44 Records of the Australian Museum (2006) Vol. 58
were similar to these, or the assumed
, butshowing variations in shape and colour. All of these typeswere female, or subadult female. Of the early authors onlySimon (1895) described a (juvenile) male from Ceylon (SriLanka), although he was unsure as to which species thisbelonged. [The description was attached to
(Ausserer)by Roewer (1942) and this was followed by Platnick (2005),but apparently this association was not intended by Simon].More recently, males of some species have been figured in anumber of works (e.g., Davies, 1988; Chikuni, 1989), but therehas been no thorough description for any species.
species have been described from most parts of the old-world tropics and sub-tropics with the greatestnumber of species from SE Asia. In Australia, nine speciesof
were described from the Australian mainland (eightspecies from Queensland, one from Western Australia) andone from Lord Howe Island in the Tasman Sea. Simon(1899) suggested several synonymies but none of these arereported by Roewer (1942) or Platnick (2005) and they havenot been followed in this study.Close to Australia, several species have been describedfrom New Guinea and the Moluccas. Unfortunately,
Chrysanthus is the only one of these species thatcan be positively identified. The types of
(Bradley) from New Guinea andof
(Doleschall) from Amboina [Ambon] havenot been found. Except for
from Borneo there is thena geographical gap in described species northwards toSingapore, the area from where
was described.From Sumatra northwards into mainland Asia there are thenanother 16 described species. All of these types aresummarized in Appendix 1.Koch was uncertain of the familial placement of
and suggested the eye pattern might align the genus withthe “Mithraen” (presumably
C.L. Koch species,which are now listed under
Walckenaer inUloboridae). As the genus became better known, its familialaffinities were recognized. Simon (1895) placed
intohis Argiopidae as the nominative member of a newsubfamily, the Poltyinae, which also included the genera
Blackwall. Later in the samework this taxon was demoted to tribal status in theArgiopinae (now essentially the family Araneidae). Thistribe is now referred to as the Poltyini to conform to theInternational Code of Zoological Nomenclature. Informaluse of this grouping has continued to the present, but asmore becomes known of these genera it now seems unlikelythat this is a monophyletic grouping (Smith, 2005).
Aims and scope
The original aim of this study was the taxonomic revisionof the Australian
species including a phylogeneticanalysis and complementary behavioural studies (which willbe reported separately). Initially, species separation wasproblematic due to unexpectedly wide intra-specificvariations in abdominal shape (Smith, 2003). Once thespecific features were better understood, and as morematerial became available, it became apparent that most of the northernmost Australian species were also presentoutside Australia, some as far north as mainland Asia. Thismeant that the original scope of the study had to be widenedto include much more of the SE Asian fauna and many moretypes needed to be examined.It was decided not to make any more formal descriptionsor redescriptions of species based on females alone. Allconfirmed Australian species have been matched to males,and most pairings have been confirmed by raising the malesfrom egg sacs. Only a few males are available for studyfrom the SE Asian region and currently, other than the newspecies described here from New Caledonia, only thoserecognisable from Australian species can be matched tofemales. Some characters of a number of named non-Australian species have been figured with a summary of their details to aid future work in this region (Appendix 1,Figs 223–247). Except where somatic details may bediagnostic, only mature types have been illustrated.A detailed generic description is not usually required fora partial generic revision. It was decided that due to thelack of previous knowledge of males and several instancesof misidentification of other genera with
, such detailwould be useful in this case.In this paper a revision of all the Australasian
species with known males is presented. Support for thesespecies’ delimitation is then examined using within andbetween-species variations in base sequences of a shortsection from two genes.
Material and methods
Specimen examinations, measurements and drawings weremade using a Wild M5 microscope with graticule anddrawing attachment. Half-tone drawings were made oncoarse-grade coquille board, using a range of graphitepencils and an ink outline. Stipple drawings are of ink ontodrafting film. All plates were made up using AdobePhotoshop® 5.0 LE, including the addition of white lineson half-tone drawings. Specimen preparations for scanningelectron microscopy (SEM) were either air dried from 70%alcohol (legs), air dried from 100% acetone afterdehydration through a series of alcohol solutions (morerobust male palps and spinnerets) or dried by critical pointdrying after the acetone/alcohol series (delicate male palps).
are often awkward to examine and draw as thelegs are often tightly bunched and the dorsally extendedabdomens may be difficult to handle. In order to damageno more specimens than necessary, the primary figuredfemale specimens of each species group are the ones thathave been used for DNA extractions, so 3–4 legs have beenremoved from one side (sometimes including coxae on smallerspecimens). All lateral views are from the left (image reversedif necessary). On dorsal and ventral drawings any missing coxaewere copied in from the entire side to balance the drawing.The point of leg excision is representational. Leg I has beenmanipulated so that a flat lateral view is shown to illustrate theproportion to the carapace; leg II femur length is in correctproportion to leg I. Legs III and IV are drawn as seen.The range of abdominal variation within each speciesmay be large but is similar in any one species group. This isillustrated for each group with exemplars drawn from thedifferent species and in addition the abdomen of eachholotype is illustrated. The particular abdominal shapeshown for any particular species should therefore NOT beconsidered specifically diagnostic within the group (but seediscussion for comments on the
-group andsome other non-Australian species).Male palpal organs are rather small and details are oftendifficult to discern under a light microscope. The drawings