Gyrinicola chabadamsoni, Brigitte, Planade, Odile, Bain, Jean-Paul, Lena & Pierre, Joly, 2008
publication ID |
https://doi.org/ 10.5281/zenodo.181991 |
DOI |
https://doi.org/10.5281/zenodo.5611237 |
persistent identifier |
https://treatment.plazi.org/id/646887D6-9309-FF89-C3DF-FA3AFC7954A1 |
treatment provided by |
Plazi |
scientific name |
Gyrinicola chabadamsoni |
status |
sp. nov. |
Gyrinicola chabadamsoni n. sp. Planade and Bain
Taxonomic summary
Type-host: Rana kl. esculenta, Linnaeus , Ranidae , tadpole 109 JW V17.
Type-locality: Vernange pond (45°56’42" N, 4°55’41" E) Saint André de Corcy, Ain, France.
Site: Intestine.
Type-material: Female holotype and male allotype, N° 108 JW V17, deposited in the collection of the Museum National d’Histoire Naturelle, Paris.
Prevalence: 17.9% in June, 6.7% in August 2005 (all parasites stages and hosts).
Collection date: 06/17/2005 and 08/01/2005.
Etymology: The authors of the name G. chabadamsoni are B. Planade and O. Bain. The species is named after our colleagues Prof. Alain Chabaud, for his outstanding work on nematode parasites of vertebrates, and Dr Martin Adamson for his enlightening study of G. batrachiensis , in which he first revealed the existence of haplodiploidy in oxyurids ( Adamson 1981b and c; 1984).
Description. Female ( Fig. 1 View FIGURE 1 , Table 1 View TABLE 1 a). Body cuticle with distinct annulations, except at both extremities. Maximum body width at the level of the excretory pore. Head: four tiny cephalic papillae; cylindrical salient amphids; triangular mouth surrounded by 12 conspicuous membranous flaps with longitudinal crests on posterior aspect; buccal cavity short, prolonged with an oesophageal cavity; junction of buccal cavity and oesophagus Y-shaped; no teeth. Oesophagus with thick bulb. Tiny excretory pore and complex vacuolated chamber; lateral canals prominent. Tail conical, almost regularly attenuated. Transverse slit of vulva at mid-body, muscuclar short vagina, ovijector 125-250 µm long, two uteri connected in a chamber lined with large epithelial cells. One long genital tract, apex of thick ovary at level of rectum (rarely anterior), directed anteriorly, oviduct with distinct enlarged section, uterus coiled posterior to oesophagus, then directed backwards with a bend before reaching the chamber in the longer females. The second genital tract is composed of a short ovary and a large uterine pouch containing subadult males and male larvae, shorter and sexually undetermined larvae and undifferentiated embryos.
(1) RL= Rana esculenta ; LL= R. lessonae
Male ( Fig. 3 View FIGURE 3 , Table 1 View TABLE 1 b). Testis directed forwards then flexed; wide ejaculatory duct, with conspicuous vacuolated walls. No spermatozoa identified in the seminal vesicle, or in the ejaculatory duct. Genital cone: distal extremity rounded in lateral view; two pairs of papillae, one precloacal, one postcloacal. Shape of the cone-tail junction and position of the caudal papillae: the posterior aspect of the cone and the tail delineate a triangle; one pair of almost joint papillae far from the acute cone-tail angle, at about mid-length of tail; phasmids not identified. Tail attenuated. Spicule thin, with bent proximal extremity and more or less lanceolate distal part and pointed extremity.
Eggs ( Fig. 1 View FIGURE 1 ). Thick-shelled eggs elliptical; dotted surface; transverse section triangular; operculum subapical, elliptical; one cell in uteri, two to 4 cells near vagina.
Taxonomic discussion. Gyrinicola chabadamsoni n. sp. is distinct from the four species already described (Tables 3 a and b). Females of G. t b a ( Dinnik 1930) have a much longer tail abruptly constricted posterior to the anus; instead of the twelve internally crested cuticular flaps, the mouth has three very thin mouth flaps, sometimes divided; the slender genital tract does not have a pouch, the eggs are less elliptical ( Fig. 1 View FIGURE 1 P and Q) with operculum as wide as long. In G. t b a males, the genital cone has a long post cloacal lip and the connection of the cone-tail is square, the third pair of joined cloacal papillae is more anterior, the spicule shape is simple ( Fig. 3 View FIGURE 3 D, H and I).
Gyrinicola batrachiensis (Walton 1929) close to G. t b a, has a longer female, a longer tail (518 ± 80 vs. 230 ± 38), a head with a hexagonal mouth with 6 flaps instead of 12 and 4 large papillae, a slender genital tract with thin tubular uterus containing infective third stage larvae, no uterine pouch and slightly smaller thickshelled eggs (90 ± 5 / 50 ± 6vs. 103-112/ 60–66). In the male, the body is twice as long, the tail is two and a half times longer and the shape of the genital cone differs in having a long salient posterior lip. The junction of the cone-tail is square; and the third caudal pair of papillae is more anterior.
Gyrinicola chabaudi Araujo and Artigas 1982 presents great variations of measurement (body and tail length, thick-shelled eggs). The female head has four large papillae and a mouth surrounded by three cuticular flaps constricted in the middle, and there is a long slender viviparous tract with no pouch ( Souza-Junior and Martins 1996). The male has a round genital cone as in our specimens, and the third pair of caudal papillae have a similar position but the tail is more filamentous ( Souza-Junior et al. 1991).
Gyrinicola japonica Yamaguti 1938 , which is the type species of the genus, is less acurately described, and appears to be close to our specimens. It differs in having slightly smaller eggs (87–96/48–54 vs. 103–112/ 60–66) and a male with a longer (800 to 870 vs. 617 ± 103) and slenderer (50–60/ 71± 15) body. The female has a uterine pouch with males and embryos as in our specimens.
Holotype | Other | Other | Other | Other | Other | Other | Other | Other | Other | Other |
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Female number V17 F I | V10 FII | V10 FIII | V11 FII | V11 FIII | V12 FI | V12 FII | V23 FI | V37 FI | V47 FI | PM5 FI |
Length 2.3 | 1.72 | 1.9 | 2.8 | 2.3 | 1.9 | 1.67 | 2.26 | 2.45 | 2.36 | 2.8 |
Maximum width 275 | 250 | 250 | 350 | 370 | 280 | 300 | 200 | 270 | 250 | 210 |
Nerve ring 170 | ND | 120 | 170 | 165 | 130 | 145 | 150 | 160 | 140 | 150 |
Oesophagus 340 | ND | 310 | 380 | 350 | 330 | 325 | 400 | 370 | 370 | 420 |
Excretory pore 490 | ND | 380 | 590 | ND | 450 | 480 | 490 | 420 | ND | 700 |
Vulva 1080 | ND | 800 | 1520 | ND | 800 | 880 | 1080 | 1230 | 1150 | 1050 |
Tail length 210 | 225 | 240 | 160 | 250 | 210 | 290 | 250 | 270 | 245 | 180 |
Eggs (L/w) ND | ND | 100/60 | 90/30 | 80/30 | ND | ND | ND | 100/40 | ND | ND |
Host (1) RL | RL | RL | LL | LL | LL | LL | LL | LL | LL | ? |
B. Males. |
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.
Kingdom |
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Phylum |
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Class |
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Order |
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SuperFamily |
Oxyuroidea |
Family |
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Genus |
Gyrinicola chabadamsoni
Brigitte, Planade, Odile, Bain, Jean-Paul, Lena & Pierre, Joly 2008 |
Gyrinicola chabaudi
Araujo and Artigas 1982 |
Gyrinicola japonica
Yamaguti 1938 |