Qu, Peng Yin, 2009) and A. parvula Thorell, 1877 are provided. Within the Artoriinae, Sinartoria gen. nov. appears to be most similar to the South American Lobizon Piacentini Grismado, 2009, but their relationship will remain contentious without a comprehensive phylogenetic analysis of artoriine genera.

Phylogeny of the orb-weaving spider family Araneidae (Araneae: Araneoidea).

We present a new phylogeny of the spider family Araneidae based on five genes (28S, 18S, COI, H3 and 16S) for 158 taxa, identified and mainly sequenced by us. This includes 25 outgroups and 133 araneid ingroups representing the subfamilies Zygiellinae Simon, 1929, Nephilinae Simon, 1894, and the typical araneids, here informally named the "ARA Clade". The araneid genera analysed here include roughly 90% of all currently named araneid species. The ARA Clade is the primary focus of this analysis. In taxonomic terms, outgroups comprise 22 genera and 11 families, and the ingroup comprises three Zygiellinae and four Nephilinae genera, and 85 ARA Clade genera (ten new). Within the ARA Clade, we recognize ten informal groups that contain at least three genera each and are supported under Bayesian posterior probabilities (≥ 0.95): "Caerostrines" (Caerostris, Gnolus and Testudinaria), "Micrathenines" (Acacesia, Micrathena, Ocrepeira, Scoloderus and Verrucosa), "Eriophorines" (Acanthepeira, Alpaida, Eriophora, Parawixia and Wagneriana), "Backobourkiines" (Acroaspis, Backobourkia, Carepalxis, Novakiella, Parawixia, Plebs, Singa and three new genera), "Argiopines" (Arachnura, Acusilas, Argiope, Cyrtophora, Gea, Lariniaria and Mecynogea), "Cyrtarachnines" (Aranoethra, Cyrtarachne, Paraplectana, Pasilobus and Poecilopachys), "Mastophorines" (Celaenia, Exechocentrus and Mastophora,), "Nuctenines" (Larinia, Larinioides and Nuctenea), "Zealaraneines" (Colaranea, Cryptaranea, Paralarinia, Zealaranea and two new genera) and "Gasteracanthines" (Augusta, Acrosomoides, Austracantha, Gasteracantha, Isoxya, Macracantha, Madacantha, Parmatergus and Thelacantha). Few of these groups are currently corroborated by morphology, behaviour, natural history or biogeography. We also include the large genus Araneus, along with Aculepeira, Agalenatea, Anepsion, Araniella, Cercidia, Chorizopes, Cyclosa, Dolophones, Eriovixia, Eustala, Gibbaranea, Hingstepeira, Hypognatha, Kaira, Larinia, Mangora, Metazygia, Metepeira, Neoscona, Paraplectanoides, Perilla, Poltys, Pycnacantha, Spilasma and Telaprocera, but the placement of these genera was generally ambiguous, except for Paraplectanoides, which is strongly supported as sister to traditional Nephilinae. Araneus, Argiope, Eriophora and Larinia are polyphyletic, Araneus implying nine new taxa of genus rank, and Eriophora and Larinia two each. In Araneus and Eriophora, polyphyly was usually due to north temperate generic concepts being used as dumping grounds for species from southern hemisphere regions, e.g. South-East Asia, Australia or New Zealand. Although Araneidae is one of the better studied spider families, too little natural history and/or morphological data are available across these terminals to draw any strong evolutionary conclusions. However, the classical orb web is reconstructed as plesiomorphic for Araneidae, with a single loss in "cyrtarachnines"-"mastophorines". Web decorations (collectively known as stabilimenta) evolved perhaps five times. Sexual dimorphism generally results from female body size increase with few exceptions; dimorphic taxa are not monophyletic and revert to monomorphism in a few cases.

The scorpion-tailed orb-weaving spiders (Araneae, Araneidae, Arachnura) in Australia and New Zealand.

The scorpion-tailed orb-weaving spiders in the genus Arachnura Vinson, 1863 (Araneidae Clerck, 1757) are revised for Australia and New Zealand. Arachnura higginsii (L. Koch, 1872) only occurs in Australia and A. feredayi (L. Koch, 1872) only in New Zealand. A single female collected in south-eastern Queensland (Australia) is here tentatively identified as A. melanura Simon, 1867, but it is doubtful that this species has established in Australia. Two juveniles from northern Queensland do not conform to the diagnoses of any of the above species and are illustrated pending a more thorough revision of the genus in South-East Asia and the Pacific region. An unidentified female from Westport (New Zealand) does not conform to the diagnoses of A. feredayi and A. higginsii, but is not described due to its poor preservation status. Arachnura caudatella Roewer, 1942 (replacement name for Epeira caudata Bradley, 1876), originally described from Hall Sound (Papua New Guinea) and repeatedly catalogued for Australia, is considered a nomen dubium.

Revision of the Australian Union-Jack wolf spiders, genus Tasmanicosa (Araneae, Lycosidae, Lycosinae).

The Australian wolf spider (Lycosidae Sundevall, 1833) genus Tasmanicosa Roewer, 1959 with Lycosa tasmanica Hogg, 1905 as type species is revised to include 14 species: T. godeffroyi (L. Koch, 1865), comb. nov. (= Lycosa tasmanica Hogg, 1905, syn. nov.; = Lycosa zualella Strand, 1907, syn. nov.; = Lycosa woodwardi Simon, 1909, syn. nov.); T. fulgor sp. nov.; T. gilberta (Hogg, 1905) comb. nov.; T. harmsi sp. nov.; T. hughjackmani sp. nov.; T. kochorum sp. nov.; T. leuckartii (Thorell, 1870), comb. nov. (= Lycosa molyneuxi Hogg, 1905, syn. nov.); T. musgravei (McKay, 1974) comb. nov.; T. phyllis (Hogg, 1905) comb. nov. (= Lycosa stirlingae Hogg, 1905, syn. nov.); T. ramosa (L. Koch, 1877), comb. nov.; T. salmo sp. nov.; T. semicincta (L. Koch, 1877) comb. nov.; T. stella sp. nov.; and T. subrufa (Karsch, 1878) comb. nov. Within the Australian wolf spider fauna, the genus Tasmanicosa can be diagnosed by the distinct pattern of radiating light and dark lines forming a "Union-Jack" pattern on the carapace. Male pedipalp morphology identifies the genus as part of the subfamily Lycosinae Sundevall, 1833 due to the presence of a transverse tegular apophysis with dorsal groove guiding the embolus during copulation. However, genital morphology is variable and a synapomorphy based on male pedipalp or female epigyne morphology could not be identified. Members of Tasmanicosa are comparatively large spiders (body length ca. 12-30 mm), that build a shallow burrow, which is sometimes covered with a flimsy trapdoor. Species of Tasmanicosa are largely a Bassian faunal element with preference for open woodlands and/or floodplains, although some species can be found into the semi-arid Australian interior. Two Australian wolf spider species may represent Tasmanicosa based on their original descriptions, but due to immature types in combination with the somatic similarities of all Tasmanicosa species, cannot be identified with certainty. They are therefore considered nomina dubia: Lycosa excusor L. Koch, 1867 and Lycosa infensa L. Koch, 1877. The type species of Orthocosa Roewer, 1960 is transferred to Tasmanicosa; however, in order to prevent some non-Australian wolf spiders in the genus Orthocosa to be transferred into Tasmanicosa, which is considered endemic to Australia, we here place these species into more appropriate genera based on their original descriptions pending a future revision of these species: Arctosa ambigua Denis, 1947 comb. reval.; Alopecosa orophila (Thorell, 1887) comb. nov.; Hygrolycosa tokinagai Saito, 1936 comb. reval. Orthocosa sternomaculata (Mello-Leitão, 1943) is considered a junior synonym of Hogna birabeni (Mello-Leitão, 1943) comb. nov.

Review of the Australian wolf spider genus Venator (Araneae, Lycosidae).

Species of the Australian wolf spider genus Venator are reviewed including the type species, V. spenceri Hogg, 1900, from south-eastern Australia and V. immansuetus (Simon, 1909) comb. nov., a common species in south-west Western Australia. Venator marginatus Hogg, 1900 is only known from two female specimens and the genital morphology of this species does not conform to the diagnosis of genus as presented here. Therefore V. marginatus is considered incerta sedis. Venator includes medium-sized (9.0-22 mm body length) wolf spiders of overall brownish colouration, and with a black patch covering the anterior three quarters of the venter. They differ from all other wolf spiders in particular by genitalic characters, namely an elevated atrium of the female epigyne that forms a raised edged against the inverted T-shaped median septum. This edge often corresponds to a retrolateral incision on the tegular apophysis of the male pedipalp. The genus is mainly a representative of the Bassian fauna of the Australian continent where it occurs predominantly in dry sclerophyll forests.

Nukuhiva Berland, 1935 is a troglobitic wolf spider (Araneae: Lycosidae), not a nursery-web spider (Pisauridae).

The monotypic genus Nukuhiva Berland, 1935 with N. adamsoni (Berland, 1933) as type species, is re-described and transferred from the Pisauridae Simon, 1890 (fishing or nursery-web spiders) to the Lycosidae Sundevall, 1833 (wolf spiders) based on genitalic and somatic characters. Nukuhiva adamsoni, originally described from French Polynesia, appears to inhabit mountainous habitats of volcanic origin. Its troglobitic morphology--comparatively small eyes and pale, uniform coloration--suggest it to be associated with subterranean habitats such as caves or lava tubes, similar to the Hawaiian troglobitic species Lycosa howarthi Gertsch, 1973 and Adelocosa anops Gertsch, 1973.

New species of mouse spiders (Araneae: Mygalomorphae: Actinopodidae: Missulena) from the Pilbara region, Western Australia.

Two new species of Mouse Spiders, genus Missulena, from the Pilbara region in Western Australia are described based on morphological features of males. Missulena faulderi sp. nov. and Missulena langlandsi sp. nov. are currently known from a small area in the southern Pilbara only. Mitochondrial cytochrome c oxidase subunit I (COI) sequence divergence failed in clearly delimiting species in Missulena, but provided a useful, independent line of evidence for taxonomic work in addition to morphology.

Predicting the post-fire responses of animal assemblages: testing a trait-based approach using spiders.

1. Developing a predictive understanding of how species assemblages respond to fire is a key conservation goal. In moving from solely describing patterns following fire to predicting changes, plant ecologists have successfully elucidated generalizations based on functional traits. Using species traits might also allow better predictions for fauna, but there are few empirical tests of this approach. 2. We examined whether species traits changed with post-fire age for spiders in 27 sites, representing a chronosequence of 0-20 years post-fire. We predicted a priori whether spiders with ten traits associated with survival, dispersal, reproduction, resource-utilization and microhabitat occupation would increase or decrease with post-fire age. We then tested these predictions using a direct (fourth-corner on individual traits and composite traits) and an indirect (emergent groups) approach, comparing the benefits of each and also examining the degree to which traits were intercorrelated. 3. For the seven individual traits that were significant, three followed predictions (body size, abundance of burrow ambushers and burrowers was greater in recently burnt sites); two were opposite (species with heavy sclerotisation of the cephalothorax and longer time to maturity were in greater abundance in long unburnt and recently burnt sites respectively); and two displayed response patterns more complex than predicted (abdominal scutes displayed a U-shaped response and dispersal ability a hump shaped curve). However, within a given trait, there were few significant differences among post-fire ages. 4. Several traits were intercorrelated and scores based on composite traits used in a fourth-corner analysis found significant patterns, but slightly different to those using individual traits. Changes in abundance with post-fire age were significant for three of the five emergent groups. The fourth-corner analysis yielded more detailed results, but overall we consider the two approaches complementary. 5. While we found significant differences in traits with post-fire age, our results suggest that a trait-based approach may not increase predictive power, at least for the assemblages of spiders we studied. That said, there are many refinements to faunal traits that could increase predictive power.

Phylogenetic reconstruction of the wolf spiders (Araneae: Lycosidae) using sequences from the 12S rRNA, 28S rRNA, and NADH1 genes: implications for classification, biogeography, and the evolution of web building behavior.

Current knowledge of the evolutionary relationships amongst the wolf spiders (Araneae: Lycosidae) is based on assessment of morphological similarity or phylogenetic analysis of a small number of taxa. In order to enhance the current understanding of lycosid relationships, phylogenies of 70 lycosid species were reconstructed by parsimony and Bayesian methods using three molecular markers; the mitochondrial genes 12S rRNA, NADH1, and the nuclear gene 28S rRNA. The resultant trees from the mitochondrial markers were used to assess the current taxonomic status of the Lycosidae and to assess the evolutionary history of sheet-web construction in the group. The results suggest that a number of genera are not monophyletic, including Lycosa, Arctosa, Alopecosa, and Artoria. At the subfamilial level, the status of Pardosinae needs to be re-assessed, and the position of a number of genera within their respective subfamilies is in doubt (e.g., Hippasa and Arctosa in Lycosinae and Xerolycosa, Aulonia and Hygrolycosa in Venoniinae). In addition, a major clade of strictly Australasian taxa may require the creation of a new subfamily. The analysis of sheet-web building in Lycosidae revealed that the interpretation of this trait as an ancestral state relies on two factors: (1) an asymmetrical model favoring the loss of sheet-webs and (2) that the suspended silken tube of Pirata is directly descended from sheet-web building. Paralogous copies of the nuclear 28S rRNA gene were sequenced, confounding the interpretation of the phylogenetic analysis and suggesting that a cautionary approach should be taken to the further use of this gene for lycosid phylogenetic analysis.

Australian wolf spider bites (Lycosidae): clinical effects and influence of species on bite circumstances.

BACKGROUND: Necrotic arachnidism continues to be attributed to wolf spider bites. This study investigates the clinical effects of bites by wolf spiders in Australia (family Lycosidae). METHODS: Subjects were recruited prospectively from February 1999 to April 2001 from participating emergency departments or state poison information centers. Subjects were included if they had a definite bite by a wolf spider and had collected the spider, which was later identified by an arachnologist. Spiders were identified to the lowest taxonomic level possible and cephalothorax width was measured to correlate bite effects and spider size. RESULTS: There were 45 definite wolf spider bites (23 male and 22 female patients; age range 1 to 69 years, median age 28 years). Species level identifications (14 species) were possible for 31 of 43 spiders belonging to seven different generic groupings. Most bites were by spiders from four generic groupings, Tasmanicosa (including 'Lycosa') (15), Venatrix (8), Venator (10), and Hogna (7). Bites occurred more commonly in south-eastern Australia and occurred throughout the year, with 7 bites (16%) in late autumn or winter. In 7 cases (16%) the person was swimming in or cleaning a pool. Seventy-two percent of bites occurred on distal parts of limbs. Pain occurred in all bites and was severe in 11 cases (24%), with a median duration of 10 min (IQR: 2-60 min). Other effects included puncture marks/bleeding (33%), swelling (20%), redness (67%), and itchiness (13%). Minor systemic effects occurred in three patients (7%): nausea (two), headache (one) and malaise (one). There were no cases of necrotic ulcers [0%; 97.5% CI 0-8%]. Tasmanicosa spider bites caused significantly more itchiness and redness, and large spiders (>5 mm) more often caused severe pain and left fang marks. CONCLUSION: Wolf spider bites cause minor effects, no more severe than most other spiders, and do not appear to cause necrotic ulcers. The effects are likely to be due to mechanical injury, although minor local envenomation occurs with Tasmanicosa bites.