Ephemerotoma buryatica Potapov, Huang & Gulgenova, 2020

Potapov, Mikhail, Huang, Cheng-Wang, Gulgenova, Ayuna & Luan, Yun-Xia, 2020, New and little known Isotomidae (Collembola) from the shore of Lake Baikal and saline lakes of continental Asia, ZooKeys 935, pp. 1-24 : 1

publication ID

https://dx.doi.org/10.3897/zookeys.935.49363

publication LSID

lsid:zoobank.org:pub:69778FE4-EAD8-4F5D-8F73-B8D666C25546

persistent identifier

https://treatment.plazi.org/id/01C359C5-F519-4B0A-9B06-8445933FD6E0

taxon LSID

lsid:zoobank.org:act:01C359C5-F519-4B0A-9B06-8445933FD6E0

treatment provided by

ZooKeys by Pensoft

scientific name

Ephemerotoma buryatica Potapov, Huang & Gulgenova
status

sp. nov.

Ephemerotoma buryatica Potapov, Huang & Gulgenova sp. nov. Figures 19-26 View Figures 19–26 , 27-31 View Figures 27–31

Type material.

Holotype: female. Russia, south-western part of Buryat Republic, Gusinoozerskaya Basin, 0.5 km SW from Tokhoy, 51.356417°N, 106.558733°E, 590 m alt., southern shore of Sul’phatnoye (= Selenginskoye) Lake, grassland with Caragana sp., Achnatherum splendens , Atriplex sp., Leymus sp., 18.X.2015, coll. M. Potapov and A. Gulgenova. 24 paratypes (sub-adult and adult males and females) from the same place. Holotype and 10 paratypes deposited in MSPU, 4 in BSU, 5 in SMNG, 5 in SEM.

Other material.

From the type locality dated 02.V.2015 and 25.VII.2015.

Description.

Size 0.6-0.9 mm. Body as common for Anurophorinae with short furca (Fig. 27 View Figures 27–31 ). Pigmentation grey, as in Proisotoma minuta (Tullberg, 1871). Cuticle finely reticulated, size of largest polygons smaller than bases of setae. Ocelli 8+8, G and H smaller (Fig. 23 View Figures 19–26 ), all ocelli usually look subequal by pigmentation. PAO with three guard setae along posterior margin, elliptical, not constricted, as long as 0.4-0.6 of Ant.1 width and 0.7-1.1 as long as U3 (Fig. 23 View Figures 19–26 ). Maxillary outer lobe with simple maxillary palp and four sublobal hairs. Labral formula as 2/554. Labium with all papillae (A-E), papillae A-D with normal number of guards (1,4,0,4), E with four guards (Fig. 21 View Figures 19–26 ). Main part of labium with three proximal, four basomedian and five basolateral setae. Ventral side of head with 4+4 postlabial setae. Ant.1 with two basal, ventral and dorsal, bms, two ventro-lateral s, and eleven setae, without p-setae (Fig. 23 View Figures 19–26 ). Ant.2 with three bms and one laterodistal s. Ant.3 without bms and with five distal s (including one lateral spine-like), inner s of AO small (Fig. 22 View Figures 19–26 ). All s-setae on Ant.1-3 very short. S-setae on Ant.4 weakly differentiated, subapical organite small. Apex of Ant.4 with bilobed bulb (Figs 24-26 View Figures 19–26 ), well visible in dorsal view (Fig. 25 View Figures 19–26 ). In fully grown animals the bulb can look trilobed due to slight secondary division of one of the lobes (Fig. 26 View Figures 19–26 ).

Body with smooth and rather short setae. Dorsal axial setal pattern of Th.II-Abd.IV: 7-8,6-7/5,5,5,7-8. Th.I and II without ventral setae, Th.III with 3-5+3-5 (usually 4+4) ventral axial setae (Fig. 31 View Figures 27–31 ). Abd.II with a pair of mid-ventral setae (Fig. 31 View Figures 27–31 ). Macrosetae weakly differentiated, medial macrosetae on Abd.V as long as 0.25-0.35 of tergal midline (Fig. 20 View Figures 19–26 ). S-setae on tergites very short (Fig. 20 View Figures 19–26 ). S-formula as 3,3/2,2,2,2,4 (s) and 1,1/1,1,1 (ms). In al-group of Th.II and III front s-seta and ms-seta set close to each other (notated as ‘ms+s’ in Fig. 21 View Figures 19–26 ). S-setae on Th.II-Abd.V set in front of p-row of setae (Fig. 1 View Figures 1–5 ). On Abd.V s-setae arranged in one transverse row, lateral pair very short (Fig. 2 View Figures 1–5 ).

Unguis of unusual shape, expanded at the middle, without teeth. Empodial appendage slender, without lamellae. Ti.1 and Ti.2 without additional setae (21), Ti.3 usually with 25 setae. B-row of setae on Ti.1-2 complete (B4 and B5 present). Male spurs (x and B5 on Ti.3) in adult males thin, stick-like. Tibiotarsal tenent setae pointed (Fig. 30 View Figures 27–31 ). Ventral tube with 4+4 distal and four posterior setae arranged in one transversal row (Fig. 31 View Figures 27–31 ). Tenaculum with 3+3 teeth and one seta. Anterior furcal subcoxae with 10-13 setae, posterior subcoxae with five or six setae (Fig. 28 View Figures 27–31 ). Anterior side of manubrium with a pair of distal setae (Fig. 28 View Figures 27–31 ), posterior side with 9-10+9-10 setae on main part, lateral edges without setae (Fig. 29 View Figures 27–31 ), laterobasal lobes with 3+3 setae. Dens short, about half as along as Ti.3. Anterior side of dens with three setae in subapical position (Figs 28 View Figures 27–31 , 29 View Figures 27–31 ). Posterior side of dens usually with large subapical hump, more proximal part without clear modifications. Dens with four posterior setae, three in basal half, one subapical. Mucro with two teeth, subapical tooth largest. Ratio of manubrium: dens: mucro = 5.5-6.5: 2.4-3.3: 1.0. Males present.

Affinity.

The species belongs to recently described genus Ephemerotoma Potapov, Kahrarian, Deharveng & Shayanmehr, 2015 due to simple maxillary palp, reduced number (four) of guards on labial papilla E, two prelabral setae, complete set of ms-setae on tergites (11/111), and tergal s-setae on abdomen set in front of p-row. Ephemerotoma buryatica sp. nov. does not share a significant character of the genus, the "two transverse rows" pattern of s-setae on Abd.V. The sexual dimorphism common for the genus Ephemerotoma [ E. porcella (Ellis, 1976), E. skarzynskii Potapov, Kahrarian, Deharveng & Shayanmehr, 2015, E. huadongensis (Chen, 1985)] is not observed in the new species. Small and rather slender body, short furca, shape of unguis, and absence of sexual dimorphism indicate a preference for deeper edaphic habitat than in its congeners.

Regarding all genera of the Proisotoma complex, a peculiarity of the new species is the bilobed apical bulb on Ant.4, which is otherwise known only in Proisotoma bulba Christiansen & Bellinger, 1980 (California, U.S.A.). The generic position of P. bulba is obscure because of lack of information on mouth parts and s-setae on body. In other characters, E. buryatica sp. nov. differs from P. bulba by fewer setae on dens (3/4 vs. 4-5/5-6), shorter dens (dens: mucro = 9: 1 in bulba ), teeth on tenaculum (3+3 vs. 4+4) and characters of unguis and tibiotarsi ( bulba has inner tooth on unguis and a clavate tenent hair). In Proisotoma complex, a similar furca is shown, for example, for Weberacantha echinodermata Potapov, Babenko & Fjellberg, 2006 and Scutisotoma robustodens Huang & Potapov, 2012, which belong to other genera. Mouth parts (two prelabral setae, simple maxillary palp and reduced number of e-guards) of E. buryatica sp. nov. resemble the " asiatica " group of the genus Subisotoma but several other characters of great value are different (e.g., presence/absence of anterior setae on manubrium).

Distribution and ecology.

Known only from one locality in SW Buryatia where it inhabits soil of dry steppe at upper part of a salt-lake catena. The species probably occurs in all seasons since it was recorded in May, July and October in the type locality. It was highly aggregated in October which that suggests a resemblance to the “ephemeral” species of the genus Ephemerotoma .

Name derivation.

It is named after the type locality.