Loxosoma (Loxosomina) aripes Borisanova & Schepetov 2023, n. comb.
- 1. Faculty of Biology, Moscow State University, Moscow 119991, Russia.
- 2. Faculty of Biology, Moscow State University, Moscow 119991, Russia. & Biological Faculty, Shenzhen MSU-BIT University, Shenzhen, 518172 China.
Description
Loxosoma (Loxosomina) aripes (Nielsen, 1964b) n. comb.
(Figs 1–8, Table 3)
Loxosomella aripes Nielsen, 1964b: 4, fig. 2.
Original description. Small species, up to 470 µm. Lophophore has six very short, stout tentacles (one specimen with 4 tentacles). Atrium narrow. Stomach big and rounded. Peduncle longer than calyx. Peduncle slender, terminating in laterally compressed expansion, which on each side bears 3–4 transverse furrows. Youngest buds formed laterally at lower level of stomach, and older buds found above this reaching upper level of stomach; up to three buds at time. Embryos very big and quite deform the calyx; 1–3 embryos at time. Usually buds and embryos found only in one side of animal. Host: Laonice cirrata. Type locality: Raunefjorden, off Sletten (60°16.5′N, 5°12′E), depth 100– 120 m. The holotype is illustrated in Fig. 1.
Material examined. Holotype (number 46395) (Fig. 1); No Uk-31 (ZMMU)— six specimens from the Kandalaksha Bay, White Sea (66°34′N, 33°08′E), 30–70 m; six specimens from the White Sea from a personal collection.
Description of the material from the White Sea. Medium-sized species with average body length of 596 µm (Figs 2, 3) (measurements for 11 specimens are provided in Table 3 on page 11). Calyx is up to one and a half times shorter than stalk (average calyx length 228 µm). Calyx bears six short tentacles directed distally when embryos are not developed. When embryos are developing the calyx strongly swells on one side and the tentacles are shifted to the side and directed disto-laterally. The tentacles are unusually wide and the frontal surface is formed by nine rows of ciliated cells (Fig. 4a, b). The frontal groove is formed by three rows of frontal cells (Fig. 4a–c). The latero-frontal cells border the frontal groove (Fig. 4b–d), and the lateral cells form two rows on each side of the frontal surface of the tentacle (Fig. 4a, b, e).
Digestive system includes esophagus, stomach, intestine and rectum (Fig. 5a). The esophagus is lined with cuboidal epithelium (Fig. 5b). The stomach is large, looks roundish (Fig. 2), but histological sections show that the stomach is three-lobed. In the lower part of the stomach lateral lobes are separated from the central zone by epithelial invaginations deeply protruding into the stomach cavity (Fig. 5a). A roof of the stomach is lined with 'liver' cells; lateral sides and lateral lobes of the stomach are glandular; epithelium from the beneath intestine and esophagus to the bottom of the stomach is cuboidal (Fig. 5b). The intestine is bulbous (Fig. 5a), lined with prismatic epithelium, the cells with granular cytoplasm and numerous cilia on the apical surface (Fig. 5c). Rectum oval, cells with long cilia (Fig. 5d). Anal cone directed upward (Fig. 2c, f, h, i).
The cylindrical stalk has average length of 377 µm. Its width is almost uniform throughout its length (average width 83 µm). The attachment organ looks like a 'beak' extended backwards, often bent to the abfrontal side (Figs 2, 3, 6a, b). Beak gradually narrows towards the apical part. At the tip of the beak there is usually a small swelling (Fig. 6a, b). The stalk gradually passes into the beak, there is no pedal gland at the base of the stalk (Fig. 6c–g, l–n). The cavity of the beak contains many muscular cells and several glandular cells, the pedal groove and accessory cells are absent (Fig. 6h–k). The cavity of the swelling is empty; several large glandular cells lie in epithelium (Fig. 6i, g).
Buds originate from lateral area only on one side of the calyx, up to seven buds at a time (Figs 2, 7a, b). Larger buds are located upper and more laterally than younger ones. The stalk of the fully developed bud ends with a rounded pedal disc (Fig. 7c–f). The bud attaches to the maternal specimen by the posterior end of the pedal disc (Fig. 7c). Specimens with fully developed buds have paired gonads on both sides of the calyx, but do not have embryos (Fig. 7b). Specimens with young buds may have embryos. Embryos, like buds, form only on one side of the calyx, and this is the same side where the buds are located (Fig. 2a–c, h, i). In some specimens embryos and buds develop on the left side of a calyx (Fig. 2a, i), in other specimens on the right side of a calyx (Figs 2h, 6a).
Most specimens that were collected at the end of August had developing embryos in the calyx. When embryos develop, the calyx becomes asymmetric—it swells on one side (Fig. 2g –i). One specimen may simultaneously have one fully developed larva in the brood chamber, one or two developing larvae and about five embryos at different stages of development (Fig. 8a–c). The creeping-type larva has a well-developed foot, a large paired frontal organ, and a small apical organ (Fig. 8d–f).
Remarks. The specimens found in the White Sea attach to the setae of the parapodia of Laonice sp. Several dozen specimens were found on one polychaete. They have some differences from those described from the Bergen area. They are slightly larger (up to 700 µm, while specimens from Bergen are up to 470 µm). The specimens from Bergen have transverse furrows on the base of the stalk caused by the setae of the polychaete (Nielsen 1964b), which are lacking on the specimens from the White Sea. In the White Sea sexually reproduced specimens were found in August, while in Bergen was September. Despite these differences, we still assume that specimens from Bergen and from the White Sea belong to the same species. They share the unique features: buds and embryos develop only on one side of the calyx, which becomes asymmetrical when embryos are large; the calyx bears six short and wide tentacles (specimens with four tentacles are also described from Bergen). Loxosomatids rarely have six tentacles. Only calyxes of Loxosoma axisadversum Konno 1972, Loxosomella sextentaculata Borisanova & Chernyshev & Ekimova, 2018 and Loxosomella discopoda Nielsen & Ryland, 1961 bear six tentacles, and calyx of Loxosomella brachystipes Franzén, 1973 can bear from six to twelve tentacles. The tentacles of Loxosoma (Loxosomina) aripes n. comb. differ from all other studied entoprocts in the structure of the frontal surface. It consists of nine rows of ciliated cells instead of five rows as in other entoprocts (Nielsen & Jespersen 1997; Riisgard et al. 2000; Borisanova 2020). There are two additional rows of cells similar in ultrastructure to the frontal cells that form the lateral walls of the frontal groove. In other entoprocts, the frontal groove is formed by a single frontal cell. There are also two additional rows of lateral cells, which create a water current.
Notes
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Linked records
Additional details
Identifiers
Biodiversity
- Collection code
- ZMMU
- Family
- Loxosomatidae
- Genus
- Loxosoma
- Kingdom
- Animalia
- Order
- Coloniales
- Phylum
- Kamptozoa
- Scientific name authorship
- Borisanova & Schepetov
- Species
- aripes
- Taxonomic status
- comb. nov.
- Taxon rank
- species
- Type status
- holotype
- Taxonomic concept label
- Loxosoma (Loxosomina) aripes (Nielsen, 1964) sec. Borisanova & Schepetov, 2023
References
- Nielsen, C. (1964 b) Entoprocta from the Bergen area. Sarsia, 17 (1), 1 - 6. https: // doi. org / 10.1080 / 00364827.1964.10409535
- Konno, K. (1972) Studies on Japanese Entoprocta. I. On four new species of loxosomatides found at Fukuara, Aomori Prefecture. Science Reports of the Hirosaki University, 19, 64 - 78.
- Borisanova, A. O. (2018) Entoprocta (Kamptozoa). In: Schmidt-Rhaesa, A. (Ed.), Handbook of Zoology. Miscellaneous Invertebrates. De Gruyter, Berlin and Boston, pp. 111 - 162. https: // doi. org / 10.1515 / 9783110489279 - 006
- Nielsen, C. & Ryland, J. S. (1961) Three new species of Entoprocta from West Norway. Sarsia, 1, 39 - 45. https: // doi. org / 10.1080 / 00364827.1961.10410243
- Franzen, A. (1973) Some Antarctic Entoprocta with notes on morphology and taxonomy in the Entoprocta in general. Zoologica Scripta, 2, 183 - 195. https: // doi. org / 10.1111 / j. 1463 - 6409.1974. tb 00751. x
- Nielsen, C. & Jespersen, A. (1997) Entoprocta. In: Harrison, F. W. & Ruppert, E. E. (Eds.), Microscopic anatomy of invertebrates. Vol. 13. Wiley-Liss, New York, pp. 13 - 43.
- Riisgard, H. U., Nielsen, C. & Larsen, P. S. (2000) Downstream collecting in ciliary suspension feeders: the catch-up principle. Marine Ecology Progress Series, 207, 33 - 51. [https: // www. jstor. org / stable / 24863777]
- Borisanova, A. O. (2020) Two types of the tentacle structure of Entoprocta and the fine structure of the vestibular groove. Zoomorphology, 139 (4), 433 - 445. https: // doi. org / 10.1007 / s 00435 - 020 - 00497 - y