Tischeria sichotensis Ermolaev
publication ID |
https://doi.org/ 10.11646/zootaxa.3884.2.3 |
publication LSID |
lsid:zoobank.org:pub:F19AB131-10FD-447B-A4C6-17D0D6649DCB |
DOI |
https://doi.org/10.5281/zenodo.6140778 |
persistent identifier |
https://treatment.plazi.org/id/03C07128-FFBF-FFDB-FF5F-EB5438EDFE99 |
treatment provided by |
Plazi |
scientific name |
Tischeria sichotensis Ermolaev |
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Tischeria sichotensis Ermolaev View in CoL
( Figs 3, 4 View FIGURES 1 – 4 , 36–47 View FIGURES 36 – 41 View FIGURES 42, 43 View FIGURES 44 – 47 )
Tischeria sichotensis Ermolaev, 1986: 7 View in CoL , 8.
Material examined. 1♂ Neotype, designated here, RUSSIAN FAR EAST, Primorskiy Kray (Primorskiy Territory), 20 km E Ussuriysk, Gornotayezhnoe, Biological Station, 43º41'38"N, 132 º09'07"E, mining larvae on Quercus mongolica Fisch. ex Turcz. , 26.vii.2011, ex pupa 30.vii.–02.viii.2011, field card no. AG7002, leg. A. Rocienė, genitalia slide no. AD580 ( ZIN); 1♀, same label data as the neotype, genitalia slide no. AD587 ( ZIN).
Diagnosis. The scale colour of Tischeria sichotensis has little or no diagnostic value. However, from all known Tischeria possessing an undivided valva, T. sichotensis differs in the combination of the broadly bifurcate phallus, the large triangular plate of the vinculum and the simple juxta comprising a pair of curved processes; from the most similar and probably closely related T. dodonaea Stainton , it differs in the broad vinculum and distally broad (broadly bifurcate) phallus.
Male ( Figs 36, 37 View FIGURES 36 – 41 ). Forewing length: about 3.5 mm. Wingspan: about 7.5 mm. Head: palpi and face cream to yellowish cream; frontal tuft and collar comprised of cream to yellowish cream, slender, lamellar scales; antenna with long piliform sensillae, cream on upper side and greyish brown on underside, slightly shorter than half of forewing. Thorax yellowish cream; tegulae ochreous cream, sometimes with a few brownish scales. Forewing ochreous cream with many sparsely distributed brownish to brown scales along costa and in the apical third of forewing; some brown scales are cream-tipped. Underside of forewing uniformly greyish brown. Cilia ochreous cream. Hindwing narrow, greyish cream, without androconia; its cilia grey-cream. Legs ochreous cream, with greyish brown darkening on upper side (except hindlegs). Abdomen pale brownish to greyish brown on upper side and underside.
Female. Antenna half the length of forewing, whitish cream or greyish cream on upper side and underside, without long sensillae. Otherwise as in male.
Male genitalia ( Figs 38–41 View FIGURES 36 – 41 ). Capsule 560 µm. Lateral lobes of uncus very large: as broad as valva and half the length of valva ( Fig. 38 View FIGURES 36 – 41 ). Socii very large, membranous, densely covered with fine spines ( Fig. 39 View FIGURES 36 – 41 ). Tegumen very broad but moderately short (shorter than length of uncus or vinculum). Valva 380 µm long, very narrow, without dorsal process; valva densely covered with short chaetae apically and on inner margin; sublateral process of valva very short; transtilla (transverse bar) absent, replaced with unusually reinforced, strongly chitinized and elaborate anterior margin of tegumen, which we refer to here as the pseudotranstilla ( Fig. 39 View FIGURES 36 – 41 ). Ventral plate of vinculum large (265 µm broad, 175 µm long), almost triangular shaped but rounded anteriorly ( Fig. 38 View FIGURES 36 – 41 ). Juxta comprising two 120 µm long bent lateral elements connected with membranous articulation ( Fig. 40 View FIGURES 36 – 41 , right side/element). Phallus 310 µm long, strongly broadening (up to 110 µm in width) on caudal half, apically bifid, with very slender and inwardly bent arms; connected with juxta by membranous articulation and forming a complex structure ( Fig. 41 View FIGURES 36 – 41 ).
Female genitalia ( Figs 42, 43 View FIGURES 42, 43 ) 1280 µm long. Antrum short, with two pointed, 125 µm long lateral lobes anteriorly ( Fig. 43 View FIGURES 42, 43 ). Ductus spermathecae membranous (chitinized coils either absent or probably lost in fig. 42). Corpus bursae about 1100 µm long, narrow, with short spine-like pectinations in caudal part of bursa.
Bionomics. Host-plant: Quercus mongolica Fisch. ex Turcz. (section Quercus , Fagaceae ). Larvae produce whitish, irregular blotch leaf-mines ( Figs 3, 4 View FIGURES 1 – 4 ) with a round, bulging central spot (a firm, silk-lined nidus inside of the mine in which larva pupate); the leaf-mine contains no frass. The material obtained by V. P. Ermolaev in 1977 was reared in laboratory conditions during mid-winter ( Ermolaev 1986), then adults were attracted to a light trap in July; larvae mine leaves from July (our rearing data) to autumn ( Ermolaev 1986).
Distribution ( Fig. 45 View FIGURES 44 – 47 ). Tischeria sichotensis occurs in deciduous, broadleaf ( Figs 46, 47 View FIGURES 44 – 47 ) or mixed forest of the Primorskiy Kray (= Primorskiy Territory) and Khabarovskiy Kray (= Khabarovskiy Territory), along the Amur and Ussuri rivers (Russian Far East) at altitudes of 50– 300 m.
Remarks. The type series of Tischeria sichotensis Ermolaev , comprising two male specimens (the holotype from Sarapul’skoe, Khabarovskiy Kray, and the paratype from Gornotayezhnoe, Primorskiy Kray) has been missing for almost the past three decades (S.V. Baryshnikova, S.Yu. Sinev, A.L. Lvovsky, V.G. Mironov, pers. comm.). Despite the fact that the type-series of T. sichotensis was described and illustrated by the author of the species ( Ermolaev 1986), we feel that it necessary to designate a neotype for two reasons: 1) the primary description and original drawings are not very precise or exhaustive so that there may be a problem with the identification of this species; 2) currently we expect ongoing investigations of the East Asiatic fauna of Tischeriidae to increase significantly in a relatively near future, particularly in China (Xiaohua Dai, pers. comm.), and prefer to avoid possible misidentifications, especially in the case of new species discoveries or descriptions from China or adjacent territories. Therefore, after discussions and consultations with Russian specialists from the Zoological Institute of the Russian Academy of Sciences, we designated a neotype for T. sichotensis . The neotype specimen was collected precisely at the same locality as the missing paratype (Gornotayezhnoe). It also seems to match the drawing of the missing holotype published in the original description of the species ( Ermolaev 1986: fig. 2).
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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Tischeria sichotensis Ermolaev
Stonis, Jonas R., Diškus, Arūnas, Rocienė, Agnė, Sruoga, Virginijus & Davis, Donald R. 2014 |
Tischeria sichotensis
Ermolaev 1986: 7 |