identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
391D8874F1485D67B6E6E652389517BB.text	391D8874F1485D67B6E6E652389517BB.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Campylomyza abjecta Mamaev 1998	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Campylomyza abjecta Mamaev, 1998</p>
            <p> Campylomyza abjecta Mamaev 1998: 6.</p>
            <p> Campylomyza abjecta Jaschhof and Jaschhof 2017: 5, fig. 2 A – C (redescription).</p>
            <p>Distribution.</p>
            <p>Russia (Primorsky), Sweden, new record for South Korea.</p>
            <p>Specimens examined.</p>
            <p> Korea • 3 ♂♂ (slides no. 19 AY-3, 7, 19 AYa-9, 10); NERC; 10–17 Apr. 2019; Y. J. Choi, H. G. Kim leg.; deposited in KU •  1 ♂ (slide no. NIBRIN 0000857557); KUF; 2–8 Apr. 2017; D. Ham leg.; deposited in NIBR •  1 ♂ (slide no. NIBRIN 0000992636); SJ 1; 13 Apr. – 4 May 2019; W. G. Kim leg.; deposited in NIBR •  1 ♂ (slide no. NIBRIN 0000992634); SJ 2; 8–24 Apr. 2020; W. G. Kim leg.; deposited in NIBR . </p>
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	https://treatment.plazi.org/id/391D8874F1485D67B6E6E652389517BB	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	Ham, Daseul;Bae, Yeon Jae	Ham, Daseul, Bae, Yeon Jae (2025): Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species. ZooKeys 1223: 221-245, DOI: 10.3897/zookeys.1223.128062
A46C5981898F53AFA9BA5002BB19AC85.text	A46C5981898F53AFA9BA5002BB19AC85.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Campylomyza aborigena Mamaev 1998	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Campylomyza aborigena Mamaev, 1998</p>
            <p>Fig. 1 C, 2 A – C</p>
            <p> Campylomyza aborigena Mamaev, 1998: 6.</p>
            <p>Specimens examined.</p>
            <p>  Korea • 1 ♂ (slide no. NIBRIN 0000992639);  Sobaek ; 6 May – 6 Jun. 2019; D. Ham, S. Park leg.; deposited in NIBR  •   2 ♂♂ (slides no. NIBRIN 0000992638, 19-38);  Odae 2 ; 23 Apr. – 11 May 2019; D. Ham, S. Park leg.; deposited in NIBR  . </p>
            <p>Diagnosis.</p>
            <p> Campylomyza aborigena closely resembles  C. aemula Mamaev, 1998 (inferred from the illustration in Jaschhof and Jaschhof 2009) and shares the following characteristics: 1) Tegmen with lamellate (Fig. 2 C, ↓ 5), tapering apical points that are rounded and strongly sclerotized anteriorly, and weakly sclerotized posteriorly; 2) Large foliate dorsal processes (Fig. 2 C, ↓ 6) with narrower, sharp points; 3) Gonostyli tapering apically and curved anteroventrally with convex apex margins (Fig. 2 B). However,  C. aborigena can be distinguished from  C. aemula by the following characteristics: tegmen with parallel-sided apical points (Fig. 2 C, ↓ 5); dorsal processes large, broad basally, pointed apically with strongly sclerotized margin (Fig. 2 C, ↓ 6). </p>
            <p>Measurements.</p>
            <p>Male adult (Slide no. NIBRIN 0000992639): Body length 1.454 mm. Wing length 1.484 mm. Hind leg coxa 0.170 mm; femur 0.547 mm; tibia 0.551 mm; tarsomere I 0.307 mm; tarsomere II 0.164 mm; tarsomere III 0.130 mm; tarsomere IV 0.067 mm; tarsomere V 0.062 mm.</p>
            <p>Redescription.</p>
            <p>Male adult. Head. Postocular bristles four or five. Antenna with 12 flagellomeres. Neck of fourth antennal flagellomeres as long as node. Node with one complete and two incomplete crenulate whorls with sensory hairs, two incompletely collar-shaped sensilla distally. Palpus 4 - segmented; fourth segment longest. Thorax. Preepisternum with eight setae. Wing length to width ratio 2.44, AntC ending beyond R 4 + 5 but before reaching M 4; ApicR 1 3.23 × length of Rs; CuA separated (Fig. 1 C). Tarsomere I longer than tarsomere II. Claws sickle-shaped, toothed; empodia longer than claws; pubescent. Terminalia. Tg 9 slightly tapered towards apex (Fig. 2 A, ↓ 1). Gonocoxites emarginated broad U-shaped ventrally. (Fig. 2 A, ↓ 2); ventromedial portion swollen, pronounced (Fig. 2 A, ↓ 3); dorsal transverse bridge narrower to apex, extending far beyond ventrobasal margin (Fig. 2 A, ↓ 4). Gonostyli curved anteroventrally; apical margin strongly convex; medial portion excavated; setae becoming denser towards apex. On tegmen, apical points long, lamellate, rounded apically (Fig. 2 C, ↓ 5); dorsal processes spoon-shaped with hollow in the center and strongly sclerotized apex; directed anteriorly (Fig. 2 C, ↓ 6). Mesal processes short, sclerotized (Fig. 2 C, ↓ 7). Tegmen shoulders inconspicuous.</p>
            <p>Distribution.</p>
            <p>Russia (Primorsky), new to South Korea.</p>
            <p>Remarks.</p>
            <p> Campylomyza aborigena Mamaev, 1998 was originally described based on a single specimen collected in Far East Russia in 1964. Mamaev’s description was limited to just seven lines of text, without any accompanying drawings or photographs. However, thanks to the observations made by Dr. Mathias Jaschhof on the holotype specimen of  C. aborigena in the Zoological Museum of Moscow State University in 2006, we now know that the Korean species is the same as the Russian  C. aborigena . This is significant because it provides further evidence supporting the existence of  C. aborigena , with the Korean finding being only the second record except for the holotype. Mamaev often described species based on a single specimen without proper illustration or depiction. Therefore, the discovery of this species in Korea and the possibility of obtaining additional specimens are of great importance for further supporting Mamaev’s species concept and advancing the taxonomy of mycophagous cecidomyiids. </p>
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	https://treatment.plazi.org/id/A46C5981898F53AFA9BA5002BB19AC85	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	Ham, Daseul;Bae, Yeon Jae	Ham, Daseul, Bae, Yeon Jae (2025): Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species. ZooKeys 1223: 221-245, DOI: 10.3897/zookeys.1223.128062
69FBE51B451C57A88F21584882A89FC7.text	69FBE51B451C57A88F21584882A89FC7.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Campylomyza ambulata Ham & Bae 2025	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Campylomyza ambulata sp. nov.</p>
            <p>Fig. 2 D – G</p>
            <p>Type material examined.</p>
            <p>  Holotype: Korea • 1 ♂ (slide no. 19 AYa-11); Gyeongsangbuk-do, Yeongyang-gun, Yeongyang-eup, Gowol-gil, 23,  National Endangered Species Restoration Center (NERC); 10–17 Apr. 2019; Y. J. Choi, H. G. Kim leg.; deposited in KU  .  Paratypes: Korea • 6 ♂♂ (slides no. 19 AY-4, 8, 9, 11, 12, 14, 19 AYa-6, 12); same data and deposition as holotype •  1 ♂ (slide no. 19 AZ-10); NERC; 3–10 Apr. 2019; Y. J. Choi, H. G. Kim leg.; deposited in KU •  1 ♂ (slide no. NIBRIN 0000919403); NERC; same data as for preceding; deposited in NIBR . </p>
            <p>Other material examined.</p>
            <p>  Korea • 2 ♂♂ (slides no. NIBRIN 0000992627, NIBRIN 0000992628);  Odae 2 ; 23 Apr. – 11 May 2019; D. Ham, S. Park leg.; deposited in NIBR  •  1 ♂ (slide no. HDS-674); GW; 8 Nov. 2017; D. Ham leg.; deposited in KU •  1 ♂ (21 AE-2-2); GP; 28 Apr. – 5 May 2019; Y. J. Bae leg.; deposited in KU •  1 ♂ (21 AG-1-5); SJ 2; 8–24 Apr. 2020; W. G. Kim leg.; deposited in KU . </p>
            <p>Diagnosis.</p>
            <p> Campylomyza ambulata sp. nov. can be distinguished from other species in the  flavipes group found in Korea through the following characteristics: 1) gonostyli curved anteroventrally, excavated ventromesally with denser setae towards the apex; 2) apical point small, short subtriangular (Fig. 2 E, ↓ 10); 3) dorsal processes strongly tapering anteriorly, moveable depending on the pressure (Fig. 2 E, ↓ 11); 4) shoulders of tegmen conspicuous (Fig. 2 E, ↓ 12); 5) parameral apodeme short. </p>
            <p>Measurements.</p>
            <p>Male adult (holotype): Body length 1.187 mm. Wing length 1.364 mm. Hind leg coxa 0.134 mm; femur 0.480 mm; tibia 0.500 mm; tarsomere I 0.290 mm; tarsomere II 0.133 mm; tarsomere III 0.112 mm; tarsomere IV 0.071 mm; tarsomere V 0.058 mm.</p>
            <p>Description.</p>
            <p>Male adult (holotype). Head. Postocular bristles 3–5. Antenna with 12 flagellomeres. Neck of fourth antennal flagellomeres as long as node. Node with one complete and two incomplete crenulate whorls with sensory hairs, two incompletely collar-shaped sensilla distally. Palpus 4 - segmented; fourth segment longest. Thorax. Preepisternum with eight setae. Wing length to width ratio 2.28, AntC ending beyond R 4 + 5 but before reaching M 4; ApicR 1 3.46 × length of Rs; CuA separated. Tarsomere I longer than tarsomere II. Claws sickle-shaped, toothed; empodia longer than claws, pubescent. Terminalia. Tg 9 tapering towards apex with five fine setae apically. Ventral emargination U-shaped; ventromedial portion of gonocoxites slightly pronounced (Fig. 2 D, ↓ 8). Gonostyli with moderately convex apical margins, excavated ventromedially, narrowly rounded apically. Dorsal transverse bridge broadly rounded apically, extending beyond ventrobasal margin (Fig. 2 D, ↓ 9). On tegmen, apical points small, subtriangular, lamellate (Fig. 2 E, ↓ 10), dorsal processes long, strongly tapering towards apex beyond midlength, blunt apically (Fig. 2 E, ↓ 11). Tegmen shoulders well-developed (Fig. 2 E, ↓ 12), Parameral apodeme short (Fig. 2 E, ↓ 15).</p>
            <p>Variation.</p>
            <p>We observed significant variation concerning apical points and tegmen shoulders (Fig. 2 F – G). Apical points bulged with round serrated surfaces (Fig. 2 G, ↓ 13); Shoulders inconspicuous, when almost in the same position or lower than apical points of tegmen (Fig. 2 G, ↓ 14). Dorsal processes moveable apically.</p>
            <p>Etymology.</p>
            <p> The species epithet  ambulata is derived from the Latin word ambulātus, which means ambulatory, referring to the movable nature of the dorsal processes. </p>
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	https://treatment.plazi.org/id/69FBE51B451C57A88F21584882A89FC7	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	Ham, Daseul;Bae, Yeon Jae	Ham, Daseul, Bae, Yeon Jae (2025): Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species. ZooKeys 1223: 221-245, DOI: 10.3897/zookeys.1223.128062
D7178C0065385A48BF28E24F28153231.text	D7178C0065385A48BF28E24F28153231.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Campylomyza angusta Ham & Bae 2025	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Campylomyza angusta sp. nov.</p>
            <p>Fig. 3 A – C</p>
            <p>Type material examined.</p>
            <p>  Holotype: Korea • 1 ♂ (slide no. NIBRIN 0000941947); Gangwon-do, Pyeongchang-gun, Jinbu-myeon, Odaesan-ro, Mt. Odae,  small valley before So-Myeong valley (Odae 1); 18 Apr. – 1 May 2020; D. Ham, S. Park leg.; deposited in NIBR. </p>
            <p>Diagnosis.</p>
            <p> Campylomyza angusta sp. nov. belongs to the ormerodi group of species where it is reminiscent of  C. pubescens (Jaschhof and Jaschhof 2009) mainly due to cerci bearing strikingly large pubescence and short dorsal transverse bridge, which is almost not protruding beyond the ventrobasal margin.  Campylomyza angusta sp. nov. is distinguished as follows. Gonostyli moderately convex posteriorly with narrowly rounded apex (Fig. 3 A, ↓ 6). Gonocoxites strongly protruding dorsomedially, ventral bridge short. The tegmen lacks shoulders (Fig. 3 C, ↓ 4), parameral apodemes long (Fig. 3 C, ↓ 5), apical points directed slightly laterally, mesal points short, weakly sclerotized, rounded apically (Fig. 3 C, ↓ 3). </p>
            <p>Measurements.</p>
            <p>Male adult (holotype): Body length 1.329 mm. Wing length 1.569 mm. Hind leg coxa 0.160 mm; femur 0.571 mm; tibia 0.567 mm; tarsomere I 0.330 mm; tarsomere II 0.153 mm; tarsomere III 0.109 mm; tarsomere IV 0.078 mm; tarsomere V 0.061 mm.</p>
            <p>Description.</p>
            <p>Male adult (holotype). Head. Postocular bristles seven. Antenna with 12 flagellomeres. Neck of fourth antennal flagellomeres shorter than node. Node with one complete and two incomplete crenulate whorls with sensory hairs, two incompletely collar-shaped sensilla distally. Palpus 4 - segmented; fourth segment longest. Thorax. Preepisternum with eight setae. Wing length to width ratio 2.53. AntC ending beyond R 4 + 5 but before reaching M 4; ApicR 1 4.18 × length of Rs. CuA separated. Tarsomere I longer than tarsomere II. Claws sickle-shaped, fine toothed; empodia shorter than claws; pubescent. Terminalia. Tg 9 tapered towards apex with 13 setae apically. Ventral bridge of gonocoxites short, dorsal transverse bridge protruding only slightly beyond the ventrobasal margin. Ventral emargination deep, U-shaped. Ventromedial portion broad rounded, not protruding medially (Fig. 3 A, ↓ 1). Gonostyli rounded apically with semi-circular apical margin; excavated ventromedially, plump dorsally; setae denser towards apex. On tegmen, apical points not lamellate, pointed apically, directed slightly posterolaterally (Fig. 3 C, ↓ 2); mesal points weakly sclerotized, short, tapered basally, broadened at apical third, rounded apically (Fig. 3 C, ↓ 3). Tegmen shoulders indistinct (Fig. 3 C, ↓ 4). Parameral apodemes long, more than half-length of tegmen (Fig. 3 C, ↓ 5).</p>
            <p>Etymology.</p>
            <p> The specific epithet  angusta in Latin means narrow, referring to the narrowness of the shoulder region of the tegmen in this species. </p>
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	https://treatment.plazi.org/id/D7178C0065385A48BF28E24F28153231	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	Ham, Daseul;Bae, Yeon Jae	Ham, Daseul, Bae, Yeon Jae (2025): Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species. ZooKeys 1223: 221-245, DOI: 10.3897/zookeys.1223.128062
AD6365B292675E2AB330779926A0ACEC.text	AD6365B292675E2AB330779926A0ACEC.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Campylomyza cavitata Mamaev 1998	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Campylomyza cavitata Mamaev, 1998</p>
            <p> Campylomyza cavitata Mamaev, 1998: 7; Jaschhof and Jaschhof 2009: 112–113, fig. 37 A – C.</p>
            <p>Specimens examined.</p>
            <p>  Korea • 1 ♂ (slide no. NIBR 0000919409);  Odae 1 ; 11–26 May 2019; D. Ham, S. Park leg.; deposited in NIBR  . </p>
            <p>Distribution.</p>
            <p>Sweden, Finland, Germany, Russia, new record for South Korea.</p>
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	https://treatment.plazi.org/id/AD6365B292675E2AB330779926A0ACEC	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	Ham, Daseul;Bae, Yeon Jae	Ham, Daseul, Bae, Yeon Jae (2025): Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species. ZooKeys 1223: 221-245, DOI: 10.3897/zookeys.1223.128062
CB1B5D206DA25D84B9D4EBA6F558C1CB.text	CB1B5D206DA25D84B9D4EBA6F558C1CB.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Campylomyza cingulata Jaschhof 2009	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Campylomyza cingulata Jaschhof, 2009</p>
            <p> Campylomyza cingulata Jaschhof, 2009: 119, fig. 41 A – E.</p>
            <p>Specimens examined.</p>
            <p>  Korea • 1 ♂ (slide no. NIBRIN 0000941946);  Odae 1 ; 18 Apr. – 1 May 2020; D. Ham, S. Park leg.; deposited in NIBR  . </p>
            <p>Distribution.</p>
            <p>Fennoscandia, Germany, new record for South Korea.</p>
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	https://treatment.plazi.org/id/CB1B5D206DA25D84B9D4EBA6F558C1CB	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	Ham, Daseul;Bae, Yeon Jae	Ham, Daseul, Bae, Yeon Jae (2025): Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species. ZooKeys 1223: 221-245, DOI: 10.3897/zookeys.1223.128062
52FC3E3F8F3D51739C8D1A6378DC38C6.text	52FC3E3F8F3D51739C8D1A6378DC38C6.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Campylomyza convexa Ham & Bae 2025	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Campylomyza convexa sp. nov.</p>
            <p>Fig. 3 D – F</p>
            <p>Type material examined.</p>
            <p>  Korea • 1 ♂ (slide no. HDS-505); Gyeonggi-do, Namyangju-si, Wabu-eup, Dosim-gil,  Korea University’s farm to practice (KUF); 2–8 Apr. 2017; D. Ham leg.; deposited in KU  .  Paratypes: Korea • 1 ♂ (slide no. HDS-504); same data and deposition as holotype •  2 ♂♂ (slides no. NIBRIN 0000857555, NIBRIN 0000919405) KUF; 2–8 Apr. 2017; D. Ham leg.; deposited in NIBR . </p>
            <p>Other material examined.</p>
            <p> Korea • 4 ♂♂ (slides no. NIBRIN 0000992649 – NIBRIN 0000992652); KUF; 2–8 Apr. 2017; Y. J. Bae leg.; deposited in NIBR . </p>
            <p>Diagnosis.</p>
            <p> Campylomyza convexa sp. nov. is most similar to  C. aemula (cf. Jaschhof and Jaschhof 2009: fig. 29 A – D), especially in having the rounded apical points on the tegmen, tapering posteriorly, the dorsal processes are broad basally, directed dorsolaterally with a strongly sclerotized triangular apex. However,  C. convexa sp. nov. can be distinguished from  C. aemula by following characteristics: 1) Gonostyli moderately convex apically, not excavated medially, broadly rounded apically, with small dorsomedial lobe (Fig. 3 E, ↓ 8); 2) Apical points of tegmen parallel-sided to rounded apically, longer than  C. aemula (Jaschhof and Jaschhof 2009: 102) ; 3) Mesal points of tegmen longer and narrower than in  C. aemula (Fig. 3 E, ↓ 11); 4) Dorsal processes lacking sclerotized ridge, strongly sclerotized apically (Fig. 3 E, ↓ 10). </p>
            <p>Measurements.</p>
            <p>Male adult (holotype): Body length 1.417 mm. Wing length 1.639 mm. Hind leg coxa 0.105 mm; femur 0.555 mm; tibia 0.574 mm; tarsomere I 0.333 mm; tarsomere II 0.170 mm; tarsomere III 0.138 mm; tarsomere IV 0.082 mm; tarsomere V 0.065 mm.</p>
            <p>Description.</p>
            <p> Male adult (holotype). Head. Postocular bristles seven. Antenna with 12 flagellomeres. Neck of fourth antennal flagellomeres shorter than node. Node with one complete and two incomplete crenulate whorls with sensory hairs, two incompletely collar-shaped sensilla distally. Palpus 4 - segmented; fourth segment longest. Thorax. Preepisternum with nine setae. Wing length to width ratio 2.24. AntC ending beyond R 4 + 5 but before reaching M 4; ApicR 1 3.82 × length of Rs. CuA separated. Tarsomere I longer than tarsomere II. Tarsomere I longer than tarsomere II. Claws sickle-shaped, slightly toothed; empodia as long as claws, slightly broaden apically; pubescent. Terminalia. Tg 9 tapered towards apex with eight fine setae. Ventral bridge of gonocoxites long, ventral emargination relatively short and broad, U-shaped, dorsal transverse bridge broad, extending far beyond ventrobasal margin. Ventromedial portion of gonocoxites broad, slightly pronounced (Fig. 3 D, ↓ 7). Gonostyli curved anteroventrally, rounded apically, moderately convex apically with small dorsomedial lobe (Fig. 3 E, ↓ 8); setae distributed evenly in ventral view, denser towards apex in dorsal view. On tegmen, apical points long, parallel-sided to rounded apically, not lamellate, sclerotized (Fig. 3 F, ↓ 9); dorsal processes strongly sclerotized apically, directed dorsolaterally (Fig. 3 F, ↓ 10); mesal points weakly sclerotized, faint apically, directed anteriorly (Fig. 3 F, ↓ 11). Shoulders of tegmen inconspicuous. Transverse brace rib-shaped without extension (Fig. 3 F, ↓ 12). Parameral apodeme sclerotized, long, slightly shorter than half of tegmen (Fig. 3 F, ↓ 13). Ejaculatory apodeme of typical  Campylomyza outline. </p>
            <p>Etymology.</p>
            <p>From the Latin word convexus, meaning ‘ a surface with rounded edges’, which refers to the rounded outline of the apex of the apical points on the tegmen.</p>
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	https://treatment.plazi.org/id/52FC3E3F8F3D51739C8D1A6378DC38C6	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	Ham, Daseul;Bae, Yeon Jae	Ham, Daseul, Bae, Yeon Jae (2025): Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species. ZooKeys 1223: 221-245, DOI: 10.3897/zookeys.1223.128062
451E00DA591F584F85A241FC1F6834CC.text	451E00DA591F584F85A241FC1F6834CC.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Campylomyza cornigera Ham & Bae 2025	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Campylomyza cornigera sp. nov.</p>
            <p>Fig. 4 A – C</p>
            <p>Type material examined.</p>
            <p>  Holotype: Korea • 1 ♂ (slide no. 19 Aya- 8); Gyeongsangbuk-do, Yeongyang-gun, Yeongyang-eup, Gowol-gil, 23,  National Endangered Species Restoration Center (NERC); 10–17 Apr. 2019; Y. J. Choi, H. G. Kim leg.; deposited in KU  .  Paratype: Korea • 1 ♂ (slide no. NIBRIN 0000857558); KUF; 2–8 Apr. 2017; D. Ham leg.; deposited in NIBR . </p>
            <p>Other material examined.</p>
            <p>  Korea • 1 ♂ (slide no. NIBRIN 0000992637);  Odae 1 ; 18 Apr. – 1 May 2020; D. Ham, S. Park leg.; deposited in NIBR  . </p>
            <p>Diagnosis.</p>
            <p> Campylomyza cornigera sp. nov. is most similar to  C. nigroliminata Mamaev, 1998 (cf. Jaschhof and Jaschhof 2021: fig. 30 A, B), especially in having lamellate apical points of the tegmen that are rounded apically and pointed processes directed anterolaterad (Fis. 4 C, ↓ 5, 6), and mesal processes are directed anteriorly (Fig. 4 C, ↓ 7). However,  C. cornigera sp. nov. can be distinguished from  C. nigroliminata by the following characteristics: 1) Pointed processes directed anterolaterally of apical points slightly curved; 2) Dorsal processes missing; 3) Tegmen shoulders indistinct. </p>
            <p>Measurements.</p>
            <p>Male adult (holotype): Body length 1.315 mm. Wing length 1.574 mm. Hind leg coxa 0.141 mm; femur 0.539 mm; tibia 0.515 mm; tarsomere I 0.302 mm; tarsomere II 0.142 mm; tarsomere III 0.105 mm; tarsomere IV 0.062 mm; tarsomere V 0.056 mm.</p>
            <p>Description.</p>
            <p> Male adult (holotype). Head. Postocular bristles seven. Antenna with 12 flagellomeres. Neck of fourth antennal flagellomeres as long as node. Node with one complete and two incomplete crenulate whorls with sensory hairs, two incompletely collar-shaped sensilla distally. Palpus 4 - segmented; fourth segment longest. Thorax. Preepisternum with 1–9 setae. Wing length to width ratio 2.58. AntC ending beyond R 4 + 5 but before reaching M 4; ApicR 1 3.08 × length of Rs. CuA separated. Tarsomere I longer than tarsomere II. Claws sickle-shaped, toothed; empodia longer than claws, slightly broaden apically; pubescent. Terminalia. Tg 9 tapered towards apex with seven or eight fine setae apically. Ventral bridge of gonocoxites long (Fig. 4 A, ↓ 1), with U-shaped emargination; dorsal transverse bridge narrowly tapering, extending far beyond basal margin (Fig. 4 A, ↓ 2). Ventromedial portion of gonocoxites almost angular (Fig. 4 A, ↓ 3). Gonostyli narrowly rounded to pointed apically (Fig. 4 A, ↓ 4), moderately convex posteriorly, and slightly excavated medially, plump dorsally; setae denser towards apex. Tegmen long and narrow, apical points sclerotized, short, stout, and broadly rounded apically (Fig. 4 C, ↓ 5); a pair of strongly sclerotized processes directed dorsolaterally (Fig. 4 C, ↓ 6); true dorsal processes missing. Mesal points of tegmen slightly sclerotized, narrowly long, directed anteriorly (Fig. 4 C, ↓ 7). Shoulders of tegmen inconspicuous; width between apices of shoulders narrower than processes directed dorsolaterally. Transverse brace rib-shaped (Fig. 4 C, ↓ 8). Parameral apodemes long (Fig. 4 C, ↓ 9). Ejaculatory apodeme of typical  Campylomyza outline. </p>
            <p>Etymology.</p>
            <p> The species epithet  cornigera , derived from Latin meaning ‘ having horns, ’ refers to the horn-shaped processes on the tegmen that are directed dorsolaterally. </p>
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	https://treatment.plazi.org/id/451E00DA591F584F85A241FC1F6834CC	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	Ham, Daseul;Bae, Yeon Jae	Ham, Daseul, Bae, Yeon Jae (2025): Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species. ZooKeys 1223: 221-245, DOI: 10.3897/zookeys.1223.128062
17378D71DA3D5C7A8255B768107F116B.text	17378D71DA3D5C7A8255B768107F116B.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Campylomyza cornuta Jaschhof 1998	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Campylomyza cornuta Jaschhof, 1998</p>
            <p> Campylomyza cornuta Jaschhof 1998 b: 260–261, Abb. 1 a – e.</p>
            <p>Specimens examined.</p>
            <p> Korea • 2 ♂♂ (slides no. NIBRIN 0000941945, NIBRIN 0000992653); HN; 3 Mar. – 12 Apr. 2019; H. S. Ahn leg.; deposited in NIBR . </p>
            <p>Distribution.</p>
            <p>Sweden, Lithuania, Germany, and new to South Korea.</p>
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	https://treatment.plazi.org/id/17378D71DA3D5C7A8255B768107F116B	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	Ham, Daseul;Bae, Yeon Jae	Ham, Daseul, Bae, Yeon Jae (2025): Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species. ZooKeys 1223: 221-245, DOI: 10.3897/zookeys.1223.128062
3668EB2BE84E53D989C67C09FC656247.text	3668EB2BE84E53D989C67C09FC656247.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Campylomyza hori Ham & Bae 2025	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Campylomyza hori sp. nov.</p>
            <p>Fig. 4 D – F</p>
            <p>Type material examined.</p>
            <p>  Holotype: Korea • 1 ♂ (slide no. 19 I-5); Gangwon-do, Jeongseon-gun, Jeongseon-eup, Hoedong-ri, 870,  Gariwangsan Recreational Forest (Gariwang); 13 Apr. – 12 May 2019; D. Ham, S. Park leg.; deposited in KU  .  Paratype: Korea • 1 ♂ (slide no. NIBRIN 0000919401); same data as holotype and deposited in NIBR . </p>
            <p>Other material examined.</p>
            <p>  Korea • 2 ♂♂ (slides no. NIBRIN 0000992654, NIBRIN 0000992655);  Sobaek ; 6 May – 6 Jun. 2019; D. Ham, S. Park leg.; deposited in NIBR  . </p>
            <p>Diagnosis.</p>
            <p> Campylomyza hori sp. nov. is most similar to  C. mohrigi Jaschhof, 2009 , especially in having the apical points divided, and the dorsal processes with sclerotized ridge, subtriangular apex on tegmen. However,  C. hori sp. nov. can be distinguished from  C. mohrigi by the following characteristics: 1) Necks of antennal flagellomeres longer than nodes; 2) Gonostyli slightly longer and narrower (Fig. 4 E); 3) Dorsal processes wider, margin sclerotized, with subtriangular apex, center membranous (Fig. 4 F, ↓ 13) vs. narrower, leaf-shaped with sclerotized ridge and points apically in  C. mohrigi . </p>
            <p>Measurements.</p>
            <p>Male adult (holotype). Body length 1.441 mm, wing length 1.645 mm. Hind leg coxa 0.156 mm; femur 0.607 mm; tibia 0.647 mm; tarsomere I 0.351 mm; tarsomere II 0.180 mm; tarsomere III 0.141 mm; tarsomere IV 0.088 mm; tarsomere V 0.070 mm.</p>
            <p>Description.</p>
            <p>Male adult (holotype). Head. Postocular bristles three. Antenna with 12 flagellomeres. Neck of fourth antennal flagellomere longer than node. Node with one complete and two incomplete crenulate whorls with sensory hairs, two incompletely collar-shaped sensilla distally. Palpus 4 - segmented; fourth segment longest. Thorax. Preepisternum with five fine setae anteriorly. Wing length to width ratio 2.47. AntC ending beyond R 4 + 5 but before reaching; ApicR 1 2.77 × length of Rs. CuA separated. Tarsomere I longer than tarsomere II. Claws sickle-shaped, weakly toothed; empodia as long as claws; pubescent. Terminalia. Tg 9 tapering towards apex with six fine setae apically. Ventral emargination deep, U-shaped, ventral bridge short. Dorsal transverse bridge broadly rounded apically, slightly extended beyond ventrobasal margin (Fig. 4 D, ↓ 10). Gonostyli elongated apically, curved anteroventrally, constricted ventrosubapically (Fig. 4 D, ↓ 11) with fine setae denser towards apex; incised dorsomesally. On tegmen, apical points pointed, directed posteriorly (Fig. 4 F, ↓ 12); dorsal processes broad basally, constricted medially, pointed apically (Fig. 4 F, ↓ 13), directed anterodorsally, with strongly sclerotized margin basally; mesal points faint, short, pointed (Fig. 4 F, ↓ 14). Tegmen shoulders almost angular, equipped with several small bumps laterally (Fig. 4 F, ↓ 15). Transverse brace with lobe-like dorsal extensions. Ejaculatory apodeme swelling medially (Fig. 4 D, ↓ 16), narrow basally.</p>
            <p>Etymology.</p>
            <p> The species epithet  hori originates from the Korean native term, pronounced  ‘ hori -  hori - hada’, an adjective describing a slender or tapered part. This name specifically denotes the narrowed part of the gonostyli. </p>
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	https://treatment.plazi.org/id/3668EB2BE84E53D989C67C09FC656247	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	Ham, Daseul;Bae, Yeon Jae	Ham, Daseul, Bae, Yeon Jae (2025): Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species. ZooKeys 1223: 221-245, DOI: 10.3897/zookeys.1223.128062
AC7C741F6FBB5CE884AFFC6BEB07096E.text	AC7C741F6FBB5CE884AFFC6BEB07096E.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Campylomyza Meigen 1818	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Genus  Campylomyza Meigen, 1818</p>
            <p>Fig. 1 C</p>
            <p> Campylomyza Meigen, 1818: 101; Westwood 1840: 126; Jaschhof 1998 b: 136; Jaschhof and Jaschhof 2009: 89.</p>
            <p>Type species.</p>
            <p> Campylomyza flavipes Meigen, 1818 (original designation by Westwood 1840). Type locality Germany. </p>
            <p>Diagnosis.</p>
            <p> The adult males of the South Korean genus  Campylomyza can be distinguished from other mycophagous cecidomyiid taxa based on the following combination of characters [adapted from Jaschhof and Jaschhof 2009]: 1) Antenna with 12 flagellomeres; 2) Node of fourth antennal flagellomere featuring one complete and two incomplete crenulate whorls with sensory hairs with two incompletely collar-shaped sensilla distally; 3) Apical part of the R 1 vein, located near wing tip (ApicR 1) elongated, approximately 4–6 times the length of Rs; 4) Gonostyli strongly convex posteriorly without apical spines; 5) Aedeagal apodeme equipped with typical head-like structure; 6) Tegmen with transverse brace (i. e., H-shaped), various processes on apex. </p>
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	https://treatment.plazi.org/id/AC7C741F6FBB5CE884AFFC6BEB07096E	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	Ham, Daseul;Bae, Yeon Jae	Ham, Daseul, Bae, Yeon Jae (2025): Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species. ZooKeys 1223: 221-245, DOI: 10.3897/zookeys.1223.128062
FB7F0A266D625ECEBE3EC29C56C9E0FF.text	FB7F0A266D625ECEBE3EC29C56C9E0FF.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Campylomyza odae Ham & Bae 2025	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Campylomyza odae sp. nov.</p>
            <p>Fig. 5 A – D</p>
            <p>Type material examined.</p>
            <p>  Holotype: Korea • 1 ♂ (slide no. NIBRIN 0000992641) Gangwon-do, Pyeongchang-gun, Jinbu-myeon, Odaesan-ro,  Mt. Odae, the road before temple (Buk-Dae-Mi-Reuk-Am) (Odae 2); 11–26 May 2019; D. Ham, S. Park leg.; deposited in NIBR  .  Paratype: Korea • 1 ♂ (slide no. NIBRIN 0000919408); same data and deposition as holotype . </p>
            <p>Diagnosis.</p>
            <p> Campylomyza odae sp. nov. is distinguishable from other  Campylomyza species by the following combination of characteristics: 1) Apical margin of gonostyli rounded (Fig. 5 A, ↓ 3); 2) Dorsal processes on tegmen with inconspicuous pair of subtriangular processes anterolaterally; 3) Dorsal processes constricted medially, forming mesal cleft (Fig. 5 C, ↓ 6); 4) Cerci visible (Fig. 5 D). </p>
            <p>Measurements.</p>
            <p>Male adult (Holotype): Body length 1.737 mm. Wing length 1.870 mm. Hind leg coxa 0.221 mm; femur 0.713 mm; tibia 0.624 mm; tarsomere I 0.369 mm; tarsomere II 0.193 mm; tarsomere III 0.134 mm; tarsomere IV 0.089 mm; tarsomere V 0.072 mm.</p>
            <p>Description.</p>
            <p> Male adult. Slightly larger than other  Campylomyza species. Head. Postocular bristles four. Antenna with 12 flagellomeres. Neck of fourth antennal flagellomere slightly shorter than node. Node with one complete and two incomplete crenulate whorls with sensory hairs, two incompletely collar-shaped sensilla distally. Palpus 4 - segmented; fourth segment longest. Thorax. Wing length to width ratio 2.39, AntC ending beyond R 4 + 5 but before reaching M 4; ApicR 1 4.31 × length of Rs; CuA separated. Tarsomere I longer than tarsomere II. Claws sickle-shaped, toothed; empodia small, shorter than claws. Terminalia. Tg 9 broadly tapered towards apex with eight fine setae. Ventral emargiantion U-shaped; ventral bridge long; dorsal transverse bridge extending far beyond ventrobasal margin (Fig. 5 A, ↓ 1); ventromedial portion of gonocoxites relatively narrow, not pronounced (Fig. 5 A, ↓ 2). Gonostyli short, stout, strongly convex posteriorly, truncated apically (Fig. 5 A, ↓ 3), directed ventrally, bearing dorsoapically numerous straight setae of various length, with denser stiff setae as it goes to apex. Tegmen narrow, shoulders inconspicuous. Parameral apodemes short. Apical points lamellated, triangular-shaped, directed posteriorly (Fig. 5 C, ↓ 4), separated by wide cleft mesally; dorsal processes subtriangular shaped, directed dorsomedially, apices crossed with spreading subtriangular extensions (Fig. 5 C, ↓ 5); each dorsal process constricted at midlength, forming mesal cleft (Fig. 5 C, ↓ 6). Cerci visible. </p>
            <p>Etymology.</p>
            <p> The species name  odae is a noun in apposition to the collection locality, Mt. Odae in Gangwon province. </p>
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	https://treatment.plazi.org/id/FB7F0A266D625ECEBE3EC29C56C9E0FF	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	Ham, Daseul;Bae, Yeon Jae	Ham, Daseul, Bae, Yeon Jae (2025): Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species. ZooKeys 1223: 221-245, DOI: 10.3897/zookeys.1223.128062
471DC710F3595A73875832F3C4581E23.text	471DC710F3595A73875832F3C4581E23.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Campylomyza salicia Ham & Bae 2025	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Campylomyza salicia sp. nov.</p>
            <p>Fig. 5 E – G</p>
            <p>Type material examined.</p>
            <p>  Holotype: Korea • 1 ♂ (slide no. 19 Aya- 2); Gyeongsangbuk-do, Yeongyang-gun, Yeongyang-eup, Gowol-gil, 23,  National Endangered Species Restoration Center (NERC); 10–17 Apr. 2019; Y. J. Choi, H. G. Kim leg.; deposited in KU  .  Paratypes: Korea • 5 ♂♂ (slides no. 19 AY-5, 10, 13, 17, 19 AYa-13); same data and deposition as holotype •  1 ♂ (slide no. NIBRIN 0000919404); same data as holotype, deposited in NIBR . </p>
            <p>Other material examined.</p>
            <p> Korea • 2 ♂♂ (slides no. 19 AZ-6, 9); NERC; 3–10 Apr. 2019; Y. J. Choi, H. G. Kim leg.; deposited in KU •  1 ♂ (slide no. 19 AX-4); NERC; 20–27 Mar. 2019; Y. J. Choi, H. G. Kim leg.; deposited in KU •  1 ♂ (slide no. NIBRIN 0000992640); NERC; 27 Mar. – 3 Apr. 2019; Y. J. Choi, H. G. Kim leg.; deposited in NIBR . </p>
            <p>Diagnosis.</p>
            <p> Campylomyza salicia sp. nov. is most similar to  C. mohrigi (cf. illustration of Jaschhof and Jaschhof 2009: 109), especially having the elongated, tapering Gonostyli ventrally, not lamellate apical points and foliate dorsal processes which reaching to transverse brace on tegmen. However,  C. salicia sp. nov. can be distinguished from  C. mohrigi by following characteristics: 1) dorsal processes of tegmen sclerotized margin without sclerotized ridge (Fig. 5 G, ↓ 9); 2) the dorsal processes are directed dorsolaterally with a strongly sclerotized triangular apex; 3) parameral apodeme shorter than that of  C. mohrigi (Fig. 5 G, ↓ 10). </p>
            <p>Measurements.</p>
            <p>Male adult (holotype): Body length 0.944 mm. Wing length 1.266 mm. Hind leg coxa 0.142 mm; femur 0.441 mm; tibia 0.463 mm; tarsomere I 0.275 mm; tarsomere II 0.123 mm; tarsomere III 0.103 mm; tarsomere IV 0.072 mm; tarsomere V 0.057 mm.</p>
            <p>Description.</p>
            <p> Male adult (holotype). Slightly smaller than other  Campylomyza species. Head. Postocular bristles five. Antenna with 12 flagellomeres. Neck of fourth antennal flagellomere longer than node. Node with one complete and two incomplete crenulate whorls with sensory hairs, two incompletely collar-shaped sensilla distally. Palpus 4 - segmented; fourth segment longest. Thorax. Preepisternum with six fine setae anteriorly. Wing length to width ratio 2.70. AntC ending beyond R 4 + 5 but before reaching M 4; ApicR 1 3.23 × length of Rs; CuA separated. Tarsomere I longer than tarsomere II. Claws slightly toothed; empodia small, narrow. Terminalia. Tg 9 tapered towards apex with 8 setae apically. Ventral bridge of gonocoxites half-length of gonocoxites; dorsal transverse bridge tapering, extending beyond ventrobasal margin. Ventral emargination U-shaped. Gonostyli elongated, blunt to slightly pointed apically, moderately convex apically; ventrosubapically constricted (Fig. 5 E, ↓ 7); excavated ventromesally; setae denser towards apex. On tegmen, apical points triangular shaped, not lamellate, pointed apically, directed posterolaterally (Fig. 5 G, ↓ 8); dorsal processes leaf-shaped, elongated slightly beyond transverse brace, with strongly sclerotized apex (Fig. 5 G, ↓ 9). Shoulders of tegmen well developed, thick. Transverse brace slightly extended, lobe shaped. Parameral apodemes short (Fig. 5 G, ↓ 10). </p>
            <p>Etymology.</p>
            <p> The species name  salicia is derived from the Latin word salici, meaning ‘ willow, ’ in reference to the dorsal processes of the tegmen, which resembles the shape of a willow leaf. </p>
            <p> Key to the Species of Korean  Campylomyza</p>
            <p>DNA barcode analysis and MOTU estimation</p>
            <p> The 658 - bp COI sequences were analyzed, revealing 234 variable sites, of which 63 were parsimony informative. Within the genus  Campylomyza , the interspecific divergences (p - distances) ranged from 6.18 % to 15.28 %. The mean distance across the entire dataset was 10.72 % (Suppl. material 1: table S 3). Intraspecific genetic distances varied from 0 % to 0.92 %. The species delimitation using the ABGD method delineated 17 Molecular Operational Taxonomic Units (MOTUs), including the outgroup. These MOTUs are illustrated by the color bars on the Neighbor Joining (NJ) tree in Fig. 6, corresponding with the delineations observed in the same NJ tree. All 17 MOTUs correspond to groups distinguished by their morphological characteristics. </p>
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	https://treatment.plazi.org/id/471DC710F3595A73875832F3C4581E23	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	Ham, Daseul;Bae, Yeon Jae	Ham, Daseul, Bae, Yeon Jae (2025): Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species. ZooKeys 1223: 221-245, DOI: 10.3897/zookeys.1223.128062
