identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
03B0650E4E2BFFE79695FAB8FA7AFA57.text	03B0650E4E2BFFE79695FAB8FA7AFA57.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Pseudosyllis Grube 1863	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> PSEUDOSYLLIS GRUBE, 1863</p>
            <p> Pseudosyllis Grube, 1863: 44 . </p>
            <p> Trypanosyllis Claparede, 1864 (partim). </p>
            <p> Type species:  Pseudosyllis brevipennis Grube, 1863 . </p>
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	https://treatment.plazi.org/id/03B0650E4E2BFFE79695FAB8FA7AFA57	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.		Plazi	Álvarez-Campos, Patricia;Giribet, Gonzalo;San Martín, Guillermo;Rouse, Greg W.;Riesgo, Ana	Álvarez-Campos, Patricia, Giribet, Gonzalo, San Martín, Guillermo, Rouse, Greg W., Riesgo, Ana (2017): Straightening the striped chaos: systematics and evolution of Trypanosyllis and the case of its pseudocryptic type species Trypanosyllis krohnii (Annelida, Syllidae). Zoological Journal of the Linnean Society 179 (3): 492-540, DOI: 10.1111/zoj.12443, URL: https://doi.org/10.1111/zoj.12443
03B0650E4E2BFFEC964AFA71FE73F998.text	03B0650E4E2BFFEC964AFA71FE73F998.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Pseudosyllis brevipennis Grube 1863	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> PSEUDOSYLLIS BREVIPENNIS GRUBE, 1863</p>
            <p>FIGS 6A – D, 7</p>
            <p> Trypanosyllis coeliaca Claparede, 1868 , 19(2): 203; San Martın, 2003: 308 – 311, Figs 169, 170. </p>
            <p>Type material examined</p>
            <p>
                  Neotype:  
                <a title="Search Plazi for locations around (long 13.616667/lat 45.066666)" href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=13.616667&amp;materialsCitation.latitude=45.066666">Rovigno</a>
                 , Croatia (45.066667, 13.616667): one specimen mounted on a slide (ZMB 797), 1912, coll. Heider (Figs 6A, B). 
            </p>
            <p>Other material examined</p>
            <p>
                 Rovigno, Croatia:  two specimens mounted on slides (ZMB 7978 a, ZMB 7978 b), collection details as for the neotype. Spain, Catalonia :   one specimen in 96% EtOH (MNCN / ADN 9622), Port de la Selva (42.3375, 3.203333),  Posidonia oceanica , 10 m, 21 September 2004, no collector data  ;  two specimens in 96% EtOH (MNCN 16.01 /16041, 16176), Barcelona, Mataro (41.5325, 2.453056), intertidal algae, March 2014, leg. M. Ballesteros ;  one specimen mounted for SEM (MNCN 16.01 /16177) Girona, Cap Falco (42.433333, 3.174722), calcareous algae, 15 September 2011, leg. G. San Martın (Figs 5C – D, 8). Spain , Alboran Sea:   one specimen in 96% EtOH (MNCN 16.01 /16040), (42.433333, 3.174722), algae, 42 – 48 m, 21 September 2011, leg. A. Luque and Alboran-INDEMARES  
                <a title="Search Plazi for locations around (long 3.174722/lat 42.433334)" href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=3.174722&amp;materialsCitation.latitude=42.433334">Oceanographic Campaign</a>
                 collecting team  ;   one specimen in 10% formalin buffered in seawater (MNCN 16.01 / 16178), (35.983333, 2.916667), calcareous algae, 68 – 70 m, 24 September 2011, leg. A. Luque AlboranINDEMARES  
                <a title="Search Plazi for locations around (long 2.916667/lat 35.983334)" href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=2.916667&amp;materialsCitation.latitude=35.983334">Oceanographic Campaign</a>
                 collecting team  ;   one specimen in 10% formalin buffered in seawater (MNCN 16.01 /16079), (35.878667, 3.077833), calcareous algae, 96 – 100 m, Alboran-INDEMARES  
                <a title="Search Plazi for locations around (long 3.077833/lat 35.878666)" href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=3.077833&amp;materialsCitation.latitude=35.878666">Oceanographic Campaign</a>
                 collecting team  . 
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            <p>Diagnosis</p>
            <p>Body of medium to small size (up to about 12 mm long) without colour pattern. Short appendages, relatively thick, with few articles (Figs 6A, 7A). Bidentate chaetae with similar teeth; with spines along margin, distalmost spines reaching the distalmost tooth (Figs 6B – D, 7B). Proventricle shorter than pharynx, occupying two or three segments (Fig. 6A). Reproduction by single tetraglene stolon (San Martın, 2003).</p>
            <p>Description</p>
            <p>Neotype, complete specimen: 5 mm long, 0.5 mm wide, 51 chaetigers, without distinct colour pattern (Fig. 6A). Oval prostomium with two pairs of eyes in trapezoidal arrangement, anterior eyes slightly larger (Figs 6A, 7A); antennae originating on anterior margin of prostomium; long median antenna with about eight articles; lateral antennae shorter, with about six articles. Oval palps shorter, completely separate. Nuchal organs as two densely ciliated semicircular areas, surrounding prostomial lobes (Fig. 7A). Segment 1 slightly smaller than subsequent segments; dorsal enlarged anterior cirri similar in length to antennae, with eight or nine articles; ventral cirri shorter with between four and six articles. Dorsal cirri similar in length to median antenna, with seven or eight articles (Figs 6A, 7A). Anterior segments with two rows of cilia, reaching cirrophores (Fig. 7A). Between ten and 12 compound bidentate, heterogomph falcigers in anterior and midbody segments, and seven or eight in posterior parapodia. All compound chaetae morphologically similar throughout body, bidentate, with distal tooth slightly larger than proximal one, and spines along margin, most distal ones larger and reaching distal tooth (Figs 6B – D, 7B). All parapodia with two protruding, acuminate, and thick aciculae (Fig. 7C). Dorsal and ventral simple chaetae not seen. Pharynx through about six segments, with an anterior tooth and a trepan with between eight and ten small teeth (Fig. 6A). Proventricle through three segments, with about 22 muscle cell rows (Fig. 6A). Reproduction by a single cephalous stolon with two pairs of eyes.</p>
            <p>Remarks</p>
            <p> San Mart � ın (2003) considered that  Trypanosyllis coeliaca Claparede, 1868 (type-locality, Naples, W Mediterranean) and  Pseudosyllis brevipennis Grube, 1863 (type-locality: Adriatic Sea) were synonymous species. Although the author noted that  Pseudosyllis Grube, 1863 had priority over  Trypanosyllis Claparede, 1864 ; he considered  Pseudosyllis as a nomen dubium, and therefore the species was named as  Trypanosyllis coeliaca for stability purposes (see remarks in San Mart � ın, 2003). Our study shows that  Trypanosyllis coeliaca , as traditionally considered, belongs to a different genus, more closely related to the genera  Xenosyllis ,  Eurysyllis , and  Plakosyllis (Figs 1, 2, 5). These results agree with the morphological features: all species included in these four genera share a small body size, short cirri and proventricle, and a trepan with minute teeth, except for  Xenosyllis , the trepan of which was secondarily lost. In addition, the species presented a large spine on the chaetae margin that is unique compared with other species of  Trypanosyllis . Therefore, we reinstate  Pseudosyllis (following ICZN requirements) to include the former  Trypanosyllis coeliaca , which should now be considered  Pseudosyllis brevipennis , the type and unique species of the genus. One of the specimens examined from the Museum f ur € Naturkunde (Berlin) from the type locality (Croatia) agrees with the characters described by Grube (1863) and also in the morphological features examined in our specimens. Since the type material is lost, we have designated a neotype for the species (ZMB 7978), but further molecular studies are required to test if the specimens collected in the Spanish coasts are the same species as the specimens from the type locality. The other two specimens examined from the ZMB, identified as  Trypanosyllis coeliaca (slides ZMB 7978a and ZMB 7978b), belonging to the same locality, might represent a different species because they have shorter chaetae with a minute proximal tooth and without spines on the margin. Nevertheless, they also share some of the morphological characters defined for  Pseudosyllis species , so it will be necessary to sequence and compare specimens of these two morphotypes from Croatia to assess if they are different species. In addition, in order to check the status of  Trypanosyllis coeliaca , further molecular studies are required including material from Naples (the type locality). Although  Pseudosyllis is currently monotypic, there are also other species traditionally considered within  Trypanosyllis that could also belong to  Pseudosyllis , as they share the synapomorphies identified for the group. This is the case for  Trypanosyllis parvidentata Perkins, 1981 from Florida (Perkins, 1981) and  Trypanosyllis microdenticulata Salcedo-Oropeza , San Martın &amp; Solis-Weiss, 2011, from the southern Mexican Pacific coast (Salcedo-Oropeza et al., 2011). Further molecular analyses are still needed in order to test whether  Trypanosyllis parvidentata and  Trypanosyllis microdenticulata are more closely related to  Pseudosyllis brevipennis than to species within  Trypanosyllis , and therefore to establish the status of  Pseudosyllis brevipennis s.s.</p>
            <p>Type locality</p>
            <p>Rovigno, Croatia (Adriatic Sea).</p>
            <p>Distribution</p>
            <p>Mediterranean Sea.</p>
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	https://treatment.plazi.org/id/03B0650E4E2BFFEC964AFA71FE73F998	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.		Plazi	Álvarez-Campos, Patricia;Giribet, Gonzalo;San Martín, Guillermo;Rouse, Greg W.;Riesgo, Ana	Álvarez-Campos, Patricia, Giribet, Gonzalo, San Martín, Guillermo, Rouse, Greg W., Riesgo, Ana (2017): Straightening the striped chaos: systematics and evolution of Trypanosyllis and the case of its pseudocryptic type species Trypanosyllis krohnii (Annelida, Syllidae). Zoological Journal of the Linnean Society 179 (3): 492-540, DOI: 10.1111/zoj.12443, URL: https://doi.org/10.1111/zoj.12443
03B0650E4E20FFEE95F7F92FFD12FABD.text	03B0650E4E20FFEE95F7F92FFD12FABD.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Trypanedenta Imajima & Hartman 1964	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> TRYPANEDENTA IMAJIMA &amp; HARTMAN, 1964 ; </p>
            <p>FIGS 6E – I, 8, 9</p>
            <p> Trypanosyllis (Trypanedenta) Imajima &amp; Hartman : 125. </p>
            <p> Trypanosyllis Claparede, 1864 (partim). </p>
            <p> Type species:  Trypanosyllis gemmipara Johnson, 1901 . </p>
            <p>Diagnosis</p>
            <p>Body variable in size, from 7 mm to more than 80 mm in length, and from 1 mm to 5 mm wide, with uniform yellowish coloration (Figs 6E, G). Unidentate or bidentate chaetae, without serration in margin or with a few, minute spines (Fig. 6F, I). Reproduction by clusters of several simultaneous tetraglene stolons (Fig. 6G, H).</p>
            <p>Remarks</p>
            <p> Trypanedenta was considered a subgenus of  Trypanosyllis , because of the lack of a middorsal tooth in the pharynx (Imajima &amp; Hartman, 1964). Our study concluded that  Trypanedenta Imajima &amp; Hartman, 1964 should be raised to genus level, although the synapomorphies for the group require a re-evaluation of pharyngeal teeth during ontogeny (San Martın, 2003). Indeed, the type of reproduction, which differs from that in the other genera analysed, seems to be one of the most important features to differentiate this genus from the remaining genera. Both species included in the genus,  Trypanedenta gemmipara comb. nov. and  Trypanedenta gigantea comb. nov. , present more than one stolon during their reproductive stages.  Trypanedenta gemmipara comb. nov. develops a cluster of stolons (Johnson, 1901; Imajima &amp; Hartman, 1964; Imajima, 1966), whereas  Trypanedenta gigantea comb. nov. forms a chain of stolons (first report, this paper; Fig. 6G). Another character that seems to be important for the diagnosis of the genus is the presence of chaetae with just a few small spines on the margin (  Trypanedenta gigantea comb. nov. ) or none (  Trypanedenta gemmipara comb. nov. ) (Figs 6F, I, 8E – F, 9F – H). Further molecular studies are required to assess if other species currently included within  Trypanosyllis , presenting similar chaetae and more than one stolon during their reproductive stage, actually belong to  Trypanedenta . That may be the case for  Trypanosyllis ingens Johnson, 1902 ,  Trypanosyllis sanmartini Cinar, 2007 , and  Trypanosyllis auranticus Nogueira &amp; Fukuda, 2008 (Johnson, 1902; Cinar, 2007; Nogueira &amp; Fukuda, 2008). In addition, the budding of numerous simultaneous stolons has also been observed in  Trypanobia asterobia Okada, 1933 , but the relationship between the recently resurrected genus  Trypanobia Imajima &amp; Hartman, 1964 (Aguado et al., 2015) and  Trypanedenta needs further study. </p>
            <p>Distribution</p>
            <p>Cosmopolitan.</p>
            <p> TRYPANEDENTA GEMMIPARA (JOHNSON, 1901)</p>
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	https://treatment.plazi.org/id/03B0650E4E20FFEE95F7F92FFD12FABD	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.		Plazi	Álvarez-Campos, Patricia;Giribet, Gonzalo;San Martín, Guillermo;Rouse, Greg W.;Riesgo, Ana	Álvarez-Campos, Patricia, Giribet, Gonzalo, San Martín, Guillermo, Rouse, Greg W., Riesgo, Ana (2017): Straightening the striped chaos: systematics and evolution of Trypanosyllis and the case of its pseudocryptic type species Trypanosyllis krohnii (Annelida, Syllidae). Zoological Journal of the Linnean Society 179 (3): 492-540, DOI: 10.1111/zoj.12443, URL: https://doi.org/10.1111/zoj.12443
03B0650E4E24FFE8968AFF70FC77FC54.text	03B0650E4E24FFE8968AFF70FC77FC54.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Trypanosyllis Claparede 1864	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> TRYPANOSYLLIS CLAPAREDE, 1864</p>
            <p> Trypanosyllis Claparede, 1864: 558 . </p>
            <p> Parautolytus Pillai, 1965: 123 . </p>
            <p> Type species:  Trypanosyllis krohnii Claparede, 1864 . </p>
            <p>Diagnosis</p>
            <p>As in San Martın et al. (2008).</p>
            <p>Remarks</p>
            <p> Although Imajima &amp; Hartman (1964) divided the genus into four subgenera, based on body shape, type of chaetae, and the presence of a pharyngeal tooth, most authors did not follow this classification, arguing that these features depended on the ontogeny (e.g., San Martın, 2003; Cinar, 2007; Nogueira &amp; Fukuda, 2008; San Martın et al., 2008). Our results show that  Trypanosyllis s.l. contains at least two clades, which we have designated as genera:  Trypanedenta Imajima &amp; Hartman, 1964 and  Pseudosyllis Grube, 1863 . These genera differ from  Trypanosyllis s.s. in the type of chaetae, body size, length of cirri, and reproductive mode (see remarks above). </p>
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	https://treatment.plazi.org/id/03B0650E4E24FFE8968AFF70FC77FC54	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.		Plazi	Álvarez-Campos, Patricia;Giribet, Gonzalo;San Martín, Guillermo;Rouse, Greg W.;Riesgo, Ana	Álvarez-Campos, Patricia, Giribet, Gonzalo, San Martín, Guillermo, Rouse, Greg W., Riesgo, Ana (2017): Straightening the striped chaos: systematics and evolution of Trypanosyllis and the case of its pseudocryptic type species Trypanosyllis krohnii (Annelida, Syllidae). Zoological Journal of the Linnean Society 179 (3): 492-540, DOI: 10.1111/zoj.12443, URL: https://doi.org/10.1111/zoj.12443
03B0650E4E24FFEA9652FC75FC5FFA4D.text	03B0650E4E24FFEA9652FC75FC5FFA4D.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Trypanosyllis krohnii Claparede 1864	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> TRYPANOSYLLIS KROHNII CLAPAREDE, 1864 ; </p>
            <p>FIGS 4B, 10A, 11</p>
            <p>Type material examined</p>
            <p>
                  Neotype. France,  
                <a title="Search Plazi for locations around (long 3.133333/lat 42.483334)" href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=3.133333&amp;materialsCitation.latitude=42.483334">Banyuls-sur-Mer</a>
                 (42.483333, 3.133333): one specimen in 96% EtOH (MNCN ADN/ 9623), Harbour on docks, snorkelling, epifauna on mussels (i.e. hydroids, sponges), 19 April 2001, no collector data (Fig. 9A). 
            </p>
            <p>Other material examined</p>
            <p>
                 Spain, Catalonia: one specimen in 96% EtOH (MNCN 16.01 /16187), Barcelona, Mataro (41.5325, 2.453056), intertidal algae, March 2014, leg. M. Ballesteros ;   one specimen in 96% EtOH (MNCN 16.01 /16066), Girona,  
                <a title="Search Plazi for locations around (long 3.320556/lat 42.32028)" href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=3.320556&amp;materialsCitation.latitude=42.32028">Cap de Creus</a>
                 (42.320278, 3.320556),  Petrosia sp. , 16 m, 16 September 2011, leg. G. San Martın  ;  one specimen mounted for SEM (MNCN 16.01 /16186), collection data as for MNCN 16.01/16066; four midbody parts (MNCN 16.01 / 16188), collection data as for MNCN 16.01/16066 . 
            </p>
            <p>Morphologically similar species examined</p>
            <p>  Italy:  Trypanosyllis zebra , one specimen (ZMB Q4428), Lesina (41.766667, 15.433333), 1874, leg. Grube.  Lessina coll. Grube. </p>
            <p>Diagnosis</p>
            <p>Colour pattern in preserved specimens as brown transverse stripes across anterior and midbody parts, one close to anterior end of segment and the other in middle of segment (Figs 4B, 10A). All stripes similar in length, reaching parapodia (Figs 4B, 10A). Large anterior cirri with about 42 articles (n = 5); dorsal cirri alternating long (30 – 32 articles) and short (20 – 22 articles).</p>
            <p>Description</p>
            <p>Neotype incomplete, 8 mm long, 1.5 mm wide, 83 chaetigers. Long dorsoventrally flattened body (Figs 10A, 11A). Colour pattern as two thin, brown, transverse stripes across limit of anterior and midbody segments (Fig. 10A). Some specimens with purple pigmentation remaining on anterior and dorsal cirri (Fig. 4B). Oval prostomium with two pairs of eyes in trapezoidal arrangement (Fig. 10A); antennae originating on anterior margin of prostomium, long median antenna with about 30 articles; lateral antennae slightly shorter, with about 25 articles (Fig. 10A, 11A, B). Oval palps shorter than prostomium, completely separated. Nuchal organs as two densely ciliated semicircular areas, extending on prostomium and surrounding prostomial lobes. In addition, ciliary bands on dorsum of anterior and midbody segments and parapodia (Fig. 11C). Segment 1 slightly smaller than subsequent segments; dorsal enlarged anterior cirri longer than antennae, with about 42 articles, longer than ventral cirri, with about 35 articles Dorsal cirri alternating long (30 – 32 articles) and short (20 – 22 articles). Ventral digitiform cirri, reaching edge of parapodia. Parapodia with two anterior, digitiform lobes. Compound bidentate, heterogomph falciger chaetae, about 15 – 17 on anterior parapodia, 13 – 15 on midbody and 12 – 14 on posterior ones. All chaetae similar throughout body, with both teeth similar in length and serrated margin (Fig. 11D – G); all parapodia with dorsal chaetae with longer blades and very short spines on the margin (Fig. 11D, F), and ventral bidentate chaetae, shorter than ventral chaetae, with minute spines on the margin of anterior and midbody chaetae (Fig. 11E), and almost smooth on posterior parapodia (Fig. 11G). Three or four anterior straight aciculae, all distally blunt; two or three midbody and posterior straight, distally pointed aciculae thicker than anterior aciculae. Dorsal and ventral simple chaetae not seen. Pharynx running through 11 segments. Proventricle running through 13 segments, with about 40 muscle cell rows.</p>
            <p>Remarks</p>
            <p> Trypanosyllis , together with the species  Trypanosyllis krohnii , were described by Claparede (1864) from Port-Vendres (France). Four years earlier,  Syllis zebra Grube, 1860 was described from the Adriatic Sea, and Marenzeller (1874) later placed it in  Trypanosyllis because it presented a trepan. In 1879, Langerhans synonymized  Trypanosyllis krohnii with  Trypanosyllis zebra on the basis of the original descriptions, without studying the type specimens (subjective synonymy, ICZN, article 61.3). All subsequent authors followed this synonymy, probably because of the similarity in the striped coloration found in both species. Many years later Hartman (1959) designed  Trypanosyllis zebra as the type species of the genus by subsequent designation (ICZN, article 69.1), and since then all the authors except Day (1967) considered this designation as valid (e.g., Imajima, 1966; Uebelacker, 1984; San Mart � ın, 2003). Our study found that Hartman’s designation is in fact not valid, because Claparede (1864) described the genus  Trypanosyllis and its monotypic type species  Trypanosyllis krohnii (ICZN, art 68.3), which is a valid species. Lineage 6, which inhabits the same geographical areas as the type species, presented enough distinctive morphological features to separate them, such as the colour pattern, the length of the dorsal cirri, and the body width (Fig. 10A, I; Table 3). In addition, the comparative material from the Adriatic deposited in the ZMB, which was collected in 1874 and identified by Grube as  Syllis zebra , also differed from lineage 6 in the same characters (Fig. 10C, I; Table 3), but was slightly more similar to  Trypanosyllis krohnii than lineage 6 (Fig. 10A, C; Table 3). The ZMB specimen did not fully agree with the original description of  Trypanosyllis zebra Grube (1860) , mainly because of the huge size of the holotype described by Grube (Table 3), and therefore we prefer not to designate it as the neotype of  Trypanosyllis zebra . Likewise, even though this ZMB specimen is similar to  Trypanosyllis krohnii , we cannot synonymize them because we have not sequenced this material. Therefore, until new material of striped  Trypanosyllis from the Adriatic is collected for further sequencing, we will regard our specimens in lineage 6 as  Trypanosyllis sp. 2 . </p>
            <p> Nevertheless, here we conclude that  Trypanosyllis krohnii is not a synonym of  Trypanosyllis zebra , but a valid and well-defined species distributed at least in the Gulf of Lion and along the north-west coast of Spain (Tables 1 and 3). In the present study we re-describe the type species of the genus, designating a neotype (as the type material is lost) following the ICZN requirements. The studied specimens agree with the original description, except for the colouration, which Claparede (1864) described as violet. As we have observed remnants of violet pigmentation in the anterior and midbody cirri of some specimens (Fig. 4B), we conclude that the coloration differences may be the result of preservation methods. Our results also suggest that the species is distributed in the same area (Gulf of Lion) as  Trypanosyllis sp. 2 , but inhabiting different bathymetric ranges, with  Trypanosyllis krohnii occurring in more shallow waters (Table 3). Marion &amp; Bobretzky (1875) reported  Trypanosyllis krohnii from the Gulf of Marseille, noting that specimens collected in shallow waters presented body coloration and length of cirri that differed considerably from those of specimens collected in deeper waters, although they considered both as the same species. Our examination agrees with their observation, and thus we conclude that there is enough molecular, morphological, and ecological evidence to consider them as two different species. </p>
            <p>Type locality</p>
            <p>Banyuls-sur-Mer, France (North-Western Mediterranean Sea).</p>
            <p>Distribution</p>
            <p>Gulf of Lion (Mediterranean Sea), including the Cap de Creus, in the north-eastern coast of Spain (Girona).</p>
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	https://treatment.plazi.org/id/03B0650E4E24FFEA9652FC75FC5FFA4D	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.		Plazi	Álvarez-Campos, Patricia;Giribet, Gonzalo;San Martín, Guillermo;Rouse, Greg W.;Riesgo, Ana	Álvarez-Campos, Patricia, Giribet, Gonzalo, San Martín, Guillermo, Rouse, Greg W., Riesgo, Ana (2017): Straightening the striped chaos: systematics and evolution of Trypanosyllis and the case of its pseudocryptic type species Trypanosyllis krohnii (Annelida, Syllidae). Zoological Journal of the Linnean Society 179 (3): 492-540, DOI: 10.1111/zoj.12443, URL: https://doi.org/10.1111/zoj.12443
03B0650E4E26FFD49652FA1CFCF2FF25.text	03B0650E4E26FFD49652FA1CFCF2FF25.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Trypanosyllis aeolis Langerhans 1879	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> TRYPANOSYLLIS AEOLIS LANGERHANS, 1879 ; </p>
            <p>FIGS 10B, 12A, B</p>
            <p> Trypanosyllis aeolis Langerhans, 1879: 558 , figs 18a, b; N u � nez ~ et al., 1992: 114; San Mart � ın, 2003: 315, figs 174 – 176. </p>
            <p>Material examined</p>
            <p>
                  Spain,  
                <a title="Search Plazi for locations around (long 2.4809/lat 39.4891)" href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=2.4809&amp;materialsCitation.latitude=39.4891">Mallorca</a>
                 , El Toro Island (39.4891, 2.4809): three specimens in 96% EtOH (MNCN 16.01 /16039, 16180, 16181),  Cladocora cespitosa and Miriapora sp., 12 m, 18 June 2012, leg. P. Alvarez-Campos  � and M. Capa.   Australia, QLD,  
                <a title="Search Plazi for locations around (long 145.45084/lat 14.657222)" href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=145.45084&amp;materialsCitation.latitude=14.657222">Lizard Island</a>
                 , Watsons Bay (14.657222, 145.450833): one specimen in 96% EtOH (AM W.41717), coral rubble, 4.5 m, 28 August 2010, leg. P. Hutchings and M. Capa. 
            </p>
            <p>Diagnosis</p>
            <p>Uniform pale pink coloration, with yellow dorsal cirri (Fig. 10B); compound bidentate chaetae, with small proximal tooth; sometimes blades unidentate on posterior parapodia (Fig. 12B).</p>
            <p>Description</p>
            <p>Longest complete specimen (MNCN 16.01/16039), 10 mm long, 1.2 mm wide, 65 chaetigers. Pale pink body coloration with yellow pigmentation in some cirri (Fig. 10B). Oval posteriorly bilobed prostomium (Figs 10B, 12A); two prostomial lobes, with two pairs of red eyes in trapezoidal arrangement (Fig. 10B). Oval palps slightly shorter than prostomium, completely separate. Nuchal organs as two densely ciliated semicircular areas, surrounding the eyes (Fig. 12A). Antennae originating on anterior margin of prostomium, median antenna long, with about 23 articles; lateral antennae distinctly shorter, with about 15 articles (Figs 10B, 12A). Segment 1 slightly shorter than subsequent segments; dorsal enlarged anterior cirri slightly longer than antennae, with about 25 articles, longer than ventral cirri, with about 20 articles. Anterior dorsal cirri as long as median antenna (25 articles); midbody and posterior dorsal cirri shorter, with 20 and 15 articles, respectively. Ventral cirri digitiform, shorter than parapodia. Compound bidentate heterogomph falciger chaetae with both teeth similar in length and with a few and minute spines on margin (Fig. 12B, C). About 13 or 14 chaetae on anterior parapodia (Fig. 12B), and with between eight and ten chaetae on midbody and posterior parapodia (Fig. 12C). One unique, thick, and straight aciculae protruding from each parapodia (Fig. 12B). Pharynx through about ten segments; trepan with eight teeth. Proventricle similar in length to pharynx, through nine segments, with about 22 muscle cell rows.</p>
            <p>Remarks</p>
            <p> See remarks for  Trypanedenta gemmipara comb. nov. One of the specimens of  Trypanosyllis aeolis analysed is from Australia, and even though we have not been able to find morphological differences with the specimens from the Iberian Peninsula, because of their disjunct distribution this may represent another case of cryptic speciation. </p>
            <p>Type locality</p>
            <p>Madeira (Atlantic Ocean).</p>
            <p>Distribution</p>
            <p>Pacific Ocean (Washington, USA); north-eastern Atlantic Ocean (UK, Portugal, and Spain); Mediterranean Sea, including Adriatic and Aegean seas.</p>
            <p> TRYPANOSYLLIS LUZONENSIS (PILLAI, 1965) COMB.</p>
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	https://treatment.plazi.org/id/03B0650E4E26FFD49652FA1CFCF2FF25	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.		Plazi	Álvarez-Campos, Patricia;Giribet, Gonzalo;San Martín, Guillermo;Rouse, Greg W.;Riesgo, Ana	Álvarez-Campos, Patricia, Giribet, Gonzalo, San Martín, Guillermo, Rouse, Greg W., Riesgo, Ana (2017): Straightening the striped chaos: systematics and evolution of Trypanosyllis and the case of its pseudocryptic type species Trypanosyllis krohnii (Annelida, Syllidae). Zoological Journal of the Linnean Society 179 (3): 492-540, DOI: 10.1111/zoj.12443, URL: https://doi.org/10.1111/zoj.12443
03B0650E4E1CFFD29435F9B1FDEFFE19.text	03B0650E4E1CFFD29435F9B1FDEFFE19.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Trypanosyllis californiensis Álvarez-Campos & Giribet & San Martín & Rouse & Riesgo 2017	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> TRYPANOSYLLIS CALIFORNIENSIS</p>
            <p> ALLVAREZ- CAMPOS &amp; ROUSE  SP. NOV.</p>
            <p>FIGS 10H, 15D – F</p>
            <p>Type material examined</p>
            <p> Holotype. California: specimen in 96% EtOH (SIO A5008), La Jolla, San Diego (32.866944, 117.255833), kelp holdfast, 5 m, 18 April 2014, leg. G.W. Rouse.</p>
            <p> Paratypes. California: one specimen mounted for SEM (SIO A5007), collection data as for the holotype ;  two specimens in 96% EtOH (SIO A5006, 5009), La Jolla, San Diego (32.866944, 117.255833), algae, 0 m, 18 April 2014, leg. G.W. Rouse.</p>
            <p>Diagnosis</p>
            <p> Similar to  Trypanosyllis krohnii except for pigmentation and body size (Fig. 10H). Dark-brown transverse stripes across anterior segments of living specimens. Fixed material appears red/pink with dark red – purple stripes: anterior stripe is situated close to anterior end of segment, whereas posterior stripe appears slightly before end of segment (anterior and posterior stripes appear as two close lines per segment, but, in fact, are on different segments; Fig. 10H). Appendages also with pigmentation only in limit of each article. </p>
            <p>Description</p>
            <p>Holotype incomplete: 12 mm long, 0.8 mm wide, 76 chaetigers. Body coloration in live specimens white/ pale, with two dark-brown thin transverse stripes across anterior and midbody segments of live specimens (Fig. 10H). Fixed material appeared red pigmented with dark red – purple stripes. Anterior stripe situated only in anterior end of segment, whereas posterior stripe slightly precedes posterior end of segment (Fig. 9H). Appendages also with pigmentation in limit of each article. Oval prostomium with two pairs of red eyes in trapezoidal arrangement (Fig. 10H). Oval palps shorter than prostomium, completely separate. Nuchal organs not seen. Segment 1 slightly smaller than subsequent segments; antennae originating on anterior margin of prostomium, median antenna with about 20 articles; lateral antennae slightly shorter, with 15 – 17 articles. Dorsal enlarged anterior cirri longer than antennae, with about 32 articles, much longer than ventral cirri, with about 17 articles. Dorsal cirri alternating between long (30 – 32 articles) and short (20 – 22 articles). Dorsal cirri of the anteriormost segments slightly longer than the rest, with 34 – 36 articles. Ventral digitiform cirri, shorter than parapodia. Compound bidentate heterogomph falciger chaetae with spines on margin, with between eight and ten spines per parapodium (Fig. 15D – F), similar throughout body, except in most posterior parapodia, that are shorter (Fig. 15F). Two or three thick, acutely pointed aciculae in all segments. Dorsal and ventral simple chaetae not seen. Pharynx through about 14 segments, proventricle through 11 segments, with about 30 muscle cell rows.</p>
            <p>Remarks</p>
            <p> The examined specimens of  Trypanosyllis californiensis sp. nov. collected in La Jolla differ markedly from those of  Trypanosyllis luquei sp. nov. , collected from San Diego Bay, in length of dorsal cirri (32 and 20 articles in the former, 20 and 14 articles the latter; four and three specimens from each species) and in coloration (  Trypanosyllis californiensis sp. nov. has stripes on each segment, whereas  Trypanosyllis luquei sp. nov. has stripes in the anterior and posterior end of the segment). In addition, there are also ecological differences:  Trypanosyllis californiensis sp. nov. occurs in association with algae, whereas  Trypanosyllis luquei sp. nov. lives in association with bryozoans. Another congeneric species described from California (from Monterey Bay),  Trypanosyllis intermedia Moore, 1909 ; differs from  Trypanosyllis californiensis sp. nov. in colour pattern, which is reddish brown in the dorsum with pale in anterior and posterior ends of segments (instead of the two brown transverse stripes of  Trypanosyllis californiensis sp. nov. ) and also in the form of midbody and posterior chaetae, which are much shorter, bidentate, and without spines, i.e. more similar to those in  Trypanedenta gemmipara comb. nov. (Fig. 7E). </p>
            <p>Type locality</p>
            <p>La Jolla, San Diego (Pacific Ocean).</p>
            <p>Distribution</p>
            <p>Only known from the type locality.</p>
            <p>Etymology</p>
            <p>Named after the state of California, where the type locality of the species is located.</p>
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	https://treatment.plazi.org/id/03B0650E4E1CFFD29435F9B1FDEFFE19	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.		Plazi	Álvarez-Campos, Patricia;Giribet, Gonzalo;San Martín, Guillermo;Rouse, Greg W.;Riesgo, Ana	Álvarez-Campos, Patricia, Giribet, Gonzalo, San Martín, Guillermo, Rouse, Greg W., Riesgo, Ana (2017): Straightening the striped chaos: systematics and evolution of Trypanosyllis and the case of its pseudocryptic type species Trypanosyllis krohnii (Annelida, Syllidae). Zoological Journal of the Linnean Society 179 (3): 492-540, DOI: 10.1111/zoj.12443, URL: https://doi.org/10.1111/zoj.12443
03B0650E4E1EFFD39473FDA0FE0DFCB5.text	03B0650E4E1EFFD39473FDA0FE0DFCB5.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Trypanosyllis leivai Álvarez-Campos & Giribet & San Martín & Rouse & Riesgo 2017	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> TRYPANOSYLLIS LEIVAI</p>
            <p> ALLVAREZ- CAMPOS, RIESGO &amp; SAN MARTIN  SP. NOV.</p>
            <p>FIGS 10G, 15G – I</p>
            <p>Type material examined</p>
            <p>  Holotype. Philippines: specimen in 96% EtOH (MNCN 16.01 /16082), Luzon Island, between Balayan Bay and Batangas  Bay , ‘  Mainif Point’ , (13.68, 120.855556), coral rubble, 2 m, 8 December 2010, leg. G. San Martın Project CGL2009-12292 BOS collecting team. </p>
            <p>
                 Paratypes. Philippines: three specimens in 96% EtOH (MNCN 16.01 /16062, 16063, 16081), collection data as for the holotype ;   one specimen mounted for SEM (MNCN 16.01 /16073) and one anterior part in 96% EtOH (MNCN 16.01 /16077), Luzon Island,  
                <a title="Search Plazi for locations around (long 120.89278/lat 13.740556)" href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=120.89278&amp;materialsCitation.latitude=13.740556">Balayan Bay</a>
                 (13.740556, 120.892778), coral rubble, 2 – 4 m, 7 December 2010, leg. G. San Martın Project CGL2009-12292 BOS collecting team  ;   one specimen in 96% EtOH (MNCN / ADN 85680), Sombrero Island (Luzon),  
                <a title="Search Plazi for locations around (long 120.82972/lat 13.697778)" href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=120.82972&amp;materialsCitation.latitude=13.697778">Balayan Bay</a>
                 , ‘  
                <a title="Search Plazi for locations around (long 120.82972/lat 13.697778)" href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=120.82972&amp;materialsCitation.latitude=13.697778">Beatrice Point’</a>
                 , (13.697778, 120.829722), unidentified sponge, 2 m, 9 December 2010, leg. G. San Martın Project CGL2009-12292 BOS collecting team  ;   one specimen in 96% EtOH (MNCN 16.01 /16075), Sombrero Island (Luzon),  
                <a title="Search Plazi for locations around (long 120.82972/lat 13.697778)" href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=120.82972&amp;materialsCitation.latitude=13.697778">Balayan Bay</a>
                 (13.697778, 120.829722), unidentified sponges, 2 m, 6 December 2010, leg. G. San Martın Project CGL2009-12292 BOS collecting team  ;   one specimen in 96% EtOH (MNCN 16.01 /16074), Luzon Island, Balayan Bay, ‘  
                <a title="Search Plazi for locations around (long 120.869446/lat 13.798889)" href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=120.869446&amp;materialsCitation.latitude=13.798889">Koala Point’</a>
                 (13.798889, 120.869444), coral rubble, 2 m, 5 December 2010, leg. G. San Martın Project CGL2009-12292 BOS collecting team  ;   1 specimen in 96% EtOH (MNCN ADN 85683, 16.01 /16061), Palawan Island,  
                <a title="Search Plazi for locations around (long 119.31722/lat 11.197222)" href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=119.31722&amp;materialsCitation.latitude=11.197222">El Nido</a>
                 (11.197222 119.317222), unidentified sponge, 12 m, 18 December 2010, leg. G. San Martın Project CGL2009-12292 BOS collecting team  . 
            </p>
            <p>Diagnosis</p>
            <p> Similar to  Trypanosyllis krohnii except for pigmentation, body size, and length of appendages (Fig. 9G). Red-brown transverse stripes across anterior segments, two per segment, one wider than the other. Stripes do not reach end of segments (Fig. 10G). Specimens considerably (0.3 – 0.4 mm; n = 10) with slender and shorter anterior cirri (14 – 19 articles). Dorsal cirri alternating in anterior and midbody segments: Segments 1 and 3 presenting longer cirri (30 – 32 articles) and segments 2 and 4 with shorter ones (16 – 18 articles). Midbody segments with an alternation pattern less evident: long cirri with 16 – 18 articles and short cirri with 12 – 14 articles; posterior dorsal cirri all short (7 – 9 articles). </p>
            <p>Description</p>
            <p>Holotype incomplete: 15 mm long, 0.4 mm wide, 144 chaetigers. Well-preserved specimens white in colour with brown transverse stripes across anterior and midbody segments; one stripe slightly thicker, in middle of each segment, and the other two stripes thinner, in both anterior and posterior ends of segment (Fig. 10G). Only these two lines are similar in length, reaching the parapodia (Fig. 10G). Appendages also white. Oval prostomium with two pairs of red eyes in trapezoidal arrangement (Fig. 10G). Oval palps shorter than prostomium, completely separate. Nuchal organs not seen. Segment 1 slightly smaller than subsequent segments; antennae originating on anterior margin of prostomium, median antenna with about 22 articles; lateral antennae slightly shorter, with 15 – 17 articles. Dorsal enlarged anterior cirri longer than antennae, with about 19 articles, longer than ventral cirri, with about 14 articles. Dorsal cirri alternating long (16 – 18 articles) and short (12 – 14 articles). Dorsal cirri of the first and third segment longer than remaining cirri, with 32 articles; those from the second and fourth segment much shorter with 14 articles. Ventral digitiform cirri, shorter than parapodia. Compound bidentate heterogomph falciger chaetae with spines on margin. Between ten and 12 chaetae on anterior parapodia (Fig. 15G), between nine and 11 chaetae on midbody parapodia (Fig. 15H), and between six and eight chaetae in posterior parapodia (Fig. 15I). Blades similar throughout body, with ventral blades shorter both in midbody and posterior chaetae (Fig. 15H, I). Three aciculae in anterior parapodia, two thick, straight, acutely pointed and one slightly thinner, distally blended; only two thick, straight, acutely pointed aciculae in midbody parapodia and one in posterior parapodia. Dorsal and ventral simple chaetae not seen. Pharynx through about 14 segments, proventricle through 15 segments, with about 45 muscle cell rows.</p>
            <p>Remarks</p>
            <p> The general aspect of specimens from the Philippines is more slender and smaller than specimens of the type species of the genus, although they both share a similar coloration pattern (Fig. 10G).  Trypanosyllis leivai sp. nov. is the second species of the genus described in the Philippines, together with  Trypanosyllis luzonensis comb. nov. , although our results showed that there are probably two other species inhabiting these waters (see Fig. 1,  Trypanosyllis sp. 1 and specimens Tz39 – Tz43). Within the Philippines, the most similar species that also presents stripes on the body is  Trypanosyllis luzonensis comb. nov. ; however, it clearly differs from  Trypanosyllis leivai sp.nov in coloration pattern, size of body, and length of the dorsal cirri (see description above). </p>
            <p>Type locality</p>
            <p>‘Mainif Point’, between Balayan Bay and Batangas Bay, Luzon Island, Philippines (Indo-Pacific Ocean).</p>
            <p>Distribution</p>
            <p> Known from the type locality and from El Nido (Palawan Island), in the Philippines . </p>
            <p>Etymology</p>
            <p>Named after Carlos Leiva, colleague and friend of P.A.-C. and A.R., for his help collecting and sorting some of the analysed material.</p>
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	https://treatment.plazi.org/id/03B0650E4E1EFFD39473FDA0FE0DFCB5	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.		Plazi	Álvarez-Campos, Patricia;Giribet, Gonzalo;San Martín, Guillermo;Rouse, Greg W.;Riesgo, Ana	Álvarez-Campos, Patricia, Giribet, Gonzalo, San Martín, Guillermo, Rouse, Greg W., Riesgo, Ana (2017): Straightening the striped chaos: systematics and evolution of Trypanosyllis and the case of its pseudocryptic type species Trypanosyllis krohnii (Annelida, Syllidae). Zoological Journal of the Linnean Society 179 (3): 492-540, DOI: 10.1111/zoj.12443, URL: https://doi.org/10.1111/zoj.12443
03B0650E4E1FFFD3941BFC14FA9EFA7A.text	03B0650E4E1FFFD3941BFC14FA9EFA7A.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Trypanosyllis luquei Álvarez-Campos & Giribet & San Martín & Rouse & Riesgo 2017	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> TRYPANOSYLLIS LUQUEI</p>
            <p> ALVAREZ- CAMPOS &amp; VERDES  SP. NOV.</p>
            <p>FIGS 10F, 16A – C</p>
            <p>Type material examined</p>
            <p> Holotype. California: specimen in 96% EtOH (SIO A5005), San Diego, Anza Cove (32.795278,</p>
            <p>117.212778), bryozoans, intertidal, October 2013, leg. A. Verdes.</p>
            <p> Paratypes. California: one specimen mounted for SEM (SIO A5004) and one specimen in 96% EtOH (SIO A5006), collection data as for the holotype . </p>
            <p>Diagnosis</p>
            <p> Similar to  Trypanosyllis krohnii except for pigmentation and length of appendages (Figs 3C, 10F). Two brown transverse stripes across anterior segments, situated next to anterior and posterior ends of segment. Appendages also with brown pigmentation only in limit of each article. Width 0.2 – 0.4 mm with slender and shorter anterior cirri (32 – 35 articles). Dorsal cirri alternating long (18 – 20 articles) and short (12 – 14 articles). </p>
            <p>Description</p>
            <p>Holotype incomplete, 12 mm long, 0.4 mm wide, 105 chaetigers. Body white with brown transverse stripes across anterior and midbody segments, situated in the anterior and posterior ends of the segment (Fig. 10G). Appendages also with brown pigmentation just in the end of each article (Fig. 10G). Oval prostomium with two pairs of red eyes in trapezoidal arrangement. Oval palps shorter than prostomium, completely separate. Nuchal organs not seen. Segment 1 slightly smaller than subsequent segments; antennae originating on anterior margin of prostomium, median antenna with about 14 articles; lateral antennae slightly shorter, with 11 articles. Dorsal enlarged anterior cirri much longer than antennae, with about 35 articles, longer than ventral cirri, with about 24 articles. Dorsal cirri alternating between long (20 articles) and short (14 articles). Dorsal cirri from the first to the fourth segment longer than those of remaining segments, with 28 articles. Ventral cirri digitiform, shorter than parapodia. Compound bidentate heterogomph falciger chaetae with spines on margin, with between ten and 12 on anterior parapodia (Fig. 16A), seven or eight on midbody parapodia (Fig. 16B), and five or six on posterior parapodia (Fig. 16C). Blades decreasing in length throughout the body, ventral blades always shorter than dorsal blades (Fig. 16A – C). Two or three aciculae in all parapodia, thick, straight, acutely pointed. Dorsal and ventral simple chaetae not seen. Pharynx through about 12 segments, proventricle also through 12 segments, with about 30 muscle cell rows.</p>
            <p>Remarks</p>
            <p> Same as those in  Trypanosyllis californiensis sp. nov.</p>
            <p>Type locality</p>
            <p>  San Diego Bay , California (Pacific Ocean)  . </p>
            <p>Distribution</p>
            <p>Only known from the type locality.</p>
            <p>Etymology</p>
            <p>Named after Dr. Angel A. Luque, colleague, friend, and mentor in our malacological endeavours.</p>
            <p> TRYPANOSYLLIS KALKIN ALVAREZ- CAMPOS &amp; </p>
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	https://treatment.plazi.org/id/03B0650E4E1FFFD3941BFC14FA9EFA7A	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.		Plazi	Álvarez-Campos, Patricia;Giribet, Gonzalo;San Martín, Guillermo;Rouse, Greg W.;Riesgo, Ana	Álvarez-Campos, Patricia, Giribet, Gonzalo, San Martín, Guillermo, Rouse, Greg W., Riesgo, Ana (2017): Straightening the striped chaos: systematics and evolution of Trypanosyllis and the case of its pseudocryptic type species Trypanosyllis krohnii (Annelida, Syllidae). Zoological Journal of the Linnean Society 179 (3): 492-540, DOI: 10.1111/zoj.12443, URL: https://doi.org/10.1111/zoj.12443
