Macropsidius kajkanus Mityaev, 1990

Tishechkin, Dmitri Yu., 2022, Macropsidius bogutensis (Mityaev, 1990) species group (Hemiptera: Auchenorrhyncha: Cicadellidae: Eurymelinae: Macropsini) in Kazakhstan: taxonomy, biology, and evolution, Zootaxa 5165 (3), pp. 405-414 : 410

Macropsidius kajkanus Mityaev, 1990

Figs. 29–33 , 70–72

Description. In appearance and coloration, indistinguishable from most other species of Macropsidius .

Aedeagus in posterior view with narrow lateral carinae slightly not reaching gonopore ( Fig. 70 ). Ventral carina with evenly curved margin, runs all along shaft from base to gonopore ( Figs. 71–72 ). Aedeagal apex somewhat expanded, with only 1–3 if any blunt denticles on each side. Shape of pygofer appendages and styles same as in most other members of genus.

Hosts. Originally collected from undetermined species of Artemisia ( Mityaev, 1990) ; later A. (Seriphidium) juncea was recorded as a host plant for specimens from the type series ( Mityaev, 2002). Specimens for this study were collected from A. (Seriphidium) juncea growing on stony slopes ( Fig. 76 ).

Calling signal. Signals of one male from Southeastern Kazakhstan (foothills of Dzhungarskiy Alatau near the gorge of the Lepsy River at its exit from the mountains to the plain, 13 km south of Kolbay Village, 45.700 N, 80.297 E, from A. (Seriphidium) juncea , 19. VI. 2017) were recorded at 29 o C .

Male calling signal is a phrase lasting for 5–10 s in the recordings and consisting of syllables following each other with a period from 0.3– 0.4 s at the beginning to 0.8– 0.9 s (occasionally, up to 1 s and more) at the end ( Figs. 29–31 ). Each syllable includes the low-amplitude rather variable initial part and the high-amplitude component consisting of 6–10 partially merged pulses ( Figs. 32–33 ). Often, low-amplitude parts of syllables gradually reduce towards the end of a phrase, so that the end syllables in a phrase sometimes consist of only high-amplitude component ( Fig. 30 ).

On the whole, in temporal pattern, the calling signal of M. kajkanus is similar to that of M. bogutensis . Syllable repetition period ranges in these species considerably overlap, and syllables share similar final component consisting of several partially merged pulses ( Figs. 26–28 and 32–33 ). Since the initial low-amplitude part of a syllable in both species is variable, occasionally, some syllables in phrases of two species are almost indistinguishable (two last syllables on Fig. 27 and on Fig. 32 ).

Distribution. All known records are restricted to the arid foothills of the eastern part of Dzhungarskiy Alatau, Southeastern Kazakhstan ( Fig. 73 ).

Remark. In appearance and genitalia shape, M. kajkanus is very similar to M. valiturus and M. araxes ( Tishechkin, 2014) . However, these two species are known only from Caucasus, Transcaucasia, and the adjacent regions of Iran, whereas M. kajkanus was never found outside the eastern part of Dzhungarskiy Alatau. For this reason, their synonymization without comprehensive investigation of Caucasian species would be premature.

Figures

FIGURES 19–33. Macropsidius spp., calling signal oscillograms. 19–23―M. karatavicus sp. n., 24–28―M. bogutensis, 29– 33―M. kajkanus. Faster oscillograms of the parts of signals indicated as “21–22”, “26–28”, and “32–33” are given under the same numbers.

FIGURES 63–76. 63―paratype of M. bogutensis, style, 64―same, male from the type locality, 65―same, drawing from the original description (after Mityaev, 1990), 66–68―same, males from Dzhungarskiy Alatau (M. zhuravlevi sensu Mityaev, 2014), 69―same, drawing from the original description of M. zhuravlevi (after Mityaev, 2014), 70―M. kajkanus, penis, back view, 71―same, frontal and lateral view, 72―same, lateral view, 73―distribution map of species of the M. bogutensis group, 74–76―biotopes,where insects were collected; localities, where photos were taken are shown with arrows, the whitish green plant in the center of each photo is Artemisia (Seriphidium) juncea.