identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
2503879EFFDA7F17FF05FE50E1B2DC71.text	2503879EFFDA7F17FF05FE50E1B2DC71.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Dysomma Alcock 1889	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Dysomma Alcock, 1889</p>
            <p> Dysomma Alcock, 1889:459 (type species,  Dysomma bucephalus Alcock, 1889 , by monotypy).  Sinomyrus Lin, 1933:93 , fig. 1 (type species,  S. angustus Lin , by monotypy;  S. angustus is a synonym of  Dysomma anguillare Barnard , fide Böhlke, 1949:34 –35). </p>
            <p> Definition. A genus of  Synaphobranchidae with a row of large compound teeth on the vomer and the following combination of characters: body stout to moderately elongate, slightly compressed in head and trunk; scales absent; pectoral fin present or not; dorsal-fin origin in front of anus; intermaxillary teeth present or not; snout projects slightly beyond lower jaw (except for  D. melanurum ); anus below pectoral fin to more than one head length behind pectoral-fin tip; and gill openings well-separated. </p>
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	https://treatment.plazi.org/id/2503879EFFDA7F17FF05FE50E1B2DC71	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.		MagnoliaPress via Plazi	Ho, Hsuan-Ching;Smith, David G.;Tighe, Kenneth A.	Ho, Hsuan-Ching, Smith, David G., Tighe, Kenneth A. (2015): Review of the arrowtooth eel genera Dysomma and Dysommina in Taiwan, with the description of a new species (Anguilliformes: Synaphobranchidae: Ilyophinae). Zootaxa 4060 (1): 86-104, DOI: 10.11646/zootaxa.4060.1.12
2503879EFFDA7F13FF05FC30E09FDEB3.text	2503879EFFDA7F13FF05FC30E09FDEB3.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Dysomma taiwanensis	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Dysomma taiwanensis sp. nov.</p>
            <p>New English name: Taiwanese arrowtooth eel Figs. 1 A–B, 2A–B; Table 1</p>
            <p>Holotype. NMMB-P11115 (496 mm TL), Daxi, Yilan, NE Taiwan, northwestern Pacific, bottom trawl, ca. 200– 400 m, 12 May 2006.</p>
            <p>Paratypes. NMMB-P 22194 (443), collected with the holotype. USNM 427172 (2, 192–248), Dong-gang, southwestern Taiwan, market, 16 Nov. 2007.</p>
            <p>Diagnosis. Pectoral fin present; dorsal-fin origin slightly in front of level of pectoral-fin base; anus well behind tip of pectoral fin; trunk very short; two intermaxillary teeth; 4 compound teeth on vomer; single row of 7–10 large compound teeth on lower jaw; head pores: IO 4, SO 3, M 6, POP 0, AD 1, F 0, ST 0; lateral-line pores: predorsal 4– 5, prepectoral 5–7, preanal 9–12, total 40–48, the last to about half of total length. Vertebrae: predorsal 9–10, preanal 13–17, total 137–139; MVF 9-15-138. Body uniformly brownish, lower part of posterior one-eighth of body darker, with black base and margin on rear part of anal fin and lower part of caudal fin.</p>
            <p>Description. Morphometric data of the holotype (in mm): total length 496; head length 63.5; predorsal length 60.1; preanal length 83; trunk length 16.5; tail length 413; depth at gill opening 23.5; width at gill opening 16.7; depth at anus 26.5; width at anus 17.4; eye diameter 3.9; interorbital width 9.4; snout length 14.1; rictus 27.4; postorbital length 47.2; gill opening 6.6; interbranchial width 9.7.</p>
            <p>The following values are given for the holotype, followed by that of paratypes in parentheses. Head relatively short, 12.8 (10.5–12.7)% TL; origin of dorsal fin slightly in front of a vertical through gill opening, predorsal length 12.1 (11.3–11.9)% TL; trunk very short, 3.3 (2.8–3.8)% TL, 26.0 (26.2–34.5)% HL; anus at one pectoral-fin length behind tip of fin; origin of anal fin immediately behind anus, preanal length 16.7 (13.3–16.5)% TL; tail long, tail length 83.3 (83.5–85.4)%TL.</p>
            <p>Body moderately slender, head and trunk somewhat cylindrical, becoming gradually compressed to rear end; body width at anus 3.5 (2.2–2.8)% TL; body depth relatively uniform, depth at anus 5.3 (2.5–4.2)% TL, narrowing gradually to caudal fin; depth of gill opening 4.7 (3.4–3.7)% TL. Dorsal and anal fins low and fleshy, continuous with a small caudal fin. Pectoral fin well-developed, at upper corner of gill opening.</p>
            <p>Head slender in profile; snout blunt anteriorly and broad dorsally, covered by many short papillae, snout length 22.2 (24.4–26.7)% HL; tip of snout projecting slightly beyond lower jaw; eye small, covered by a thick and semitransparent membrane; eye diameter 6.1 (4.7–7.5)% HL; interorbital space broad, slightly elevated, its width 14.8 (13.9–15.1)% HL; postorbital space very wide. Anterior nostrils tubular, directed anteroventrally. Posterior nostril rounded, below anterior margin of eye, opening directed posteroventrally. Lower jaw shorter than upper, its tip reaching first pore of supraorbital series. Mouth gape far behind eye, upper jaw length 43.1 (41.1–42.2)% HL. Tongue well-attached to mouth floor. Gill opening a narrow slit.</p>
            <p>Head and lateral-line pores large (Fig. 2 A). Supraorbital pores 3, all restricted to anterior portion of snout; infraorbital pores 4, 2 pores between nostrils and 2 below eye; mandibular pores 6, all under mouth gape; preopercular pores 0; adnasal 1; supratemporal commissure 0; frontal 0. Lateral line incomplete, extending to midbody, predorsal 5 (4 or 5), prepectoral 7 (4 or 5), preanal 12 (9–12) and total 45 (right)/48 (left) (40–45).</p>
            <p>Teeth (Fig. 2 B) small and pointed. Intermaxillary teeth 2, side-by-side, followed by 4 large compound vomerine teeth, uniserial, the third one largest. Maxillary with 3 to 4 irregular rows of small teeth, those in inner row slightly larger than the rest. Lower jaw with single row of 7 (7–10) large compound teeth; two smaller paratypes with 1–3 much smaller embedded compound teeth behind these exposed teeth, which can only be seen on the x-ray.</p>
            <p>* Values in brackets from a single 312 mm specimen (part of NMMB-P 11121).</p>
            <p>Mean vertebral formula 9-13-139; predorsal vertebrae 9–10, preanal vertebrae 13–17 and total vertebrae 137– 139.</p>
            <p>Coloration. Fresh color unknown. When preserved (Figs. 1 A–B), uniformly brownish including all fins; lower part of posterior one-eighth of body darker, with black base and margin on rear part of anal fin and lower part of caudal fin. Peritoneum dark grayish. Mouth cavity light brownish.</p>
            <p>Distribution. Known from the type specimens collected from off Taiwan at depths around 200–400 meters. Etymology. The specific name is derived from its type locality, Taiwan.</p>
            <p> Comparison.  Dysomma taiwanensis sp. nov. is closely similar to  D. anguillare in its body proportions and dentition. It differs from  D. anguillare in having more total vertebrae (137–139 vs. 119–128, 119– 130 in Robins &amp; Robins,1989) and fewer total lateral-line pores (40–48 vs. 57–75). </p>
            <p> The coloration of  D. taiwanensis is somewhat different from  D. anguillare ; the type specimens of  D. taiwanensis have uniformly brown coloration whereas  D. anguillare usually has a darker dorsal surface and a paler ventral surface to uniformly black. However, many specimens of  D. anguillare collected by midwater trawl (e.g. epipelagic zone less than 100 meters) may have paler body coloration. </p>
            <p> Although  D. taiwanensis co-occurs with  D. anguillare in Taiwan, only four specimens were found among hundreds specimens in the collection, which may suggest either that  D. taiwanensis is a rare species and its population is far smaller than that of  D. anguillare , or that  D. taiwanensis is more abundant at other depths and localities. </p>
            <p> It is also similar to  D. polycatodon but can be distinguished by the dentition on the lower jaw (single row of large compound teeth in  D. taiwanensis vs. single row of two large anterior teeth followed by 22–31 small teeth) and by the total lateral-line pores (40–48 vs. 65–78). Moreover,  D. taiwanensis has a uniformly brown body, whereas that of  D. polycatodon is pale to light brown, and the posterior margin of the anal fin and lower half of the caudal fin are black in  D. taiwanensis , whereas they are white in  D. polycatodon . </p>
            <p> Dysomma taiwanensis can also be distinguished from  D. bucephalus Alcock, 1889 by having single row of 7– 10 large compound teeth on the lower jaw (vs. single row of many small teeth) and 137–139 total vertebrae (vs. 107), and from  Dysomma fuscoventralis Karrer &amp; Klausewitz, 1982 by having 137–139 total vertebrae (vs. 119– 124), 40–48 total lateral-line pores (vs. 57–63), and 7–13 teeth on the lower jaw (vs. 16–21). </p>
            <p> The new species differs from  D. brevirostre (Facciolà, 1887) ,  D. muciparus (Alcock, 1891) ,  D. dolichosomatum and  D. tridens Robins, Böhlke &amp; Robins, 1989 by the presence of well-developed pectoral fins (vs. without pectoral fin) and total vertebrae 137–139 (vs. 146–204); from  D. longirostrum ,  D. goslinei , and  D. melanurum by the presence of two intermaxillary teeth (vs. without intermaxillary teeth) and a single row of large compound teeth on the lower jaw (vs. multiple series of small teeth); and from  D. opisthoproctus by having the anus below the pectoral fin (vs. far behind the tip of pectoral fin) and 137–139 total vertebrae (vs. 120). </p>
            <p>Remarks. It is notable that two large specimens (443–496 mm TL) have only 7 compound mandibular teeth, whereas two small paratypes (192–248 mm TL) have 8–10 larger teeth anteriorly and 1–3 much smaller posterior teeth which can only be seen on the x-ray, not with direct observation of the specimens, at least without damaging the rear of the jaws. This variation may be attributed to change with growth.</p>
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	https://treatment.plazi.org/id/2503879EFFDA7F13FF05FC30E09FDEB3	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.		MagnoliaPress via Plazi	Ho, Hsuan-Ching;Smith, David G.;Tighe, Kenneth A.	Ho, Hsuan-Ching, Smith, David G., Tighe, Kenneth A. (2015): Review of the arrowtooth eel genera Dysomma and Dysommina in Taiwan, with the description of a new species (Anguilliformes: Synaphobranchidae: Ilyophinae). Zootaxa 4060 (1): 86-104, DOI: 10.11646/zootaxa.4060.1.12
2503879EFFDE7F10FF05FE73E650D8B3.text	2503879EFFDE7F10FF05FE73E650D8B3.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Dysomma anguillare Barnard 1923	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Dysomma anguillare Barnard, 1923</p>
            <p>Figure 3; Table 1</p>
            <p> Dysomma anguillaris Barnard, 1923:443 (type locality: off Tugela River mouth, KwaZulu-Natal, South Africa, southwestern Indian Ocean, depth 63 fathoms [115 meters]). </p>
            <p> Dysomma anguillare: Böhlke, 1949:36 . Nelson, 1966:392. Robins &amp; Robins, 1976:263. Robins &amp; Robins, 1989:245. Chen &amp; Mok, 1995:930. Chen &amp; Mok, 2001:79. </p>
            <p> Sinomyrus angustus Lin, 1933:93 (type locality: Hoitow, Hainan). Böhlke, 1949:34 –36. </p>
            <p> Dysomma japonicus Matsubara, 1936:900 , fig. (description, relationships; type locality: Japan, southeast of Kii Peninsula). Böhlke, 1949:34, 36. </p>
            <p> Dysomma zanzibarensis Norman, 1939:44 , fig. 17 (description; type locality: 5º38'54"S, 39º15'42"– 39º17'36"E). Böhlke, 1949:34. </p>
            <p> Dyssoma  anguillaris : Smith, 1949:394. Smith, 1961:394. </p>
            <p> Dysomma aphododera Ginsburg, 1951:452 , fig. 7 (type locality: off Padre Island, Texas, in 50 fms., 26 º 30'N, 96 º 26' W). </p>
            <p> Dysomma angustum: Kamohara, 1950:49 . Kamohara, 1952:20. Kamohara,1958:15. Kamohara, 1964:18. </p>
            <p>Specimens examined. Collected from Tainan, southwestern Taiwan: NMMB-P5709 (1 spec., 392 mm TL), 20 Feb. 1966. Collected from Kaohsiung, southwestern Taiwan: NMMB-P5716 (2, 260–286), 23 Jan. 1960. Collected from Fong-gang, southwestern Taiwan: NMMB-P14566 (1, 239), 200 m, 28 Feb. 2001. Collected from Dong-gang fishing port, southwestern Taiwan: NMMB-P7144 (1, 332), 26 Dec. 2003. NMMB-P7994 (1, 279), 17 Jun. 2004. NMMB-P11124 (6, 305–360), 13 Sep. 2010. NMMB-P11125 (9, 334–455), 13 Sep. 2010. NMMB-P12065 (1, 235), 18 Feb. 2011. NMMB-P13799 (1, 450), 2 Jul. 2011. NMMB-P13840 (2, 185–265), 5 Oct. 2010. NMMB- P13842 (1, 260), 5 Oct. 2010. NMMB-P13844 (2, 330–420), 5 Oct. 2010. NMMB-P15568 (2 of 4, 153–191), 25 Oct. 2011. NMMB-P16176 (1, 262), 10 Nov. 2009. NMMB-P16453 (1, 135), 2 Feb. 2012. NMMB-P16536 (1, 385), 23 Feb. 2012. NMMB-P18108 (3, 386–466), 8 Aug. 2012. USNM 395054 (1, 363), 16 Nov 2007. USNM 398733 (1, 300), 14 Nov. 2009. USNM 398734 (1, 282), 14 Nov. 2009. USNM 398735 (1, 315), 14 Nov. 2009. Collected from Daxi fishing port, NE Taiwan, bottom trawl: NMMB-P4517 (1, 385), 23 Jan. 1994. NMMB- P16175 (1, 310), 20 May 2010. NMMB-P11113 (1, 515), no date. NMMB-P11114 (4, 345–434), no date. NMMB- P11118 (3, 308–370), 5 Jan. 2010. NMMB-P11119 (1, 460), 8 Dec. 2010. NMMB-P12067 (4, 345–434), 2 Oct. 2011. NMMB-P12068 (2, 401–413), 20 Jan. 2011. NMMB-P12069 (3, 401–477), 21 Jan. 2011. NMMB-P22059 (9, 300–417), 1 Dec. 2014. USNM 371927 (1, 521), 4 Mar 1999. USNM 398516 (1, 378), 6 Nov. 2009. USNM 398517 (1, 333), USNM 401058 (1, 370), 6 Nov. 2009. Collected from Nan-fang-ao fishing port, NE Taiwan, bottom trawl: NMMB-P16288 (1, 202), 16 Mar. 2012. Collected from Tong-shih, Chia-yi, Taiwan: USNM 396128 (3, 362–421), 14 Nov 2008). Collected from Taiwan, no precise locality: USNM 396129 (1, 388), 2009. Plus many others in NMMB-P collection.</p>
            <p>Other localities. Da Nang, Vietnam: NMMB-P12592 (1, 148), 13 Apr. 2011. Nha Trang, Vietnam: USNM 396163 (6, 332–450), 16 Apr 2009. China: CAS-SU 32403 (20, 280–426). MNHN 1978-0078 (formerly CAS-SU 32403, 2, 273–365), Oct. 1936. Luzon, Philippines: MNHN 1998-0655 (1, 210), 13°23'N, 122°21'E, 760–820 m, 26 Nov. 1980. Madagascar: MNHN 1987-1226 (3, 337–458), 23°36'3.6"S, 43°32'2.4"E, 250 m, 28 Feb. 1973. MNHN 1987-1227 (2, partly dry), 25°2'6"S, 47°5'6"E, 65– 60 m, 4 Mar. 1973. Solomon Islands: MNHN 2002- 3921 (1, 364), 9°31'58.8''S. 160°37'1.2"E, 2 Oct. 2001.</p>
            <p>Diagnosis. Pectoral fin present; dorsal-fin origin slightly anterior to pectoral-fin base, predorsal length 10.7– 13.1% TL; anus anterior, below tip of pectoral fin, preanal length 15.9–18.9% TL; trunk very short, 2.8–5.5% TL; two intermaxillary teeth; 4 compound teeth on vomer; single row of 9–11 large compound teeth on lower jaw; head pores: IO 4, SO 3; M 6; POP 0; AD 1, F 0, ST 0; lateral-line pores: predorsal 3–6, prepectoral 6–9, preanal 8–12, total 57–75, the last at posterior two-thirds of total length; MVF 8-14-124, total vertebrae 119–128 (119–130 in Robins &amp; Robins, 1989).</p>
            <p>Body light brown to blackish dorsally, paler ventrally. Dorsal fin and most part of anal fin white; posterior margin of anal fin with black and white color. Caudal fin black with upper margin white.</p>
            <p> Distribution. Widespread in the Indo-west Pacific and Atlantic oceans, although the taxonomic status of the various geographic populations is still to be determined. In Taiwan, it is the most abundant species of  Dysomma and can be collected by bottom and midwater trawls from near the surface (&lt;50 m) to as deep as 600 m. </p>
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	https://treatment.plazi.org/id/2503879EFFDE7F10FF05FE73E650D8B3	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.		MagnoliaPress via Plazi	Ho, Hsuan-Ching;Smith, David G.;Tighe, Kenneth A.	Ho, Hsuan-Ching, Smith, David G., Tighe, Kenneth A. (2015): Review of the arrowtooth eel genera Dysomma and Dysommina in Taiwan, with the description of a new species (Anguilliformes: Synaphobranchidae: Ilyophinae). Zootaxa 4060 (1): 86-104, DOI: 10.11646/zootaxa.4060.1.12
2503879EFFDC7F1EFF05FF37E393DA2E.text	2503879EFFDC7F1EFF05FF37E393DA2E.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Dysomma dolichosomatum Karrer 1983	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Dysomma dolichosomatum Karrer, 1983</p>
            <p>Figs. 4 A–B; Table 1</p>
            <p> Dysomma dolichosomatum Karrer, 1983:93 (type locality: Madagascar, 22°25'S, 43°04.5'E, 550–555 m). Robins &amp; Robins, 1989:249. Chen &amp; Mok, 2001:79. </p>
            <p>Specimens examined. Collected from Fong-gang, SW Taiwan: NMMB-P2861 (1 spec., 242 mm TL), 8 Nov. 2001. Collected from Dong-gang fishing port, SW Taiwan: NMMB-P9098 (1, dry), 13 Jun. 2008. NMMB-P9241 (1, 349), 18 Sep. 2008. NMMB-P11121 (6, 209–312), 16 Jul. 2009. NMMB-P11130 (2, 231–269), 13 Sep. 2010. NMMB-P12066 (1, 336), 28, Jan. 2011. NMMB-P13794 (1, 197), 21 Jul. 2011. NMMB-P14189 (4, 166–301), 20 Oct. 2011. NMMB-P15568 (2 of 4, 218–294), 25 Oct. 2011. NMMB-P16134 (1, 189), 9 Feb. 2012. NMMB- P16404 (4, 264–320), 28 Jan. 2012. NMMB-P16422 (1, 357), 21 Feb. 2012. NMMB-P17820 (1, 357), 2 Nov. 2012. NMMB-P17881 (1, 263), 25 Jan. 2012. NMMB-P18083 (1, 336), 7 Sep. 2012. NMMB-P21733 (2, 215– 221), 18 Feb. 2011. NMMB-P21799 (1, 227), 7 Nov. 2013. NMMB-P21928 (1, 343), 1 Nov.2014. NMMB-P22126 (1, 242), 12 Dec. 2013. USNM 270682 (2, 172–187), 23 Nov. 1969. USNM 398567 (1, 317), 10 Nov. 2009. USNM 401019 (1, 197), 26 Feb. 2011. USNM 401036 (1, 345), 8 Nov. 2009.</p>
            <p>Other localities. Madagascar: MNHN 1979-0004, holotype, 22°25'1.2"S, 43°4'4.8"E, 550–555 m, 27 Nov. 1973. Philippines: MNHN 1978-0717, paratype, 14°1'1.2"N, 120°22'1.2"E, 223 m, 21 Mar. 1976. Solomon Islands: MNHN 2006-0734 (1, 203), 8°24'28.8"S, 159°28'22.8"E, 105–897 m, 24 Oct. 2004.</p>
            <p>Diagnosis. No pectoral fin; dorsal-fin origin about 0.8–1 HL behind gill opening, predorsal length 16.5–19.1% TL; anus posterior, about 1.5 time of HL behind gill opening, preanal length 23.3–28.6% TL; trunk long, trunk length 14.3–17.7% TL; two intermaxillary teeth; 2 irregular rows of small blunt teeth on upper jaw; 2 or 3 (mainly 3) compound teeth on vomer; single row of 4 or 5 small compound teeth followed by 1 or 2 irregular rows of small blunt teeth on lower jaw; short cirri on surfaces of chin and jaws; head pores: IO 4, SO 3, M 6 (1 with 7), POP 1, AD1, F 0, ST 0; lateral-line pores large, prepectoral 5 or 6, total 9–11, the last at slightly beyond the gill opening posteriorly; MVF 18-27-153, total vertebrae 146–156.</p>
            <p>Body light pinkish to light grayish dorsally when fresh with a black margin at posterior portion of anal fin; light brownish to grayish when preserved.</p>
            <p>Distribution. Indo-west Pacific off Madagascar, Taiwan, Philippines, and Solomon Islands at depth 105– 897 m.</p>
            <p> Remarks. This species is common in the by-catch in Taiwan. It is usually collected by midwater trawlers together with many mesopelagic fishes, which would indicate pelagic living. However, many specimens are also found to feed on polychelids, a demersal shrimp family.  Dysomma dolichosomatum is the only species found to possess one preopercular pore and a very short lateral line, with only 9–11 pores, among all Taiwanese species. It is similar to  D. brevirostre ,  D. muciparus and  D. tridens in lacking a pectoral fin. It differs from  D. brevirostre by having tiny papillae on the head and snout (vs. large papillae and ridges) and total vertebrae 146–156 (vs. 195–205 in Robins &amp; Robins, 1989); from  D. muciparus by having trunk 1.4–1.9 times in head length (vs. less than 1 time in head length) and 146–156 total vertebrae (vs. 153–157); and from  D. tridens by having 2 intermaxillary teeth (vs. three large compressed teeth) and by having 146–156 total vertebrae (vs. 175). </p>
            <p> Our specimens have a broader range of total vertebrae (146–156) compared to 151–152 reported for the types by Karrer (1983). One 312 mm specimen out of NMMB-P 11121 had a relatively long predorsal measurement (23.4 % of TL) and high predorsal vertebral count (25 vertebrae). While it is possible that this specimen may represent a different species, the close correspondence of all other counts and measurements with the other specimens of  D. dolichosomatum from Taiwan indicates that it is probably a specimen with an aberrant dorsal origin. </p>
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	https://treatment.plazi.org/id/2503879EFFDC7F1EFF05FF37E393DA2E	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.		MagnoliaPress via Plazi	Ho, Hsuan-Ching;Smith, David G.;Tighe, Kenneth A.	Ho, Hsuan-Ching, Smith, David G., Tighe, Kenneth A. (2015): Review of the arrowtooth eel genera Dysomma and Dysommina in Taiwan, with the description of a new species (Anguilliformes: Synaphobranchidae: Ilyophinae). Zootaxa 4060 (1): 86-104, DOI: 10.11646/zootaxa.4060.1.12
2503879EFFD37F1CFF05FACFE02ED9C8.text	2503879EFFD37F1CFF05FACFE02ED9C8.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Dysomma goslinei Robins & Robins 1976	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Dysomma goslinei Robins &amp; Robins, 1976</p>
            <p>Table 2</p>
            <p> Dysomma goslinei Robins &amp; Robins, 1976:261 (type locality: Indian Ocean, 14°52'N, 96°39'W). Robins &amp; Robins, 1989:249. Smith, 1999:1661. Chen &amp; Mok, 2001:79. </p>
            <p>Diagnosis. Pectoral fin present; dorsal-fin origin before pectoral-fin base, predorsal length 10.7% TL; anus anterior, just below pectoral fin, preanal length 16.2% TL; trunk very short, trunk length 4.0% TL; no intermaxillary teeth; multiple rows of teeth on upper jaw; 4 compound teeth on vomer; teeth on lower jaw multiserial, those on inner row slightly enlarged; lateral line short; and MVF 10-15-123. [Data adapted from Chen &amp; Mok, 2001].</p>
            <p>Remarks. No specimen from Taiwan is available for this study. Mok in Shen et al. (1993) first recorded the present species from Taiwan, but no voucher was mentioned. One specimen (NSYSU 2607, 207 mm TL) examined by Chen &amp; Mok (2001) has only 123 total vertebrae, less than 130–131 provided by Robins &amp; Robins (1989). However, we could not locate this specimen. More investigations are needed of the population in Taiwan.</p>
            <p> Dysomma longirostrum Chen &amp; Mok, 2001:79 (type locality: Nan-fang-ao, NE Taiwan). Ho &amp; Shao, 2011:22. </p>
            <p>Specimens examined. Holotype: NSYU 2732 (196), Nan-fang-ao fish market, NE Taiwan, bottom trawl, 100–150 m, 12 Sep. 1992, coll. Y.- Y. Chen.</p>
            <p>Other locality. MNHN 2003-1515 (1, 285), R/V Alis, stn. CP8, 24°54'S, 168°21'E, Norfolk Ridge, New Caledonia, Coral Sea, 540 m, 11 Aug. 1999.</p>
            <p>Diagnosis. Pectoral fin present; origin of dorsal fin above tip of pectoral fin, predorsal length 17.9–18.6% TL; no intermaxillary teeth; snout very long, its length 25.7–32.1% HL; jaw long and slender, upper jaw length 42.0– 52.1% HL; anus posterior, far behind pectoral fin, preanal length 24.0–24.3% TL; trunk moderately long, trunk length 9.7–10.3% TL; multiple rows of teeth on upper jaw; 5 compound teeth on vomer; multiple rows of small teeth on lower jaw, those on inner row larger than the rest; head pores: SO 5, IO 8 (2 between nostrils, 2 below eye, 4 behind eye), M 7, POP 2, AD 1, ST 0, F 1; lateral-line pores: predorsal 11, prepectoral 3–6, preanal 20, total ca. 77 or ca. 96, the last at 2/3 HL before caudal fin; MVF 14-24-130 (holotype only). Body uniformly brown when preserved. [Data adapted from Chen &amp; Mok, 2001 and based on present study].</p>
            <p>Remarks. One additional specimen was found in the MNHN collection that represents the second record of the species, in New Caledonia.</p>
            <p> Dysomma longirostrum is the only member with four head pores behind the eye and two POP pores among all congeners. There is one frontal pore in the holotype whereas the MNHN specimen has none. The count of total lateral-line pores is not accurate because the posterior portion of the lateral line (behind anus) is broken into small canals, each canal connects two pores. These canals are not evenly spaced and sometimes have additional pores in the space between two canals. However, this may be used as a diagnostic character because the other congeners examined in the present work all have a continuous lateral line. </p>
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	https://treatment.plazi.org/id/2503879EFFD37F1CFF05FACFE02ED9C8	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.		MagnoliaPress via Plazi	Ho, Hsuan-Ching;Smith, David G.;Tighe, Kenneth A.	Ho, Hsuan-Ching, Smith, David G., Tighe, Kenneth A. (2015): Review of the arrowtooth eel genera Dysomma and Dysommina in Taiwan, with the description of a new species (Anguilliformes: Synaphobranchidae: Ilyophinae). Zootaxa 4060 (1): 86-104, DOI: 10.11646/zootaxa.4060.1.12
2503879EFFD17F1AFF05F8A9E0D3DFE6.text	2503879EFFD17F1AFF05F8A9E0D3DFE6.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Dysomma melanurum Chen & Weng 1967	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Dysomma melanurum Chen &amp; Weng, 1967</p>
            <p>Figs. 6 A–B; Table 2</p>
            <p> Dysomma melanurum Chen &amp; Weng, 1967:84 , fig. 63 (Type locality: Tungkang [Dong-gang], Taiwan). Chen &amp; Mok, 2001:79. Ho et al. 2010:26. Ho &amp; Shao, 2011:22. </p>
            <p>Specimens examined. Lectotype: NMMB-P5284 (formerly THUP 1687), Tungkang [Dong-gang], SW Taiwan.</p>
            <p>Paralectypes: NMMB-P3885 and NMMB-P5470, same as lectotype. Non-types: collected from Dong-gang, SW Taiwan by midwater trawl: NSYU 2732 (1, 237 mm TL). NMMB-P3885 (1, 191, partly dry), 13 Feb. 1962. NMMB-P10949 (3, 271–285), 4 Sep. 2010. NMMB-P11122 (2, 258–261), 13 Sep. 2010. NMMB-P13741 (1, 265), 29 Jul. 2011. NMMB-P13841 (1, 260), 5 Oct. 2010. NMMB-P14044 (7, 206–285), 3 Nov. 2011. NMMB-P14213 (1, 255), 20 Oct. 2011. NMMB-P15471 (3, 281–297), 2 Jul. 2011. USNM 398473 (1, 165), 13 Nov. 2009. USNM 398474 (1, 178), 13 Nov. 2009.</p>
            <p>Diagnosis. Pectoral fin present; dorsal-fin origin above middle of pectoral fin, predorsal length 11.5–15.0% TL; lower jaw longer than upper jaw, slightly curved and not appressed to upper jaw when mouth closed; anus anterior, below pectoral fin, preanal length 15.4–17.3% TL; trunk very short, trunk length 3.0–5.3% TL; no intermaxillary teeth; multiple rows of teeth on upper jaw, those on innermost row about twice the size of the rest; 5 or 6 (mainly 5) compound teeth on vomer; multiple rows of teeth on lower jaw, those on innermost row about twice the size of the rest; head pores: IO 4, SO 3, M 7 (1 with 8), POP 0, AD 1, F 0, ST 0. Lateral-line pores very large, predorsal 10–13, prepectoral 8–11, preanal11–17, total pores 107–117, the last to 1/2 HL before the caudal-fin base. MVF 13-14-135, total vertebrae 131–138. Body uniformly light pinkish to grayish with numerous melanophores, posterior margin of anal fin and caudal fin black.</p>
            <p>Remarks. This species has a very different morphology of its lower jaw, strongly curved and not appressed to the upper jaw when the mouth is closed. This may reflect its pelagic living. Many specimens are found to feed on pelagic shrimps. This is a small species; the largest specimen examined was only 297 mm TL.</p>
            <p>Robins &amp; Robins (1976:263) suggested that the projecting lower jaw of this species was an artifact, based on the damaged condition of the specimen they examined (THUP 1687, now the lectotype). We have examined 25 specimens, however, and they all have a clearly projecting lower jaw.</p>
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	https://treatment.plazi.org/id/2503879EFFD17F1AFF05F8A9E0D3DFE6	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.		MagnoliaPress via Plazi	Ho, Hsuan-Ching;Smith, David G.;Tighe, Kenneth A.	Ho, Hsuan-Ching, Smith, David G., Tighe, Kenneth A. (2015): Review of the arrowtooth eel genera Dysomma and Dysommina in Taiwan, with the description of a new species (Anguilliformes: Synaphobranchidae: Ilyophinae). Zootaxa 4060 (1): 86-104, DOI: 10.11646/zootaxa.4060.1.12
2503879EFFD77F1BFF05FE87E00DDC0B.text	2503879EFFD77F1BFF05FE87E00DDC0B.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Dysomma opisthoproctus Chen & Mok 1995	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Dysomma opisthoproctus Chen &amp; Mok, 1995</p>
            <p>Table 3</p>
            <p> Dysomma opisthoproctus Chen &amp; Mok, 1995:930 (type locality: Nan-fang-ao, NE Taiwan, 200 m). Chen &amp; Mok, 2001:79. </p>
            <p>Diagnosis. Pectoral fin present; dorsal-fin origin in front of level of pectoral-fin base, predorsal length 10.6% TL; anus posterior, far behind tip of pectoral fin, preanal length 35.1% TL; trunk very long, trunk length 20.2% TL; 2 intermaxillary teeth; 4 compound teeth on vomer; multiple rows of small teeth on upper jaw; single row of 7 or 8 large compound teeth on lower jaw; head pores: IO 4, SO 3, M 7, POP 0, AD 1; lateral-line pores: prepectoral 6, preanal 24, lateral line runs to more than 2 head length before caudal fin; preanal vertebrae 35, total vertebrae 120. Body brownish dorsally and paler ventrally with lower part of posterior margin of anal fin and caudal fin black. [Data adapted from Chen &amp; Mok, 1995]</p>
            <p> Remarks. The holotype and only known specimen was not available for our study because its whereabouts is unknown.  Dysomma opisthoproctus can be separated from all Taiwanese congeners except  D. dolichosomatum and  D. longirostrum by the posterior position of the anus. It differs from  D. dolichosomatum by having a pectoral fin (vs. absent) and 7 or 8 larger compound teeth on lower jaw (vs. 4 or 5 small compound teeth followed by 1 or 2 irregular rows of small blunt teeth on lower jaw) and 120 total vertebrae (vs. 147–156). It differs from  D. longirostrum by having 2 intermaxillary teeth (vs. 0), a relatively short snout (22.0% vs. 32.1% HL), 7 or 8 large compound teeth (vs. small multiserial teeth) on lower jaw, 120 (vs. 130) total vertebrae, and lacking POP pores (vs. 2 POP pores). It is also similar to  Dysommina rugosa in the posterior position of its anus and a similar external appearance, but differs by having lateral-line pores (vs. absent), a single row of compound teeth (vs. small multiserial teeth) on the lower jaw, 120 (vs. 127–134) total vertebrae, presence of intermaxillary teeth (vs. absent), and well-developed papillae on both jaws (vs. slightly developed). </p>
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	https://treatment.plazi.org/id/2503879EFFD77F1BFF05FE87E00DDC0B	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.		MagnoliaPress via Plazi	Ho, Hsuan-Ching;Smith, David G.;Tighe, Kenneth A.	Ho, Hsuan-Ching, Smith, David G., Tighe, Kenneth A. (2015): Review of the arrowtooth eel genera Dysomma and Dysommina in Taiwan, with the description of a new species (Anguilliformes: Synaphobranchidae: Ilyophinae). Zootaxa 4060 (1): 86-104, DOI: 10.11646/zootaxa.4060.1.12
2503879EFFD67F1BFF05FCEBE766D8B0.text	2503879EFFD67F1BFF05FCEBE766D8B0.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Dysomma polycatodon Karrer 1983	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Dysomma polycatodon Karrer, 1983</p>
            <p>Fig. 7; Table 3</p>
            <p> Dysomma polycatodon Karrer, 1983:89 (type locality: Northwestern Madagascar, 15°21'S, 46°11'E, depth 170–175 m). Robins &amp; Robins, 1989:250. Smith, 1999:1661. Chen &amp; Mok, 2001:79. </p>
            <p>Specimens examined. Collected from Daxi fishing port, NE Taiwan, bottom trawl: ASIZP 60188 (1 spec., 453 mm TL), 15 Oct. 1997. NMMB-P384 (1, 326), 23 Jan. 1994. NMMB-P11120 (1, 544), 6 Sep. 2010. USNM 372011 (1, 362), 12 Sep 1998. USNM 398475 (1, 384), 10 Sep. 2007. Collected from Dong-gang fishing port, SW Taiwan, bottom trawl: ASIZP 55560 (1, 358), 15 Jan. 1981. NMMB-P2843 (1, 505), 100 m, 8 Nov. 2001. NMMB- P3652 (1,321), 150 m, 28 May 2012. NMMB-P9076 (1, 250), 13 Jun. 2008. NMMB-P11128 (2, 310–333), 13 Sep. 2010. NMMB-P11129 (1, 400), 13 Sep. 2011. NMMB-P11132 (1, 365), 6 Sep. 2010. NMMB-P12070 (1, 550), 18 Feb. 2011. NMMB-P12625 (2, 372–375), 25 Mar. 2011. NMMB-P15256 (1, 407), 28 Oct. 2011. NMMB-P15625 (2, 367–371), 25 Mar. 2011. NMMB-P16388 (1, 274), 21 Feb. 2012. NMMB-P17776 (1, 344), 9 Aug. 2012. NMMB-P17783 (1, 544), 9 Aug. 2012. NMMB-P18040 (3, 500–600), no date. NMMB-P19278 (1, 260), 10 Nov. 2011. USNM 398736 (1, 196), 14 Nov. 2009. USNM 398737 (1, 265), 14 Nov. 2009. USNM 402447 (5, 275–362), Nov. 2009. USNM 410020 (1, 382), 26 Feb. 2011. USNM 427171 (1, 311), 16 Nov. 2011. Collected from Shiaoliu-chiu, SW Taiwan: NMMB-P3415 (1, 355), 26 Dec. 2003.</p>
            <p>Other localities. Philippines: USNM 344108 (1, 436), 23 Sep. 1995. Madagascar: MNHN 1979–0003 (1, 523), holotype, 15°19'58.8"S, 46°11'2.4"E, 170–175 m, 19 Jan. 1979.</p>
            <p>Diagnosis. Pectoral fin present; dorsal-fin origin anterior tolevel of pectoral fin base, predorsal length 10.0– 12.9% TL; anus anterior, just below pectoral fin, preanal length 15.5–18.2% TL; trunk very short, trunk length 2.4– 3.9% TL; 2 intermaxillary teeth; 3 compound teeth on vomer; 3 or 4 rows of small sharp teeth on upper jaw; single row of 2 large anterior teeth followed by 22–31 small sharp teeth on lower jaw; head pores: IO 4, SO 3, M 6, POP 0 (1 with 1), AD 1 (1with 0); lateral-line pores: predorsal 3–5, prepectoral 5–7, preanal 8–11, and total 65–78, the last at about anterior two-thirds of total length; MVF 8-13-130, total vertebrae 128–133 (1 with 120). Body light grayish to brown dorsally, paler ventrally; posterior half of anal-fin base deep brown, and dorsal and anal fins with white margins.</p>
            <p>Remarks. The holotype of this species, collected off Madagascar, has 140 vertebrae (Karrer, 1983), significantly more than the specimens from Taiwan (128–133). One of two specimens in NMMB-P18040 has only 120 total vertebrae. However, no other difference can be observed and the vertebrae appear to be complete. This specimen may represent a different species when more specimens are available.</p>
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	https://treatment.plazi.org/id/2503879EFFD67F1BFF05FCEBE766D8B0	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.		MagnoliaPress via Plazi	Ho, Hsuan-Ching;Smith, David G.;Tighe, Kenneth A.	Ho, Hsuan-Ching, Smith, David G., Tighe, Kenneth A. (2015): Review of the arrowtooth eel genera Dysomma and Dysommina in Taiwan, with the description of a new species (Anguilliformes: Synaphobranchidae: Ilyophinae). Zootaxa 4060 (1): 86-104, DOI: 10.11646/zootaxa.4060.1.12
2503879EFFD57F18FF05FB39E734DAD4.text	2503879EFFD57F18FF05FB39E734DAD4.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Dysommina Ginsburg 1951	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Dysommina Ginsburg, 1951</p>
            <p> Dysommina Ginsburg, 1951:450 (type species:  Dysommina rugosa Ginsburg 1951 , by monotypy). </p>
            <p> Definition. A genus of  Synaphobranchidae with a row of large compound teeth on the vomer and the following combination of characters: body moderately elongate, slightly compressed in head and trunk; scales absent; pectoral fin present; dorsal-fin origin over or slightly behind tip of pectoral fin; pores in lateral line absent; intermaxillary teeth absent; snout projects slightly beyond lower jaw; anus more than 1 head length behind pectoral-fin tip; multiple serial teeth on lower jaw; and gill openings well-separated. </p>
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	https://treatment.plazi.org/id/2503879EFFD57F18FF05FB39E734DAD4	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.		MagnoliaPress via Plazi	Ho, Hsuan-Ching;Smith, David G.;Tighe, Kenneth A.	Ho, Hsuan-Ching, Smith, David G., Tighe, Kenneth A. (2015): Review of the arrowtooth eel genera Dysomma and Dysommina in Taiwan, with the description of a new species (Anguilliformes: Synaphobranchidae: Ilyophinae). Zootaxa 4060 (1): 86-104, DOI: 10.11646/zootaxa.4060.1.12
2503879EFFD57F19FF05FA56E1E6DAAC.text	2503879EFFD57F19FF05FA56E1E6DAAC.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Dysommina rugosa Ginsburg 1951	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Dysommina rugosa Ginsburg, 1951</p>
            <p>Fig. 8; Table 3</p>
            <p> Dysommina rugosa Ginsburg, 1951:450 (type locality: off Cumberland Island, Georgia, U.S.A., western North Atlantic, 30°53'00"N, 79°42'30"W, depth 273 fathoms [499 m]). Karrer, 1983:96. Robins &amp; Robins, 1989:242. Smith, 1999:1661. </p>
            <p>Specimens examined. Collected from Dong-sha Island, South China Sea: ASIZP 57954 (1 spec., 238 mm TL), 17 Aug. 1991. Collected from Dong-gang fishing port, SW Taiwan, bottom trawl: NMMB-P8361 (1, 258), 16 Mar. 2005. NMMB-P11131 (1, 413), 13 Sep. 2010. NMMB-P14012 (1, 316), 20 Oct. 2011. NSYU uncat. (2, twisted).</p>
            <p>Other localities. Solomon Islands: MNHN 2006-0017 (1, 350), 8°16’26.4”S, 160°4’33.6”E, 23 Oct. 2004. MNHN 2006-0461 (1), 7°45'S, 156°28'22.8"E, 582–609 m, 1 Nov. 2004. MNHN 2006-0509 (1), 8°16'33.6"S, 160°4'33.6"E, 430 m, 23 Oct. 2004. Madagascar: MNHN 1979-0005 (1), 18°54’S, 43°55’1.2”E, 24 Nov. 1973. Philippines: MNHN 1998-0641 (1), 13°49’1.2”N, 120°49’58.8”E, 23 Nov. 1980. USNM 343985 (1, 362+), 12°54’29"N, 12°57’30”E, 376–382 m, 23 Sep. 1995. New Caledonia: MNHN 1995-0329 (1, 140), 22°6’S, 167°10’1.2”E, 550 m, 3 Oct. 1985. MNHN 2003-1529 (1, 198), 23°42’S, 168°15’E, 12 Aug. 1999.</p>
            <p>Diagnosis. Pectoral fin present; dorsal-fin origin over tip of pectoral fin, predorsal length 14.0–17.1% TL; anus posterior, more than 1 head length behind pectoral fin, preanal length 26.8–28.8% TL; trunk long, trunk length 12.8–16.4% TL; no intermaxillary teeth; 4 compound teeth on vomer; multiple rows of teeth on upper jaw and lower jaw; head pores: IO 4, SO 3, M 6, POP 0, AD 1, ST 0, F 0; lateral-line pores absent; MVF 11-28-136, total vertebrae 133–141.</p>
            <p>Body light brownish dorsally, paler ventrally; dorsal and anal fins with white margin, posterior one third of anal-fin base and posterior one-seventh of anal fin black.</p>
            <p>Distribution. Widespread in tropical Atlantic and Indo-West Pacific Oceans. Specimens examined in present study were collected at depths of 376– 609 m.</p>
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	https://treatment.plazi.org/id/2503879EFFD57F19FF05FA56E1E6DAAC	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.		MagnoliaPress via Plazi	Ho, Hsuan-Ching;Smith, David G.;Tighe, Kenneth A.	Ho, Hsuan-Ching, Smith, David G., Tighe, Kenneth A. (2015): Review of the arrowtooth eel genera Dysomma and Dysommina in Taiwan, with the description of a new species (Anguilliformes: Synaphobranchidae: Ilyophinae). Zootaxa 4060 (1): 86-104, DOI: 10.11646/zootaxa.4060.1.12
2503879EFFCB7F07FF05FA2BE6EEDE1A.text	2503879EFFCB7F07FF05FA2BE6EEDE1A.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Dysomma	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Key to species of  Dysomma and  Dysommina in Taiwan </p>
            <p> As mentioned above,  Dysommina shares many external characters with  Dysomma and is thus included in this key. </p>
            <p> 1A. Pectoral fin absent; about 2 rows of teeth on upper jaw.........................................  D. dolichosomatum</p>
            <p>1B. Pectoral fin present; 4 or more rows of teeth on upper jaw...................................................... 2</p>
            <p>2A. Intermaxillary teeth present; uniserial teeth on dentary......................................................... 3</p>
            <p>2B. Intermaxillary teeth absent; multiserial teeth on dentary........................................................ 6</p>
            <p>3A. Anus anterior, trunk shorter than head length................................................................4</p>
            <p> 3B. Anus posterior, trunk much longer than head length.............................................  D. opisthoproctus</p>
            <p> 4A. Two large compound teeth followed by row of 22–31 smaller ones on lower jaw.........................  D. polycatodon</p>
            <p>4B. Single row of 7 to 11 large compound teeth on lower jaw...................................................... 5</p>
            <p> 5A. Total vertebrae 137–139; total lateral-line pore 40–48.......................................  D. taiwanensis sp. nov.</p>
            <p> 5B. Total vertebrae 119–130; total lateral-line pores 57–75..............................................  D. anguillare</p>
            <p>6A. Anus anterior, just below pectoral fin...................................................................... 7</p>
            <p>6B. Anus posterior, well behind pectoral fin.................................................................... 8</p>
            <p> 7A. Lower jaw projects beyond snout, not appressed to upper jaw when mouth fully closed; lateral line extends to 1/2 HL before the caudal-fin base..........................................................................  D. melanurum</p>
            <p> 7B. Lower jaw included, not projecting beyond snout, appressed to upper jaw when mouth fully closed; lateral line extends to about anterior 23% of body......................................................................  D. goslinei</p>
            <p> 8A. Five compound teeth on vomer; lateral-line pores present; head pores present on frontal, infraorbital posterior to eye and preopercular.................................................................................  D. longirostrum</p>
            <p> 8B. Four compound teeth on vomer; pores absent onlateral line, frontal, infraorbital posterior to eye and preopercular...............................................................................................  Dysommina rugosa</p>
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	https://treatment.plazi.org/id/2503879EFFCB7F07FF05FA2BE6EEDE1A	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.		MagnoliaPress via Plazi	Ho, Hsuan-Ching;Smith, David G.;Tighe, Kenneth A.	Ho, Hsuan-Ching, Smith, David G., Tighe, Kenneth A. (2015): Review of the arrowtooth eel genera Dysomma and Dysommina in Taiwan, with the description of a new species (Anguilliformes: Synaphobranchidae: Ilyophinae). Zootaxa 4060 (1): 86-104, DOI: 10.11646/zootaxa.4060.1.12
