Capitella
publication ID |
https://doi.org/ 10.5281/zenodo.215310 |
publication LSID |
lsid:zoobank.org:pub:07C06068-9160-4AB4-AAF4-0451679D9F13 |
DOI |
https://doi.org/10.5281/zenodo.6175602 |
persistent identifier |
https://treatment.plazi.org/id/03913362-FF80-FF9B-99BE-FB3E9EC54FC6 |
treatment provided by |
Plazi |
scientific name |
Capitella |
status |
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Capitella View in CoL sp.
Figures 6 View FIGURE 6 C–D, 11 A–D, 12 A–F
Material examined. Oahu Island: Moanalua Stream, 21°21ʹ7.2ʺ N, 157°53ʹ45.6ʺ W, Environmental Monitoring and Assessment Program ( EMAP), state of Hawaii estuaries and bays, Oct. 2002, Sta. 16, (2, BPBM R3598; 9 on stub).
Comparative material examined. 2 males and two females of Capitella teleta Blake, Grassle & Eckelbarger, 2009 removed from laboratory cultures on Feb/2012, donated by Dr. E. Seaver (see notes in Blake et al. (2009) concerning stock’s origin).
Description. All specimens incomplete fragments; largest female (mature) 13 mm long, 0.6 mm wide for 32 chaetigers; largest male with 29 chaetigers. Body elongate, wider on mid-thoracic chaetigers, especially on chaetiger 5 of females, gradually narrowing on abdomen; body rounded dorsally and flattened ventrally with shallow ventral groove on thoracic chaetigers 5–9. Color in alcohol pale yellow.
Prostomium triangular, broad, longer than wide, shovel–shaped with dorsal depression extending through peristomium ( Figs 11 View FIGURE 11 A–D, 12A–C); large nuchal organs postero-lateral to prostomium ( Fig. 12 View FIGURE 12 B), eyespots not observed. Peristomium distinct from prostomium, wider in dorsal view and slightly shorter than chaetiger 1 ( Fig. 12 View FIGURE 12 B). Proboscis not observed.
Thorax with nine segments; males and females with chaetigers 1–7 unilimbate capillaries only, 10–12 per fascicle. Segments of females increasing in width to chaetiger 5, tapering to end of thorax; chaetigers 8 and 9 slightly longer than other thoracic chaetigers, with 10–12 hooded hooks ( Figs 11 View FIGURE 11 C–D, 12A). Thoracic segments 1–7 of males subequal, discretely wider on chaetigers 5 and 6, but chaetiger 5 not as distinct as in females ( Figs 11 View FIGURE 11 A–D, 12C); chaetigers 8 and 9 highly modified, muscular, with notochaetae replaced by genital spines ( Figs 11 View FIGURE 11 A, B, 12C, D); spines of chaetiger 8 directed posteriorly and those of chaetiger 9 directed anteriorly; chaetiger 8 with two sets of 3–4 short spines and chaetiger 9 with two robust spines ( Fig. 12 View FIGURE 12 D).
Abdominal chaetae all hooded hooks; anteriorly with 10–12 hooks per fascicle, reducing posteriorly to 3–6 hooks. Abdominal segments multi-annulated at least 3x wider than anterior thoracic segments ( Fig. 12 View FIGURE 12 A). Noto- and neuropodia with well separated glandular tori pads; posterior parapodial tori glandular. Hooded hooks similar on thorax and abdomen, with short hood extending slightly beyond main fang and crenulated margin ( Fig. 12 View FIGURE 12 E, F). Hooks with moderate anterior shaft, slight node and multiple teeth. In frontal view with at least 3 rows of teeth, with three teeth in basal position, four in middle row and 4–5 in superior row ( Fig. 12 View FIGURE 12 E, F). Posterior abdominal segments and pygidium not observed.
Methyl green staining pattern. Males without a distinct staining pattern, with a solid light green throughout ( Fig. 6 View FIGURE 6 D) and females with chaetiger 4 darkly stained and chaetigers 7–8 intensely stained with lateral glandular patches ( Fig. 6 View FIGURE 6 C; genital duct? see Blake 2009). Abdominal region uniformly light green; parapodial tori with sparse green speckles. Comparative material of C. teleta with chaetiger 6 in females darkly stained and a distinct band on anterior half of chaetiger 9 ( Fig. 6 View FIGURE 6 E, F) as described in Blake et al. (2009).
Distribution. Specimens collected in Oahu, Hawaii.
Remarks. This Capitella species may belong to one of the sibling species identified by Grassle & Grassle (1976) but since a detailed description of the external morphology of these species is only available for Capitella teleta ( Capitella sp. I) and Capitella jonesi ( Capitella sp. III) it is impossible to identify to which species the Hawaiian material belongs. Blake et al. (2009) point out that these sibling species may be readily separated on the basis of prostomial shape, nature of the peristomium, shape of posterior end, distribution of hooded hooks, and several reproductive and developmental characteristics. We provide a full description of the Hawaiian material including photographs of the distinct MGSP of the females for future identification. The most similar sibling species is Capitella sp. IIIa, based on the shape of prostomium, peristomium and number of genital spines. The MGSP is unknown for these undescribed sibling species of Capitella , although Wu et al. (1991) illustrated it for Capitella sp. I and Capitella sp. II; however, as pointed out by Blake (2009), many more undescribed species of Capitella may exist and, as the Chinese material reported in Wu et al. (1991) could still be undescribed, delimitation of species using MGSP only would be unwise.
Biology. Tubes not observed. Mature females filled with eggs 40–50 µm in diameter.
BPBM |
Bishop Museum |
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.