Targets of black cloth with or without flanking netting panels (ca. 1 m tall x 1.7 m) baited with acetone (130 mg/h) and l-octen-3-ol (0.5 mg/h), coated with deltamethrin suspension concentrate and deployed at 4/km 2 , produced a decline of 3% per day in the apparent density of the tsetse fly Glossina morsitans centralis Machado in 500 km 2 of the Western Province of Zambia. Hies were eradicated in a year as evidenced by the absence of catches from flyrounds and traps and the elimination of the transmission of trypanosomiasis. The promise of the target technique is confirmed but the need for its further development is emphasized.
Four aspects of olfaction in host location by tsetse flies, Glossina spp., are discussed as follows: (1) host location and its mechanism, (2) factors affecting host location, (3) kairomones and host location, and (4) kairomones and host selection. Flight behavior in the various phases of host location (i.e., ranging, activation, orientation, and landing) in the absence and presence of olfactory cues is summarized. Movement toward an odor source is effected inter alia through optomotor-steered, upwind anemotaxis. It is still unclear how tsetse employ upwind anemotaxis to realize host location, considering the often highly variable wind direction. Olfactorily induced activation is governed by the olfactory cue perceived and threshold levels set by the internal state of the fly. The former depends on the odor source and distance from it; the latter is determined by species, sex, and physiological state. Wind direction and speed, as well as vegetation and the mobility of the host, interfere with successful completion of odor-induced host location. Close-range olfactory cues (including composition and concentration gradients), visual cues, and nutritional state determine whether a fly, having reached the host animal, will land on it. Carbon dioxide is important in host location because it induces landing and long-range attraction. The role of the other kairomones (acetone, 1-octen-3-ol, 4-methyl-phenol, and 3-n-propyl-phenol) is less clear. Apart from the complacency of various host species under tsetse attack, host choice by tsetse is predominantly opportunistic and primarily the result of the frequency of successful tsetse-host encounters. Nevertheless, host selection based on olfactory cues cannot be ruled out.
After successful laboratory rearing of both males and females from a single clutch of eggs, the genus Nanophyllium Redtenbacher, 1906 (described only from males) and the frondosum species group within Phyllium (Pulchriphyllium) Griffini, 1898 (described only from females) are found to be the opposite sexes of the same genus. This rearing observation finally elucidates the relationship of these two small body sized leaf insect groups which, for more than a century, have never been linked before. This paper synonymizes the frondosum species group with Nanophyllium Redtenbacher, 1906 in order to create a singular and clearly defined taxonomic group. Five species are transferred from the Phyllium (Pulchriphyllium) frondosum species group and create the following new combinations: Nanophyllium asekiense (Größer, 2002), comb. nov.; Nanophyllium chitoniscoides (Größer, 1992), comb. nov.; Nanophyllium frondosum (Redtenbacher, 1906), comb. nov.; Nanophyllium keyicum (Karny, 1914), comb. nov.; Nanophyllium suzukii (Größer, 2008), comb. nov. The only taxon from this species group not transferred from the frondosum species group to Nanophyllium is Phyllium (Pulchriphyllium) groesseri Zompro, 1998. Based on protibial exterior lobes, this species belongs in the schultzei species group as described in Hennemann et al. 2009 and is therefore excluded from further discussion here. The rearing of Nanophyllium also yielded the male Nanophyllium asekiense (Größer, 2002), comb. nov. thus, enabling comparison of this male to the other previously known Nanophyllium species. Two new species of nano-leaf insects are described within, Nanophyllium miyashitaisp. nov., from Morobe Province, Papua New Guinea, and Nanophyllium daphnesp. nov., from Biak Island, Papua Province, Indonesia. With such distinct sexual dimorphism in Nanophyllium between sexes, which have only now been matched up via captive rearing, illustrated within are numerous specimens which might represent the unknown opposite sexes of the many currently known species of Nanophyllium. Due to pronounced sexual dimorphism in Nanophyllium, only future captive rearing or molecular analysis will match up the many unknown sexes. To conclude, with the description of two new Nanophyllium species, dichotomous keys to species for known males and females are presented.
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