Branchinotogluma Pettibone, 1985
publication ID |
https://doi.org/ 10.3897/zookeys.1215.129623 |
publication LSID |
lsid:zoobank.org:pub:4A593809-AE76-458F-B085-0D34B29105CC |
DOI |
https://doi.org/10.5281/zenodo.13928939 |
persistent identifier |
https://treatment.plazi.org/id/D20B503F-7044-5D35-86AE-3FE2A9BE060C |
treatment provided by |
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scientific name |
Branchinotogluma Pettibone, 1985 |
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Genus Branchinotogluma Pettibone, 1985 View in CoL
Branchinotogluma bipapillata Zhou, Wang, Zhang & Wang, 2018: 528–533, figs 1–7; table 1. View in CoL View Cited Treatment
Material examined.
Indian Ocean • 2 ♂; Cheoeum ; 12°37.1'S, 66°07.6'E; depth 3018 m; 28 Mar. 2023; W-K Lee leg.; hydrothermal vent; GenBank: PP 600168 – PP 600169; KRIBB 310101 to KRIBB 310102 GoogleMaps • 2 ♂, 2 ♀, 1 undetermined; Onnuri; 11°24.9'S, 66°25.4'E; depth 2009 m; 1–2 Apr. 2023; W-K Lee leg.; hydrothermal vent; GenBank: PP 600170 – PP 600174; KRIBB 310103 to KRIBB 310107 GoogleMaps • 1 ♀, 2 undetermined; Onnare; 9°47.4'S, 66°41.9'E; depth 2993 m; 3 Apr. 2023; W-K Lee leg.; hydrothermal vent; GenBank: PP 600175 – PP 600177; KRIBB 310108 to KRIBB 310110 GoogleMaps • 1 ♂, 1 ♀; Onbada; 9°48.9'S, 66°40.6'E; depth 2563 m; 4 Apr. 2023; W-K Lee leg.; hydrothermal vent; GenBank: PP 600178 – PP 600179; KRIBB 310111 to KRIBB 310112 GoogleMaps • 2 ♂, 2 ♀; Saero; 11°19.7'S, 66°26.9'E; depth 3256 m; 7 Apr. 2023; W-K Lee leg.; hydrothermal vent; GenBank: PP 600180 – PP 600183; KRIBB 310113 to KRIBB 310116 GoogleMaps .
Description.
Specimens relatively well preserved, with 21 segments, 12.0–51.0 mm in length and 5.0– 16.6 mm in width. Body shape fusiform, tapered anteriorly and posteriorly (Fig. 2 A, B View Figure 2 , Table 2 View Table 2 ). Pairs of elytra on elytrophores on segments 2, 4, 5, 7, 9, 11, 13, 15, 17, and 19; elytra oval to subreniform, white, slightly transparent, with a smooth surface (Fig. 2 C – E View Figure 2 ). Dorsal cirri on segments 3, 6, 8, 10, 12, 14, 16, 18, 20, and 21, extending beyond the tips of neurochaetae. Branchiae arborescent; grouped in two, one at base of the notopodia and another at base of dorsal tubercles or elytrophores; starting from segment 3 and ending between segments 18 or 21 (Table 2 View Table 2 ).
Prostomium bilobed, triangular anterior lobes with slender frontal filaments (Fig. 2 F View Figure 2 ). Median antennae on anterior notch, with a cylindrical ceratophore and subulate style; palps thick, smooth, and end in subulate tips; lateral antennae and eyes absent (Fig. 2 F View Figure 2 ). Tentacular segment fused to prostomium, with pair of tentacular cirri on each side, and a small acicular lobe at the base of tentaculophore; tentacular cirri slender (Fig. 2 F View Figure 2 ).
First segment not distinct, fused to prostomium. Pharynx with five dorsal and four ventral papillae in one immature individual, but not seen in others (Fig. 2 G View Figure 2 ). Second segment with first pair of elytrophores, ventral cirri, and biramous parapodia. Third segment with ventral cirri and first pair of branchiae. Fourth to last segments with ventral cirri and biramous parapodia. Notopodia smaller than neuropodia; notochaetae stout, few, arranged in radiating bundles; neurochaetae slender, numerous, forming a fan shape (Fig. 2 H – K View Figure 2 ).
Sexual dimorphism evident. In males, posterior segments modified (Fig. 3 A View Figure 3 ) with 10 th elytra and elytrophores much smaller than 9 th (Figs 2 D View Figure 2 , 3 A View Figure 3 , Table 2 View Table 2 ); ventral papillae present on segments 12–13, long, tapering, with slender tips extending to next segment; ventral lamellae on segments 14–17, round (Fig. 3 B View Figure 3 ). In females, posterior segments not modified (Fig. 3 C View Figure 3 ), with 10 th elytra and elytrophores similar to 9 th (Figs 2 E View Figure 2 , 3 C View Figure 3 , Table 2 View Table 2 ); ventral papillae present on segments 11–15, short and blunt (Fig. 3 D View Figure 3 ).
Distribution.
Indian Ocean (depth 1732–3256 m): Longqi and Duanqiao vent fields on the southern Southwest Indian Ridge; Tiancheng vent field on the northern Southwest Indian Ridge; Edmond vent field on the southern Central Indian Ridge; Onnare, Onbada, Saero, Onnuri, and Cheoeum vent fields on the northern Central Indian Ridge.
Remarks.
Comparisons of key morphological characters between the geographically distant populations are present in Table 2 View Table 2 . The key characters of the nCIR specimens of B. bipapillata largely correspond with those of the SWIR specimens ( Zhang et al. 2018). However, the two populations differ in the last segment with branchiae in females (segment 19 in sSWIR compared with segment 18 or 21 in nCIR; Table 2 View Table 2 ).
Among the 16 specimens from the nCIR population, 10 specimens with body length greater than 20 mm were well-developed in all features indicating adult morphology, while characters of sexual dimorphism were not observed in 6 specimens shorter than 20 mm.
DNA barcoding and phylogenetic analysis.
Partial sequences of CO 1, 16S, and 18 S were recovered from 16 specimens collected from the nCIR. As shown in Table 1 View Table 1 , 48 newly obtained sequences have been deposited in GenBank.
In CO 1, the mean intra-population variation was 0.56 % for nCIR and 0.65 % for SWIR, with an inter-population variation of 1.00 % (Table 3 View Table 3 ). In 16 S, the mean intra-population variation was 0.27 % for nCIR and 0.33 % for SWIR, with an inter-population variation of 0.39 %. In 18 S, the mean intra-population variation was 0.01 % for nCIR and 0.00 % for SWIR, with an inter-population variation of 0.004 %.
The interspecific variation between B. bipapillata and other congeners ranged from 18.63 % to 21.88 % in CO 1, and from 13.11 % to 19.08 % in 16 S (Suppl. material 1: table S 2). In 18 S, the interspecific variation ranged from 1.69 % to 3.80 %.
The maximum likelihood phylogenetic tree, constructed with concatenated sequences of CO 1, 16S, and 18 S (Fig. 4 View Figure 4 ), shows the SWIR and nCIR populations of B. bipapillata clustering together as a single clade, indicating no significant divergence between populations from different ridges. Within the Branchinotogluma genus, B. bipapillata is closely related to a clade including B. kaireiensis , B. pettiboneae Wu et al., 2019 , and B. robusta Wu et al., 2023 .
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.
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Lepidonotopodinae |
Branchinotogluma Pettibone, 1985
Lee, Won-Kyung & Kim, Se-Joo 2024 |