identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
7192603A349E59CA904CEC3FA7C2605A.text	7192603A349E59CA904CEC3FA7C2605A.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Barantolla multibranchia Lin & García-Garza & Zhang & Lin 2026	<div><p>Barantolla multibranchia sp. nov.</p><p>Figs 2 A – R, 3 A – I</p><p>Material examined.</p><p>Holotype: China • TIO-Poly 153, complete; <a href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=118.68&amp;materialsCitation.latitude=24.83" title="Search Plazi for locations around (long 118.68/lat 24.83)">Quanzhou Bay; sta. Q 18</a>; 24.83°N, 118.68°E; 2 m depth, muddy sand; 23 Sep. 2022; Jun-Hui Lin leg. Paratypes: China • TIO-Poly 154, 4 specs., complete or incomplete; same site as holotype; one used for DNA extraction . • TIO-Poly 159, 5 specs, incomplete; <a href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=118.68&amp;materialsCitation.latitude=24.9" title="Search Plazi for locations around (long 118.68/lat 24.9)">Quanzhou Bay; sta. Q 7</a>; 24.90°N, 118.68°E; 2 m depth, mud; 18 May 2022; Jun-Hui Lin leg. • TIO-Poly 160, 4 specs, complete or incomplete; <a href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=118.3&amp;materialsCitation.latitude=24.57" title="Search Plazi for locations around (long 118.3/lat 24.57)">Xiamen Bay</a>; 24.57°N, 118.30°E; intertidal mud; 16 May 2025; Jun-Hui Lin leg. • TIO-Poly 161, 4 specs, incomplete; <a href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=118.31&amp;materialsCitation.latitude=24.58" title="Search Plazi for locations around (long 118.31/lat 24.58)">Xiamen Bay</a>; 24.58°N, 118.31°E; intertidal mud; 29 Jan. 2024; Jun-Hui Lin leg.</p><p>Non-type material.</p><p>China • TIO-Poly 155, 1 spec., incomplete; <a href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=121.63&amp;materialsCitation.latitude=29.09" title="Search Plazi for locations around (long 121.63/lat 29.09)">Sanmen Bay</a>; 29.09°N, 121.63°E; intertidal mud; 26 Dec. 2022; Wen-Sheng Lin leg. • TIO-Poly 156, 12 specs, complete or incomplete; <a href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=121.64&amp;materialsCitation.latitude=29.17" title="Search Plazi for locations around (long 121.64/lat 29.17)">Sanmen Bay</a>; 29.17°N, 121.64°E; intertidal mud; 31 Mar. 2020; Wen-Sheng Lin leg. • TIO-Poly 157, 2 specs, incomplete; <a href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=120.19&amp;materialsCitation.latitude=27.21" title="Search Plazi for locations around (long 120.19/lat 27.21)">Shacheng Harbor</a>; 27.21°N, 120.19°E; intertidal mud; 30 May 2025; Wen-Sheng Lin leg. • TIO-Poly 158, 2 specs, incomplete; <a href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=119.68&amp;materialsCitation.latitude=26.48" title="Search Plazi for locations around (long 119.68/lat 26.48)">Luoyuan Bay</a>; 26.48°N, 119.68°E; intertidal mud; 10 Jan. 2026; Wen-Sheng Lin leg. • TIO-Poly 162, 1 spec., incomplete; <a href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=117.49&amp;materialsCitation.latitude=23.92" title="Search Plazi for locations around (long 117.49/lat 23.92)">Dongshan Bay</a>; 23.92°N, 117.49°E; intertidal mud; 24 Feb. 2019; Wen-Sheng Lin leg. • TIO-Poly 163, 1 spec., incomplete; <a href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=111.27&amp;materialsCitation.latitude=21.5" title="Search Plazi for locations around (long 111.27/lat 21.5)">Maoming</a>; 21.50°N, 111.27°E; mangrove, mud; 2 Nov. 2025; Wen-Sheng Lin leg. • TIO-Poly 164, 4 specs, incomplete; <a href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=109.8&amp;materialsCitation.latitude=21.47" title="Search Plazi for locations around (long 109.8/lat 21.47)">Lianjiang</a>; 21.47°N, 109.80°E; mangrove, muddy sand; 13 May 2023; Wen-Sheng Lin leg. • TIO-Poly 165, 1 spec., incomplete; <a href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=108.22&amp;materialsCitation.latitude=21.52" title="Search Plazi for locations around (long 108.22/lat 21.52)">Bailong</a>; 21.52°N, 108.22°E; intertidal mud; 15 May 2023; Wen-Sheng Lin leg.</p><p>Description.</p><p>Holotype complete (Fig. 2 A), measuring 47.78 mm long by 1.20 mm wide (widest at chaetiger 13) for about 173 chaetigers. Paratypes complete or incomplete, ranging from 18.64–36.13 mm long, 0.92–1.15 mm wide for 47–152 chaetigers. Body nearly cylindrical, widest in anterior abdomen. Colour in alcohol tan (Fig. 2 B). Epithelium clearly areolated from peristomium to chaetiger 3, and smooth on following segments (Figs 2 D, 3 A). Abdominal segments with transverse wrinkles (Fig. 2 G). Ventral and lateral grooves present from anterior thorax (Fig. 2 A, D). Nuchal organs not observed.</p><p>Prostomium conical with short palpode (Figs 2 B, 2 D, 3 B). Proboscis everted in holotype, covered with numerous minute papillae (Fig. 2 B, D). Eyespots absent. Peristomium achaetous, separated from chaetiger 1, 2 times wider than long, longer than chaetiger 1.</p><p>Thorax consisting of achaetous peristomium and 11 chaetigers (Figs 2 A, 2 D, 3 A); intersegmental grooves distinct throughout. Lateral organs located between noto- and neuropodia, closer to notopodia, as small pores (Fig. 2 D, E). Genital pores not observed. First chaetiger biramous, 2.0 times wider than long (Fig. 2 B, D). Following segments 1.5–2.5 times wider than long. Chaetigers 1–5 with only capillaries in both rami, 14–24 per fascicle in notopodia and 16–30 per fascicle in neuropodia. Chaetiger 6 with mixed chaetae in both rami (Fig. 2 L, N, O), around 21 per fascicle in notopodia and 26 per fascicle in neuropodia. Chaetigers 7–11 with only long-handled hooks (Fig. 2 J, K, Q), 18–30 per fascicle in notopodia and 20–34 per fascicle in neuropodia. Notopodia inserted dorso-laterally, moving to dorsal side gradually, and neuropodia ventro-laterally. Chaetal fascicles inserted near midline of thoracic segments.</p><p>Transition between thorax and abdomen marked by abrupt broadening of anterior abdominal segments and chaetal change (Figs 2 D, 2 E, 3 C). Abdominal segments longer and wider than last thoracic chaetigers in anterior abdomen (Fig. 2 E), tapering gradually towards pygidium (Fig. 2 C). Notopodial lobes well separated in anterior abdomen. Elevated tori pad forming a thin membrane surrounding the segment like a collar in posterior abdomen (Fig. 2 G). Posterior abdominal segments crowded (Figs 2 I, 3 F). Abdominal chaetigers with hooded hooks throughout, with 24–40 hooks per fascicle in anterior abdomen, increasing to 50–80 hooks in posterior abdomen, decreasing to 2 or 3 hooks in posterior end (Fig. 2 P). In anterior abdomen, notopodial lobes dorsally located and neuropodial lobes ventro-lateral. From middle abdomen, notopodial lobes dorsal and neuropodial lobes ventral (Figs 2 F – H, 3 D, 3 E). Chaetal fascicles positioned posterior to midsegment in anterior abdomen, and near posterior edge of segment toward the pygidium (Fig. 2 H).</p><p>Thoracic long-handled hooks without angled node, distal 1 / 6 to 1 / 5 hooded (Fig. 2 J); hoods around 5 times longer than wide (Figs 2 K, 3 H). Abdominal hooded hooks much shorter than thoracic ones, with angled node, developed shoulder, posterior shaft slightly longer than anterior one, attenuated at terminal end (Figs 2 M, 3 I). Hood slightly longer than wide. Hooded hooks with 3 rows of teeth above main fang (Fig. 2 R): 3 teeth in basal row, 3 teeth in middle row, 2 teeth in apical row (smaller than in basal row). Main fang subtriangular, longer than wide.</p><p>Dorsal branchiae commencing from around chaetiger 74 in middle abdomen, located behind notopodial tori. Anterior branchiae consisting of 2 or 3 nipple-like lobes (Fig. 2 G). Towards the tail branchial lobes increasing in number and length, the largest with 14 finger-like lobes (Figs 2 H, 2 I, 3 F). Near pygidium branchial lobes decreasing to 1 or 2 spherical lobes (Figs 2 C, 3 G).</p><p>Pygidium adorned with a mid-ventral cirrus (Figs 2 C, 3 G).</p><p>Methyl green staining pattern.</p><p>(Figs 2 A, 2 D, 2 F, 2 H) Chaetigers 1–4 stained with medium green. Abdominal segments with sparse green speckles on areas behind parapodial tori.</p><p>DNA sequences.</p><p>Twelve specimens of B. multibranchia sp. nov. from nine sampling localities were sequenced in this study. This yielded eight partial COI sequences (PZ 487945 – PZ 487952), 11 partial 16 S sequences (PZ 486615 – PZ 486625), 12 partial 18 S sequences (PZ 486637 – PZ 486648), 11 partial 28 S sequences (PZ 486626 – PZ 486636), and 12 partial H 3 sequences (PZ 499943 – PZ 499954).</p><p>Distribution.</p><p>Widely distributed along the southern coasts of China, spanning from Zhejiang Province in the east to Guangxi Province in the west.</p><p>Ecology.</p><p>The new species mainly inhabits intertidal or shallow waters in estuarine areas or inner bays, where the sediment consists of mud, muddy sand, or sandy mud.</p><p>Etymology.</p><p>The specific epithet multibranchia is composed of the Latin prefix multi- (many) and the Latin noun branchia (gills), referring to the presence of numerous branchiae in the new species. It is used as a noun in apposition and is indeclinable.</p><p>Remarks.</p><p>Barantolla multibranchia sp. nov. is assigned to the genus Barantolla based on the presence of an achaetous peristomium and 11 thoracic chaetigers, with the first six chaetigers bearing capillary chaetae. Since Southern (1921) erected the genus, five species have been formally described worldwide (Hartman 1963; Hutchings 1974; Yabe and Mawatari 1998; Çinar et al. 2022). Among these, only B. sculpta, described from a brackish lake near Calcutta, India, has been reported to bear dorsal branchiae on the abdomen. The new species closely resembles B. sculpta in sharing dorsal branchiae on the abdomen, an areolated epithelium on the anterior thorax, and a complete chaetiger 1. However, it differs from the latter in details of the chaetae at chaetiger 6 and in epithelial texture. Barantolla multibranchia sp. nov. has mixed chaetae in both rami of chaetiger 6 and lacks the thoracic sculpturing. Whereas the unique sculpturing of the thorax was characteristic of B. sculpta, which possesses only capillaries on the first six thoracic chaetigers. Owing to the absence of a detailed description of hooded hooks in the original reference, a comparison of this character is not possible.</p><p>Genetic divergence.</p><p>Within B. multibranchia sp. nov. the intraspecific K 2 P genetic distances among specimens sequenced in this study varied across gene markers (Suppl. material 1): COI (0–4.3 %), 16 S (0–0.9 %), 18 S (0 %), 28 S (0–0.1 %), and H 3 (0–1.6 %). Notably, the COI-based genetic distances between specimens from Guangxi and those from other localities are substantially higher, suggesting that the Guangxi population may be undergoing divergence.</p><p>The Hainan specimen (accession number PQ 010756) exhibits a K 2 P genetic distance of 1.3 % from the paratype of B. multibranchia sp. nov. (PZ 487946), a value well within the intraspecific range, indicating that the Hainan specimen belongs to the new species described herein. The COI-based genetic distance between B. multibranchia sp. nov. and other species with available molecular sequences ranged from 22.3 % to 44.6 %, greater than the intraspecific genetic distance (Table 2). Additionally, the 18 S-based K 2 P genetic distance between B. lepte Hutchings, 1974 (AB 106265) and B. multibranchia sp. nov. is 1.2 %, which exceeds the intraspecific divergence (0 %) in B. multibranchia, confirming the distinction of the new species from B. lepte .</p></div>	https://treatment.plazi.org/id/7192603A349E59CA904CEC3FA7C2605A	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Lin, Jun-Hui;García-Garza, María E.;Zhang, Shu-Yi;Lin, He-Shan	Lin, Jun-Hui, García-Garza, María E., Zhang, Shu-Yi, Lin, He-Shan (2026): Two new species of Capitellidae (Annelida, Polychaeta) from the southern coasts of China. ZooKeys 1292: 227-241, DOI: 10.3897/zookeys.1292.203560
03CF3E4E7D1752D9A409AB83602CB4AE.text	03CF3E4E7D1752D9A409AB83602CB4AE.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Barantolla Southern 1921	<div><p>Genus Barantolla Southern, 1921</p><p>Type species.</p><p>Barantolla sculpta Southern, 1921</p><p>Generic diagnosis.</p><p>(amended after Magalhães and Blake 2020) Prostomium conical, palpode present or absent; eyespots absent, nuchal organs present. Peristomium clearly distinct from prostomium; achaetous segment absent. First chaetiger uniramous or biramous. Eleven thoracic chaetigers. Chaetigers 1–6 with capillaries; one transitional thoracic chaetiger may be present on chaetiger 6 or chaetiger 7; remaining thoracic chaetigers with notopodial and neuropodial hooks. Thorax clearly demarcated from abdomen. Abdominal segments with hooded hooks in both rami, different in shape and size than thoracic hooks. Branchiae present or absent; when present, branched and dorsal. Genital pores not observed. Lateral organs present on thorax. Pygidium may be adorned with ventral cirrus.</p><p>Remarks.</p><p>The current generic diagnosis of Barantolla encompasses interspecific variation in chaetal details. Most species bear only capillaries on the first six chaetigers and hooks on subsequent thoracic chaetigers, while B. americana uniquely possesses mixed chaetae on chaetiger 7. The new species differs in having mixed chaetae in both rami on chaetiger 6 and a short palpode at the prostomial tip, which is not seen in congeneric species. To accommodate these new features, we have expanded the generic diagnosis.</p></div>	https://treatment.plazi.org/id/03CF3E4E7D1752D9A409AB83602CB4AE	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Lin, Jun-Hui;García-Garza, María E.;Zhang, Shu-Yi;Lin, He-Shan	Lin, Jun-Hui, García-Garza, María E., Zhang, Shu-Yi, Lin, He-Shan (2026): Two new species of Capitellidae (Annelida, Polychaeta) from the southern coasts of China. ZooKeys 1292: 227-241, DOI: 10.3897/zookeys.1292.203560
A73C99EA4F21592DAD69A07E172EA4E2.text	A73C99EA4F21592DAD69A07E172EA4E2.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Parheteromastus Monro 1937	<div><p>Genus Parheteromastus Monro, 1937</p><p>Type species.</p><p>Parheteromastus tenuis Monro, 1937 .</p><p>Diagnosis.</p><p>(amended after Magalhães and Blake 2020) Prostomium conical, eyespots absent. Peristomium clearly distinct from prostomium; achaetous segment absent. First chaetiger biramous. Eleven thoracic chaetigers. Chaetigers 1–4 with only capillaries and chaetigers 5–11 with only hooded hooks. Thorax may or may not be clearly demarcated from abdomen. Abdominal segments with only hooded hooks. Branchiae absent. Genital pores and lateral organs not described. Pygidium adorned with a single short cirrus.</p></div>	https://treatment.plazi.org/id/A73C99EA4F21592DAD69A07E172EA4E2	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Lin, Jun-Hui;García-Garza, María E.;Zhang, Shu-Yi;Lin, He-Shan	Lin, Jun-Hui, García-Garza, María E., Zhang, Shu-Yi, Lin, He-Shan (2026): Two new species of Capitellidae (Annelida, Polychaeta) from the southern coasts of China. ZooKeys 1292: 227-241, DOI: 10.3897/zookeys.1292.203560
611437D0905B5DDCA5F29E958148FB9E.text	611437D0905B5DDCA5F29E958148FB9E.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Parheteromastus simplex Lin & García-Garza & Zhang & Lin 2026	<div><p>Parheteromastus simplex sp. nov.</p><p>Figs 4 A – J, 5 A – F</p><p>Material examined.</p><p>Holotype. China • TIO-Poly 165, complete; <a href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=118.3&amp;materialsCitation.latitude=24.57" title="Search Plazi for locations around (long 118.3/lat 24.57)">intertidal zone near Dadeng Island</a>; 24.57°N, 118.30°E; intertidal mud; 16 March 2025; Jun-Hui Lin leg. Paratypes. China • TIO-Poly 166, 1 spec., incomplete; same site as TIO-Poly 165 . China • TIO-Poly 167, 1 spec., incomplete; <a href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=118.34&amp;materialsCitation.latitude=24.57" title="Search Plazi for locations around (long 118.34/lat 24.57)">intertidal zone near Dadeng Island</a>; 24.57°N, 118.34°E; intertidal mud; 11 March 2020; Jun-Hui Lin leg.</p><p>Description.</p><p>Holotype complete with posterior part heavily coiled (Fig. 4 A), measuring 20.11 mm long by 0.55 mm wide (at chaetiger 14) for about 104 chaetigers. Paratypes incomplete, ranging from 13.48–22.83 mm long, 0.56–0.61 mm wide for 47–52 chaetigers. Body thread-like, widest in anterior abdomen. Lateral and ventral grooves present in thorax. Colour in alcohol tan. Nuchal organ not observed.</p><p>Prostomium conical with short palpode, eyespots absent. Proboscis everted in holotype, covered with numerous minute papillae (Figs 4 A – C, 5 A, 5 B). Peristomium achaetous, longer than wide, longer than chaetiger 1. Peristomium clearly demarked from chaetiger 1 (Fig. 4 B, C).</p><p>Thorax with achaetous peristomium and 11 chaetigers in holotype; thoracic chaetigers biannulate; first chaetiger biramous (Fig. 4 B). Thoracic segments wider than long, with epithelium areolated from peristomium up to chaetiger 3 (Fig. 4 C), and smooth on following segments (Fig. 4 D). Intersegmental grooves distinct. Lateral organs located between noto- and neuropodia, closer to notopodia, as small pores (Fig. 4 D). Genital pores not observed. First chaetiger 1.2 times wider than long; following segments 1.3–2.2 times wider than long. Chaetigers 1–4 with only capillaries in both rami, 5–10 per fascicle in notopodia and 6–10 per fascicle in neuropodia. Chaetigers 5–11 with only long-handled hooks (Fig. 4 G), 8–10 per fascicle in notopodia and 8–12 per fascicle in neuropodia. Notopodia inserted dorso-laterally, moving to dorsal side posteriorly; neuropodia inserted ventro-laterally throughout. Chaetal fascicles inserted near midline of thoracic segments.</p><p>Transition between thorax and abdomen marked by constriction and chaetal change (Figs 4 D, 5 C). Abdominal segments longer and wider than last thoracic chaetiger in anterior abdomen, tapering gradually towards pygidium (Fig. 4 F). Parapodial lobes reduced, well separated in entire abdomen (Fig. 4 D, E). Abdominal chaetigers with hooded hooks throughout, with about 10 hooks per fascicle in abdomen, decreasing to 1 or 2 hooks per fascicle in posterior end. Notopodial lobes located dorsally and neuropodial lobes ventral. Chaetal fascicles positioned posterior to mid-segment in anterior abdomen (Fig. 4 D), and near posterior edge of segment toward the pygidium (Fig. 4 E).</p><p>Thoracic hooded hooks without angled node, distal 1 / 6 to 1 / 5 hooded; hoods about 5 times longer than wide (Fig. 4 H). Abdominal hooded hooks much shorter than thoracic ones, with angled node, developed shoulder, posterior shaft slightly longer than anterior one, attenuated at terminal end (Figs 4 I, 5 E). Hood slightly longer than wide. Hooded hooks with 3 rows of teeth above main fang (Figs 4 J, 5 F): 2 teeth in basal row, 3 teeth in middle row, 3 teeth in apical row. Main fang subtriangular, longer than wide.</p><p>Branchiae absent. Pygidium adorned with a mid-ventral cirrus (Figs 4 F, 5 D).</p><p>Methyl green staining pattern.</p><p>(Fig. 4 A – E) Anterior three chaetigers stained with dense green speckles. Sparse dark spots of stain scattered on anterior two abdominal chaetigers, and on posterior quarter of each following segment.</p><p>DNA sequences.</p><p>Two Parheteromastus specimens collected from two sampling sites were sequenced, and all five gene fragments were successfully obtained. No intraspecific genetic variation was detected between the two specimens across all markers, except for a single nucleotide substitution in the COI gene. These sequences represent the first molecular data for species of the genus Parheteromastus .</p><p>Distribution.</p><p>Currently known from the intertidal zones near Dadeng Island, Xiamen Bay, and possibly present in the mangrove wetlands of Fujian Province.</p><p>Ecology.</p><p>The new species inhabits intertidal sediment characterized by mud, muddy sand, or sandy mud.</p><p>Etymology.</p><p>This species was named after its plain external morphology: the Latin adjective referring to a plain state.</p><p>Remarks.</p><p>Parheteromastus was initially erected by Monro (1937) based on specimens collected from the coasts of Myanmar. To date, species of Parheteromastus have been sparsely documented worldwide. Prior to this study, the genus was considered monotypic, with only Parheteromastus tenuis having been described. The new species described herein agrees well with the generic diagnosis: its thorax has an achaetous peristomium and 11 chaetigers, of which the anterior four chaetigers possess capillaries and the remaining seven chaetigers bear only long-handled hooks. Parheteromastus simplex sp. nov. is similar to P. tenuis in several respects: both species are small worms with reduced abdominal parapodial tori, lack branchiae, and possess a short cirrus on the pygidium. However, the two species differ in the appearance of the anterior thorax and the transition of the thorax and abdomen. Parheteromastus simplex sp. nov. has an areolated epithelium from the peristomium to chaetiger 3, and the transition between the thorax and abdomen is clearly demarcated by a constriction. In contrast, P. tenuis has a smooth thorax and the transition is indistinct. With respect to the dental formula, no description or illustration of abdominal hooks is available for P. tenuis, which prevents a detailed comparison between the two species.</p></div>	https://treatment.plazi.org/id/611437D0905B5DDCA5F29E958148FB9E	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Lin, Jun-Hui;García-Garza, María E.;Zhang, Shu-Yi;Lin, He-Shan	Lin, Jun-Hui, García-Garza, María E., Zhang, Shu-Yi, Lin, He-Shan (2026): Two new species of Capitellidae (Annelida, Polychaeta) from the southern coasts of China. ZooKeys 1292: 227-241, DOI: 10.3897/zookeys.1292.203560
