Window, Lake Weyba House, Sunshine Coast

Vinyl window to daybed alcove, bedroom pavilion, South-West elevation.

Window, Lake Weyba House, Sunshine Coast

Vinyl window to bath house pavilion, South-West elevation.

Main Pavilion, Lake Weyba House, Sunshine Coast

As seen from West, looking towards front of main pavilion. Standard roller doors to clerestory.

Pivoting vent, Lake Weyba House, Sunshine Coast

Bedroom pavilion, South-East elevation. Day bed alcove on left.

Pavilions and outdoor seating area, Lake Weyba House, Sunshine Coast

As seen from back of bedroom pavilion, looking towards main pavilion. Day bed alcove to bedroom in foreground.

South-West elevation, Lake Weyba House, Sunshine Coast

Bath house and bedroom pavilions, with outdoor seating area in foreground.

Main pavilion, Lake Weyba House, Sunshine Coast

South-West elevation of main pavilion - living, kitchen, dining and study/guest areas.

Bedroom pavilion, Lake Weyba House, Sunshine Coast

As seen from outdoor seating area. Pivoting vent on left and day bed alcove on right. Standard roller doors to clerestory.

Bath house pavilion, Lake Weyba House, Sunshine Coast

South-West elevation. Paved seating area in foreground.

Bath house pavilion, Lake Weyba House, Sunshine Coast

Link to bedroom pavilion on right; roof of main pavilion on left.

North-East elevation, Lake Weyba House, Sunshine Coast

Bedroom pavilion on left, bath house pavilion centre and main pavilion on right.

North-East elevation, Lake Weyba House, Sunshine Coast

As seen from East, looking along pavilions. Bedroom pavilion and day bed alcove in foreground.

The Genus Wolbachia

Numerous invertebrate species form long lasting symbioses with bacteria (Buchner, 1949; Buchner, 1965). One of the most common of these bacterial symbionts is Wolbachia pipientis, which has been estimated to infect anywhere from 15–75% of all insect species (Werren et al., 1995a; West et al., 1998; Jeyaprakash and Hoy, 2000; Werren and Windsor, 2000) as well as many species of arachnids, terrestrial crustaceans and filarial nematodes (O’Neill et al., 1997a; Bandi et al., 1998). In most arthropod associations, Wolbachia act as reproductive parasites manipulating the reproduction of their hosts to enhance their own vertical transmission. There appears to be little direct fitness cost to the infected host besides the costs arising from the reproductive manipulations. However instances have been reported where Wolbachia can be either deleterious (Min and Benzer, 1997; Bouchon et al., 1998) or beneficial (Girin and Boultreau, 1995; Stolk and Stouthamer, 1995; Wade and Chang, 1995; Vavre et al., 1999b; Dedeine et al., 2001) to their hosts. Wolbachia were first described as intracellular Rickettsia-like organisms (RLOs), infecting the gonad cells of the mosquito, Culex pipiens (Hertig and Wolbach, 1924), and were later named 'Wolbachia pipientis' (Hertig, 1936). It was not until the work of Yen and Barr (Yen and Barr, 1971; Yen and Barr, 1973) that Wolbachia were implicated in causing crossing incompatibilities between different mosquito populations (Laven, 1951; Ghelelovitch, 1952). When polymerase chain reaction (PCR) diagnostics for Wolbachia became available, it became clear that this agent was both extremely widespread and also responsible for a range of different reproductive phenotypes in the different hosts it infected (O’Neill et al., 1992; Rousset et al., 1992; Stouthamer et al., 1993). The most common of these are cytoplasmic incompatibility, inducing parthenogenesis, overriding host sex-determination, and male-killing (O’Neill et al., 1997a). As of the time of this writing, more than 450 different Wolbachia strains with unique gene sequences, different phenotypes, and infecting different hosts have been deposited in GenBank and the Wolbachia host database (http://www.wolbachia.sols. uq.edu.au).