identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
2D86E8F6AE1353E392493FA4C40ED071.text	2D86E8F6AE1353E392493FA4C40ED071.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Calicotis atricosta Lee & Terada 2026	<div><p>Calicotis atricosta sp. nov.</p><p>Figs 1 C, 1 D, 3 C, 4 B, 7</p><p>Korean name.</p><p>Geom-eun-tti-hol-ssi-kkok-ji-na-bang.</p><p>Type material.</p><p>Holotype: Korea • ♂; Jeju-do, Seogwipo-si, Topyeong-dong; 27. VIII. 2021; Ga-Eun Lee leg.; genitalia slide no. LGE 22020 (JNU); DNA voucher no. LGE-G 901 . Paratype: Korea • 1 ♂; same original data as holotype; genitalia slide no. LGE 22019 (NIBR); DNA voucher no. LGE-G 549 .</p><p>Additional species examined.</p><p>Calicotis latebrifica: Korea • 7 ♂ 10 ♀; Jeju-si, Aewol-eup, Gwakji-ri; 28. IV – 15. V. 2021; Ga-Eun Lee leg.; genitalia slide nos LGE 21025 m, LGE 21030 f; DNA voucher no. LGE-G 552 • 3 ♂ 8 ♀; Aewol-eup, Aewol-ri; 8, 10. V. 2021; Ga-Eun Lee leg. • 1 ♀; Jeju-si, Hangyeong-myeon, Chengsu-ri; 2. VI. 2021; Ga-Eun Lee leg.; genitalia slide no. LGE 22086 f; DNA voucher no. LGE- G 899 • 1 ♀; Seogwipo-si, Namwon-eup, Sumang-ri; 21. VI. 2023; Ga-Eun Lee leg.; genitalia slide no. LGE 24021 f; DNA voucher no. LGE-G 900 (all deposited in JNU) • 1 larva ex Cyrtomium falcatum var. devexiscapulae; Seogwipo-si, Daejeong-eup; 7. VI. 2025; Ga-Eun Lee leg.; DNA voucher no. LGE-G 1006 • 1 larva ex Cyrtomium falcatum var. devexiscapulae; Jeju-si, Yeon-dong; 10. VI. 2025; Ga-Eun Lee leg.; DNA voucher no. LGE-G 1015 • 1 larva ex Arachniodes aristata; Seogwipo-si, Andeok-myeon, Seogwang-ri; 22. VI. 2025; Ga-Eun Lee leg.; DNA voucher no. LGE-G 1038.</p><p>Diagnosis.</p><p>This new species can be readily distinguished by the whitish forewing with a black basal costa and a broad black antemedian fascia. While many congeneric species have a dark blotch or streak beyond the middle of the wing, no markings are present in the distal part of the forewing in this species. In the male genitalia, the oval cucullus and anellar lobe, and the rounded juxta are diagnostic.</p><p>Description.</p><p>Adult. Head: Vertex and occiput mixed creamy white and black, frons creamy white. Labial palpus creamy white, outer margin of segment II tinged with dark grey. Antenna with scape creamy white, posterior margin of scape black; flagellum cream, with short fine ciliation in male.</p><p>Thorax: Dorsum of thorax and tegula creamy white, anterior margin of tegula black. Legs creamy white; fore-femur, - tibia and - tarsus black along dorsal margin; mid-tibia tinged with black near base and apex of outer surface, with white bristles dorsally; hind-tibia with white bristles dorsally, slightly mixed with grey beyond middle, apex with whorls of ochreous white bristles; hind-tarsomeres I – IV with whorls of ochreous white bristles at apexes.</p><p>Wings (Fig. 1 C, D): Forewing span 7.5 mm (n = 2). Forewing ground color creamy white, slightly mixed with grey toward apex; costa black in 1 / 4 wing length, this dark shadow expanded as a basal patch and nearly reaching fold; beyond this, a broad, inwardly oblique black antemedian fascia running from costa to dorsum, broadest near costa and narrowest on fold; fringe scales greyish white. Hindwing dark grey except base white; fringe scales greyish white.</p><p>Abdominal segments (Fig. 3 C): Terga with a row of spines on segments II – VII in male.</p><p>Male genitalia (Fig. 4 B): Uncus stout, gradually tapering, with long lateral setae from base to near apex; apex blunt, slightly curved downward. Gnathos slightly shorter than uncus, tongue-shaped, apex rounded. Tegumen simple. Valva somewhat narrowed toward apex; costa slightly convex near base, with long sparse setae at ~ 1 / 3 length; cucullus oval, covered with dense setae on inner surface; sacculus nearly straight from base to near apex, rounded apically, with long sparse setae ventrally. Vinculum narrow and elongate, leading to rounded saccus. Juxta rounded. Anellar lobe developed, oval, with short setae. Aedeagus ~ 3 × as long as uncus, stout, distal half tapering toward apex; a narrow apical spatulate projection present, ~ 1 / 3 length of aedeagus, with apex rounded; cornutus absent.</p><p>Female genitalia. Unknown.</p><p>Host plant and biology.</p><p>Unknown.</p><p>Distribution.</p><p>(Fig. 7) Korea (Jeju-do).</p><p>Etymology.</p><p>The species name is derived from the Latin ater (black) and costa (costa), referring to the black basal costa of the forewing.</p><p>Remarks.</p><p>Due to the limited number of available specimens, no wing venation slide was prepared for the new species in order to avoid destructive sampling of the type material.</p></div>	https://treatment.plazi.org/id/2D86E8F6AE1353E392493FA4C40ED071	Public Domain	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.		Pensoft via Plazi	Lee, Ga-Eun;Terada, Takeshi	Lee, Ga-Eun, Terada, Takeshi (2026): Two new species and three new records of Cuprininae (Lepidoptera, Stathmopodidae) from Jeju Island, Korea, with molecular evidence for their placement. ZooKeys 1287: 253-272, DOI: 10.3897/zookeys.1287.194473
0BC62FA9D3975309B52F0A7E4072BA49.text	0BC62FA9D3975309B52F0A7E4072BA49.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Cuprina porphyrantha (Meyrick 1913)	<div><p>Cuprina porphyrantha (Meyrick, 1913)</p><p>Figs 1 E, 3 D, 4 C, 7</p><p>Stathmopoda porphyrantha Meyrick, 1913: 90 . TL: Ceylon (Sri Lanka). TD: NHMUK.</p><p>Cuprina porphyrantha (Meyrick): Shen and Hsu 2020: 118; Kobayashi and Terada 2022: 112; Shen et al. 2024: 10.</p><p>Cuprina flaviscapella Sinev, 1988: 126; Terada 2016: 150. Synonymized by Sinev (2015: 24).</p><p>Korean name.</p><p>Gwan-jung-ae-gi-kkok-ji-na-bang.</p><p>Material examined.</p><p>Korea • 1 ♂; Jeju-do, Seogwipo-si, Topyeong-dong; 27. VIII. 2021, Ga-Eun Lee leg.; genitalia slide no. LGE 22033 (NIBR); DNA voucher no. LGE-G 548 • 1 larva ex Arachniodes aristata; Seogwipo-si, Andeok-myeon, Seogwang-ri; 22. VI. 2025; Ga-Eun Lee leg.; DNA voucher no. LGE-G 1023 .</p><p>Additional species examined.</p><p>Cuprina fuscella: Korea • 2 ♂; Jeju-do, Seogwipo-si, Topyeong-dong; 22. IV, 23. V. 2021; Ga-Eun Lee leg.; genitalia slide no. LGE 21029 (JNU); DNA voucher no. LGE-G 738 • 4 larvae ex Arachniodes sporadosora, Cyrtomium falcatum var. devexiscapulae, Dryopteris uniformis and Polystichum polyblepharum; Jeju-do, Seogwipo-si, Topyeong-dong; 30. V. – 19. VI. 2025; DNA voucher nos LGE-G 1000, - G 1001, - G 1014, - G 1021 • 1 larva ex Dryopteris uniformis; Jeju-do, Jeju-si, Ara-dong; 6. VI. 2025; Ga-Eun Lee leg.; DNA voucher no. LGE-G 1005 • 1 larva ex Dryopteris uniformis; Jeju-do, Jeju-si, Yeon-dong; 10. VI. 2025; Ga-Eun Lee leg.; DNA voucher no. LGE-G 1016 • 3 larvae ex Dryopteris uniformis and Polystichum polyblepharum; Jeju-do, Jeju-si, Jocheon-eup, Gyorae-ri; 11. VI. 2025; Ga-Eun Lee leg.; DNA voucher nos LGE-G 1017, - G 1018, - G 1019.</p><p>Diagnosis.</p><p>Forewing span 6.9 mm (n = 1). This species closely resembles C. fuscella in both external appearance and genitalia. It is difficult to distinguish the two species based on superficial appearance, as both have dark forewings without distinct markings. However, antennal coloration provides a useful diagnostic character. The scape of C. porphyrantha is ochreous yellow dorsally (Fig. 1 E); in C. fuscella it is fuscous to dark grey. Also, the apical portion of the antennae is more broadly pale in C. porphyrantha, although this character may sometimes be indistinct. In the male genitalia (Fig. 4 C), the basal sclerotized structure of the aedeagus is larger in C. porphyrantha than in C. fuscella . The female genitalia of the two species were not examined in this study; however, according to Terada (2016), the signum of C. porphyrantha is smaller.</p><p>Host plants.</p><p>Dryopteridaceae: Dryopteris crassirhizoma Nakai (Terada 2016), D. hondoensis Koidz. (Kobayashi and Terada 2022), Dryopteris sp. (Sawamura et al. 2009; C. porphyrantha was identified as Stathmopodinae sp.), Arachniodes aristata (G. Forst.) Tindale (this study).</p><p>Biology.</p><p>Larvae are found in silky galleries on the underside of fern fronds. Adults fly between May and August in Japan (Terada 2016). In Korea, the larvae are found in June and adults in August.</p><p>Distribution.</p><p>(Fig. 7) Korea (new record), Japan, Russia, Sri Lanka, Taiwan.</p><p>Remarks.</p><p>Detailed descriptions of the adults and genitalia are provided in Terada (2016). The larvae of C. porphyrantha are specialists on Dryopteridaceae whereas the closely related species C. fuscella feeds not only on Dryopteridaceae but also on two other families Athyriaceae and Onocleaceae (Sinev 1988; Sawamura et al. 2009; Terada 2016). Shen and Hsu (2020) listed Theyriaceae and Woodsiaceae as host plants of C. fuscella, but these were included in error (Shen pers. comm. 6 Jun 2025).</p></div>	https://treatment.plazi.org/id/0BC62FA9D3975309B52F0A7E4072BA49	Public Domain	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.		Pensoft via Plazi	Lee, Ga-Eun;Terada, Takeshi	Lee, Ga-Eun, Terada, Takeshi (2026): Two new species and three new records of Cuprininae (Lepidoptera, Stathmopodidae) from Jeju Island, Korea, with molecular evidence for their placement. ZooKeys 1287: 253-272, DOI: 10.3897/zookeys.1287.194473
5D6FF8BA8C5854449795B43D8282D1EC.text	5D6FF8BA8C5854449795B43D8282D1EC.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Pediformis astathmeta Lee & Terada 2026	<div><p>Pediformis astathmeta sp. nov.</p><p>Figs 1 A, 1 B, 2, 3 A, 3 B, 4 A, 5 A, 6, 7</p><p>Korean name.</p><p>Je-ju-go-sa-ri-kkok-ji-na-bang.</p><p>Type material.</p><p>Holotype: Korea • ♂; Jeju-do, Seogwipo-si, Topyeong-dong; 23. V. 2021; Ga-Eun Lee leg.; genitalia slide no. LGE 25031 (JNU); DNA voucher no. LGE-G 988 . Paratypes: Korea • 12 ♂ 11 ♀, same original data as holotype; genitalia slide nos LGE 22021 m, LGE 22022 f, LGE 25014 m, LGE 25015 f, LGE 25016 f, LGE 25031 m, LGE 25042 m (all deposited in JNU except for one female in NIBR); wing slide nos LGE 25042 W, LGE 25043 W, LGE 25044 W; DNA voucher nos LGE-G 550, - G 895 • 3 ♂ 1 ♀, same original data as holotype except for 30. V. 2021 • 3 ♂, same original data as holotype except for 27. V. 2025; DNA voucher no. LGE-G 1040 • 4 larvae ex Arachniodes sporadosora; same original data as holotype except for 16. VI. 2025; DNA voucher nos LGE-G 1020, - G 1022, - G 1039, - G 1062 .</p><p>Diagnosis.</p><p>This new species can be distinguished from its two congeners P. cuneiformis (Guan &amp; Li, 2016) and P. fushana (Shen &amp; Hsu, 2024) by the shape of the cucullus and aedeagus. In P. astathmeta, the cucullus is gradually narrowed and rounded apically; in P. cuneiformis it is rectangular, and in P. fushana the apex bears a pointed projection. The aedeagus of P. astathmeta is much narrower and longer than the latter two species. The female genitalia of P. astathmeta have two signa as in P. cuneiformis, but the signum near the ductus bursae is smaller and rounded (rather than triangular), and the median signum is narrower than that of P. cuneiformis .</p><p>Description.</p><p>Adult. Head: Vertex, frons, and occiput white, sometimes slightly tinged with pale ochre. Labial palpus white, outer margin of segment II rarely mixed with grey. Antenna with scape white; flagellum ochreous white, with short fine ciliation in male.</p><p>Thorax: Dorsum of thorax and tegula white, sometimes tinged with pale ochre. Legs white, tarsi strongly mixed with light ochre; fore-femur, - tibia and - tarsus black along dorsal margin, this dark coloration sometimes very weak on fore-femur; mid-tibia with a black spot at apex of outer surface and with white bristles dorsally; hind-tibia with whorls of black bristles at apex and with white bristles dorsally, slightly mixed with black beyond middle; hind-tarsus with each tarsomere tipped with dark grey on outer surface.</p><p>Wings (Figs 1 A, 1 B, 2): Forewing span 8.0–10.0 mm (n = 31; holotype = 8.5 mm). Forewing ground color white, sometimes sprinkled with grey; costa black in 1 / 4 wing length, often with a large, indistinct pale ochre patch at middle, this patch sometimes obliquely extended toward dorsal spot; dorsum usually with an elliptical dark grey spot beyond middle, sometimes reduced to a narrow streak along fold; apex tinged with pale ochre; fringe scales greyish white. Hindwing white to grey; fringe scales white to greyish white. Venation: Forewing with 12 veins: Sc reaching basal 1 / 3 of costa; R 1 and R 2 separate but both arising from near upper angle of discal cell; R 2 parallel to R 3–5; R 3 short-stalked with long-stalked R 4 + 5; M 1 weak; M 2 and M 3 separate and approximately parallel; CuA 1 arising from near lower angle of discal cell; CuA 2 absent; 1 A + 2 A unbranched. Hindwing with 10 veins: discal cell open; Rs weak and nearly reaching apex; CuA 1 and CuA 2 parallel; CuP and 1 A + 2 A weak.</p><p>Abdominal segments (Fig. 3 A, B): Terga with a row of spines on segments II – VII in male, II – VI in female.</p><p>Male genitalia (Fig. 4 A): Uncus narrow, tapering toward apex, with long lateral setae from base to near apex; apex blunt, slightly curved downward. Gnathos as long as uncus, elongate-triangular, apex rounded. Tegumen simple. Valva narrowest at base, curved from middle; costa strongly convex near base, with long sparse setae from ~ 1 / 3 length; cucullus foot-shaped (pediform), covered with dense setae on inner surface, narrowed apically; sacculus nearly straight, with sparse setae ventrally. Vinculum simple, slightly broadened toward saccus; saccus large, tongue-shaped. Juxta trapezoidal. Anellar lobe developed, narrow, with long sparse setae. Aedeagus ~ 3.5 × as long as uncus, rod-shaped, apical 1 / 3 constricted and rugose, apex rounded; cornutus absent.</p><p>Female genitalia (Fig. 5 A): Papillae anales weakly sclerotized, covered with setae of various lengths. Intersegmental membrane between papillae anales and segment VIII slightly shorter than papillae anales. Tergum VIII somewhat weakly sclerotized, trapezoidal, with long sparse setae along posterior margin. Sternum VIII forming a shield-shaped plate, slightly concave posteriorly, gradually narrowed anteriorly, with long sparse setae along near posterior margin. Apophyses anteriores as long as apophyses posteriores. Ostium bursae large, opening at posterior margin of sternum VII. Antrum broad, cup-shaped, with longitudinal furrows. Ductus bursae shorter than antrum, slightly broadened beyond middle. Corpus bursae elliptical, twice as long as antrum + ductus bursae, with numerous minute spines near entrance of corpus bursae. Two signa present; one near the spined area of corpus bursae, round and deeply emarginated anteriorly; the other situated before middle of corpus bursae, forming a transverse band, broadly convex medially, narrowed and strongly curved laterally toward the former signum. Bulla arising from posterior margin of corpus bursae, stout. Ductus seminalis long, with minute spines apically.</p><p>Host plant.</p><p>Dryopteridaceae: Arachniodes sporadosora (Kunze) Nakaike .</p><p>Biology.</p><p>(Fig. 6) Larvae make silky galleries on the underside of fern fronds. Adults fly in May, and larvae are found only in June, suggesting that the species is likely univoltine.</p><p>Distribution.</p><p>(Fig. 7) Korea (Jeju-do).</p><p>Etymology.</p><p>The species name is derived from the Greek astathmetos (unstable), referring to the indistinct forewing markings.</p><p>Remarks.</p><p>Pediformis is a small genus currently comprising only two species, P. cuneiformis and P. fushana (Guan and Li 2016; Shen et al. 2024), and P. astathmeta is the third taxon described within the genus. Based on a host plant survey conducted on Jeju Island, P. astathmeta shares its host plant with Cuprina fuscella in the same habitat. However, larvae of P. astathmeta were found only on Arachniodes sporadosora whereas C. fuscella feeds not only on A. sporadosora but also on three other fern species of Dryopteridaceae .</p></div>	https://treatment.plazi.org/id/5D6FF8BA8C5854449795B43D8282D1EC	Public Domain	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.		Pensoft via Plazi	Lee, Ga-Eun;Terada, Takeshi	Lee, Ga-Eun, Terada, Takeshi (2026): Two new species and three new records of Cuprininae (Lepidoptera, Stathmopodidae) from Jeju Island, Korea, with molecular evidence for their placement. ZooKeys 1287: 253-272, DOI: 10.3897/zookeys.1287.194473
67BB030A4308550383D28158AD4F18E5.text	67BB030A4308550383D28158AD4F18E5.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Petala aedificatrix (Terada 2016)	<div><p>Petala aedificatrix (Terada, 2016)</p><p>Figs 1 F, 3 E, 4 D, 7</p><p>Pachyrhabda aedificatrix Terada, 2016: 111 . TL: Honshu, Japan. TD: OMU.</p><p>Petala aedificatrix: Shen et al. 2024: 20.</p><p>Korean name.</p><p>Nam-bang-go-sa-ri-kkok-ji-na-bang.</p><p>Material examined.</p><p>Korea • 1 ♂; Jeju-do, Jeju-si, Jocheon-eup, Gyorae-ri; 6. VI. 2023; Ga-Eun Lee leg.; genitalia slide no. LGE 24019 (NIBR); DNA voucher no. LGE-G 897 .</p><p>Diagnosis.</p><p>Forewing span 10.0 mm (n = 1). This species is superficially similar to P. margaritacea (Terada 2016), but the forewing span is larger and the markings are somewhat indistinct in P. aedificatrix (Fig. 1 F). In addition, P. aedificatrix has black bristles at the apex of the hind-tibia; those of P. margaritacea are white to pale grey. In the male genitalia of P. aedificatrix (Fig. 4 D), the cucullus is slightly curved outward apically and the sacculus is indistinct; in P. margaritacea, the cucullus is not curved apically and the sacculus has a rounded apex. The aedeagus of P. aedificatrix is distinctive in having a needle-like cornutus with a sharply pointed apex, situated in the distal half of the aedeagus.</p><p>Host plants.</p><p>Dryopteridaceae: Arachniodes amabilis (Blume) Tindale, Cyrtomium fortune J. Sm., Dryopteris erythrosora (D. C. Eaton) Kuntze, D. hondoensis Koidz., D. nipponensis Koidz., D. pacifica (Nakai) Tagawa; Athyriaceae: Cornopteris decurrenti-alata (Hook.) Nakai (Terada 2016).</p><p>Biology.</p><p>Larvae spin a forking silky gallery on the underside of fern fronds. Adults have been collected in May and June in Japan (Terada 2016).</p><p>Distribution.</p><p>(Fig. 7) Korea (new record), Japan.</p><p>Remarks.</p><p>Detailed descriptions of the adult and genitalia are provided in Terada (2016). The genus Petala currently includes three species, P. aedificatrix, P. margaritacea, and P. shida .</p></div>	https://treatment.plazi.org/id/67BB030A4308550383D28158AD4F18E5	Public Domain	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.		Pensoft via Plazi	Lee, Ga-Eun;Terada, Takeshi	Lee, Ga-Eun, Terada, Takeshi (2026): Two new species and three new records of Cuprininae (Lepidoptera, Stathmopodidae) from Jeju Island, Korea, with molecular evidence for their placement. ZooKeys 1287: 253-272, DOI: 10.3897/zookeys.1287.194473
4080631567FC5979B80B1A47236F0EF3.text	4080631567FC5979B80B1A47236F0EF3.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Petala margaritacea (Terada 2016)	<div><p>Petala margaritacea (Terada, 2016)</p><p>Figs 1 G, 1 H, 3 F, 4 E, 5 B, 7</p><p>Pachyrhabda margaritacea Terada, 2016: 115 . TL: Kyushu, Japan. TD: OMU.</p><p>Petala margaritacea: Shen et al. 2024: 20.</p><p>Korean name.</p><p>Byeol-go-sa-ri-kkok-ji-na-bang.</p><p>Material examined.</p><p>Korea • 6 ♂ 4 ♀; Jeju-do, Jeju-si, Yeon-dong; 24. VIII. 2020 – 24. VI. 2024; Ga-Eun Lee leg.; genitalia slide nos LGE 20014 m, LGE 20015 f, LGE 24022 m; DNA voucher nos LGE-G 551, LGE-G 894 • 1 ♂; Jeju-do, Jeju-si, Hallim-eup, Gwideok-ri; 12. VII. 2022; Ga-Eun Lee leg.; genitalia slide no. LGE 20018; DNA voucher no. LGE-G 896 • 1 ♀; Jeju-do, Jeju-si, Hallim-eup, Dongmyeong-ri; 22. VI. 2023; Ga-Eun Lee leg.; genitalia slide no. LGE 24020; DNA voucher no. LGE-G 898 (all deposited in JNU except for one male in NIBR) .</p><p>Diagnosis.</p><p>Forewing span 6.5–7.5 mm (n = 12). Petala margaritacea is closely related to P. aedificatrix and the differential diagnosis between the two species is stated under the latter.</p><p>Host plant.</p><p>Thelypteridaceae: Christella acuminata (Houtt.) Holttum (Terada 2016).</p><p>Biology.</p><p>Larvae make silky galleries on the underside of fern fronds as in P. aedificatrix . Adults have been collected from April to October in Japan (Terada 2016).</p><p>Distribution.</p><p>(Fig. 7) Korea (new record), Japan.</p><p>Remarks.</p><p>Detailed descriptions of the adult and genitalia are provided in Terada (2016). The host plant has been referred to as Thelypteris acuminata (Houtt.) Morton in Japan (Terada 2016) and as Cyclosorus acuminatus (Houtt.) Nakai in Korea (National Institute of Biological Resources 2025). Here, we adopt Christella acuminata (Houtt.) Holttum following recent global taxonomic treatments (WFO 2026).</p></div>	https://treatment.plazi.org/id/4080631567FC5979B80B1A47236F0EF3	Public Domain	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.		Pensoft via Plazi	Lee, Ga-Eun;Terada, Takeshi	Lee, Ga-Eun, Terada, Takeshi (2026): Two new species and three new records of Cuprininae (Lepidoptera, Stathmopodidae) from Jeju Island, Korea, with molecular evidence for their placement. ZooKeys 1287: 253-272, DOI: 10.3897/zookeys.1287.194473
