Research Article |
Corresponding author: Volker W. Framenau ( volker.framenau@murdoch.edu.au ) Academic editor: Danilo Harms
© 2018 Volker W. Framenau, Barbara C. Baehr.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Framenau VW, Baehr BC (2018) The wolf spider genus Artoria in New South Wales and the Australian Capital Territory, Australia (Araneae, Lycosidae, Artoriinae). Evolutionary Systematics 2: 169-241. https://doi.org/10.3897/evolsyst.2.30778
|
The wolf spider (Lycosidae Sundevall, 1833) genus Artoria Thorell, 1877 is revised for New South Wales and the Australian Capital Territory, Australia, to include 34 species, 21 of which are new to science: A. albopilata (Urquhart, 1893), A. alta
Taxonomy, systematics, arachnology, forest spiders
The genus wolf spider genus Artoria Thorell, 1877 includes small, free-roaming spiders with a fairly uniform morphology. They are overall brown in colouration, with variably lighter central and marginal areas on the carapace and often with a light cardiac mark on an otherwise variably mottled abdomen (Fig.
Life images of Artoria species. A, A. mckayi Framenau, 2002 (male from Avon River, Victoria); B, A. mckayi (female with eggsac from Avon River, Victoria); C, A. flavimana Simon, 1909 (female from Capel, Western Australia); D, A. taeniifera Simon, 1909 (female from Ravensthorpe, Western Australia). All species occur in New South Wales; A. mckayi has also been found in the Australian Capital Territory.
Artoria has an Oriental-Pacific distribution and currently includes 32 species (
In Australia, species of the genus Artoria are most common in the Bassian and Torresian bioregions, i.e. along the eastern coast, in the south-east (including Tasmania), in south-western Western Australia and in the tropical northern parts of the country. Very few records are from the interior and these are often from near intermittent or permanent water bodies (
Prior to this study, 13 species of Artoria were known from New South Wales (NSW) and the Australian Capital Territory (ACT). The Bush Blitz survey to Mungo National Park in 2017 (see http://www.bushblitz.org.au; accessed 20 October 2018) resulted in the discovery of a new species of Artoria which provided the opportunity to apply for funding to resolve the taxonomy of the genus in the region. Previous studies by the senior author suggested a considerable biodiversity of the genus in the eastern part of Australia. Therefore, the aim of this study was to comprehensively revise all species of Artoria in NSW and the ACT.
This study is based on the examination of 1,580 records (vials) including 2,760 males and 1,389 females of Artoria from NSW (1,554 records) and the ACT (26 records) in mainly the Australian Museum, Sydney, and the Australian National Insect Collection, Canberra, supplemented by material from other Australian and overseas institutions (see abbreviations of institutions below). Descriptions are based on spiders stored in 70% ethanol, preferable using recent and representative material in lieu of poorly preserved historical type specimens.
For examination and illustration, female internal genitalia were placed in a Pancreatin solution for a few hours as described in
Digital images were taken using a Leica DFC 500 digital camera attached to a Leica MZ16A stereo microscope. To increase depth of field, multiple images were merged using the software package AutoMontage Pro Version 5.02 (p).
All measurements are in millimetres (mm). Morphological nomenclature follows
Life history data as described for each species generally refer to populations from New South Wales or the Australian Capital Territory. If species are more widespread and occur in different climatic zones (i.e. in Queensland or Tasmania), it is possible phenological data varies from those described here.
Distribution data of all Artoria species are interpreted and mapped based on the Interim Biogeographical Regionalisation of Australia (IBRA) (
Anatomy
AE anterior eyes
ALE anterior lateral eyes
AME anterior median eyes
PLE posterior lateral eyes
PME posterior median eyes
TA tegular apophysis
BA basoembolic apophysis
SAM South Australian Museum, Adelaide
ZSMH Zoologisches Institut und Zoologisches Museum, Universität Hamburg (today CeNak, Centrum für Naturkunde, Universität Hamburg), Germany
This revision recognizes 34 species of Artoria in NSW, five of which currently also known from the ACT (Table
The distribution of Artoria species in NSW and the ACT corresponds largely with the forests east and west of the Great Dividing Range, although some species are clearly coastal (for example A. booderee sp. n. and A. strepera sp. n.). Some occur further into central NSW (for example A. victoriensis Framenau, Gotch & Austin, 2006 and A. howquaensis Framenau, 2002). Twelve species are currently known only from their type localities or from very small ranges and should be considered short- or narrow range endemic species (
This regional review focussing on a single geographic state and one territory doubles the number of species of Artoria in Australia, demonstrating the high diversity of the genus in this country. At least 15 undescribed species of Artoria are known from Western Australia (V.W. Framenau, unpublished data) and similar ratios of undescribed to described species can be expected from other states. A conservative estimate for the total number of species of Artoria in Australia is 150–180 species, thereby likely representing the largest genus of Australian wolf spiders and a considerable challenge for taxonomic research.
Distribution of Artoria species currently known from New South Wales and Australian Capital Territory.
Species | Current known distribution | Sexes known | Comments |
---|---|---|---|
A. albopilata (Urquhart, 1893) | ACT, NSW–Qld, SA, Tas, Vic | M, F | |
A. alta Framenau, 2004 | NSW | M, F(?) | conspecifity of female with type material unclear; SRE |
A. barringtonensis sp. n. | NSW | M | Known only from type locality; SRE |
A. beaury sp. n. | NSW | M, F | |
A. belfordensis sp. n. | NSW | M, F | |
A. berenice (L. Koch, 1877) | NSW–Qld, Tas, Vic; also, Vanuatu and New Caledonia | M, F | |
A. bondi sp. n. | NSW | M | Known only from type locality; SRE |
A. booderee sp. n. | NSW | M, F | SRE |
A. comleroi sp. n. | NSW | M, F | Known only from type locality; SRE |
A. corowa sp. n. | NSW | M, F | |
A. equipalus sp. n. | NSW | M, F | Known only from type locality; SRE |
A. extraordinaria sp. n. | NSW | M, F | |
A. flavimana Simon, 1909 | ACT, NSW–SA, Tas, Vic, WA | M, F | |
A. gloriosa (Rainbow, 1920) | NSW | M, F | Endemic to Lord Howe Island; SRE |
A. grahammilledgei sp. n. | NSW–Qld | M, F | |
A. helensmithae sp. n. | NSW–Vic | M, F | |
A. howquaensis Framenau, 2002 | NSW–SA, Vic | M, F | |
A. kanangra sp. n. | NSW | M | SRE |
A. kerewong sp. n. | NSW | M | Known only from type locality; SRE |
A. lineata (L. Koch, 1877) | ACT, NSW–Qld, SA, Tas, Vic | M, F | |
A. maroota sp. n. | NSW | M | |
A. mckayi Framenau, 2002 | ACT, NSW–Qld, SA, Tas, Vic | M, F | |
A. mungo sp. n. | NSW | M, F | |
A. munmorah sp. n. | NSW | M, F | |
A. myallensis sp. n. | NSW | M | Known only from type locality; SRE |
A. quadrata Framenau, 2002 | ACT, NSW–Qld, Vic | M, F | |
A. slatyeri sp. n. | NSW | M | SRE |
A. strepera sp. n. | NSW | M | SRE |
A. taeniifera Simon, 1909 | NSW–SA, WA | M, F | |
A. terania sp. n. | NSW–Qld | M, F | |
A. triangularis Framenau, 2002 | NSW–Qld, SA, Tas, Vic | M, F | |
A. ulrichi Framenau, 2002 | NSW–Vic | M, F | |
A. victoriensis Framenau, Gotch & Austin, 2006 | NSW–Qld, SA, Tas, Vic | M, F | |
A. wilkiei sp. n. | NSW | M, F |
This study documents a considerable morphological diversity of Artoria in NSW and the ACT. Some informal species groups of putatively more closely-related species can be distinguished, for example a ‘lineata-group’, including A. lineata, A. quadrata and A. ulrichi, in which males have a spoon-shaped tegular apophysis, or a booderee-group (A. booderee sp. n., A. corowa sp. n., A. equipalus sp. n. and A. munmorah sp. n.), having small spiders in which males have a two-lobed tegular apophysis. Other species, such as A. extraordinaria sp. n., have an unusual genital morphology for Artoria, with no known similar species. It is possible future phylogenetic research will consider these groups or species discernible at the genus level. However, as the currently described fauna of Artoria only represents a fraction of the species present in Australia based on artificial geographic boundaries, a more comprehensive taxonomic documentation is required to formulate testable phylogenetic hypotheses at the genus level. This analysis should include representatives from the total distribution range of Artoria and other genera of the Artoriinae, a subfamily that reaches into China and the Pacific Ocean (
Artoriella Roewer, 1960 (synonymy established in Framenau, 2002: 210)
Lycosula
Roewer, 1960 (synonymy established in
Trabaeola
Roewer, 1960 (synonymy established in
Artoria parvula Thorell, 1877, by original designation (
In NSW and the ACT, five genera of the subfamily Artoriinae have been found: Artoria, Artoriopsis Framenau, 2007, Diahogna Roewer, 1960, Kangarosa Framenau, 2010 and Tetralycosa Roewer, 1960. The row of the anterior eyes in the latter three genera is generally wider than the row of the posterior median eyes and therefore these genera are thought to form a natural group (
Artoria males, anterior eye row, frontal view: A, A. strepera sp. n. (
(after
Chelicerae with three (rarely one or two) promarginal and three (rarely one or two) retromarginal teeth; labium as long as or slightly longer than wide; leg formula IV>I>I>III; tegular apophysis located apically at tegulum and of variable shape; basoembolic apophysis broad, heavily sclerotised and bent ventrally; embolus of varying shape (slim to very thick); terminal apophysis functioning as conductor, sometimes forming a groove for the resting embolus; most species with varying number of macrosetae at tip of male cymbium; a scopulate patch of setae occasionally present dorsally on cymbium. Epigyne variable, a simple opening of varying shape or covered by a sclerotised ovoid plate.
1 | Males | 2 |
– | Females (unknown for A. barringtonensis sp. n., A. bondi sp. n., A. kanangra sp. n., A. kerewong sp. n., A. maroota sp. n., A. myallensis sp. n., A. slatyeri sp. n., A. strepera sp. n.) | 35 |
2 | Anterior eye row straight (Fig. |
3 |
– | Anterior eye row procurved, i.e. anterior lateral eyes are lower than anterior median eyes in frontal view (Fig. |
8 |
3 | Distance between AME/AME at least twice of AME/ALE (Fig. |
A. barringtonensis sp. n. |
– | Anterior eyes evenly spaced (Fig. |
4 |
4 | Dorsal scopula patch on cymbium absent (Fig. |
A. bondi sp. n. |
– | Dorsal scopula patch on cymbium present (Fig. |
5 |
5 | Palea about twice as long as wide, basoembolic apophysis large rounded (Fig. |
A. slatyeri sp. n. |
– | Palea shorter (Figs |
6 |
6 | Palea about 1.5 times as long as wide, basoembolic apophysis large triangular (Fig. |
A. booderee sp. n. |
– | Palea about as long as wide (Figs |
7 |
7 | Basoembolic apophysis (BA) rounded (Fig. |
A. albopilata |
– |
BA triangular (Fig. |
A. strepera sp. n. |
8 | Anterior eye row strongly procurved (Fig. |
9 |
– | Anterior eye row slightly procurved (Fig. |
16 |
9 | Distance between AME/ALE at least twice of AME/AME (Fig. |
A. extraordinaria sp. n. |
– | Anterior eye row evenly spaced (Fig. |
10 |
10 | Dorsal scopula patch on cymbium absent (Figs |
11 |
– | Dorsal scopula patch on cymbium present (Figs |
14 |
11 | Palea about as long as wide (Fig. |
A. equipalus sp. n. |
– | Palea about twice as long as wide (Figs |
12 |
12 | Tegular apophysis (TA) three-lobed (Fig. |
A. belfordensis sp. n. |
– |
TA distinctly two-pronged (Fig. |
A. taeniifera |
14 | Palea about as long as wide (Fig. |
A. comleroi sp. n. |
– | Palea about 1.5 times as long as wide (Figs |
15 |
15 |
BA large triangular, embolus straight (Fig. |
A. corowa sp. n. |
– |
BA rounded, embolus apically coiled (Fig. |
A. howquaensis |
16 | Dorsal scopula patch on cymbium absent (Figs |
17 |
– | Dorsal scopula patch on cymbium present (Figs |
24 |
17 | Anterior spinnerets ventrally pale (Fig. |
A. flavimana |
– | Anterior spinnerets ventrally dark grey (Figs |
18 |
18 | Palea about twice as long as wide (Figs |
19 |
– | Palea about 1.5 times as long as wide (Fig. |
20 |
– | Palea about as long as wide (Figs |
21 |
19 | Embolus broad, basally curved (Fig. |
A. kerewong sp. n. |
– | Embolus thin and basal edge straight, tegular apophysis large spoon-shaped (Fig. |
A. lineata |
20 |
TA without retrolateral hook (Fig. |
A. beaury sp. n. |
– |
TA with strong retrolateral hook (Fig. |
A. helensmithae sp. n. |
21 |
TA distally scooped, basally not narrowed, tip with central spike (Fig. |
A. berenice |
– |
TA distally widely scooped, basally narrowed to 1/4 (Figs |
22 |
22 |
TA rounded, without retrolaterally pointed tip (Fig. |
A. ulrichi |
– |
TA with retrolaterally pointed tip (Figs |
23 |
23 |
TA tip prolaterally semicircular (Fig. |
A. quadrata |
– |
TA tip prolaterally s-shaped (Fig. |
A. victoriensis |
24 | Anterior spinnerets ventrally pale (Figs |
25 |
– | Anterior spinnerets ventrally dark grey (Fig. |
30 |
25 |
TA finger-shaped, basally not narrowed (Fig. |
A. gloriosa |
– |
TA basally narrowed (Figs |
26 |
26 |
TA tip without appendices, nearly semi-circular, with central hook (Fig. |
A. alta |
– |
TA tip with appendices, not semi-circular (Fig. |
27 |
27 |
BA triangular, TA inverted L-shaped with distal hook (Fig. |
A. maroota sp. n. |
– |
BA rounded (Figs |
28 |
28 |
BA large occupies prolateral part of palea (Fig. |
A. wilkiei sp. n. |
– |
BA smaller only in dorso-prolateral part of palea (Figs |
29 |
29 |
TA tip long pointed directed prolaterally (Fig. |
A. mckayi |
– |
TA tip distally deeply indented building 2 appendices (Fig. |
A. myallensis sp. n. |
30 | Palea about twice as long as wide, basoembolic apophysis triangular (Figs |
31 |
– | Palea shorter (Figs |
32 |
31 |
TA distally widely scooped, basally narrowed to 1/3 (Fig. |
A. terania sp. n. |
– |
TA basally narrowed to 1/2 (Fig. |
A. grahammilledgei sp. n. |
32 | Palea about 1.5 times as long as wide, basoembolic apophysis triangular (Figs |
33 |
– | Palea about as long as wide (Figs |
34 |
33 |
TA inverted L-shaped (Fig. |
A. mungo sp. n. |
– |
TA birdhead-shaped (Fig. |
A. kanangra sp. n. |
34 |
TA medially widened, tip distally pointed, not reaching cymbium (Fig. |
A. triangularis |
– |
TA medially constricted, tip bent deeply indented, reaching cymbium (Fig. |
A. munmorah sp. n. |
35 | Anterior eye row straight, anterior eyes evenly spaced (Fig. |
36 |
– | Anterior eye row procurved (Fig. |
38 |
36 | Atrium narrow, inverted U-shaped, spermathecal heads 2x diameter apart (Fig. |
A. booderee sp. n. |
– | Atrium wide semicircular, spermathecal heads 1 diameter apart (Figs |
37 |
37 | Spermathecal heads globular (Fig. |
A. equipalus sp. n. |
– | Spermathecal heads sausage-shaped (Fig. |
A. albopilata |
38 | Anterior eye row strongly procurved (Fig. |
39 |
– | Anterior eye row slightly procurved (Fig. |
43 |
39 | Distance between AME/ALE at least twice of AME/AME (Fig. |
A. extraordinaria sp. n. |
– | Anterior eye row evenly spaced (Fig. |
40 |
40 | Atrium with 2 large oval copulatory openings, stalks connected medially (Fig. |
A. comleroi sp. n. |
– | Atrium different, stalks not medially connected (Figs |
41 |
41 | Atrium inverted U-shaped or obscure, without scapus (Figs |
42 |
– | Atrium with w-shaped scapus (Fig. |
A. corowa sp. n. |
42 | Stalks short, connected posteriorly to spermathecal head (Fig. |
A. equipalus sp. n. |
– | Stalks long, connected laterally to spermathecal heads (Fig. |
A. taeniifera |
– | Stalks slightly S-shaped, connected postero-laterally to spermathecal heads (Fig. |
A. belfordensis sp. n. |
43 | Spermathecal heads massive, almost touching medially (Figs |
44 |
– | Spermathecal heads smaller, not touching medially (Figs |
46 |
44 | Spermathecal heads massive globular (Fig. |
A. wilkiei sp. n. |
– | Spermathecal heads massive ellipsoid (Figs |
45 |
45 | Atrium almost rectangular (Fig. |
A. grahammilledgei sp. n. |
– | Atrium almost bell-shaped (Fig. |
A. terania sp. n. |
46 |
Epigyne with scapus (Figs |
47 |
– |
Epigyne without well-developed scapus (Figs |
51 |
47 | Scapus tongue-shaped (Figs |
48 |
– | Scapus of varying shape, not tongue-shaped (Fig. |
49 |
48 | Spermathecal heads sausage-shaped, not separated from stalks (Fig. |
A. gloriosa |
– | Spermathecal head more globular, separated from stalks (Fig. |
A. mckayi |
49 | Scapus broadly w-shaped (Fig. |
A. lineata |
– | Scapus inverted T-shaped (Figs |
50 |
50 | Spermathecal stalks long and convoluted, heads connected medially (Fig. |
A. victoriensis |
– | Spermathecal heads connected to stalks laterally (Fig. |
A. ulrichi |
51 | Spermathecal heads triangular or ellipsoid (Fig. |
A. triangularis |
– | Spermathecal heads globular (Figs |
52 |
52 | Spermathecal heads at least 3 x diameter apart (Fig. |
A. flavimana |
– | Spermathecal heads 1diameter or less apart (Figs |
53 |
53 | Spermathecal heads 1 diameter (Figs |
54 |
– | Spermathecal heads ½ diameter or less apart (Figs |
56 |
54 | Stalks short, connected to spermathecal heads posteriorly (Fig. |
A. alta |
– | Stalks long, connected to spermathecal heads laterally (Figs |
55 |
55 |
Epigyne posterior tips massive, strongly sclerotized (Fig. |
A. quadrata |
– |
Epigyne posterior tips less sclerotized (Fig. |
A. helensmithae sp. n. |
56 | Atrium semicircular (Fig. |
A. mungo sp. n. |
– | Atrium different (Figs |
57 |
57 | Atrium bell-shaped (Fig. |
A. munmorah sp. n. |
– | Atrium obscure (Fig. |
A. beaury sp. n. |
Lycosa
albo-pilata
Urquhart, 1893: 123–125.-
Lycosa
albopilata
, Urquhart.-
Artoria
albopilata
(Urquhart).-
Syntypes male and female of Lycosa albo-pilata Urquhart, 1893, no exact locality given [Tasmania, AUSTRALIA]. As many other Urquhart types, considered lost (
Artoria albopilata (Urquhart, 1893) male, female (
588 males, 128 females and 45 juveniles in 152 records (146 NSW, 5 ACT). AUSTRALIA: Australian Capital Territory: 8 males, 1 female, Blundells Creek, 3 km E of Piccadilly Circus, 35°22’S, 148°50’E (
Artoria albopilata is most similar to A. gloriosa, a species endemic to Lord Howe Island. Males differ in the shape of the tegular apophysis, which ends in three lobes in A. albopilata (Fig.
Artoria albopilata has been described in detail (
Artoria albopilata is a forest species occurring in leaf litter. In NSW and the ACT, it has been found in open to closed dry to wet sclerophyll forests, with one record from a Hoop Pine plantation.
Mature males and females appear in spring in October with the highest number of records in November. There is a much smaller peak around March. A single female with eggsac was found in January. Mature spiders can be found until May. There are also few records of mature spiders from July.
In NSW and ACTA. albopilata is particularly found east of the Great Dividing Range (Fig.
Artoria
alta
Framenau, 2004: 28–30, Figs
Holotype male, Kosciuszko National Park, near Smiggins Hole (36°24’S, 148°26”E, New South Wales, AUSTRALIA), 1,700 m alt., alpine moor, D. Bickel (
Distribution records of Artoria albopilata (Urquhart, 1893) (full circles), A. alta Framenau, 2004 (grey triangles) and A. barringtonensis sp. n. (grey square) in NSW and ACT. IBRA bioregions with spider records: AUA – Australian Alps; NET – New England Tablelands; NNC – NSW North Coast; SEQ – South East Queensland; SHE – South Eastern Highlands; SYB – Sydney Basin.
AUSTRALIA: New South Wales: 1 female, Kosciuszko National Park, Three Mile Dam, 35°53’S, 148°27”E (
The tegular apophysis in male A. alta has a distinctive shape with a terminal part that resembles, in ventral view of the pedipalp, a bicycle seat (Fig.
Artoria alta (Framenau, 2004) male (
The male of A. alta has been described in detail (
Artoria alta is known only from subalpine or alpine habitats in Kosciuszko National Park in New South Wales. Mature males and females have so far only been found in summer, between end of November and end of December.
Known only from Kosciuszko National Park, NSW, in the Australian Alps (AUA) IBRA region (Fig.
Holotype male, 180 m off Barrington Tops Forest Road, Barrington Tops National Park [31°57’S, 151°25’E, New South Wales, AUSTRALIA], 11–21 Jan 2012, J.R. Gollan, M.A. Ashcroft, pitfall trap, edge of upland swamp (
Known only from type specimen.
The specific name is an adjective in apposition derived from the type locality, Barrington Tops National Park.
The tegular apophysis in males of A. barringtonensis sp. n. is distinct amongst the known species of the genus due to the presence of a row of apical teeth, which are visible in lateral view (Fig.
Male (based on holotype,
Total length 3.6.
Prosoma. Length 2.3, width 1.5; carapace yellow-brown, dusted with grey and with an indistinct dark radial pattern; lateral margin and central band pale yellow, broader in cephalic area (Fig.
Eyes (Fig.
Anterior eye row. Straight, distance between AME/AME at least twice of AME/ALE.
Chelicerae. Medium brown.
Labium. Dark brown, with lighter anterior rim (Fig.
Pedipalp coxae. Dark brown, with lighter anterior rim (Fig.
Legs. Femora and tibiae of leg I very dark; other legs yellow brown, with no annulations (Fig.
Opisthosoma. Length 1.6, width 1.3; dark grey with light yellow-brown anterior cardiac mark, reaching end of opisthosoma and light irregular pattern (Fig.
Pedipalps. Tibia as long as broad; cymbium tip with 4–5 macrosetae (Fig.
Female unknown.
A–D, Artoria barringtonensis sp. n., male holotype (
The single male of this species was found at the edge of an upland swamp in summer (January).
Artoria barringtonensis sp. n. is known only from its type locality, the Barrington Tops National Park in the south-eastern NSW North Coast (NNC) IBRA region (Fig.
Holotype male, Beaury State Forest, Tooloom Scrub [28°35’S, 152°22’E, New South Wales, AUSTRALIA], sheltered ridge, 600–900 m alt., 12 December 1988, H. Smith et al., pitfall trap (
Artoria beaury sp. n., male holotype (
92 males, 48 females and 2 juveniles in 58 records (all NSW). AUSTRALIA: New South Wales: 4 males, Acacia Plateau, Wilsons Peak area, Koreelah State Forest, 28°16’S, 152°27’E (
The specific epithet is a noun in apposition and refers to the type locality, Beaury State Forest.
Pedipalps of male Artoria beaury sp. n. are most similar to Artoria helensmithae sp. n.; however, the basoembolic apophysis is broadly rounded (Fig.
Male (based on holotype,
Total length 3.9.
Prosoma. Length 2.1, width 1.5; carapace light reddish-brown with dark radial pattern and black V-shaped pattern between cephalic and thoracic region; indistinct and irregular broad lighter marginal band (Fig.
Eyes. Diameter of AME: 0.08; ALE: 0.05; PME: 0.23; PLE: 0.18.
Anterior eye row. Slightly procurved, evenly spaced.
Chelicerae. Dark brown, darker apically.
Labium. Dark brown, with lighter anterior rim (Fig.
Pedipalp coxae. Dark brown, with lighter anterior rim (Fig.
Legs. Femora and tibiae of leg I very dark to almost black; other legs brown, femora and tibia with darker annulations, particularly ventrally; tarsi and metatarsi lighter reddish-brown (Fig.
Opisthosoma. Length 1.8, width 1.1; cinnamon-brown with light yellow-brown anterior cardiac mark and dark grey irregular pattern mainly in posterior half (Fig.
Pedipalps. Tibia as long as broad; Cymbium tip with 4–5 macrosetae (Fig.
Female (based on paratype,
Total length 5.0.
Prosoma. Length 2.4, width 1.6; carapace and sternum colouration as male (Fig.
Eyes. Diameter of AME 0.06, ALE 0.05, PME 0.25, PLE 0.16.
Anterior eye row. Slightly procurved, evenly spaced.
Chelicerae, labium, pedipalp coxae, legs and opisthosoma. Opisthosoma length 2.6, width 1.9; otherwise as male, but legs I not darker and opisthosoma pattern more obscure (Fig.
Epigyne about as long as wide, poorly sclerotized at posterior tips, atrium lighter (Fig.
Artoria beaury sp. n. is a forest species most commonly collected in litter from dry sclerophyll and subtropical forests or rainforests. Records also include Bunya and Hoop Pine plantations.
Mature males have only been found in November and December, mature females from November to May, with peaks in December and April. A single female with eggsac was found in March.
In NSW, Artoria beaury sp. n. occurs in the north-east, principally in the NSW North Coast (NNC), New England Tablelands (NET) and South Eastern Queensland (SEQ) IBRA regions with a single isolated record also from the South East Coastal (SEC) region (Fig.
Holotype male, Belford National Park, 60 m from Kirkton Road and 2.5 km east of Belford (32°39’S, 151°18’E, New South Wales, AUSTRALIA), 17–27 June 2012, J.R. Gollan, M.A. Ashcroft, pitfall trap, canopy of trees but moderate condition, (
18 males 13 records (all NSW). AUSTRALIA : New South Wales: 1 male, Currawong, 33°36’S, 151°18’E (
The specific name is an adjective in apposition derived from the type locality, Belford National Park.
Males of A. belfordensis sp. n. differ from all other Artoria species, except A. taeniifera, by the base of the basoembolic apophysis, which is drawn out into an apical tip (Fig.
Male (based on holotype
Total length 4.3.
Prosoma. Length 2.5, width 1.8; carapace light yellow-brown with indistinct dark radial and black V-shaped pattern between cephalic and thoracic region; covered with dark setae centrally and marginally with a band of lighter setae (Fig.
Eyes (Fig.
Anterior eye row. Strongly procurved, evenly spaced.
Chelicerae. Dark brown darker apically.
Labium. Dark brown, with lighter anterior rim (Fig.
Pedipalp coxae. Dark brown, with lighter anterior rim (Fig.
Legs. Yellow brown with darker annulations tibiae, metatarsi and tarsi darker, less annulated (Fig.
Opisthosoma. Length 1.8, width 1.3; yellow-brown with light yellow-brown anterior cardiac mark covered with white setae, and dark grey irregular pattern mainly in posterior half (Fig.
Pedipalps. Tibia globular, as long as broad; Cymbium tip without macrosetae (Fig.
Female (based on paratype,
Total length 3.4.
Prosoma. Length 1.9, width 1.3; carapace and sternum colouration as male, although somewhat lighter (Fig.
Eyes. Diameter of AME 0.05, ALE 0.04, PME 0.19, PLE 0.16.
Anterior eye row. Strongly procurved, evenly spaced.
Chelicerae, labium, pedipalp coxae, legs and opisthosoma. Opisthosoma length 1.9, width 1.2; otherwise as male, but legs I not darker and opisthosoma pattern more obscure (opisthosoma deflated due to preservation) (Fig.
Epigyne slightly wider than long, obscure, with heavily sclerotized posterior tips (Fig.
Artoria belfordensis sp. n., male holotype (
Artoria belfordensis sp. n. was collected in undisturbed or moderately disturbed forest. Mature males were collected in June, October and November and the single female in October, indicating winter to spring maturity.
This species is known from central eastern NSW, principally the Sydney Basin (SYB) and NSW North Coast (NNC) IBRA regions (Fig.
Lycosa
berenice
L. Koch, 1877: 937–938, pl. 81, figs 3, 3A.-
Pardosa
versicolor
L. Koch, 1877: 966–968, pl. 84., fig. 4.-
Lycosa
naevia
L. Koch, 1878: 978–979, pl. 85, figs 5, 5A (preoccupied by Lycosa naevia L. Koch, 1875; = Pardosa naevia (
Lycosa
ambrymiana
Berland, 1938: 184–185, figs 153–156.-
Tarentula naeviella (Roewer, 1951): 442 (replacement name for Lycosa naevia L. Koch, 1878).
Avicosa
berenice
(L. Koch).-
Hogna
naeviella
(Roewer).-
Lycosa
naeviella
(Roewer).-
Schizocosa
berenice
(L. Koch).-
Artoria
versicolor
(L. Koch).-
Artoria
berenice
(L. Koch).-
Holotype female of Lycosa berenice L.
A, B, E, F, Artoria lineata (L. Koch, 1877), male holotype (ZSMH A0000052); C, D, G, H, A berenice (L. Koch, 1877), female holotype (ZSMH A0000051). A, habitus, dorsal view; B, habitus, ventral view; C, habitus dorsal view; D, habitus ventral view; E, male pedipalp, ventral view; F, male pedipalp, retrolateral view; G, epigyne, ventral view; H, epigyne, dorsal view. Scale bars: habitus 1.0 mm; pedipalp, epigyne 0.1 mm.
237 males, 239 females (1 with eggsac, 1 with spiderlings) and 27 juveniles in 152 records (all NSW). AUSTRALIA : New South Wales: 1 male, 4 km NE of Mount Wog Wog, 17 km SE Bombala, 37°04’30”S, 149°28’00”E (
Males of A. berenice can easily be distinguished from all other species of Artoria by the presence of a small tooth on the ventral side of the tegular apophysis (Fig.
Artoria berenice has been described in detail (
Artoria berenice (L. Koch, 1877), male and female (
In NSW males and females appear from late August with highest numbers throughout October to January. Males are rarely found in March but then appear again in April and May. Females occur throughout summer and autumn until May, with two activity peaks in November/December and April and can sometimes be found into the winter months. A female with eggsac was found in November and one with spiderlings in December.
Artoria berenice is a forest species. Habitat descriptions found on collection labels include ‘wet sclerophyll’, ‘semi-cleared woodland near Pinus plantation’, ‘grassy forest’, ‘Eucalyptus botryoides-Allocasuarina torulosa, open forest’, ‘Angophora costata woodland ridge top, open forest’, but also ‘gravel pit’, and ‘cave entrance, cave in doline’.
In NSW, A. berenice is particularly found east of the Great Dividing Range, i.e. in the coastal South Eastern Queensland (SEQ), NSW North Coastal (NNC), Sydney Basin (SYB), and South East Corner (SEC) IBRA bioregions. It has been found west of the Great Dividing Range, with one single isolated record from central NSW (Fig.
Holotype male, Bondi State Forest, woodlot 3 (37°08’S, 149°09’E, New South Wales, AUSTRALIA), 26 Nov 1980 G. Gowing et al., pitfall trap, Banksia (
Known only from type material.
The specific name is a noun in apposition referring to the type locality, Bondi State Forest.
Similar to other species in the lineata-group, the tegular apophysis of the male pedipalp is spoon-shaped (Fig.
Male (based on holotype,
Total length 3.6.
Prosoma. Length 2.0, width 1.3, carapace yellow-brown, dusted with grey and indistinct dark radial pattern; lateral margin and central band pale yellow, broader in cephalic area, constricted halfway between cephalic area and fovea (Fig.
Eyes. Diameter of AME: 0.08; ALE: 0.10; PME: 0.24; PLE: 0.15.
Anterior eye row. Straight, evenly spaced.
Chelicerae. Dark brown.
Labium. Dark brown, with lighter anterior rim (Fig.
Pedipalp coxae. Dark brown, with lighter anterior rim (Fig.
Legs. Yellow brown with darker annulations; tibiae, metatarsi and tarsi darker, less annulated (Fig.
Opisthosoma. Length 1.6, width 1.2; cinnamon-brown with pale anterior cardiac mark and dark grey irregular pattern (Fig.
Pedipalps. Tibia globular, as long as broad; cymbium tip with 4–5 macrosetae (Fig.
Female unknown.
The type material of Artoria bondi sp. n. has been found in Banksia woodland in November.
Artoria bondi sp. n. is currently known only from its type locality, the Bondi State Forest in south-eastern NSW in the South Eastern Highlands (SEH) IBRA region (Fig.
Distribution records of Artoria berenice (L. Koch, 1877) (grey circles), A. bondi sp. n. (full circle) and A. booderee sp. n. (full squares) in NSW. IBRA bioregions with spider records: BBS – Brigalow Belt South; MDD – Murray Darling Depression; NAN – Nandewar; NET – New England Tablelands; NNC – NSW North Coast; SEQ – South East Queensland; SEH – South Eastern Highlands; SEC – South East Corner; SYB – Sydney Basin.
Holotype male, Booderee National Park, southern headland of Jervis Bay (35°08’49”S, 150°45’05”E, New South Wales, AUSTRALIA), 20–25 August 1999, L. Gibson, pitfall trap (
4 males and 6 females in 6 records (all NSW). AUSTRALIA: New South Wales: 1 male, Beecroft Peninsula, northern headland of Jervis Bay, 35°03’03”S, 150°47’21”E (
The specific name is a noun in apposition referring to the type locality, Booderee National Park.
Males of A. booderee sp. n. share with A. corowa sp. n., A. munmorah sp. n. and A. equipalus sp. n. a distinctly bi-lobed tegular apophysis. They differ by having a more elongated cymbium with ca. 2–3 distinct macrosetae on its tip, with 4–5 present in A. equipalus sp. n. and absent in both other species of this group. The epigyne of female A. booderee sp. n. is incised posteriorly and most similar to that of A. corowa sp. n., but the anterior edge of the epigyne in A. booderee sp. n. is distinctly semi-circular, not so in A. corowa sp. n.
Male (based on holotype,
Total length 3.9.
Prosoma. Length 2.3, width 1.6; carapace light yellow-brown with indistinct darker radial pattern; indistinct broad lighter central band and narrow lighter marginal band (Fig.
Eyes. Diameter of AME: 0.09; ALE: 0.10; PME: 0.28; PLE: 0.22.
Anterior eye row. Straight, evenly spaced.
Chelicerae. Dark brown.
Labium. Dark brown, with lighter anterior rim (Fig.
Pedipalp coxae. Dark brown, with lighter anterior rim (Fig.
Legs. Yellow brown with darker annulations; tibiae, metatarsi and tarsi darker, less annulated (Fig.
Opisthosoma. Length 1.6, width 1.2; yellow-brown with light yellow-brown anterior cardiac mark and dark grey irregular pattern laterally (Fig.
Pedipalps. Tibia globular, as long as broad; cymbium tip with 3 macrosetae (Fig.
Female (based on paratype
Total length 4.3.
Prosoma. Length 2.2, width 1.5; carapace and sternum colouration as male (Fig.
Eyes. Diameter of AME 0.07, ALE 0.09, PME 0.23, PLE 0.16.
Anterior eye row. Strongly procurved, evenly spaced.
Opisthosoma. Length 2.1, width 1.8; opisthosoma darker and cardiac mark smaller and less distinct (Fig.
Epigyne: atrium narrow, inverted u-shaped, strongly sclerotized at posterior tips (Fig.
A. booderee sp. n., male holotype (
Artoria booderee sp. n. appears to be a coastal species, as it has so far only been found on the northern and southern headlands around Jervis Bay and near Sydney. No habitat data were included on the locality labels.
All mature males at Jervis Bay were collected in August. The one from Sydney specimen was collected in December. Mature females were found in August, December and February suggesting that A. booderee sp. n. is a not tightly synchronised with any specific season.
Known only from around Jervis Bay and the Mt Kembla Basin in the Sydney Basin (SYB) IBRA region (Fig.
Artoria corowa sp. n., male holotype (
Holotype male, 40 m from Comleroi Road and 2 km N of Warkworth, private land [32°32’59”S, 151°01’22”E, New South Wales, AUSTRALIA, 27 Jun 2012, J.R. Gollan, M.A. Ashcroft, pitfall trap, She-oak forest no understory (
Known only from type material.
The specific name is a noun in apposition referring to the type locality, Comleroi Road.
Distribution records of Artoria comleroi sp. n. (full circle), A. corowa sp. n. (open circles), A. equipalus sp. n. (grey circle), A. extraordinaria sp. n. (grey squares) and A. flavimana Simon, 1909 (full squares) in NSW and ACT. IBRA bioregions with spider records: AUA – Australian Alps; COP – Cobar Peneplain; DRP – Darling River Plains; NET – New England Tablelands; NNC – NSW North Coast; RIV – Riverina; SEH – South Eastern Highlands; SEC – South East Corner; SYB – Sydney Basin.
Males of A. comleroi sp. n. are most similar to those of A. slatyeri sp. n. based on the elongated spoon-shaped tegular apophysis. They differ by an apical small lobe being present in A. comleroi sp. n. Females of A. comleroi sp. n. display an epigyne shape with the atrium forming two distinct ovoid depressions in ventral view.
Male (based on holotype,
Total length 3.6.
Prosoma. Length 2.0, width 1.5; carapace dark grey; with distinct narrow lighter marginal band and narrow central band, widening towards posterior margin (Fig.
Eyes. Diameter of AME: 0.08; ALE: 0.09; PME: 0.23; PLE: 0.21.
Anterior eye row. Strongly procurved, evenly spaced.
Chelicerae. Dark brown curved outwards.
Labium. Dark brown, with lighter anterior rim (Fig.
Pedipalp coxae. Dark brown, with lighter anterior rim (Fig.
Legs. Pale, with darker annulations; metatarsi and tarsi darker, less annulated (Fig.
Opisthosoma. Length 1.6, width 1.2; dark grey with light yellow-brown anterior cardiac mark and lighter irregular markings (Fig.
Pedipalps. Tibia about twice long as broad; cymbium tip with 4–5 macrosetae (Fig.
Female (based on paratype,
Total length 3.7.
Prosoma. Length 2.0, width 1.6; carapace and sternum colouration as male (Fig.
Eyes. Diameter of AME 0.08, ALE 0.07, PME 0.24, PLE 0.17.
Anterior eye row. Strongly procurved, evenly spaced.
Opisthosoma. Length 1.7, width 1.2; otherwise as male, (Fig.
Epigyne about as long as wide, strongly sclerotized at posterior rim, atrium formed by two distinct ovoid depressions (Fig.
No habitat data were found with the type specimens. The male and female types were collected in June suggesting Artoria comleroi sp. n. to be winter mature.
Known only from its type locality in the north-central Sydney Basin (SYB) IBRA region (Fig.
Artoria comleroi sp. n., male holotype (
Holotype male, 14.5 km NW of Corowa, roadside (35°54’33”S,146°16’11”E, New South Wales, AUSTRALIA), November 2000, D. Freudenberger, pitfall trap (
7 males and 22 females in 16 records (all NSW). AUSTRALIA: New South Wales: 1 female, 50 m E of Boonal Road, 4.4 km N from site DRRP026, travelling stock route adjacent to ‘Mooreland’ station, 28°50’26”S, 149°42’07”E (
The specific name is a noun in apposition referring to the type locality, NW of Corowa.
Males of A. corowa sp. n. share with A. booderee sp. n., A. munmorah sp. n. and A. equipalus sp. n. a distinctly bi-lobed tegular apophysis. They differ from these by the tegular apophysis not protruding past the cymbium edge in ventral view and the presence of a disto-ventral cluster of macrosetae. The epigyne of female A. corowa sp. n. is incised posteriorly and therefore most similar to that of A. booderee sp. n., but lacking the distinct semi-circular anterior edge of the epigyne of A. booderee sp. n.
Male (based on holotype,
Total length 3.6.
Prosoma. Length 1.9, width 1.4; carapace dark grey; with no lighter marginal band and broad central band, constricted between eye region and fovea (Fig.
Eyes. Diameter of AME: 0.08; ALE: 0.09; PME: 0.24; PLE: 0.18.
Anterior eye row. Strongly procurved, evenly spaced.
Chelicerae. Medium brown darker apically.
Labium. Dark brown, with lighter anterior rim (Fig.
Pedipalp coxae. Dark brown, with lighter anterior rim (Fig.
Legs. Yellow-brown, with darker annulations; tibiae and metatarsi I darker, less annulated (Fig.
Opisthosoma. Length 1.7, width 1.2; dark grey with light yellow-brown anterior cardiac mark and lighter irregular markings (Fig.
Pedipalps. Tibia globular, as long as broad; Cymbium tip with cluster of macrosetae distal-ventrally (Fig.
Female (based on paratype
Total length 4.9.
Prosoma. Length 2.6, width 1.8; carapace and sternum colouration as male (Fig.
Eyes. Diameter of AME 0.09, ALE 0.08, PME 0.28, PLE 0.23.
Anterior eye row. Strongly procurved, evenly spaced.
Opisthosoma. Length 2.6, width 2.1; opisthosoma similar colour as male but cardiac mark less distinct (Fig.
Epigyne: slightly wider than long, strongly sclerotized lateral posterior tips, atrium shaped like an inverted love-heart with posterior incision (Fig.
There was little but varied habitat data available with the specimens, including ‘roadside’, ‘Eucalyptus largiflorens patch’, ‘Eucalyptus camaldulensis patch’, Casuarina cristata patch’ and ‘native grassland’, are insufficient to form a clear account of the habitat preferences of A. corowa sp. n. remain unclear. All specimens were collected between November and December, suggesting the species is largely summer mature. The single coastal record of the species, a mature male and female, is from May (autumn).
Artoria corowa sp. n. is known from locations in central NSW from the Cobar Peneplain (COB), Darling River Plains (DRP) and Riverina (RIV) IBRA regions, with one isolated coastal record from the NSW North Coast (NNC) IBRA region (Fig.
Holotype male, Barrington Tops National Park, 100 m from Horse Swamp Track (31°56’00”S, 151°23’04”E, New South Wales, AUSTRALIA), 11–21 January 2012, J.R. Gollan, M.A. Ashcroft, pitfall trap, upland swamp (
Known only from type material.
The specific epithet is a compound noun in apposition derived from the Latin equus (= horse) and palus (= swamp) and refers to the type locality, near Horse Swamp Track.
Males of A. equipalus sp. n. share with A. booderee sp. n., A. corowa sp. n. and A. munmorah sp. n. a distinctly bi-lobed tegular apophysis, but differ from these by the basal lobe of the tegular apophysis being more sclerotized and oriented more ‘horizontally’ in ventral view. The cymbium tip in A. equipalus has 4–5 macrosetae, which are absent in A. corowa sp. n. and A. munmorah sp. n. Artoria booderee sp. n. has 2–3 macrosetae on the cymbium tip which is more elongate than that of A. equipalus sp. n. The epigyne of female A. equipalus sp. n. is most similar to that of A. mungo sp. n., but the shape of the spermathecal heads is very different in both species with in particular with respect to the insertion of the spermathecal stalks (postero-medial in A. equipalus sp. n., lateral in A. mungo sp. n.).
Male (based on holotype,
Total length 3.0.
Prosoma. Length 1.7, width 1.2; carapace dark grey; with distinct broad lighter marginal band and broad lighter central band, widening towards eye region (Fig.
Eyes. Diameter of AME: 0.07; ALE: 0.08; PME: 0.23; PLE: 0.16.
Anterior eye row. Strongly procurved, evenly spaced.
Chelicerae. Dark brown.
Labium. Dark brown, with lighter anterior rim (Fig.
Pedipalp coxae. Dark brown, with lighter anterior rim (Fig.
Legs. Tibiae, metatarsi and tarsi of leg I very dark to almost black; other legs light brown, annulated (Fig.
Opisthosoma. Length 1.3, width 1.0; cinnamon-brown with light yellow-brown anterior cardiac mark and dark grey irregular pattern (Fig.
Pedipalps. Tibia as long as broad; cymbium tip with 4–5 macrosetae (Fig.
Female (based on
Total length 5.3.
Prosoma. Length 2.5, width 1.8; carapace and sternum colouration as male (Fig.
Eyes. Diameter of AME 0.10, ALE 0.14, PME 0.26, PLE 0.17.
Anterior eye row. Straight, evenly spaced.
Opisthosoma. Length 2.8, width 2.1; otherwise as male, but legs I not darker, not annulated and opisthosoma pattern more obscure (Fig.
Epigyne slightly wider than long, poorly sclerotised at posterior tips, atrium lighter inverted u-shaped (Fig.
The habitat description with the type material is ‘upland swamp’. Spiders were found in January suggesting Artoria equipalus sp. n. to be summer mature.
Artoria equipalus sp. n. is known only from its type locality in Barrington Tops National Park in the NSW North Coast (NNC) IBRA region (Fig.
Artoria equipalus sp. n., male holotype (
Holotype male, Macquarie Road, 70 m S from junction with Milo Road, Buckenbowra State Forest (35°38’S, 149°53’E, New South Wales, AUSTRALIA], 16 Mar 1999, R. Harris, H.M. Smith, leaf litter sample (
10 males in 9 records (all NSW). AUSTRALIA: New South Wales : 1 male, 30 km SE of Braidwood, 250 m along Corn Trail Road from junction with Highway 54, 35°33’43”S, 150°00’32”E (
The specific epithet is an adjective in apposition derived from Latin (extraordinaria – unusual) and refers to the unusual shape of the basoembolic apophysis of the male pedipalp.
The male pedipalp of A. extraordinaria sp. n. is highly unusual within the genus owing to the shape of the basoembolic apophysis, which forms an almost 360-degree circle (Fig.
Male (based on holotype,
Total length 3.6.
Prosoma. Length 2.1, width 1.4; carapace light reddish-brown with dark radial pattern and black V-shaped pattern between cephalic and thoracic region; indistinct and irregular broad lighter central and marginal band (Fig.
Eyes (Fig.
Anterior eye row. Strongly procurved, distance between AME/ALE at least twice AME/AME.
Chelicerae. Dark brown.
Labium. Dark brown, with lighter anterior rim (Fig.
Pedipalp coxae. Dark brown, with lighter anterior rim (Fig.
Legs. Yellow brown with darker annulations; metatarsi and tarsi darker, less annulated (Fig.
Opisthosoma. Length 1.5, width 1.1; dark grey with pale anterior cardiac mark and light irregular pattern (Fig.
Pedipalps. Tibia as long as broad; cymbium tip with cluster of macrosetae (Fig.
Female (based on
Total length 3.8.
Prosoma. Length 2.0, width 1.4; carapace and sternum colouration as male (Fig.
Eyes. Diameter of AME 0.08, ALE 0.09, PME 0.30, PLE 0.21.
Anterior eye row. Strongly procurved, distance between AME/ALE at least twice AME/AME.
Opisthosoma. Length 1.8, width 1.2; otherwise as male, but opisthosoma pattern more obscure (Fig.
Epigyne. About as long as wide, poorly sclerotised at posterior tips, atrium lighter (Fig.
Based on locality data, Artoria extraordinaria sp. n. is a forest species. Detailed habitat data were not available on locality labels of the specimens. Most specimens were collected between February and April, with one male recorded from June, suggesting Artoria extraordinaria sp. n. to be autumn to winter mature.
This species was found some distance from the coast at scattered localities in the NSW North Coast (NNC), Sydney Basin (SYB) and South Easter Corner (SEC) IBRA bioregions (Fig.
Artoria extraordinaria sp. n., male holotype (
Artoria
flavimanus
Simon, 1909: 192, fig. 9.-
Artoria flavimana Simon.- Bonnet 1955: 750.
Artoriella
flavimanus
(Simon).-
Lycosa
neboissi
McKay, 1976: 413–416, fig. 1E–I.-
Holotype female of Artoria flavimanus Simon, 1909, Mundaring Weir (‘Station 101’) (31°57’S 116°10’E, Western Australia, AUSTRALIA], collected during the ‘Hamburger südwest-australische Forschungsreise 1905’ (
41 males, 9 females and 1 juvenile in 32 records (2 from the ACT, 30 from NSW). AUSTRALIA: Australian Capital Territory: 1 female, 1 juv., Piccadilly Circus, 35°22’S, 148°48’E (
Amongst currently described Artoria, A. flavimana is most similar to A. avona Framenau, 2002, a species not yet recorded from NSW or the ACT (
A flavimana Simon, 1909, male and female (
Artoria flavimana has been described in detail (
Artoria flavimana occurs predominantly in eucalypt forests. In NSW and ACT, most males were recorded in May and August and females also into November. Reproductive activity appears to occur mostly in winter.
Artoria flavimana occurs in south-eastern NSW and the ACT in the South East Corner (SEC), South Eastern Highlands (SEH) and Australian Alps (AUA) IBRA regions (Fig.
Lycosa
gloriosa
Rainbow, 1920: 261–262, pl. 30, figs 94–95.-
Artoria
gloriosa
(Rainbow).-
Holotype female, Lord Howe Island, (31°31’S, 159°04’E, New South Wales, AUSTRALIA), A.M. Lea, December 1915–January 1916 (SAM NN038) (examined).
Aroria gloriosa (Rainbow, 1920), male and female (
153 males, 67 females (1 with eggsac, 3 with spiderlings) and 51 juveniles in 114 records (all NSW). AUSTRALIA: New South Wales: Lord Howe Island: 7 males. 4 female, 2 juv., no exact locality (
Artoria gloriosa is similar to A. albopilata; however, the tegular apophysis of the male pedipalp of A. gloriosa lacks the apical lower tip present in A. albopilata. The tip of the embolus of A. gloriosa is blunt (Fig.
Artoria gloriosa has been described in detail (
Artoria gloriosa is a forest species dwelling in litter in a variety of forest types on Lord Howe Island. Mature males and females have largely been found between November and February, with two records of males from May and a female with spiderlings in July. Two females with spiderlings were found in December.
Artoria gloriosa is endemic to Lord Howe Island (PSI – Pacific Subtropical Island IBRA region) (Fig.
Holotype male, Awabakal Nature Reserve, 120 m off Redhead Road and 1 km S of Dudley (32°59’44”S, 151°42’58”S, New South Wales, AUSTRALIA], 22 June–1 July 2012, J.R. Gollan, M.A. Ashcroft, pitfall trap, under tree canopy (
Artoria grahammilledgei sp. n., male holotype (
378 males, 147 females (1 with eggsac, 7 with spiderlings) and 32 juveniles in 184 records (all NSW). AUSTRALIA : New South Wales: 1 male, 4 km SW of Mt Vincen, approx. 10 m from creek, 32°55’41”S, 151°26’30”E (
Species name is a patronym in honour of Mr Graham Milledge, the Collection Manager of the Australian Museum, Sydney, for his support of this and many other of the present authors’ studies on Australian spiders.
Males of Artoria grahammilledgei sp. n. are most similar to those of A. terania sp. n., but the tegular apophysis of Artoria grahammilledgei sp. n. is lobed apically (Fig.
Male (based on holotype,
Total length 5.8.
Prosoma. Length 3.3, width 2.5; carapace light yellow-brown with dark radial pattern and black V-shaped pattern between cephalic and thoracic region; indistinct and irregular broad lighter central band (Fig.
Eyes. Diameter of AME: 0.14; ALE: 0.13; PME: 0.41; PLE: 0.32.
Anterior eye row. Slightly procurved, evenly spaced.
Chelicerae. Dark brown.
Labium. Dark brown, with lighter anterior rim (Fig.
Pedipalp coxae. Dark brown, with lighter anterior rim (Fig.
Legs. Light yellow brown with slightly darker annulations. (Fig.
Opisthosoma. Length 2.5, width 1.8; dark grey with light anterior cardiac mark and light grey irregular pattern mainly in anterior half (Fig.
Pedipalps. Tibia longer than broad; cymbium tip without macrosetae (Fig.
Female (based on
Total length 6.9.
Prosoma. Length 2.8, width 2.0; carapace and sternum colouration as male (Fig.
Eyes. Diameter of AME 0.12, ALE 0.14, PME 0.37, PLE 0.29.
Anterior eye row. Slightly procurved.
Chelicerae, labium, pedipalp coxae, legs and opisthosoma. Opisthosoma length 4.1, width 2.7; otherwise as male, but opisthosoma pattern more obscure (Fig.
Epigyne about as long as wide, with rectangular atrium (Fig.
Habitat descriptions on collection labels with Artoria grahammilledgei sp. n. suggest the species to be a woodland and forest dweller in litter, i.e. ‘dry sclerophyll forest’, ‘Angophora costata woodland ridge top’, ‘Eucalyptus botryoides–Allocasuarina torulosa open forest’ and ‘litter & soil beneath Casuarina’.
Mature male Artoria grahammilledgei sp. n. have been found almost throughout the year, except November, February and March with two distinct activity periods in April and July. Mature females have been found in all months with a first peak from April to August, and a second in November. A female with eggsac was found in October/November and females with spiderlings in January, April, November and December. Therefore, the species appears largely autumn to winter mature, but with wide seasonal variation in relation to its reproductive behaviour.
In NSW, Artoria grahammilledgei sp. n. appears common east of the Great Dividing Range but has also been found along its west (Fig.
Holotype, Booti Booti National Park, S of Forster, southern end of park (32°16’47”S, 152°31’28”E, New South Wales, AUSTRALIA), 30 September–9 October 1997, L. Wilkie, pitfall trap (
Distribution records of Artoria grahammilledgei sp. n. (open circles), A. helensmithae sp. n. (full circles) and A. howquaensis Framenau, 2002 (grey squares) in NSW. IBRA bioregions with spider records: BBS – Brigalow Belt South; NAN – Nandewar; NET – New England Tablelands; NNC – NSW North Coast; SEQ – South East Queensland; SEH – South Eastern Highlands; SEC – South East Corner; SYB – Sydney Basin.
175 males, 100 females (2 with spiderlings) and 1 juvenile 134 records. AUSTRALIA: New South Wales: 2 males, 4 km NE of Mt Wog Wog, 17 km SE Bombala, 37°04’30”S, 149°28’00”E (
The specific epithet is a matronym honouring Dr Helen Smith of the Australian Museum, Sydney, for her ongoing support of our spider research.
Artoria helensmithae sp. n. males and females are very similar to those of A. beaury sp. n. (see diagnosis above).
Male (based on holotype,
Total length 3.9.
Prosoma. Length 2.2, width 1.5; carapace light yellow-brown with dark radial pattern and black V-shaped pattern between cephalic and thoracic region; indistinct and irregular lighter central and marginal band (Fig.
Eyes. Diameter of AME: 0.10; ALE: 0.07; PME: 0.28; PLE: 0.20.
Anterior eye row. Slightly procurved, evenly spaced.
Chelicerae. Dark brown darker apically.
Labium. Dark brown, with lighter anterior rim (Fig.
Pedipalp coxae. Dark brown, with lighter anterior rim (Fig.
Legs. Femora, tibiae and metatarsi of leg I very dark to almost black; other legs brown, with darker annulations; tarsi and metatarsi lighter brown (Fig.
Opisthosoma. Length 1.7, width 1.3; dark grey with light yellow-brown anterior cardiac mark and light irregular pattern (Fig.
Pedipalps. Tibia as long as broad; cymbium tip with 8–10 macrosetae (Fig.
Female (based on
Total length 3.8.
Prosoma. Length 2.2, width 1.6; carapace and sternum colouration as male (Fig.
Eyes. Diameter of AME 0.08, ALE 0.08, PME 0.26, PLE 0.19.
Anterior eye row. Slightly procurved, evenly spaced.
Opisthosoma. Length 1.6, width 1.5; otherwise as male, but legs I not darker and opisthosoma pattern more obscure (Fig.
Epigyne about slightly longer than wide, strongly sclerotized at posterior tips (Fig.
A helensmithae sp. n., male holotype (
Habitat descriptions found on the collection labels of A. helensmithae sp. n. include ‘under tall shrubs’, ‘sand dunes’, open forest, litter’, ‘rainforest’ and ‘dry forest’. A single record is from the dark zone of a cave. Therefore, A. helensmithae sp. n. seems to show some variation in its habitat preferences. Most records also state ‘litter’.
Artoria helensmithae sp. n. appears to have three peaks of reproductive activity, the first around April/May, then in July and again from October to December. Females with spiderlings were found in December. This is an unusual phenology for wolf spiders, i.e. this species appears to be reproductively active in autumn, winter and summer.
In NSW, A. helensmithae sp. n. has generally been found east of the Great Dividing Range, with records from the NSW North Coast (NNC), Sydney Basin (SYB), South East Corner (SEC) and South East Highlands (SHE) IBRA regions (Fig.
Artoria
howquaensis
Framenau, 2002: 217–218, figs 9A–G, 10;
Holotype male, Howqua River at Mansfield–Woods Point Road Bridge (37°13’S 146°10’E, Victoria), 11 February 1998, riparian gravel bank, V. W. Framenau (
7 males and 1 female in 3 records (all NSW). AUSTRALIA: New South Wales: 3 males, 1 female, Private land ‘Camp Cobark’, 80 m off Scone Road and 3 km SE of Cobark, 31°56’05”S, 151°42’27”E (
Amongst Australian Artoria, A. howquaensis is most similar to A. parvula, a tropical species not yet found in NSW or the ACT. This species most easily diagnosed by its body colouration, being very dark brown to black with distinct white lateral bands on the carapace (Fig.
Artoria howquaensis has been described in detail (
Artoria howquaensis Framenau, 2002, male (
Artoria howquaensis is a riparian species which has previously been found in open habitats along the margins of rivers and springs. The records in NSW are consistent with this habitat preference as the species was found in open, grassy and swampy areas.
Mature males and females were found in December, with further records of males in March.
In NSW, A. howquaensis has been found in scattered records in the northern half of the state east and west of the Great Dividing Range in the Nandewar (NAN), NSW North Coast (NNC) and Sydney Basin (SYB) bioregion (Fig.
Holotype male, Kanangra-Boyd National Park, Boyd River (34°03’S, 150°05’E, New South Wales, AUSTRALIA), 26 November 1994, D. Bickel, pans, 1200 m, creek sphagnum (
AUSTRALIA: New South Wales: 1 male, Barren Grounds Nature Reserve, 14 km NW Jamberoo, Illawarra Escarpment, 34°40’28”S, 150°42’45”E (
The specific epithet is a noun in apposition referring to the type locality, Kanangra-Boyd National Park.
Males of A. kanangra sp. n. are most similar to those of the booderee-group (A. booderee sp. n., A. corowa sp. n., A. munmorah sp. n. and A. equipalus sp. n.), but differ in the shape of the tegular apophysis, which is birdhead-shaped in A. kanangra sp. n. (Fig.
Male (based on holotype,
Total length 4.5.
Prosoma. Length 2.4, width 1.7; carapace yellow-brown dusted with grey and indistinct dark radial pattern; lateral margin and central band pale yellow, broader in cephalic area, constricted halfway between cephalic area and fovea (Fig.
Eyes (Fig.
Anterior eye row. Slightly procurved, evenly spaced.
Chelicerae. Dark brown.
Labium. Dark brown, with lighter anterior rim (Fig.
Pedipalp coxae. Dark brown, with lighter anterior rim (Fig.
Legs. Femora and tibiae of leg I very dark; other legs brown, femora and tibia with darker annulations, particularly ventrally; tarsi and metatarsi lighter yellow-brown (Fig.
Opisthosoma. Length 2.1, width 1.4; cinnamon-brown with light anterior cardiac mark and dark grey irregular pattern (Fig.
Pedipalps. Tibia globular, as long as broad; cymbium tip with cluster of macrosetae (Fig.
A–D, Artoria kanangra sp. n., male holotype (
Female unknown.
The holotype was found in creek sphagnum at 1,200 m altitude suggesting the species to be riparian. Adult males were found in August and December.
Artoria kanangra sp. n. is currently known only from two localities in eastern-central NSW, from the Sydney Basin (SYB) and South Eastern Highlands (SHE) IBRA bioregions (Fig.
Holotype male, Kerewong State Forest, near Lorne (31°36’S, 152°34’E, New South Wales, AUSTRALIA], 20 November 1978, D. Milledge, pitfall trap site 108(3), FN1561 (
Known only from type material.
The specific epithet is a noun in apposition referring to the type locality, Kerewong State Forest.
The pedipalp morphology of males of A. kerewong sp. n. is distinct within the genus, with the terminal section of the tegular apophysis having both a pointed apical and a pointed basal tip. The basoembolic apophysis is the longest amongst the known Artoria species. The female of A. kerewong sp. n. is currently unknown.
Male (based on holotype,
Total length 4.6.
Prosoma. Length 2.6, width 1.9; carapace dark grey; with distinct broad lighter marginal band and broad lighter central band, constricted at posterior 1/3 (Fig.
Eyes. Diameter of AME: 0.11; ALE: 0.12; PME: 0.29; PLE: 0.20.
Anterior eye row. Slightly procurved, evenly spaced.
Chelicerae. Medium brown darker apically.
Labium. Dark brown, with lighter anterior rim (Fig.
Pedipalp coxae. Dark brown, with lighter anterior rim (Fig.
Legs. Yellow brown with darker annulations; metatarsi and tarsi darker, less annulated (Fig.
Opisthosoma. Length 2.0, width 1.5; cinnamon-brown with light yellow-brown anterior cardiac mark and dark grey irregular pattern (Fig.
Pedipalps. Tibia as long as broad; cymbium tip with distal cluster of macrosetae (Fig.
Female unknown.
No habitat data were on the collection label of the holotype, which was found in November/December suggesting it is summer mature.
Artoria kerewong sp. n. is known only from the type locality, the Kerewong State Forest in the NSW North Coast (NNC) IBRA region (Fig.
Distribution records of Artoria kanangra sp. n. (full circles), A. kerewong sp. n. (grey square) and A. lineata (L. Koch, 1877) (open circles) in NSW and ACT. IBRA bioregions with spider records: AUA – Australian Alps; BBS – Brigalow Belt South; NAN – Nandewar; NET – New England Tablelands; NNC – NSW North Coast; SEQ – South East Queensland; SEH – South Eastern Highlands; SEC – South East Corner; SYB – Sydney Basin.
Trabea
lineata
L. Koch, 1877: 970–971, pl. 84, figs 7, 7A–B.-
Trabaea
lineata
(L. Koch).-
Trabaeosa
lineata
(L. Koch).-
Trabaeola
lineata
(L. Koch).-
Artoria
lineata
(L. Koch).-
Holotype male, Sydney (33°53’S, 151°13’E, New South Wales, AUSTRALIA], Museum Godeffroy Nr. 14606 (ZSMH A0000052) (examined; contra
421 males, 135 females and 25 juveniles in 149 records (143 NSW, 6 ACT). Australian Capital Territory: 2 males, Black Mountain, 35°16’S, 149°06’E (
(after
The female epigyne in both A. lineata and A. ulrichi has an inverted, T-shaped median septum, however, the posterior border is light or transparent along its whole length in A. lineata, whereas the lateral tips of the medium septum are dark all around in A. ulrichi.
Artoria lineata (L. Koch, 1877), male and female (
Artoria lineata has been described in detail (
Artoria lineata is a forest species and has been found in the leaf litter of dry and wet sclerophyll forests and rainforest. Mature males and females can be found all year round with peaks of activity in August and October. Females can also be found in high numbers through summer and into autumn.
Artoria lineata appears to be widespread in all IBRA regions immediately east and west of the Great Dividing Range (Fig.
Holotype male, Maroota State Forest (33°31’S, 150°59’E, New South Wales, AUSTRALIA), 26 October 1979, G.A. Webb, pitfall trap (
8 males in 7 records (all NSW). AUSTRALIA: New South Wales: 1 male, Beecroft Peninsula, northern headland of Jervis Bay, 35°03’03”S, 150°47’21”E (
The specific name is a noun in apposition referring to the type locality, Maroota State Forest.
Males of Artoria maroota sp. n. are able to be distinguished from all other species of the genus by the black setal brushes on the tibia of leg I and the inverted L-shaped tegular apophysis (Fig.
Male (based on holotype,
Total length 2.5.
Prosoma. Length 1.4, width 1.0; carapace shiny, light dark grey with darker radial pattern and black V-shaped pattern between cephalic and thoracic region; indistinct and irregular lighter central and marginal band (Fig.
Eye. Diameter of AME: 0.06; ALE: 0.08; PME: 0.17; PLE: 0.14.
Anterior eye row. Slightly procurved, evenly spaced.
Chelicerae. Medium brown.
Labium. Dark brown, with lighter anterior rim (Fig.
Pedipalp coxae. Dark brown, with lighter anterior rim (Fig.
Legs. Distal part of femora and tibiae dark; other legs brown, femora and tibiae with darker annulations; tarsi and metatarsi less annulated (Fig.
Opisthosoma. Length 1.1, width 0.8; dark grey with pale anterior cardiac mark and pale irregular pattern (Fig.
Pedipalps. Tibia as long as broad; cymbium tip with cluster of macrosetae (Fig.
Female unknown.
A–D, Artoria maroota sp. n., male holotype (
No detailed habitat data were available from the locality labels. As the species was mainly collected during a forest survey it appears to be a forest dweller.
Mature males were collected from October to December suggesting it is spring/summer mature.
This species was found in the Sydney Basin (SYB) IBRA region in eastern central NSW (Fig.
Artoria mckayi Framenau, 2002: 220–222, figs A–F, 14.
Holotype male, Ovens River near Smoko (36°48’S, 147°02’E, Victoria, AUSRALIA), 16 December 1998, riparian gravel bank at the water’s edge, V.W. Framenau (
13 males, 15 females (3 with eggsac) and 2 juveniles in 15 records (14 NSW, 1 ACT). AUSTRALIA: Australian Capital Territory: 1 male, Tidbinbilla, 35°26’S, 148°56’E (SAM NN13548). New South Wales: 1 female, Brookvale Creek, 33°46’10”S, 151°16’04”E (
Artoria mckayi is most similar to A. albopedipalpis Framenau, 2002, a species which has only been recorded from Victoria (Framenau, 2002). The ventrally-pointing tegular apophysis of the male pedipalp (Fig.
Artoria mckayi has been described in detail (
Artoria mckayi is a riparian habitat specialist and can mainly be found along the edges of rivers and creeks on both muddy and rocky banks. In NSW and the ACT mature spiders have been found between October and May. In Victoria, the adult spiders (species ‘A’ in
Artoria mckayi occurs at rivers and creeks of the Great Dividing Range (Fig.
Distribution records of Artoria maroota sp. n. (full circles), A. mckayi Framenau, 2002 (open circles) and A. mungo sp. n. (grey squares) in NSW and ACT. IBRA bioregions with spider records: MDD – Murray Darling Depression; NNC – NSW North Coast; SEQ – South East Queensland; SEH – South Eastern Highlands; SEC – South East Corner; SYB – Sydney Basin.
Artoria mckayi Framenau, 2002, male (
Holotype male, Lake Mungo National Park (33°41’S, 143°03’E, New South Wales, AUSTRALIA), 26 August–1 September 2017, B.C. Baehr, pitfall trap, chenopod scrub, 66 m alt. (
3 males in 3 records (all NSW). AUSTRALIA: New South Wales: 3 males, Newnes Plateau, 31°10’S, 150°15’E (
The specific name is a noun in apposition referring to the type locality.
Based on the shape of the tegular apophysis, males of A. mungo sp. n. are most similar to A. helensmithae sp. n. and A. beaury sp. n. Artoria beaury sp. n. differs distinctly in the shape of the basoembolic apophysis which is much broader than that of A. mungo sp. n. In A. helensmithae sp. n. the apical edge of the tegular apophysis is much more indented than in A. mungo sp. n. Female A. mungo sp. n. are most similar to A. wilkiei sp. n. based on the shape of the epigyne in ventral view, but the spermathecal heads of the latter are much larger and touching medially.
Male (based on holotype,
Total length 3.6.
Prosoma. Length 2.0, width 1.4; carapace greyish with dark radial pattern; indistinct lighter narrow marginal band and v-shaped central band constricted between PME (Fig.
Eyes. Diameter of AME: 0.08; ALE: 0.09; PME: 0.25; PLE: 0.16.
Anterior eye row. Slightly procurved, evenly spaced.
Chelicerae. Medium brown.
Labium. Dark brown, with lighter anterior rim (Fig.
Pedipalp coxae. Dark brown, with lighter anterior rim (Fig.
Legs. Yellow-brown, with darker annulations; tibiae, metatarsi and tarsi I darker, less annulated, lighter (Fig.
Opisthosoma. Length 1.6, width 1.2; cinnamon-brown with light yellow-brown anterior cardiac mark and dark grey irregular pattern (Fig.
Pedipalps. Tibia as long as broad; cymbium tip with few smaller distoventral macrosetae (Fig.
Female (based on
Total length 3.5.
Prosoma. Length 1.4, width 1.1; carapace and sternum colouration as male (Fig.
Eyes. Diameter of AME 0.08, ALE 0.07, PME 0.19, PLE 0.13.
Anterior eye row. Slightly procurved, evenly spaced.
Opisthosoma. Length 2.1, width 1.7; otherwise as male, but legs less annulated and opisthosoma pattern more obscure (Fig.
Epigyne. About 1 ½ times longer than wide, strongly sclerotised at posterior tips, atrium semicircular (Fig.
Artoria mungo sp. n., male holotype (
It appears that this species has affinities to at least intermittently flooded areas, as it has been found near swamps and creeks in dry sclerophyll bushland and scrubland. Mature spiders have been found in August, September and January suggesting it is spring- to summer-mature.
Artoria mungo sp. n. is currently known from two widely separate locations in the Murray Darling Depression (MDD) and Sydney Basin (SYD) IBRA regions (Fig.
Holotype male, Munmorah State Recreation Reserve (33°12’26”S, 151°34’37”E, New South Wales, AUSTRALIA), 11 October 1997, L. Wilkie, pitfall trap, MUNC01/06 (
19 males and 32 females in 35 records. AUSTRALIA: New South Wales: 1 male, Bungonia Caves area near Information Centre, 34°48’02”S, 150°00’57”E (
The specific name is a noun in apposition referring to the type locality, Munmorah State Recreation Reserve.
Males of A. munmorah sp. n. share with A. booderee sp. n., A. corowa sp. n. and A. equipalus sp. n. a distinctly bi-lobed tegular apophysis (see also diagnosis for these species). They differ from A. booderee sp. n. by the less elongate cymbium, from A. corowa sp. n. by the tegular apophysis reaching past the cymbium edge in ventral view and from A. equipalus sp. n. by the basal lobe of the tegular apophysis being less sclerotised. Females of A. munmorah sp. n. have a poorly sclerotised epigyne most similar to that of A. equipalus sp. n. and A. mungo sp. n., but differ distinctly in the shape of the spermathecal heads, specifically in the postero-lateral attachment of the spermathecal ducts (lateral in A. mungo sp. n. and postero-medial in A. equipalus sp. n.).
Male (based on holotype KS128070).
Total length 2.9.
Prosoma. Length 1.7, width 1.2; carapace yellow-brown dusted with grey and indistinct dark radial pattern; lateral margin and central band pale yellow, broader in cephalic area, constricted halfway between cephalic area and fovea (Fig.
Eyes. Diameter of AME: 0.06; ALE: 0.05; PME: 0.19; PLE: 0.15.
Anterior eye row. Slightly procurved, evenly spaced.
Chelicerae. Dark brown.
Labium. Dark brown, with lighter anterior rim (Fig.
Pedipalp coxae. Dark brown, with lighter anterior rim (Fig.
Legs. Femora and tibiae of leg I, II dark; other legs yellow-brown, with slightly darker annulations (Fig.
Opisthosoma. Length 1.2, width 0.9; yellow-brown with light yellow-brown anterior cardiac mark and dark grey irregular pattern (Fig.
Pedipalps. Tibia globular, as long as broad; dorsal scopula patch absent; tegular apophysis distally scooped, deeply indented, basally narrowed to 1/2, retrolateral tip rounded reaching margin of cymbium (Fig.
Female (based on
Total length 3.4.
Prosoma. Length 1.7, width 1.2; carapace and sternum colouration as male (Fig.
Eyes. Diameter of AME 0.08, ALE 0.05, PME 0.23, PLE 0.17.
Anterior eye row. Slightly procurved, evenly spaced.
Opisthosoma. Opisthosoma length 1.7, width 2.1; otherwise as male, but opisthosoma pattern more obscure (Fig.
Epigyne about as long as wide, poorly sclerotised at posterior tips, atrium lighter, bell-shaped (Fig.
Artoria munmorah sp. n., male (
There is only a single record with habitat information, ‘canopy of trees with grass under’; therefore, habitat preferences of A. munmorah sp. n. remain unclear.
Mature spiders have been found between October and January, therefore this species appears to be spring- to summer-mature.
Artoria munmorah sp. n. is currently known from eastern central NSW along both sides of the Great Dividing Range and occurs in the NSW North Coast (NNC), Sydney Basin (SYB), South Eastern Highlands (SHE), NSW South Western Slope (NSS) and Brigalow Belt South (BBS) IBRA regions (Fig.
Holotype male, Myall Lakes (32°26’S, 152°24’E, New South Wales, AUSTRALIA), September 1922, A. Musgrave (
Known only from holotype.
The specific name is an adjective in apposition derived from the type locality, Myall Lakes.
Males of A. myallensis sp. n. differ from all other Artoria by the deeply indented, three-lobed tegular apophysis (Fig.
Male (based on holotype,
Total length 3.9.
Prosoma. Length 2.2, width 1.5; carapace greyish with slightly dark radial pattern; indistinct lighter marginal band and v-shaped central band constricted between PME (Fig.
Eyes. Diameter of AME: 0.10; ALE: 0.09; PME: 0.28; PLE: 0.21.
Anterior eye row. Slightly procurved, evenly spaced.
Chelicerae. Light brown.
Labium. Medium brown, with lighter anterior rim (Fig.
Pedipalp coxae. Medium brown, with lighter anterior rim (Fig.
Legs. Yellow-brown, with darker annulations; metatarsi and tarsi less annulated, lighter (Fig.
Opisthosoma. Length 1.7, width 1.2 dark grey with light yellow-brown anterior cardiac mark and light irregular pattern (Fig.
Pedipalps. Pedipalp globular, tibia as long as broad; cymbium tip with cluster of disto-ventral macrosetae (Fig.
Female unknown.
Habitat preferences of A. myallensis sp. n. are not known. The holotype was found at the beginning of spring (September).
Artoria myallensis sp. n. is known only from the type locality, the coastal Myall Lakes in the southern NSW North Coast (NNC) IBRA region (Fig.
Distribution records of Artoria munmorah sp. n. (full circles), A. myallensis sp. n. (grey square) and A. quadrata Framenau, 2002 (open circles) in NSW and ACT. IBRA bioregions with spider records: AUA – Australian Alps; BBS – Brigalow Belt South; NAN – Nandewar; NET – New England Tablelands; NNC – NSW North Coast; NSS – NSW South Western Slopes; SEQ – South East Queensland; SEH – South Eastern Highlands; SEC – South East Corner; SYB – Sydney Basin.
Lycosa
pruinosa
L. Koch, 1877: 925–927, pl. 80, figs 2, 2a;
Dingosa
pruinosa
(L. Koch).-
Artoria
pruinosa
(L. Koch).-
Holotype male, Sydney (33°45’S, 151°06’E, New South Wales, AUSTRALIA), Bradley Collection (considered lost (
The transfer of Lycosa pruinosa to Artoria was based on the morphology of the male pedipalp as illustrated in the original description (L.
Artoria quadrata Framenau, 2002: 224–226, figs 19A–F, 20.
Holotype male, Avon River near Valencia Creek (37°48’S 146°27’E, Victoria, AUSTRALIA], 18 December 1996, riparian gravel bank, V.W. Framenau (
152 males, 88 females (3 with eggsac) and 30 juveniles in 91 records (85 NSW, 6 ACT). AUSTRALIA: Australian Capital Territory: 1 male, Black Mountain, 35°16’S, 149°06’E (
Artoria quadrata is part of the lineata-group, to which also A. lineata and A. ulrichi belong. A detailed diagnosis for these three species can be found above under the treatment of A. lineata.
Artoria quadrata has been described in detail (
Artoria quadrata Framenau,2002, male (
Artoria quadrata appears to be versatile with respect to its habitat preferences, reported from a variety of environments including woodland and forest habitats (e.g. ‘undisturbed forest’, ‘scattered trees’, ‘semi-cleared woodland adjacent to pine plantations’, ‘temperate rainforest’ ‘Nothofagus rainforest’, ‘dry subtropical rainforest’), and also open habitats – some near water – (‘open grassy field, swampy’, ‘open grassy field, edge of river’, ‘in grass’, ‘garden’, ‘bare limestone outcrop’). In NSW and the ACT mature spiders have been found all year round, with a peak from October to January. Three females with eggsacs were found in November.
Artoria quadrata is common east and west of the Great Dividing Range, from coastal areas into the Brigalow Belt South (BBS) and NSW South Western Slopes (NSS) IBRA regions (Fig.
Holotype male, Bondi State Forest, woodlot 2 (37°07’S, 149°08’E, New South Wales, AUSTRALIA), 3 February 1980, G. Gowing et al., pitfall trap (
AUSTRALIA: New South Wales: 1 male, Wadbilliga National Park, 9.6 km N on Bumberry Creek Fire Trail, 36°14’20”S, 149°34’00”E (
Species name is a patronym in honour of Dr Cameron Slatyer, Head of Natural Science Collections and Branch Manager of Life Sciences at the Australian Museum, who contributed significantly to Australian biodiversity knowledge of conservation reserves through the foundation of Bush Blitz.
The shape of the tegular apophysis in males of A. slatyeri sp. n. is distinctive within Artoria (Fig.
Male (based on holotype
Total length 5.1.
Prosoma. Length 2.7, width 2.0; carapace yellow-brown dusted with grey and indistinct dark radial pattern; with pale yellow lateral broad margin and central band, broader in cephalic area constricted just behind PLE (Fig.
Eyes. Diameter of AME: 0.10; ALE: 0.11; PME: 0.28; PLE: 0.21.
Anterior eye row. Straight, evenly spaced.
Chelicerae. Dark brown.
Labium. Dark brown, with lighter anterior rim (Fig.
Pedipalp coxae. Dark brown, with lighter anterior rim (Fig.
Legs. Yellow brown with darker annulations; tibiae, metatarsi and tarsi darker, less annulated (Fig.
Opisthosoma. Length 2.4, width 1.6; yellow-brown with light yellow-brown anterior cardiac mark and dark grey irregular pattern (Fig.
Pedipalps. Tibia globular, as long as broad; cymbium tip with 4–5 short macrosetae (Fig.
Female unknown.
A–D, Artoria slatyeri sp. n., male holotype (
Artoria slatyeri sp. n. is apparently a forest species, the type material being found in a forest reserve. Mature males were found in pitfall traps in December and February suggesting the species is summer-mature.
Artoria slatyeri sp. n. is currently known only from the Bondi State Forest and Wadbilliga National Park in southern NSW in the South Eastern Highlands (SEH) IBRA region (Fig.
Distribution records of Artoria slatyeri sp. n. (full circle), A. strepera sp. n. (grey square), A. taeniifera Simon, 1909 (full triangle) and A. terania sp. n. (open circles) in NSW. IBRA bioregions with spider records: COP – Cobar Peneplain; MDD – Murray Darling Depression; NNC – NSW North Coast; SEQ – South East Queensland; SEH – South Eastern Highlands; SEC – South East Corner; SYB – Sydney Basin.
Holotype male, Currawong (33°36’S, 151°18’E, New South Wales, AUSTRALIA], 2 October 1966, R. Mascord (
Known only from type material.
The specific epithet refers to the scientific genus-group name of the Australian Currawong birds, Strepera Lesson, 1831. Currawong is also the name of the type locality.
Males of A. strepera sp. n. most closely resemble A. bondi sp. n. as both have a small, spoon-shaped tegular apophysis; however, the embolus and terminal apophysis in A. strepera sp. n. are much longer and protruding distinctly apically from the tegulum (Fig.
Male (based on holotype
Total length 3.8.
Prosoma. Length 2.3, width 1.7; carapace light yellow-brown with indistinct dark radial pattern; indistinct and irregular broad lighter central band (Fig.
Eyes (Fig.
Anterior eye row. Straight, evenly spaced.
Chelicerae. Dark brown.
Labium. Dark brown, with lighter anterior rim (Fig.
Pedipalp coxae. Dark brown, with lighter anterior rim (Fig.
Legs. Yellow brown with no annulations; tibiae, metatarsi and tarsi darker (Fig.
Opisthosoma. Length 1.5, width 1.1; yellow-brown with light yellow-brown anterior cardiac mark and dark grey irregular pattern laterally (Fig.
Pedipalps. Tibia as long as broad; cymbium tip with 4–5 macrosetae (Fig.
Female unknown.
The habitat preferences of A. strepera sp. n. are unknown. The male types were found in spring (October).
Artoria strepera sp. n. is currently known only from the type locality, Currawong, north of Sydney in the Sydney Basin (SYB) IBRA region (Fig.
Artoria
taeniifera
Simon, 1909: 193–194, fig. 11. –
Artoriella
taeniifera
(Simon).-
Holotype female, Bunbury (‘Station 142’) (33°20’S 115°39’E, Western Australia, AUSTRALIA], collected during the ‘Hamburger südwest-australische Forschungsreise 1905’ (
AUSTRALIA: New South Wales: 1 female, Round Hill, Euabalong, 32°57’S, 146°09’E (
The male of A. taeniifera is most similar to that of A. belfordensis sp. n. based on the structure of the basoembolic apophysis, which is basally drawn out into a tip or sharp edge and apically truncated. However, these species differ in the shape of the tegular apophysis, which is two-pronged in A. taeniifera and three lobed in A. belfordensis sp. n. The epigyne of female A. taeniifera is distinctive within Artoria, with its atrium semicircular along its anterior border and strongly sclerotised posterior edges that point medially.
The female of A. taeniifera has been described in detail (
Male (based on
Total length 4.8.
Prosoma. Length 2.6, width 2.0; carapace brown with darker radial pattern; light brown elongated V-shaped median band and indistinct light brown submarginal bands (Fig.
Eyes. Diameter of AME: 0.09; ALE: 0.09; PME: 0.25; PLE: 0.21.
Anterior eye row. Strongly procurved, evenly spaced.
Chelicerae. Dark brown.
Labium. Brown, with lighter anterior rim (Fig.
Pedipalp coxae. Brown, with lighter anterior rim (Fig.
Legs. Yellow brown with darker annulations; tibiae, metatarsi and tarsi darker, less annulated (Fig.
Opisthosoma. Length 2.1, width 1.6; olive-brown with irregular darker pattern, centrally darker in particular in posterior half, light yellow-brown anterior cardiac mark (Fig.
Pedipalps. Tibia slightly longer than broad; cymbium apically with ca. 10 stronger setae (Fig.
Artoria taeniifera Simon, 1909, male (
The habitat of A. taeniifera in NSW is unknown. In Western Australia, from where most records of this species have been reported, A. taeniifera prefers open habitats such as coastal dunes, gardens and open woodlands. The single female from NSW was found in March suggesting the species to be autumn-mature. In south-western Western Australia, mature spiders have been found in winter and early spring.
Artoria taeniifera has only been found once in NSW, centrally in the Cobar Plain (COP) IBRA region (Fig.
Holotype male, Terania Creek, N of Lismore, (28°34’S, 153°19’E, New South Wales, AUSTRALIA), 30 April 1976, M.R. Gray, C. Horseman, litter, 340 m alt., rainforest survey site 52, FN767 (
49 males, 59 females and 52 juveniles in 41 records (all NSW). AUSTRALIA: New South Wales: 1 male, 3 females, 14 juv., Beaury State Forest, Bennetts Road ca. 10 km NW Urbenville, 28°25’32”S, 152°27’46”E (
The specific epithet is a noun in apposition referring to the type locality, Terania Creek.
Males of A. terania sp. n. most closely resemble those of A. grahammilledgei sp. n. based on the shape of the tegular apophysis, which is apically truncated (Fig.
Artoria terania sp. n., male holotype (
Male (based on holotype,
Total length 5.4.
Prosoma. Length 3.0, width 2.3; carapace yellow-brown dusted with grey and indistinct dark radial pattern; lateral margin and central band pale yellow, broader in cephalic area and posterior margin (Fig.
Eyes. Diameter of AME: 0.10; ALE: 0.11; PME: 0.36; PLE: 0.29.
Anterior eye row. Slightly procurved, evenly spaced.
Chelicerae. Dark brown.
Labium. Dark brown, with lighter anterior rim (Fig.
Pedipalp coxae. Dark brown, with lighter anterior rim (Fig.
Legs. Yellow brown with darker annulations; tibiae, metatarsi and tarsi darker, less annulated (Fig.
Opisthosoma. Length 2.4, width 1.7; yellow-brown with light yellow-brown anterior cardiac mark and dark grey irregular pattern (Fig.
Pedipalps. Tibia longer as broad; cymbium tip without macrosetae (Fig.
Female (based on
Total length 5.6.
Prosoma. Length 2.9, width 2.1; carapace and sternum colouration as male (Fig.
Eyes. Diameter of AME 0.12, ALE 0.10, PME 0.34, PLE 0.28.
Anterior eye row. Straight, evenly spaced.
Chelicerae, labium, Pedipalp coxae, legs and opisthosoma. Opisthosoma length 2.7, width 2.1; otherwise as male, but opisthosoma pattern more obscure (Fig.
Epigyne. Atrium bell-shaped with rectangular anterior margin (Fig.
Habitat descriptions on locality labels of A. terania sp. n. include ‘rainforest’, ‘microphyll vine forest’, ‘dry rainforest’ and ‘Hoop Pine plantation’, where the species seems to be litter-dwelling.
Mature males of A. terania sp. n. were mostly found in April and October, suggesting two reproductive periods. Females were found from December to May with a peak in April, but also in October.
Artoria terania sp. n. has been mostly found in north-eastern NSW in the NSW North Coast (NNC) and South Eastern Queensland (SEQ) IBRA regions, with isolated records around Sydney (Sydney Basin – SYB) and in the south-east of the state (South East Corner – SEC) (Fig.
Artoria triangularis Framenau, 2002: 227–228, figs 23A–E, 24.
Holotype male, Avon River near Valencia Creek (37°48’S 146°27’E, Victoria, AUSTRALIA], 3–17 September 1997, riparian sclerophyll forest, pitfall trap, V.W. Framenau (
60 males and 61 females in 66 records (all NSW). AUSTRALIA: New South Wales: 2 females, 14.5 km NW of Corowa, 35°54’33”S, 146°16’11”E (
The tegular apophysis of the male pedipalp is distinctive in A. triangularis in that it is almost straight and pointed apically (Fig.
Artoria triangularis has been described in detail (
Artoria triangularis Framenau, 2002, male (
In NSW, A. triangularis has mostly been found in open forests and woodlands, with two records from spinifex grassland and one from a road verge.
Mature males were generally found in October and November, with two records from May. Females were also most often encountered in October and November, but were also found in January, March–May and July. Artoria triangularis therefore appears largely spring-mature.
In NSW, A. triangularis has been found east and west of the Great Dividing Range. In the west, it reaches into the NSW South Western Slopes (NSS), Cobar Peneplain (COP) and Riverina (RIV) IBRA regions (Fig.
Artoria ulrichi Framenau, 2002: 228–229, figs 25A–F, 26.
Holotype male, Gerringong ‘Scalloway’’ (34°45’S 150°50’E, New South Wales), 18 November 1986, G. Wishart (
28 males, 12 females and 3 juveniles in 13 records (all NSW). AUSTRALIA: New South Wales: 1 male, Cambewarra Mt, 6 miles N by W of Nowra, 34°47’S, 150°35’E (
Artoria ulrichi is part of the lineata-group, to which also A. lineata and A. quadrata belong. A detailed diagnosis for these three species can be found above under the treatment of A. lineata.
Artoria ulrichi has been described in detail (
In NSW, A. ulrichi has been found in forest habitats, including rainforests. Mature spiders were found from November through to June.
In NSW, A. ulrichi has been found east and west of the Great Dividing Range in the NSW North Coast (NNC), Sydney Basin (SYB) and South Eastern Highlands (SHE) IBRA regions (Fig.
Distribution records of Artoria triangularis Framenau, 2002 (open circles) and A. ulrichi Framenau, 2002 (full circles) in NSW. IBRA bioregions with spider records: COP – Cobar Peneplain; NET New England Tablelands; NNC – NSW North Coast; NSS – NSW South Western Slopes; RIV – Riverina; SEH – South Eastern Highlands; SEC – South East Corner; SYB – Sydney Basin.
Artoria ulrichi Framenau, 2002, male and female (
Artoria victoriensis Framenau, Gotch & Austin, 2006: 28–32, figs 63–70.
Holotype male, Melbourne (37°49’S, 144°58’E, Victoria, AUSTRALIA), 8 October 1956, A Neboiss (
91 males, 59 females and 8 juveniles in 79 records (all NSW). AUSTRALLIA: New South Wales: 1 male, ‘Ashleigh Park’ Farm, 21 km S of Berrigan, 35°51’12”S, 145°49’17”E (
(after
The specimens illustrated here vary somewhat from those originally described, in particular with respect to the internal female genitalia. It is possible, that A. victoriensis may include more than one species pending a more detailed evaluation of its intraspecific variation across its wider range.
Artoria victoriensis has been described in detail (
Artoria victoriensis Framenau, Gotch & Austin, 2006, male (
Artoria victoriensis can typically be found in open, moderately moist habitats, including suburban garden and parks.
Males of the species were predominantly found from October to December, with a single record from April. Female activity is similar, although mature females are not uncommon in the later summer months.
In NSW, A. victoriensis has been found mainly east of the Great Dividing Range where it occurs into the Darling Riverine Plains (DRP), Cobar Peneplain (COP) and Riverina (RIV) IBRA regions (Fig.
Distribution records of Artoria victoriensis Framenau, Gotch & Austin, 2006 (open circles) and A. wilkiei sp. n. (full squares) in NSW. IBRA bioregions with spider records: BBS – Brigalow Belt South; DRP – Darling Riverine Plains; COP – Cobar Peneplain; NAN – Nandewar; NNC – NSW North Coast; NSS – NSW South Western Slopes; RIV – Riverina; SEH – South Eastern Highlands; SEC – South East Corner; SEQ – South East Queensland; SYB – Sydney Basin.
Holotype male, Wyrrabalong National Park (33°16’48”S, 151°32’45”E, New South Wales, AUSTRALIA), 2 June 1997, L. Wilkie, pitfall trap (
32 males, 1 female in 26 records (all NSW). AUSTRALIA: New South Wales: 1 male, Booderee National Park, southern headland of Jervis Bay, 35°08’49”S, 150°45’05”E (
The specific epithet is a patronym in honour of Mr Lance Wilkie, who collected the holotype.
The pedipalp morphology in males of A. wilkiei sp. n. is most similar to that of A. barringtonensis sp. n. and A. bondi sp. n. based on the small, spoon-shaped tegular apophysis. However, A. wilkiei sp. n. is the only species amongst these in which the tegular apophysis has a small tooth pointing ventrally, visible in retrolateral view (Fig.
Male (based on holotype
Total length 4.3.
Prosoma. Length 2.3, width 1.7; carapace yellow-brown dusted with grey and indistinct light radial pattern; lateral margin and central band pale yellow, broader in cephalic area (Fig.
Eyes. Diameter of AME: 0.09; ALE: 0.07; PME: 0.30; PLE: 0.22.
Anterior eye row. Straight, evenly spaced.
Chelicerae. Dark brown.
Labium. Dark brown, with lighter anterior rim (Fig.
Pedipalp coxae. Dark brown, with lighter anterior rim (Fig.
Legs. Femur of leg I very dark to almost black; other legs pale, femora and tibia with darker annulations; tarsi and metatarsi lighter (Fig.
Opisthosoma. Length 2.0, width 1.2; with pale anterior cardiac mark and dark grey irregular pattern (Fig.
Pedipalps. Tibia as long as broad; cymbium tip with 4–5 macrosetae (Fig.
Female (based on paratype
Total length 5.1.
Prosoma. Length 2.6, width 1.8; carapace and sternum colouration as male (Fig.
Eyes. Diameter of AME 0.09, ALE 0.07, PME 0.32, PLE 0.25.
Anterior eye row. Strongly procurved, evenly spaced.
Opisthosoma. Length 2.8, width 1.6; opisthosoma similar colour as male but cardiac mark indistinct (Fig.
Epigyne. Wider than long, strongly sclerotised lateral posterior tips, atrium whitish (Fig.
Artoria wilkiei sp. n., male holotype (
Artoria wilkiei sp. n. appears to prefer open, coastal habitats such as sand dunes and heath. The species is autumn- to winter-mature with males collected from April to August. A single female was collected in June.
Artoria wilkiei sp. n. has so far only been found in coastal NSW in the South Eastern Queensland (SEQ), NSW North Coast (NNC) and Sydney Basin (SYB) IBRA regions (Fig.
Artoria spp., palea of male pedipalp, ventral view: A, A. lineata (L. Koch, 1877) (
Artoria spp., palea of male pedipalp, ventral view: A, A. barringtonensis sp. n. (
Artoria spp., palea of male pedipalp, ventral view: A, A. kerewong sp. n. (
We are indebted to a variety of curators, collection managers and museum staff for assistance in accessing their collections either as loan or during visits to the respective institutions: Graham Milledge and Helen Smith (
This paper was completed with support from the Australian Government’s Australian Biological Resources Study (ABRS) Bush Blitz Strategic Taxonomy Grants Scheme Grant Nr: TTC216-05 to study the new wolf spiders of Artoria (Lycosidae) from ACT and NSW: integrating Bush Blitz specimens into taxonomic research on an abundant predator.
We are thankful to Robert Whyte and Robert Raven for constructive suggestions that greatly improved the quality of the manuscript.
Volker Framenau acknowledges the continuing support by Mark Harvey and Julianne Waldock (
Barbara Baehr would like to thank Jo Harding (Manager), Kate Gillespie (Senior Project Officer), Mim Jambrecina (Senior Project Officer), Beth Tully and Brian Hawkins (Bush Blitz Data Manager) for their great support in the field.