The genus Tinocallis Matsumura, 1919 (Hemiptera: Aphididae: Calaphidinae) includes 19 species of 4 subgenera, EotinocallisQuednau, 2003, OrientinocallisQuednau, 2003, Sappocallis Matsumura, 1919 and Tinocallis Matsumura, 1919 (Favret, 2016; Quednau 2001) in the world. Tinocallis species have been described throughout Asia and Eastern Europe (Blackman & Eastop, 2016), among which T. saltans (Nevsky, 1929), T. takachihoensis Higuchi, 1972, T. ulmiparvifoliae Matsumura, 1919 and T. zelkowae Takahashi, 1919 have caused economic damages on ornamental trees, by invading into Western Europe, North America and Australia (Blackman & Eastop, 2016; d’Acier et al., 2010). It has been known that Tinocallis spp. take monoecious and holocyclic lifecycle on various host-plants belonging to the Betulaceae, Fabaceae, Lythraceae, Juglandaceae, Sapindaceae, Sonneratiaceae and Ulmaceae (Quednau, 2003).
In this study, the genus Tinocallis is reported for the first time from Laos, based on the specimen of Tinocallis himalayensis Ghosh, Ghosh & Raychaudhuri, 1971. Currently, this species has been described from Bangladesh, India, Malaya, Singapore and Thailand (Gosh et al., 1971; Danielsson & Robinson 1978; Blackman & Eastop, 2016). In Laos, this species caused severe damages on Queen’s crape-myrtle, Lagerstroemia speciosa (Lythraceae), which has been widely cultivated as an ornamental plant and a folk medicine in tropical region throughout Southeast Asia such as Cambodia, China, Indonesia, Laos, Malaysia, Myanmar, Philippines, Singapore, Thailand and Vietnam (Orwa et al., 2009; Wahi et al., 1982). Sarucallis kahawaluokalani Kirkaldy 1907, the other famous aphid pest on Lagerstroemia spp., has been invaded into foreign countries such as Africa, Europe and America (Yovkova, 2011). Since Lagerstroemia spp. from Southeast Asia are steadily exported to many countries, it is worth to study on the relatively little known pest, T. himalayensis. In this paper, a diagnostic note, biometric data and illustrations are given for the alate viviparous female.
Materials and Methods
Tinocallis himalayensis samples were collected in Laos from 2013 to 2014. Samples were preserved in 90% ethanol for a month, and then mounted in Canada balsam, following the method of Blackman & Eastop (2000) and Martin (1983). Illustrations for the species were taken by a digital camera attached to the microscope (Leica 400B, Leica Microsystems, Germany) at a resolution of 600 dpi. Measurements for each specimen are taken from the digital images by using image analysis software (Active measure ver. 3.0.3 from Mitani Co. Ltd, Japan). All specimens were preserved in the College of Agriculture and Life sciences, Seoul National University Korea (CALS).
Abbreviations used for diagnosis are: Ant.I, Ant.II, Ant.III, Ant.IV, Ant.V and Ant.VIb, antennal segments I, II, III, IV, V and base of VI, respectively; PT, processus terminalis; BDAnt.III, basal diameter of antennal segment III; AbdT.I, AbdT.II, AbdT.III, AbdT.IV, abdominal tergite I-IV; 2HT, second segment of hind tarsus; HFM, hind femur; HTB, hind tibiae; SIPH, siphunculus; SIPH-bw, basal width of SIPH; URS, ultimate rostral segment; URS-bw, basal width of URS; Cauda-bw, basal width of Cauda.
Results and Discussion
Taxonomy
Genus Tinocallis Matsumura, 1919
Tinocallis Matsumura, 1919: 100.
Type species: Tinocallis ulmiparvifoliae Matsumura, 1919: 101.
Diagnosis. Head vertex with 4 pointed setae, mostly shorter than BDAnt.III, median tubercle on frons well developed; Antennae six segmented with pointed setae, shorter than BDAnt.III, secondary sensoria narrow elliptical or of slit-like annular form without ciliate margins; Pronotum always with two anterior and two posterior spinal setae, spinal setae on wart- or finger-like processes in some species; Wing veins sometimes with black pigmentations; Abdominal margin with single pairs of setae, those on tergites I-IV often on wart- or finger-like processes, marginal setae on tergite V-VII not on processes; SIPH cylindrical, truncated; Cauda knobbed, anal plate bilobate.
Tinocallis (Orientinocallis) himalayensis Gosh, Ghosh & Raychaudhuri, 1971 (Fig. 1-2; Table 1)
Tinocallis himalayensis Gosh, Ghosh & Raychaudhuri, 1971: 218.
Tinocallis khonkaenensisDanielsson & Robinson, 1978: 101.
Tinocallis (Tinocallis) himalayensis Remaudière & Remaudière, 1997; Quednau, 2001.
Tinocallis (Orienticallis) himalayensisQuednau, 2003; Favret, 2016.
Materials examined. 5 alate viviparous female, Morning market, Vientiane, Laos, 22.xii.2013, on Lagerstroemia speciosa (Lythraceae), Y. Lee (CALS); 5 alate viviparous female, Singha road, Viangchan, Vientiane, Laos, 22.xii.2013, on L. speciosa (Lythraceae), Y. Lee (CALS); 5 alate viviparous female, Banna village forest, Phou khao khouay National Biodiversity Conservation Area, Thaphabath, Bolikhamsai, Laos, 24.xii.2013, on L. speciosa (Lythraceae), Y. Lee (CALS); 5 alate viviparous female, 9.ii.2014, Lane Xang street, Vientiane, Laos, on L. speciosa (Lythraceae), S. Lee (CALS).
Host plant. Previously described on Peltophorum fleragineum (Leguminosae) and Duabanga sonneratioides in India (Chakrabarti, 1998), the species severely attacked Lagerstroemia speciosa in Laos (this study) and Thailand (Danielsson & Robinson, 1978).
Distribution. Laos, Bangladesh, India, Malaya, Singapore and Thailand. Fig. 1, Table 1
Diagnosis. Head vertex with three pairs of processes. Ant.III with 7-9 elliptical secondary rhinaria which are barely occupying basal half (Fig. 2K); Subcosta and branches of media bordered with brown pigments, radial sector weakly developed or absent (Fig. 2F). AbdT.I and II with pair of finger-like processes with one spinal seta on each tip (Fig. 2B), AbdT.III-VIII with low, wart like processes, marginal processes on AbdT. I and IV dark sclerotic with one marginal seta (Fig. 2J).
Remarks. This species can be easily distinguished from congeneric species by having unique brown pigments on fore wings. The life cycle of this species is unclear. In India and Thailand, apterous oviparae were collected together with alate viviparae in December (Blackman & Eastop, 2016). However, we only found alate viviparous females in Laos. In the almost every urban area in Laos, we found a heavy infestation of this species on Lagerstroemia speciosa. On a heavily infested plant, black sooty molds were occurred.