Cephalodella jersabeki Smet & Verolet, 2016, n. sp.
Cephalodella jersabeki n. sp. (Figs 1, 2) Diagnosis. Female about 160−170 µm long. Body stout, arched dorsally, almost flat ventrally, weakly compressed laterally. Tail rather small, rounded. Toes short, less than 1 / 5 total length, more or less conical, in dorsal view broadest and arched near base...
| Main Authors: | , |
|---|---|
| Format: | Text |
| Language: | unknown |
| Published: |
Zenodo
2016
|
| Subjects: | |
| Online Access: | https://dx.doi.org/10.5281/zenodo.6091369 https://zenodo.org/record/6091369 |
| Summary: | Cephalodella jersabeki n. sp. (Figs 1, 2) Diagnosis. Female about 160−170 µm long. Body stout, arched dorsally, almost flat ventrally, weakly compressed laterally. Tail rather small, rounded. Toes short, less than 1 / 5 total length, more or less conical, in dorsal view broadest and arched near base, tapering to rather long, blunt tips; median and ventral margin almost straight; tips weakly recurved dorsally. Two colourless eyespots (?) at end of brain. Trophi type B, moderately asymmetric. Rami composed of three well developed and sclerified chambers; fairly acute and long alulae of almost equal length. Flabella rami small, fan and shaft reduced, composing sclerite elements fused. Pectines rami with left 7 large appressed distal teeth and ~ 4−5 very short appressed proximal knobs, and right 9 large appressed distal teeth and ~ 15−20 short appressed proximal knobs. Manubria straight, characteristic asymmetrical distal crutches; crutch of left manubrium sickle-shaped, outer margin of sickle with short, acute lateral projection; crutch of right manubrium smaller, more or less crooked, outer margin without acute projection; manubrial chambers lamellar, dorsal lamella pointed distally. Type locality. Canal Font Rome, Aubenas, France; 20 May 2009; epibiotic on G. pulex (L.). Holotype. A female in a permanent, glycerine glass slide mount deposited in the Royal Belgian Institute of Natural Sciences (RBINS), Brussels, Belgium, IG 33143, RIR 258. Paratypes. One female from type locality in RBINS, IG 33143, RIR 259; 3 mounted paratypes and 4 SEM trophi preparations in Department of Biology, University of Antwerp. Etymology. The species is dedicated to Dr Christian Jersabek in recognition of his rotifer studies and impressive Rotifer World Catalog (http://www.rotifera.hausdernatur.at). Description of female. Body (Figs 1 A, B, E) stout; in lateral view dorsal margin gibbous, ventral margin almost straight; in dorsal view weakly compressed laterally, widest near mid-length. Head moderately large, slightly deflexed, offset by distinct neckfold. Integument soft, no trace of lorica plates. Tail rather small, rounded, may reach up to midlength of foot. Foot stout, irregular conical, very slightly deflexed. Toes (Figs 1 C, D) short, less than 1 / 5 total length, more or less conical, in dorsal view broadest and arched near base, tapering to rather long, blunt tips; medial and ventral margin almost straight; tips weakly recurved dorsally; proximal part of toes with reservoir, separated from distal duct by minute light refracting structures. Corona fairly oblique. Eyespots (?) two colourless globules at end of brain. Dorsal antenna in posterior third of head. Brain large, saccate, extending till neckfold. Proventriculus present. Gastric glands large, short-stalked, lobed. Stomach large, indistinctly separated from short intestine. Pedal glands large, extending into trunk, with small accessory glands (?). Vitellarium with 8 nuclei. Trophi (Figs 1 F −H, 2) virgate, moderately asymmetrical; type B according Wulfert (1937, 1938). Rami composed of subbasal, basal and dorsal chambers. Subbasal rami chambers (Fig. 2 G: sc) elongate, fairly narrow with moderately large, rounded-triangular ventral fenestra proximally (Fig. 2 G: sf), and comb of 4 strong (left) to 5 smaller (right) strong distal teeth (Fig. I: dt); subdistal lateral apophysis absent. Basal rami chambers (Fig. 2 G: bc) very shallow with large ventro-lateral fenestra; dorsal margin of chambers extending into fairly acute and long, posteriorly projecting alulae of almost equal length. Dorsal chambers (Fig. 2 G: dc) very shallow with very large lateral fenestra, anteriorly with distal comb of teeth, the pecten rami (Figs 2 H, I: p); pectines more or less oriented in the dorso-ventral plane, left one (Figs 2 K, L) with 7 large appressed distal teeth and ~ 4−5 less obvious very short appressed proximal knobs, right one (Figs 2 M, N) with 9 large appressed distal teeth and ~ 15−20 short appressed proximal knobs; distal teeth with seam at outer margin; most distal (ventral) teeth largest; apical rami apophyses absent. Flabella rami (Figs 2 F, G: f; J) fairly small, with reduced fan and shaft, the composing sclerite elements fused. Fulcrum long, in dorsal view slightly expanding towards distal end; in lateral view parallel-sided the greatest part of its length, and slightly expanding proximally and distally; basal fulcrum apophysis absent. Unci with single, acute tooth, and dorsal broadly expanded shaft (Figs 2 G, I: u); tooth shaft-length; unci with small ventral apophysis near mid-length, dorsally and opposite of it a small apophysis incorporated in expansion of shaft; left tooth with blunt inner lamellar expansion (Fig. 2 L: u), right tooth (Figs 2 M, N: u) with 2 large and at least 2 small acute subunci (Figs 2 M, N: su). Manubria straight, with characteristic asymmetrical distal crutches. Crutch of left manubrium (Fig. 2 D) sickle-shaped, near its mid-length transversely placed on manubrial shaft; concave side of sickle towards trophi axis; ventral half of sickle widest; outer margin of sickle with short, acute lateral projection. Crutch of right manubrium (Fig. 2 E) smaller, more or less crooked, ventral half weakly curved, dorsal half weakly expanded dorso-ventrally; outer margin without acute projection. Dorsal and ventral manubrial chambers lamellar, extending till mid-length of shaft; ventral ones distally rounded, dorsal ones terminating into acute, caudally directed and weakly reinforced projection, with lateral opening. Measurements. Body (N= 5): total length 156−170 µm, toe 22−24 µm; trophi (N= 4) 27.7−28.6 µm, ramus (incl. alula) 12.2−14.6 µm, fulcrum 18.4−19.4 µm, uncus (l & r) 8.6−8.9 & 6.4 −7.0 µm, manubrium (l & r) ~ 14.2−16.2 & 14.5−15.8 µm, flabellum ~ 3.5 × 0.9 µm. Distribution and ecology. Cephalodella jersabeki n. sp. is to date only known from its type locality as epibiont of G. pulex . Comments. The overall more or less similar habitus suggests that Cephalodella jersabeki n. sp. may be related to C. jakubskii Wiszniewski described from Pínsk, Byelorussia, and likewise living in association with G. p u l e x (Wiszniewski 1953). It is easily distinguished from the latter by the characteristic shape of the crutches of the manubria, especially the left sickle-shaped one with lateral spine (even obviously recognizable by transparency using light microscopy at lower magnification), which are simply T-shaped in C. jakubskii . Other differences concern the toes which are slightly recurved dorsally (straight in C. jakubskii ), and the presence of a tail (lacking in C. jakubskii ). Another species, C. donneri Hauer, described as epibiont of the crayfish Potamobius torrentium Schrank (Hauer 1959), was treated as possibly synonymous with C. crassipes (Lord) by Koste (1978) and Nogrady et al. (1995), and considered a junior subjective synonym of C. jakubskii by Jersabek (2002), Jersabek & Leitner (2013) and Jersabek et al . (2015). However, if the descriptions and figures of Wiszniewski (1953) and Hauer (1959) are reliable, C. donneri might be a valid species adapted to another basibiont. In C. jakubskii the manubrial crutches are T-shaped, the left smaller than the right one and without spine, whereas in C. donneri the ventral branches of the crutch are apparently a caudal continuation of the manubrial shaft, and the dorsal branches are pointing antero-dorsally with the left branch bearing a terminal spine; the unci are apparently much longer in C. donneri the toes are conical in both species, straight in C. jakubskii and, similar to C. jersabeki n. sp. , slightly dorsally recurved distally in C. donneri. In the most recent revision of the genus Cephalodella by Nogrady et al . (1995), C. jersabeki n. sp. keys out to C. crassipes , but the trophi type of the latter was erroneously called type B in the key, whereas it was described as type A in the species description. They also considered C. jakubskii and C. donneri as possible synonyms of C. crassipes , notwithstanding the significant differences of their diagnostic features (for a discussion of the nomenclatorial confusion concerning these species see Jersabek (2002)). Inclusion of C. jersabeki n. sp. in the C. crassipes complex, as Jersabek (2002) did for C. jakubskii , is not followed here in view of the obvious differences in trophi structure, i.e. the presence of crutched manubrial cauda and the pronounced alulae on the rami which are both lacking in C. crassipes, and the unambiguously differently shaped rami teeth which are distal instead of medial as in the latter. The study by light microscopy of the rami structure in Cephalodella is difficult and even in the few studies by SEM there is some disagreement in the interpretation and naming of the different composing structures (Markevich 1989; Segers & Pholpunthin 1997; De Smet 1998 a; Segers & Chittapun 2001; Sørensen 2002; Jersabek et al . 2011; Fischer & Ahlrichs 2006, 2011). In the present paper we recognize three chambers composing the rami (Fig. 2 G): subbasal, basal and dorsal, which can be traced in all species studied to date (unpubl. res.). The subbasal chambers (basal chambers in Markevich (1989), De Smet (1998 a); basal apophyses in Segers & Pholpunthin (1997), Segers & Chittapun (2001); subbasal chambers in Sørensen (2002: Fig. 6), Jersabek et al . (2011), Fischer & Ahlrichs (2006, 2011)) are the much isolated, often long and narrow ventral chambers (Fig. 2 G: sc) with proximal ventral or ventro-lateral basifenestra and distal (Fig. 2 I: dt) or medial (Fig. 4 C: mt) teeth. The basal chambers (subbasal in Markevich (1989), De Smet (1998 a); basal in Jersabek et al . (2011), Fischer & Ahlrichs (2011); rami in Segers & Pholpunthin (1997), Fischer & Ahlrichs (2006)) form the medio-ventral section of the widely arched part of the rami (Fig. 2 G: bc). They are elongate and more or less rounded-triangular and fairly shallow to deep chambers with very large opening, separated from the dorsal chambers by a pronounced rim running from the base of the fulcrum or caudal ramus margin towards the dorso-apical ramus margin. This rim is also easily recognized by LM and shown in most of the pictures obtained by the latter research method (e.g. Wulfert 1937, 1938; Nogrady et al . 1995). The dorsal chambers (Fig. 2 G: dc) form the much arched plate-shaped part of the rami with dorsally rounded margin and very large shallow to moderately deep fenestra. The term pecten rami (Latin pecten , comb) is introduced to denote the comb of appressed projections at the medio-frontal margin of the dorsal rami chambers (Figs 2, 3: p). Three types of rami pecten may be grossly distinguished. The combs can be composed of a fairly large series of similar delicate projections (Figs 3 A, B: p), particularly present in Cephalodella having type A trophi, e.g. C. hoodii (Gosse), C. delicata Wulfert, C. ventripes (Dixon-Nutall) and C. acidophila Jersabek, Weithoff & Weisse (Jersabek et al. 2011; Jersabek, pers. comm.), but may also be present in species of trophi type C such as C. maior (Zavadovski) (Fig. 3 C: p). Fusion of the projections results in a medially more or less strongly crenate plate, such as in C. panarista Myers (Fig. 3 E: p).The ramus pecten can also be shaped as a comb of stout teeth of more or less similar shape (Fig. 3 F: p, C. stenroosi Wulfert), or as a differentiated comb with a stout major ventral tooth, followed by a series of smaller stout teeth, and terminating in a series of short dorsal knobs such as in C. jersabeki n. sp . (Figs 2 H, I, K −N) and C. boettgeri Koste (Fig. 3 D: p). Teeth of this third pecten type are provided with a longitudinal seam at their outer surface. Species with plate-shaped or toothed pectines are most common in species of trophi types B and C. The term apical ramus apophysis is proposed for the protuberance at the outer surface/margin of the dorsal rami chamber posterior or off the pecten. Depending on the species the apical apophyses can be absent (e.g. C. jersabeki n. sp .) or present. If present, they may be thorn-shaped such as in C. theodora Koch-Althaus (Fig. 4 H: aa), tooth-like as in C. edax Hollowday (Jersabek 2003, Fig. 2), or irregularly shaped as in C. boettgeri (Fig. 3 D: aa). The term subdistal lateral ramus apophysis is proposed for the lateral apophysis posterior from the distal comb of teeth of the subbasal chambers (Fig. 4 G: la), and apparently connected with the unci. The term flabellum (diminutive of Latin flabrum , fan) rami is introduced for the fan-shaped elements associated with the dorsal margin of the dorsal rami chambers (Figs 4 A −E). The flabella are basically composed of a series of elongate sclerite elements forming the rays of the fan. The sclerite elements are provided with a seam, and grouped into a more or less developed stalk caudally, and more or less diverging into a unilaterally fanned structure antero-dorsally. Their ventral margin is closely connected to the dorsal margin of the dorsal chambers, but in species showing flabella with long stalk, the stalk may become more or less free from the rami (Fig. 4 C: f). The rays of the fan may be simple, bifid at their free end, or more or less strongly branching (Fig. 4 B: f); they may be spread (Fig. 4 B: f) or compacted into a broom-like structure (Fig. 4 C: f). In species with reduced flabellum the composing sclerite elements are usually fused into a platelet (Fig. 2 J). Apparently, flabella rami are present only in the genus Cephalodella , and have been called subunci (e.g. Wulfert 1937; Donner 1950; Koste 1978; Nogrady et al. 1995; Fischer & Ahlrichs 2011), or pleural rods (e.g. De Smet 2001; Sørensen 2002, Fig. 6). The latter terms are also used to denote other, different and unrelated structures. The Figs 4 A −G clearly show that the flabella are not associated with the unci, and the term subunci should only be used for the hard structures situated distally at the inner side of the unci (Figs 2 M, N; 4 A: su). The term pleural rod has been used for the long, rod-shaped straight (in numbers of one, 2 or 3), U, V, or Y-shaped structures found laterally to medio-ventrally from the incus and more or less in line with the trophi axis, and hitherto only demonstrated in the genus Cephalodella. They easily dissolve in hypochlorite solution, suggesting that they may belong to the ligamentous system of the trophi or supporting structure of the mastax. The term pleural rod has been used in other Notommatidae as well (e.g. Eothinia , Notommata , Resticula ) to denote the paired and strongly sclerified, straight or slightly bent rod-shaped trophi elements (Figs 4 I: ts, 4 J, K), often with small terminal widening dorsally, situated between the head of the manubria and the rami, and more or less perpendicular to the trophi axis. We propose to keep ‘pleural rod’ for the long, longitudinally oriented and easily dissolving structures in Cephalodella , and to use ‘transversal sclerite’ for the elements located transversally between malleus and incus in the other notommatid genera. Fischer & Ahlrichs (2011) introduced a new definition scheme for the trophi of Cephalodella based on SEM to identify the six types originally described by Wulfert (1937, 1938). However, this new scheme, based on trophi preparations obtained with the dithio-dl-threitol method modified after Kleinow et al. (1990), can be confusing as some delicate trophi parts may be missed by this method. For example, they do not mention flabella in their group with trophi types A, E and F, but use this feature to differentiate these types with trophi type D species, notwithstanding that these structures are clearly seen in preparations obtained by the NaOCl method (e.g. C. hoodii (Fig. 3 A: f) and C. megalocephala (Glascott), (Figs 4 E, F: f), respectively type E and F according Fischer & Ahlrichs l.c .). : Published as part of De Smet, Willem H. & Verolet, Michel, 2016, Epibiotic rotifers of Gammarus pulex (L.) (Crustacea, Amphipoda), with descriptions of two new species and notes on the terminology of the trophi, pp. 301-320 in Zootaxa 4107 (3) on pages 302-306, DOI: 10.11646/zootaxa.4107.3.1, http://zenodo.org/record/255018 : {"references": ["Wulfert, K. (1937) Beitrage zur Kenntnis der Radertierfauna Deutschlands. Teil III. Archiv fur Hydrobiologie, 31, 592 - 636, 6 pls.", "Wulfert, K. (1938) Die Radertiergattung Cephalodella Bory de Vincent. Bestimmungsschlussel. Archiv fur Naturgeschichte, 7, 137 - 152.", "Wiszniewski, J. (1953) O wrotkach-komensalach niektorych skorupiakow. Polskie Archiwum Hydrobiologii, 1, 25 - 41.", "Hauer, J. (1959) Raumparasitische Rotatorien aus der Kiemenhohle des Steinkrebses (Potamobius torrentium Schrank). Beitrage zur naturkundlichen Forschung in Sudwest-Deutschland, 18, 92 - 105.", "Koste, W. (1978) Rotatoria. Die Radertiere Mitteleuropas. Ein Bestimmungswerk, begrundet von Max Voigt. Ueberordnung Monogononta. 2 nd Edition. Gebr. Borntraeger, Berlin, Stuttgart, I. Textband, 673 pp., II. Tafelband, 234 Taf.", "Nogrady, T. & Pourriot, R. (1995) The Notommatidae. In: Nogrady, T., Pourriot, R. & Segers, H. (Eds.), Rotifera 3. Notommatidae and Scaridiidae. In: Nogrady, T. & Dumont, H. J. (Eds.), Guides to the Identification of the Microinvertebrates of the Continental Waters of the World. Vol. 8. SPB Academic Publishers bv., Amsterdam, pp. 1 - 248.", "Jersabek, C. D. (2002) A case of considerable confusion in rotifer taxonomy: the Cephalodella crassipes complex. Archiv fur Hydrobiologie Supplement, 139 / 2, 265 \u0336 274.", "Jersabek, C. D. & Leitner, M. F. (2013) The Rotifer World Catalog. World Wide Web", "Jersabek, C. D., De Smet, W. H., Hinz, C., Fontaneto, D., Michaloudi, E., Wallace, R. L. & Segers, H. (2015) List of Available Names in Zoology, candidate part Phylum Rotifera, species-group names established before 1 Januari 2000. Revised version 2015 - 12 - 04. 355 pp. Available from: http: // rotifera. hausdernatur. at / Home / RotiferLAN (accessed 24 January 2016)", "Markevich, G. I. (1989) Morphology and principal organization of the sclerite system of rotifer mastax. In: Shilova, A. I. (Ed.), Biological and Functional Morphology of Freshwater Animals. Proceedings of the Institute of the Biology of Inland Waters, 56, pp. 27 - 82. [in Russian]", "Segers, H. & Pholpunthin, P. (1997) New and rare Rotifera from Thale-Noi Lake, Pattalang Province, Thailand, with a note on the taxonomy of Cephalodella (Notommatidae). Annales de Limnologie, 33, 13 - 21. http: // dx. doi. org / 10.1051 / limn / 1997001", "De Smet, W. H. (1998 a) Cephalodella segersi n. sp. (Notommatidae, Monogononta), a new rotifer from Belgium, with notes on C. catellina (O. F. Muller, 1786), C. fluviatilis (Zavadovsky, 1926) and C. maior Zavadovsky, 1926 stat. nov. Hydrobiologia, 367, 1 - 13. http: // dx. doi. org / 10.1023 / A: 1003199004604", "Segers, H. & Chittapun, S. (2001) The interstitial Rotifera of a tropical freshwater peat swamp on Phuket Island, Thailand. Belgian Journal of Zoology, Supplement, 131, 65 - 71.", "Sorensen, M. V. (2002) On the evolution and morphology of the rotiferan trophi, with a cladistics analysis of Rotifera. Journal of Zoological Systematics and Evolutionary Research, 40, 129 - 154. http: // dx. doi. org / 10.1046 / j. 1439 - 0469.2002.00188. x", "electronic publication. Available from: http: // www. rotifera. hausdernatur. at / Species / Index / 222 (accessed 24 January 2016) Jersabek, C. D., Weithoff, G. & Weisse, T. (2011) Cephalodella acidophila n. sp. (Monogononta: Notommatidae), a new rotifer species from high acidic mining lakes. Zootaxa, 2939, 50 58.", "Fischer, C. & Ahlrichs, W. H (2006) Cephalodella ungulata n. sp. (Monogononta: Notommatidae), a new rotifer from North- West Germany, with notes on C. tenuiseta (Burn, 1890). Zootaxa, 1378, 49 - 59.", "Fischer, C. & Ahlrichs, W. H (2011) Revisiting the Cephalodella trophi types. Hydrobiologia, 662, 205 - 209. http: // dx. doi. org / 10.1007 / s 10750 - 010 - 0497 - z", "Jersabek, C. D. (2003) Additions to the rotifer fauna of Central Europe: new records of rare species from Austria. Archiv fur Hydrobiologie Supplement, 139 / 3, 433 \u0336 448.", "Donner, J. (1950) Radertiere der gattung Cephalodella aus Sudmahren. Archiv fur Hydrobiologie, 42, 304 - 328, pls. 11 - 18.", "De Smet, W. H. (2001) Freshwater Rotifera from plankton of the Kerguelen Islands (Subantarctica). Hydrobiologia, 446 / 447, 261 - 272. http: // dx. doi. org / 10.1023 / A: 1017580129530", "Kleinow, W., Klusemann J. & Wratil, H. (1990) A gentle method for the preparation of hard parts (trophi) of the mastax of rotifers and scanning electron microscopy of the trophi of Brachionus plicatilis (Rotifera). Zoomorphology, 109, 329 - 336. http: // dx. doi. org / 10.1007 / BF 00803573"]} |
|---|