Structure of female genitalia of glassy-winged sharpshooter, Homalodisca coagulata (Say) (Hemiptera: Cicadellidae).

The functional reproductive morphology of the female glassy-winged sharpshooter, Homalodisca coagulata (Say), is described at both light microscopy and scanning electron microscopy levels. The female has nine abdominal segments; the seventh to the ninth abdominal segments are modified for reproduction; the eighth tergite is reduced to two segments, with the ovipositor partially exposed from the modified ninth segment-the pygofer. The pygofer, covered with trichoid and coeloconic sensilla, almost completely encloses the ovipositor, which consists of three pairs of valvulae and two pairs of valvifers. The first and second valvulae function together for oviposition. The first valvulae are located exterior to the second valvulae, both of which bear many trichoid, campaniform, and coeloconic sensilla. The third valvulae, possessing many coeloconic sensilla, envelope the first and second valvulae. Seven major muscles are found to be associated with the ovipositor and the pygofer. The oviposition process is described with respect to the activity of the valvulae and their associated musculature. The female morphology follows the general pattern of cicadellids as a group.

Virulence and site of infection of the fungus, Hirsutella thompsonii, to the honey bee ectoparasitic mite, Varroa destructor.

The Varroa mite, Varroa destructor, is recognized as the most serious pest of both managed and feral Western honey bee (Apis mellifera) in the world. The mite has developed resistance to fluvalinate, an acaricide used to control it in beehives, and fluvalinate residues have been found in the beeswax, necessitating an urgent need to find alternative control measures to suppress this pest. Accordingly, we investigated the possibility of using the fungus, Hirsutella thompsonii, as a biocontrol agent of the Varroa mite. Among the 9 isolates of H. thompsonii obtained from the University of Florida and the USDA, only the 3 USDA isolates (ARSEF 257, 1947 and 3323) were infectious to the Varroa mite in laboratory tests. The mite became infected when it was allowed to walk on a sporulating H. thompsonii culture for 5 min. Scanning electron micrographs revealed that the membranous arolium of the mite leg sucker is the focus of infection where the fungal conidia adhered and germinated. The infected mites died from mycosis, with the lethal times to kill 50% (LT(50)s) dependent on the fungal isolates. Thus, the LT(50)s were 52.7, 77.2, and 96.7h for isolates 3323, 257, and 1947, respectively. Passage of H. thompsonii through Varroa mite three times significantly reduced the LT(50)s of isolates 257 and 1947 (P<0.05) but not the LT(50) of isolate 3323. The fungus did not infect the honey bee in larval, prepupal, pupal, and adult stages under our laboratory rearing conditions. Our encouraging results suggest that some isolates of H. thompsonii have the potential to be developed as a biocontrol agent for V. destructor. However, fungal infectivity against the mites under beehive conditions needs to be studied before any conclusion can be made.