Rhabdochona kisutchi Margolis, Moravec & McDonald, 1975
publication ID |
https://doi.org/ 10.11646/zootaxa.4185.1.1 |
publication LSID |
lsid:zoobank.org:pub:0D054EDD-9CDC-4D16-A8B2-F1EBBDAD6E09 |
DOI |
https://doi.org/10.5281/zenodo.5626734 |
persistent identifier |
https://treatment.plazi.org/id/038FB248-FFF9-FFFD-89B9-C19324239DF0 |
treatment provided by |
Plazi |
scientific name |
Rhabdochona kisutchi Margolis, Moravec & McDonald, 1975 |
status |
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Rhabdochona kisutchi Margolis, Moravec & McDonald, 1975
Description (after Margolis et al. 1975). With characteristics of the genus.
Medium-sized worms with rudimentary pseudolabia. Mouth opening roughly hexagonal. Two fairly large lateral amphids and eight small submedian cephalic papillae arranged in an inner and outer circle of four each; papillae of inner circle at mouth margin. Prostom funnel-shaped with distinct basal teeth, and its anterior margin with 10 conical teeth ( Fig. 47 View FIGURE 47 A,B). Vestibule relatively long, straight (but S-shaped in specimens that the authors claim to be “older’). Deirids medium-sized, bifurcate, located near mid-point of vestibule ( Fig. 47 View FIGURE 47 B). Tail of both sexes “ending in blunt point”.
Males (11 specimens, allotype in parentheses): 6.61–8.41 (6.90) long, 0.110–0.150 (0.150) maximum width. Prostom 0.024–0.027 (0.024), vestibule including prostom 0.108–0.153 (0.123), muscular oesophagus 0.225– 0.270 (0.233) and glandular oesophagus 1.35–2.29 (1.69) long. Deirids 0.060–0.075 (0.066), nerve ring 0.168– 0.240 (0.195) and excretory pore 0.249–0.351 (0.286) from anterior end. Subventral pre-cloacal papillae variable in number: allotype has nine on each side, paratypes with the combinations 7+8, 8+8, 8+9, 7+9, 8+10, and 10+10. Additional pair of lateral pre-cloacal papillae at level of 3rd subventral pair or slightly posterior to it. One paratype had two pairs of lateral papillae. Six pairs of post-cloacal papillae—five subventral and one lateral ( Fig. 47 View FIGURE 47 C). Left
spicule 0.564–0.660 (0.627) long, with shaft representing about its distal half; proximal end slightly widened, distal
tip lanceolate, with wide cuticular membrane; ventral process seen on distal tip when spicule protruding from
cloacal opening ( Fig. 47 View FIGURE 47 D). Right spicule variable in shape, 0.087–0.135 (0.120) long; dorsal barb feebly
developed, usually indistinct, its apparent presence depending perhaps on angle from which it is viewed. Length
ratio of right to left spicule 1:4.80 to 1:6.48 (1:5.22). Tail 0.300–0.390 (0.360) long, “ending in blunt point”.
Females (nine specimens, holotype in parentheses): gravid worms 12.04–17.38 (13.59) long, 0.190–0.272 (0.231)
maximum width. Prostom funnel–shaped 0.030–0.036 (0.033), vestibule including prostom 0.126–0.198 (0.192),
muscular oesophagus 0.285–0.361 (0.330), and glandular oesophagus 2.34–3.36 (2.87) long. Deirids 0.060–0.096
(0.090), nerve ring 0.174–0.276 (0.261) and excretory pore 0.411–0.420 (0.411) from anterior end. Tail 0.351–
0.450 (0.351) long, ending in “a blunt point”. Vulva slightly post-equatorial located 6.16–8.02 (6.25) from
posterior end. Amphidelphic. Mature eggs oval, embryonated, always with gelatinous “formations” most often in
shape of caps or lobes covering egg poles and partly their lateral surfaces; rarely polar “formations” tendril-shaped
and as long as 0.045; in some eggs a long filiform filament, about 0.45 long, arises from proximo-lateral corner of
one polar cap ( Fig. 47 View FIGURE 47 E,F,G). Eggs, excluding polar “formations”, “0.039–0.042 x 0.024 (0.039–0.042 x 0.024)
[sic]”, polar caps usually 0.006–0.009 high.
Sites: intestine, pyloric caeca
Hosts: Oncorhynchus kisutch (1); Oncorhynchus mykiss (2, 3); Oncorhynchus nerka (2, 3); Prosopium williamsoni (2, 3); Salvelinus malma (2, 3, 4)
Distribution: British Columbia
Records: 1. Margolis et al. 1975; 2. Anon. 1978; 3. Arai & Mudry 1983; 4. Anon. 1984
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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