Multitestis paramagnacetabulum, Bray, Rodney A., Cribb, Thomas H. & Justine, Jean-Lou, 2010

Bray, Rodney A., Cribb, Thomas H. & Justine, Jean-Lou, 2010, Multitestis Manter 1931 (Digenea: Lepocreadiidae) in ephippid and chaetodontid fishes (Perciformes) in the south-western Pacific Ocean and the Indian Ocean off Western Australia, Zootaxa 2427, pp. 36-46 : 42-44

publication ID

https://doi.org/ 10.5281/zenodo.294252

publication LSID

lsid:zoobank.org:pub:A41D1538-1D85-43CE-9612-50E6A5708ACE

DOI

https://doi.org/10.5281/zenodo.5629693

persistent identifier

https://treatment.plazi.org/id/84E00168-E83A-4E46-84EE-06482D7A3DF7

taxon LSID

lsid:zoobank.org:act:84E00168-E83A-4E46-84EE-06482D7A3DF7

treatment provided by

Plazi

scientific name

Multitestis paramagnacetabulum
status

sp. nov.

Multitestis paramagnacetabulum View in CoL n. sp.

( Figs 9–10 View FIGURES 7 – 10. 7 – 8 )

Type-host: Platax orbicularis (Forsskål) , orbicular batfish (juv) ( Ephippidae ).

Site: Intestine.

Type-locality: Ningaloo Reef, Western Australia (22°42’S. 113°40’E, April, 2000).

Prevalence: 1 of 2 (50%).

Voucher specimens: Holotype QM G 231079, paratypes QM G 231080 – 231085, BMNH 2010.2.10.1-5.

Description: Based on 11 specimens. Measurements in Table 2 View TABLE 2 . Soma almost circular but with slightly protuberant anterior region, short posterior dorsosubterminal ‘tail’. Tegument spinous throughout most of soma; spines minute, not detected on ‘tail’. Oral sucker subterminal, cup-shaped. Ventral sucker large, oval, aperture in form of depressed central region along length of sucker. Prepharynx short. Pharynx subglobular. Oesophagus short. Intestinal bifurcation in posterior forebody. Caeca arcuate, reaching around body parallel to margin, terminating blindly fairly close to posterior extremity of soma, not extending into ‘tail’, termination often obscured by vitelline follicles.

Testes 11, oval, in 2 rosette-like clusters, ventral and overlapping caeca in region between mid-ventral sucker and mid-hindbody, poral field with 6 testes; aporal field with 5. External seminal vesicle saccular, posterodorsal to cirrus-sac. Cirrus-sac claviform, passing transversely dorsal to anterior part of ventral sucker. Internal seminal vesicle oval. Pars prostatica oval or bipartite, lined with anuclear cell-like bodies. Ejaculatory duct long, relatively wide. Genital atrium large, pocketed. Genital pore sinistral, bifurcal, ventral to left caecum.

Ovary multilobate, just posterior to ventral sucker, median. Canalicular seminal receptacle oval, dorsal to ovary. Laurer’s canal not detected. Uterus initially passes posteriorly over ventral surface of ovary, reaches to about mid-hindbody, then passes anteriorly over ventral surface of ovary and into space between ovary and ventral sucker. Eggs relatively few, weakly tanned, operculate. Metraterm muscular, wide, shorter than cirrussac. Vitellarium follicular; dorsal field almost continuous in soma, absent in around edge of worm, anterior to level of pharynx and in median region from mid-ventral sucker posteriorly; not reaching into tail.

Excretory pore dorsally subterminal, on ‘tail’. Excretory vesicle I-shaped, initially narrow, widens in posterior soma, mostly obscured by other internal organs, extent not detected.

Discussion. The worms from Ningaloo are similar to those described by Mamaev (1970) and Bray & Cribb (2003) as Multitestis magnacetabulum , but differ consistently in the testes always being situated a little more posteriorly ( Fig. 9 View FIGURES 7 – 10. 7 – 8 ). Both Mamaev (1970) and Bray and Cribb (2003) stated that the testicular follicles are lateral to the ventral sucker, whereas in the Ningaloo specimens the testes are mostly in the hindbody, although overlapping the ventral sucker. This means that the post-testicular region is relatively shorter in the Ningaloo specimens. Giving dimensions is a problem as the specimens illustrated in detail by Mamaev (1970) lack the distinctive tail-like appendage which always occurs in well-fixed specimens of this species. Mamaev (1970) gives outline illustrations of the shapes taken up by this species, including specimens with ‘tails’, indicating that the fixation method he used often caused contraction or distortion. Nevertheless several dimensions can be quoted from our own measurements (Bray & Cribb 2003 and original data) to indicate the distinctness of the specimens from Ningaloo: pre-testicular distance (34–43% of body length vs 17–27% (our data) and 34–37% (from Mamaev’s illustrations of tailless specimens)), post-testicular distance (22–33% of body-length vs 37–51% (our data) and 21–26% (from Mamaev’s illustrations of tailless specimens)). Measurements of these worms are included in Table 2 View TABLE 2 where they are compared with a series of measurements taken from M. magnacetabulum from Platax teira from Heron Island and New Caledonia. The specimens from Ningaloo, Heron Island and New Caledonia were fixed in the same way, so the slight differences found can be considered genuine local variation.

TABLE 2. Dimensions and ratios of Multitestis magnacetabulum and M. paramagnacetabulum n. sp.

Species Multitestis magnacetabulum Multitestis magnacetabulum Multitestis paramagnacetabulum n.sp.
Host Platax teira Platax teira Platax orbicularis
Locality Heron Island New Caledonia Ningaloo
n 18 1 11
Length 636–1,351 (874) 781 520–625 (603)
Width 570–957 (722) 748 419–621 (500)
Forebody 217–366 (277) 295 176–219 (202)
Pre-oral lobe 8–18 (11) 7 0–5 (2)
Oral sucker 98–148 × 118–168 (114 × 140) 136 × 155 68–92 × 85–109 (75 × 97)
Prepharynx 0 0 7–21 (15)
Pharynx 57–99 × 60–103 (74 × 80) 100 × 122 45–60 × 55–71 (52 × 63)
Oesophagus 0–17 (2) 0 0–28 (11)
Intestinal bifurcation to ventral sucker 64–172 (118) 90 0–56 (15)
Vitellarium to ventral sucker (V-VS) 117–221 (163) 201 74–132 (92)
Ventral sucker (VS) 141–225 × 192–318 (175 × 250) 182 × 267 87–142 × 141–186 (103 × 157)
Cirrus-sac 205–347 × 58–140 (255 × 86) 274 × 82 196–293 × 60–88 (253 × 75)
Extent of external seminal vesicle into hindbody (EESSH) 0 0 0–78 (35)
VS to Ovary 0 0 0–36 (9)
Ovary 88–184 × 102–219 (126 × 162) 98 × 132 46–131 × 83–149 (88 × 120)
Testicular field Distance between testicular fields 222–407 × 164–330 (290 × 228) 102–275 (155) 254–276× × 226–236 158 151–229 × 99–205 (186 × 147) 115–232 (147)
Post-testicular region 247–642 (383) 301 121–207 (158)
Post-caecal length 120–310 (215) ? 146–159 (152)
Eggs 49–58 × 20–31 (54 × 25) 52 × 27 49–62 × 28–39 (57 × 34)
Width as % of body-length 71–94 (84) 96 78–93 (83)
Forebody as % of body-length 27–37 (32) 38 30–39 (34)
Sucker-length ratio 1:1.36–1.70 (1.53) 1:1.3 1:1.2–1.9 (1.4)
Sucker-width ratio 1:1.6–1.9 (1.8) 1:1.7 1:1.5–1.8 (1.6)
Pharynx: oral sucker ratio 1:1.5–2.0 (1.8) 1:1.3 1:1.4–1.6 (1.5)
VS-Ovary as % of body-length 0 0 0–5.4 (1.5)
EESVH as % of VS-Ovary N/A N/A N/A
Post-testicular region 37–51 (43) 39 22-33 (26)
Cirrus-sac length% of body-length 25–34 (30) 35 36–46 (42)
Pre-vitelline distance % of body- length 10–17 (13) 12 14–22 (18)
Testicular field length% of body- length 30–38 (34) 33–35 24–35 (31)
Pretesticular distance% of body-length 17–25 (22) 27 34–43 (38)
Post-uterine distance% of body-length 22–40 (30) 20 17–29 (24)
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