identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
183387E3FFC8FFC8FF20FA54FCA4F90E.text	183387E3FFC8FFC8FF20FA54FCA4F90E.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Selachinematidae Cobb 1915	<div><p>Family Selachinematidae Cobb, 1915</p><p>Diagnosis. (from Leduc (2013)). Body usually stout. Cuticle punctated with or without lateral differentiation. Head sensilla may be jointed. Amphideal fovea usually spiral, rarely loop-shaped. Buccal cavity spacious, divided into two compartments, either reinforced by cuticularised rhabdions in both portions (Choniolaiminae), or with posterior rhabdions modified into protrusible mandibles (Selachinematinae). Pharynx with or without posterior bulb, anterior bulb sometimes present. Males usually with two outstretched testes, either on same or different sides of the intestine; pre-cloacal supplements usually present, usually cup-shaped, sometimes setose, papilliform, rarely tubular. Female didelphic-amphidelphic with reflexed ovaries.</p></div>	https://treatment.plazi.org/id/183387E3FFC8FFC8FF20FA54FCA4F90E	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	Leduc, Daniel;Zhao, Zeng Qi	Leduc, Daniel, Zhao, Zeng Qi (2016): Molecular characterisation of five nematode species (Chromadorida, Selachinematidae) from shelf and upper slope sediments off New Zealand, with description of three new species. Zootaxa 4132 (1): 59-76, DOI: 10.11646/zootaxa.4132.1.5
183387E3FFC9FFC9FF20FF08FCE9FD76.text	183387E3FFC9FFC9FF20FF08FCE9FD76.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Cheironchus Cobb 1917	<div><p>Genus Cheironchus Cobb, 1917</p><p>Diagnosis. (from Tchesunov &amp; Okhlopkov (2006)) Six inner labial sensilla in form of conical papillae. Outer labial and cephalic sensilla in a single crown with cephalic setae much longer than outer labial setae. Amphideal fovea multispiral. Short somatic setae or papillae and pores in irregular rows along body. Anterior buccal cavity (cheilostom) unarmed. Posterior buccal cavity (pharyngostom) with three mandibles; two large lateroventral mandibles equal in shape and size and shifted laterally; dorsal mandible vestigial. Pharynx with anterior and posterior bulbs. Male with cup-shaped precloacal supplements. Tail short, ranging from bluntly conical to conical with short cylindrical portion.</p><p>Type species. Cheironchus vorax Cobb, 1917</p><p>Other valid species</p><p>C. conicaudatus Tchesunov &amp; Okhlopkov, 2006</p><p>C. dactylocaudatus Tchesunov &amp; Okhlopkov, 2006</p><p>C. paravorax Castillo-Fernandez &amp; Decraemer, 1993</p></div>	https://treatment.plazi.org/id/183387E3FFC9FFC9FF20FF08FCE9FD76	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	Leduc, Daniel;Zhao, Zeng Qi	Leduc, Daniel, Zhao, Zeng Qi (2016): Molecular characterisation of five nematode species (Chromadorida, Selachinematidae) from shelf and upper slope sediments off New Zealand, with description of three new species. Zootaxa 4132 (1): 59-76, DOI: 10.11646/zootaxa.4132.1.5
183387E3FFC9FFCDFF20FD46FBDBFEE9.text	183387E3FFC9FFCDFF20FD46FBDBFEE9.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Cheironchus haurakiensis	<div><p>Cheironchus haurakiensis n. sp.</p><p>(Figures 1 &amp; 2, Table 1)</p><p>Diagnosis. Cheironchus haurakiensis n. sp. is characterised by cephalic setae 9–12 µm long, multispiral amphids with five turns, lateroventral mandibles 49–61 µm long with central arm curved distally and bearing 4–5 pointed projections, and each palm bearing 4–5 pointed projections, ten precloacal supplements in a 1 + 9 arrangement (posteriormost supplement 60 µm from 2nd posteriormost supplement and remaining supplements 33–43 µm apart), spicules 78 µm long, and blunt conical tail with thickened cuticle.</p><p>Etymology. This species is named after the type locality.</p><p>Material examined. Holotype male (NIWA 99777), collected 10 May 2015 (NIWA cruise TAN 1506, station 45), continental shelf off Hauraki coast, New Zealand (175.1495º E, 35.8243º S); water depth: 127 m. One paratype female (NIWA 99778), same data as holotype.</p><p>Description. Male Body cylindrical, stout. Cuticle 4–5 µm thick, gradually thickening posteriorly in tail region, up to 14 µm thick at posterior extremity (Fig. 2 B); transverse rows of punctations without lateral differentiation. Anteriormost punctations noticeably smaller on remainder of body. Somatic setae short and sparse, arranged irregularly. Head not set off from body. Mouth opening wide, surrounded by six fleshy, conical lips, each bearing a conical inner labial papilla terminally; labial region surrounded by cuticular fold. Six conical outer labial papillae, ~2 µm long, and four markedly longer cephalic setae (~0.3 cbd) situated in one circle. Amphideal fovea situated near anterior extremity, multispiral with 5.0–5.25 turns and circular outline. Anterior buccal cavity (cheilostom) small, cup shaped, with fine rugae. Posterior buccal cavity (pharyngostom) with three mandibles; lateroventral mandibles well-developed, with central arm and two lateral arms. Central arm curved distally and with four or five inward pointed projections; each palm with broad anterior portion bearing five (four in one case) pointed projections, and thin, pointed posterior portion (Fig. 1 B, C). Dorsal mandible short and difficult to distinguish, without differentiated anterior tip or palms. Pharynx short, muscular, with large, oval anterior bulb and smaller spherical posterior bulb. Nerve ring situated slightly posterior to middle of pharynx length. Cardia short, 9 µm long, not surrounded by intestinal tissue. Small renette cell present at level of cardia; excretory pore not observed.</p><p>Reproductive system diorchic with short outstretched testes (Fig. 2 C). Anterior and posterior testes both on right of intestine. Sperm cells globular to oval-shaped, ~5-6 × 9–10 mm. Spicules paired, curved, 1.5 cloacal body diameters long, with narrow, strongly curved proximal portion and pointed distal portion. Gubernaculum short, without crurae or apophyses. Mid-ventral row of ten cup-shaped precloacal supplements in a 1 + 9 arrangement; posteriormost and 2nd posteriormost supplements 60 µm apart, distance between other supplements 33–43 mm. Tail short, bluntly conical, with sparse, very short lateral, subventral, and subdorsal setae and three terminal setae. Caudal glands extending slight anterior to cloaca; spinneret present.</p><p>Females Similar to male. Reproductive system didelphic-amphidelphic with reflexed ovaries both on right side of intestine. Vulva situated slightly post-median. Proximal portion of vagina surrounded by constrictor muscle.</p><p>Species Cheironchus haurakiensis n. sp.</p><p>Male Female Holotype Paratype Differential diagnosis. Cheironchus haurakiensis n. sp. differs from most species of the genus except C. vorax in the shape of the tail, which is conical with blister in C. paravorax, conical and gradually tapering in C. conicaudatus, and conicocylindrical in C. dactylocaudatus . C. haurakiensis n. sp. resembles C. vorax in the shape and size of the lateroventral mandibles and spicules, and blunt conical tail, but can be differentiated from the latter in the number and arrangement of precloacal supplements (10 supplements in a 1 + 9 arrangement vs 12–20 regularly-spaced supplements in C. vorax). C. haurakiensis n. sp. also differs from the original description of C. vorax by Cobb (1917) and re-description by Tchesunov &amp; Okhlopkov (2006) from the western Atlantic coast by the shorter spicules (78 vs 113–125 mm) and higher values of c (32–38 vs 24–29).</p></div>	https://treatment.plazi.org/id/183387E3FFC9FFCDFF20FD46FBDBFEE9	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	Leduc, Daniel;Zhao, Zeng Qi	Leduc, Daniel, Zhao, Zeng Qi (2016): Molecular characterisation of five nematode species (Chromadorida, Selachinematidae) from shelf and upper slope sediments off New Zealand, with description of three new species. Zootaxa 4132 (1): 59-76, DOI: 10.11646/zootaxa.4132.1.5
183387E3FFCDFFCDFF20FDD5FA93FC88.text	183387E3FFCDFFCDFF20FDD5FA93FC88.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Halichoanolaimus De Man 1886	<div><p>Genus Halichoanolaimus De Man 1886</p><p>Diagnosis. (modified from Tchesunov (2014)) Cuticle with lateral differentiation in the form of larger and more widely spaced punctations. All anterior sensilla papilliform. Cuticularised rhabdions of anterior buccal cavity with pointed teeth (denticles) at posterior extremity. Pharynx without anterior or posterior bulb. Intestine of adult stages blind. Precloacal supplements papilliform or setiform (except in H. anisospermus n. sp.). Tail with conical proximal portion and often elongated cylindrical distal portion.</p><p>Synonym. Smalsundia Allgén, 1929 .</p><p>Remarks. A key to males of all 22 valid Halichoanolaimus species was provided by Zograf et al. (2015).</p></div>	https://treatment.plazi.org/id/183387E3FFCDFFCDFF20FDD5FA93FC88	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	Leduc, Daniel;Zhao, Zeng Qi	Leduc, Daniel, Zhao, Zeng Qi (2016): Molecular characterisation of five nematode species (Chromadorida, Selachinematidae) from shelf and upper slope sediments off New Zealand, with description of three new species. Zootaxa 4132 (1): 59-76, DOI: 10.11646/zootaxa.4132.1.5
183387E3FFCDFFC1FF20FC5FFBBCFDED.text	183387E3FFCDFFC1FF20FC5FFBBCFDED.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Halichoanolaimus anisospermus	<div><p>Halichoanolaimus anisospermus n. sp.</p><p>(Figures 3 &amp; 4, Table 2)</p><p>Diagnosis. Halichoanolaimus anisospermus n. sp. is characterised by having an amphideal fovea with six (males) or five turns (female) and ~0.9 cbd from anterior end, anterior portion of buccal cavity with cuticularised rhabdions terminating in three sets of seven pairs of teeth (denticles), with central pair of each set positioned above the other six, pore of secretory-excretory system situated slightly posterior to nerve ring, dimorphism in size of sperm cells between anterior and posterior testes, spicules 1.6–1.9 cloacal body diameters long, with gland protruding from proximal extremity, gubernaculum consisting of two detached lateral pieces (crurae) tapering distally, three small precloacal supplements present, consisting of slightly thickened and raised cuticle, and conicocylindrical tail with conical portion 32–38% of total tail length.</p><p>Etymology. The species name is derived from the Greek terms anisos (= unequal) and sperma (= seed), and refers to the dimorphism in the size of the sperm cells between the anterior and posterior testes.</p><p>Material examined. Holotype male (NIWA 99779), collected 8 May 2015 (NIWA cruise TAN 1506, station 14), upper continental slope off Hauraki coast, New Zealand (175.3163º E, 35.5402º S); water depth: 432 m. One paratype male and one paratype female (NIWA 99780, NNCNZ 3201), same data as holotype.</p><p>Description. Male Body cylindrical. Cuticle with transverse rows of punctations; lateral differentiation consisting of larger, more widely-spaced punctations. Somatic setae short, 1–2 µm long, sparse, irregularly arranged along body. Head rounded, with slight constriction immediately posterior to cephalic setae. Lip region not conspicuously differentiated. Six inner labial papillae; six short outer labial papillae, 2 µm long, at same level as four cephalic sensilla of similar length. Amphideal fovea multispiral with 6.0 turns, situated ~0.9 cbd from anterior end. Buccal cavity large, 21–28 µm deep, divided into anterior (cheilostom) and posterior portions (pharyngostom). Anterior portion of buccal cavity cup-shaped, with cuticularised rhabdions terminating in three sets of seven pairs of teeth (denticles), with central pair of each set positioned above the other six; posterior portion of buccal cavity narrower, cylindrical, surrounded by three Y-shaped pairs of cuticularised rhabdions. Pharynx cylindrical, muscular, without anterior or posterior bulb. Nerve ring at 40% of pharynx length from anterior. Secretory-excretory system present, renette cell small, 19 × 12 mm, situated at anterior extremity of intestine; ampulla small, pore situated slightly posterior to nerve ring.</p><p>Reproductive system diorchic with short outstretched testes. Anterior testis to the right or left of intestine, posterior testis on opposite side. Sperm cells globular, conspicuously larger in anterior testis (6–7× 8 mm) than in posterior testis (3–4 × 5–6 mm). Spicules paired, curved, tapering distally, 1.6–1.9 cloacal body diameters long, with gland protruding from proximal extremity; gubernaculum consisting of two detached lateral pieces (crurae) tapering distally, median portion of gubernaculum (corpus and cuneus) apparently absent. Three precloacal supplements present, consisting of slightly thickened and raised cuticle (Fig. 3 C). Tail conicocylindrical, conical portion 32–38% of total tail length; a few short and sparse somatic setae present. Caudal glands not observed, spinneret present.</p><p>*tail length was measured from, and anal body diameter at, the posterior-most extremity of the intestine.</p><p>Species Halichoanolaimus anisospermus n. sp. Bendiella longicauda n. sp.</p><p>Male Female Male Holotype Paratype Paratype</p><p>Female Similar to males but amphideal fovea slightly smaller with 5.0 turns. Reproductive system didelphicamphidelphic, with reflexed ovaries. Anterior ovary to the left of intestine and posterior ovary to the right of intestine. Vulva situated at mid-body. Mature eggs 22–26 × 26–27 mm. Proximal portion of vagina surrounded by constrictor muscle, vaginal glands not observed. Intestine blind, anus not observed.</p><p>Differential diagnosis. Halichoanolaimus anisospermus n. sp. differs from most other species of the genus by the unusual shape of the precloacal supplements, which are usually papilliform or setiform, but which consist of areas of slightly thickened and raised cuticle in this species. H. anisospermus n. sp. is most similar to H. macrophallus Gourbault &amp; Vincx, 1985 in the number of amphid turns, tail shape, and spicule shape, but differs from the latter by the markedly shorter spicules (45 vs 115 mm) and gubernaculum (13–14 vs 45 mm), and the number (3 vs 4) and shape of precloacal supplements. H. anisospermus n. sp. is also similar to H. brandtae Zograf et al., 2015 but can be distinguished from the latter by the different spicule size and shape (45 µm long with gland protruding from proximal extremity vs 81–94 µm long and without gland), number (3 vs 5) and shape of precloacal supplements, and absence of lateral rows of cuticular pores (present in H. brandtae).</p></div>	https://treatment.plazi.org/id/183387E3FFCDFFC1FF20FC5FFBBCFDED	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	Leduc, Daniel;Zhao, Zeng Qi	Leduc, Daniel, Zhao, Zeng Qi (2016): Molecular characterisation of five nematode species (Chromadorida, Selachinematidae) from shelf and upper slope sediments off New Zealand, with description of three new species. Zootaxa 4132 (1): 59-76, DOI: 10.11646/zootaxa.4132.1.5
183387E3FFC1FFC1FF20FDFCFE3BFC8A.text	183387E3FFC1FFC1FF20FDFCFE3BFC8A.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Bendiella Leduc 2013	<div><p>Genus Bendiella Leduc, 2013</p><p>Diagnosis. (from Leduc (2013)) Cuticle with lateral differentiation in the form of longitudinal rows of larger punctations. Outer labial sensilla and cephalic setae in one circle; cephalic setae slightly longer or of similar length to outer labial sensilla. Buccal cavity large; anterior portion of buccal cavity cylindrical to funnel-shaped, with twelve or fifteen cuticularised rhabdions, each with pointed projections at posterior extremity. Posterior buccal cavity narrower, cylindrical, surrounded by three Y-shaped pairs of rhabdions. Pre-cloacal supplements absent. Long conicocylindrical tail.</p></div>	https://treatment.plazi.org/id/183387E3FFC1FFC1FF20FDFCFE3BFC8A	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	Leduc, Daniel;Zhao, Zeng Qi	Leduc, Daniel, Zhao, Zeng Qi (2016): Molecular characterisation of five nematode species (Chromadorida, Selachinematidae) from shelf and upper slope sediments off New Zealand, with description of three new species. Zootaxa 4132 (1): 59-76, DOI: 10.11646/zootaxa.4132.1.5
183387E3FFC1FFC5FF20FC42FC20FD05.text	183387E3FFC1FFC5FF20FC42FC20FD05.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Bendiella longicauda	<div><p>Bendiella longicauda n. sp.</p><p>(Figures 5 &amp; 6, Table 2)</p><p>Diagnosis. Bendiella longicauda n. sp. is characterised by having a long body (length 2762 mm), two dorsosublateral rows of pores from midbody to level of cloaca, amphideal fovea with 4.5 turns, anterior portion of buccal cavity with three sets of five cuticularised rhabdions, each with two pairs of pointed projections at posterior extremity, except for central rhabdion of each set which bears two pairs of pointed projections and an additional central projection situated above the other four, rhabdions of posterior buccal cavity with numerous small denticles, spicules 2.1 cloacal body diameters long, tail 13.3 cloacal body diameters long, conicocylindrical, and with conical portion 8% of tail length.</p><p>Etymology. The species name is derived from the Latin longus (= long) and cauda (= tail), and refers to the length of the tail.</p><p>Material examined. Holotype male (NIWA 99781), collected 10 May 2015 (NIWA cruise TAN 1506, station 45), continental shelf off Hauraki coast, New Zealand (175.1495º E, 35.8243º S); water depth: 127 m.</p><p>Description. Male Body cylindrical. Cuticle with transverse rows of punctations, lateral differentiation beginning at one third of pharynx length from anterior extremity, consisting of three longitudinal rows of more widely spaced, larger punctations, gradually decreasing in size posteriorly from level of cloaca. Somatic setae short and sparse, 2 µm long, situated on either side of cuticle lateral differentiation (Fig. 6 C). Two dorsosublateral rows of pores visible from midbody to slightly posterior to level of cloaca (Figs. 5 E &amp; 6C). Head rounded, not set off. Six minute inner labial papillae; six small outer labial setae situated in same circle as four cephalic setae of similar length. Amphideal fovea multispiral with 4.5 turns, situated ~0.4 cbd from anterior extremity. Buccal cavity large, divided into anterior (cheilostom) and posterior portions (pharyngostom). Anterior portion of buccal cavity cylindrical to barrel-shaped, with three sets of five cuticularised rhabdions; each with two pairs or pointed projections at posterior extremity, except for central rhabdion of each set which bears two pairs of pointed projections and an additional central projection situated above the other four (Fig. 5 E). Posterior buccal cavity narrower, surrounded by three Y-shaped pairs of rhabdions fused from two thirds of distance from anterior end; posterior rhabdions with numerous small denticles near anterior extremity (Fig. 5 E). Pharynx cylindrical, muscular, without anterior or posterior bulb. Nerve ring at ~40% of pharynx length from anterior. Secretory-excretory system not observed.</p><p>Reproductive system diorchic with short, outstretched testes. Anterior testis on right of intestine, posterior testis on left of intestine; mature sperm cells round or globular, larger in anterior testis (11–13 × 23–27 mm) than posterior testis (8–9 × 8–9 mm). Spicules paired, 2.1 cloacal body diameters long, curved, tapering distally. Gubernaculum consisting of two detached lateral pieces (crurae) tapering distally; median portion of gubernaculum (corpus and cuneus) apparently absent. Four ventral setae present immediately anterior to cloaca; precloacal supplements absent. Tail long, conicocylindrical; conical portion short, 8% of tail length, with few, sparse setae. Caudal glands not observed.</p><p>Differential diagnosis. Bendiella longicauda n. sp. can be differentiated from the only other species of the genus, B. thalassa Leduc, 2013, by the larger body size (2762 vs 975–1118 mm), higher value of a (38 vs 28–34), presence of cuticle pores (absent in B. thalassa), fewer amphid turns (4.5 vs 5.25), presence of denticles on posterior rhabdions (vs no denticles in B. thalassa), longer spicules (2.1 vs 1.4 cloacal body diameters), dimorphism in sperm size between anterior and posterior testes (no dimorphism in B. thalassa), and longer tail (13.3 vs 7.0 cloacal body diameters).</p><p>Molecular sequence data. The SSU and D2–D3 of LSU phylogenetic trees comprised 15 and 11 sequences, respectively (Figs 7 &amp; 8). In the SSU tree, Cheironchus haurakiensis n. sp. was the most divergent sequence and was placed well away from the other two Cheironchus sequences. This degree of divergence among Cheironchus sequences is somewhat surprising given the close morphological similarities among species of this genus, however it is not possible to ascertain the identity of the other Cheironchus sequences due to lack of vouchers (Armenteros et al. 2014). In the D2–D3 of LSU tree, Cheironchus haurakiensis n. sp. was placed in a clade together with Choanolaimus and Latronema (subfamily Choniolaiminae) and well away from Pseudocheironchus and Synonchiella (Selachinematinae) . Pseudocheironchus ingluviosus and Synonchiella rotundicauda appear to be relatively closely related (89% posterior probability support in D2–D3 of LSU tree), although the genus Synonchiella is polyphyletic according to the SSU tree. These data do not support the monophyly of the two selachinematid subfamilies, which is consistent with the findings of Leduc &amp; Zhao (2015).</p><p>Analyses of SSU and D2–D3 of LSU sequences suggest a close relationship between Halichoanolaimus anisospermus n. sp. and Bendiella longicauda n. sp. (100% posterior probability support in the D2–D3 of LSU tree), consistent with the close morphological similarities between the two genera. In the SSU tree, Bendiella longicauda n. sp. differed from Halichoanolaimus dolichurus by 1% (12 in 850 base pairs including zero gap). In the D2–D3 of LSU tree, Bendiella longicauda n. sp. differed from Halichoanolaimus anisospermus n. sp. by 29% (141 in 747 base pairs including 28 gaps).</p><p>The sequences provided herein are the first sequences obtained from beyond subtidal depths for the Selachinematidae . Our preliminary analyses do not provide evidence of clustering according to depth (intertidal/ subtidal vs shelf/upper slope) or geographical location (New Zealand vs Northern Hemisphere). The number of available Selachinematidae sequences, however, remains limited and comprehensive analyses based on a larger number of sequences will be necessary to provide more solid conclusions.</p></div>	https://treatment.plazi.org/id/183387E3FFC1FFC5FF20FC42FC20FD05	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	Leduc, Daniel;Zhao, Zeng Qi	Leduc, Daniel, Zhao, Zeng Qi (2016): Molecular characterisation of five nematode species (Chromadorida, Selachinematidae) from shelf and upper slope sediments off New Zealand, with description of three new species. Zootaxa 4132 (1): 59-76, DOI: 10.11646/zootaxa.4132.1.5
