Enterostomula densissimabursa, Omi, 2020

Omi, Nao, 2020, A novel Enterostomula (Platyhelminthes, Prolecithophora) species from two brackish lakes in Japan, Biodiversity Data Journal 8, pp. 47161-47161 : 47161

Enterostomula densissimabursa sp. n.

Materials

Type status: Holotype. Taxon: scientificName: Enterostomuladensissimabursa sp. nov.; kingdom: Animalia; phylum: Platyheminthes; order: Prolecithophora; family: Pseudostomidae; genus: Enterostomula; taxonRank: species; Location: waterBody: Shinji Lake; island: Honshu (Main island of Japan); country: Japan; countryCode: Japan/JP; stateProvince: Shimane; Identification: identifiedBy: Nao Omi; Event: year: 2014; month: 8; habitat: Sand and seaweed; Record Level: language: en; institutionID: NMST-Pl 6300 (sagittal serial section) Type status: Paratype. Record Level: scientificName: Enterostomuladensissimabursa sp. nov.; institutionID: NMST-Pl 6298 (Frontal serial setion), NMST-Pl 6299 (Sagittal serial section)

Description

Body is short and cylindrical, 0.28-0.42 mm (average 0.34 mm, n = 12) long and 0.12-0.33 mm (average 0.17 mm, n = 12) wide. Anterior end is rounded; no ciliated grooves or pits; posterior end is sharpened slightly. Body colour is white; two black pigmented bands located at the dorsal anterior and opposite to end; posterior pigment band extends to the ventral side through the flank; the pigment lies just below the basement membrane of the epidermis (Fig. 1 a, b, c). The basement membrane under the body surface is thick. The intestine is pale orange or white in the living specimen. The eyes, surrounded by black pigment, are located anteriorly and partially embedded in the brain. Each eye consists of a heart-shaped posterior part of two lenses and a single anterior lens (Fig. 2 a). The brain has a weak tunic and is situated under the testis and posteriorly to the eyes; pigment granules can be seen on the brain surface (Fig. 2 a). The testis is follicular, with a tunic near the anterior end. Two vasa deferentia from the testis pass lateral to the intestine. No distinct vesicula seminalis is present. The male copulatory organ, dorsal to the intesitine, is long and cylindrical, 80 µm × 20 µm, with thick-walls of circular and longitudinal muscles; vesicular granulorum is located anteriorly within the male copulatory organ and the penis is located internally within the copulatory organ and extends beyond the penis sheath (Fig. 2 b). The penis sheath is flexible and thick. The ovary is unpaired, not fully separated from the vitellarium and lies dorsally to and posterior to the testis (Fig. 2 c). The vitellarium is an unpaired structure extending dorsally from just behind the testes to the posterior part of the body. The bursa is long and large and is located on the posterior dorsal part of the animal. The posterior portion of the bursa is swollen with thick walls consisting of fibre bundles around a narrow lumen (Fig. 2 b). The anterior portion of the bursa has a columnar structure. The bursa connects to a sclerotised portion of the spermatic duct. The rest of this duct has a swollen portion that opens through a sclerotic bursal mouthpiece (Fig. 2 d, f). The vagina externa opens into the bursa and connects to the vaginal pore at the posterior end of the animal’s body (Fig. 2 e). The pharynx is small and tube-shaped and is located near the posterior ventral end. The oesophagus is short. The common oral-genital opening is located near the posterior ventral end. The intestine with weak tunic lies posterior to the testis.

Etymology

The name of the new species refers to its thick-walled bursa.

Distribution

Lakes Shinji and Nakaumi near the coast of Shimane Prefecture, Japan

Taxon discussion

By having a common gonopore, a short droplet body shape, a tubular pharynx, a brain and intestine with a weak tunic and an ovary that is not fully separated from the vitellarium, E. densissimabursa sp. nov. belongs to the family Pseudostomidae . Its unpaired ovary, unpaired spermatic duct, bursa, vagina externa and unpaired vitellarium more specifically place this species in the genus Enterostomula . Amongst pseudostomids, both genera Allostoma and Enterostomula have a vaginal pore and a bursa; however, Allostoma has a paired spermatic duct, while Enterostomula has an unpaired spermatic duct ( Reisinger 1926, Ruffin Jones Jr. 1941).

Enterostomula densissimabursa sp. nov. has two black pigment bands on its dorsal side. The pigment is typical in prolecithophorans. Allostoma amoenum Karling, 1962 and Enterostomula graffi (Beauckamp, 1913), also have pigmented bands ( Beauchamp 1913, Ma et al. 2014, Karling 1962). In addition, although E. graffi is considered a marine species, it has been reported in the brackish waters of the Marmara Sea, some European seas,and the Atlantic ( Ruffin Jones Jr. 1941, Ax 1959, Ax 2008).

Enterostomula graffi has two pairs of eyes, a short globular male copulatory organ and a thin-walled bursa, whereas E. densissimabursa sp. nov. has one pair of eyes, its male copulatory organ is long and cylindrical in form and its bursa is thick-walled ( Ma et al. 2014, Ruffin Jones Jr. 1941, Beauchamp 1913).

Allostoma amoenum superficially resembles E. densissimabursa sp. nov. Both species have dorsal pigment bands, cylindrical male copulatory organs and a large bursa. In A. amoenum , the vesicula seminalis connects to the male copulatory organ; however, a distinct vesicula seminalis is not observed in E. densissimabursa sp. nov. The bursa of A. amoenum directly connects to the ovary without a spermatic duct; however, in E. densissimabursa sp. nov., the bursa connects to the ovary via the spermatic duct. The bursa of A. amoenum is a large cellular body, whereas the wall of the bursa of E. densissimabursa sp. nov. consists mainly of thick fibres of extracellular matrix and muscle bundles. Although E. densissimabursa sp. nov. has one distinct pair of black eyes, A. amoenum lacks eyes entirely ( Karling 1962). In addition, while A. amoenum has a groove on the anterior body surface, E. densissimabursa sp. nov. does not have a distinct groove.

Allostoma amoenum is considered endemic to California, USA and is found in marine environments ( Karling 1962). The new species, reported in the present study, inhabits brackish lakes at low salinities ranging between 1‰ and 20‰.

In addition to bursa and male copulatory organs, spermatic ducts were observed in 11 individuals amongst the 17 E. densissimabursa sp. nov. specimens collected. Additionally, the bursal mouthpiece, which is connected to a single ovary, was observed in only one specimen. The development of a bursal mouthpiece could be the final stage in the development of the genital system of the organisms.

Enterostomula graffi and Allostoma catinosum (Beklemischev, 1927) (see Beklemischev 1927) have been collected only from brackish waters, but are considered to stem from ancestors in the marine environment ( Ruffin Jones Jr. 1941, Beauchamp 1913, Mack-Fira 1974, Ax 1959, Ax 2008), while Allostoma pallidum Beneden, 1861 (see Ax 2008) is a marine-euhaline immigrant, collected from both marine and brackish habitats. Enterostomula densissimabursa sp. nov. was collected from the brackish waters of Lakes Shinji and Nakaumi with salinities ranging between 1‰ and 20‰ and not from the high salinity (> 27‰) outlets of the Sea of Japan, suggesting that it is a genuine brackish water species, as Ax 2008 would call it. Nonetheless, I found at least seven other pseudostomid species in marine waters just outside the lakes, whereas only E. densissimabursa was found within the lakes. Therefore, E. mursubursa potentially occupies a niche to which other local pseudostomids have not adapted. To date, few studies have reported Pseudostomids in environments with such low salinities. Future studies on the genus should not only explore it in seawater environments but also in low-salinity environments.