Ephemerotoma skarzynskii, Potapov, Mikhail, Kahrarian, Morteza, Deharveng, Louis & Shayanmehr, Masoumeh, 2015

Potapov, Mikhail, Kahrarian, Morteza, Deharveng, Louis & Shayanmehr, Masoumeh, 2015, Taxonomy of the Proisotoma complex. V. Sexually dimorphic Ephemerotoma gen. nov. (Collembola: Isotomidae), Zootaxa 4052 (3), pp. 345-358 : 347-351

publication ID

https://doi.org/ 10.11646/zootaxa.4052.3.4

publication LSID

lsid:zoobank.org:pub:E746140C-2239-4425-9007-31AC036D852C

DOI

https://doi.org/10.5281/zenodo.6110111

persistent identifier

https://treatment.plazi.org/id/03F06833-FFAF-647A-8CC6-F741FCDBFD87

treatment provided by

Plazi

scientific name

Ephemerotoma skarzynskii
status

sp. nov.

Ephemerotoma skarzynskii sp. nov.

Figs 1–16 View FIGURES 1 – 10 View FIGURES 11 – 14 View FIGURES 15 – 16 , 41 View FIGURES 34 – 41

Material. Holotype subadult male: Iran, SE Kermanshah Province, Osmanvand rural district, Cheshmeh Sorkh village, 33°58.319' 047°18.018', 1913 m elev., oak forest, in leaf litter, 31. i. 2014, leg. M. Kahrarian. Paratypes (adult and subadult females): 20 specimens, same locality as for holotype. Type specimens deposited in IAU, MSPU, and MNHN.

Description. Size of fully developed adult unknown, from 1.5 to 1.7 mm in subadult individuals. Colour brown. Cuticle finely reticulated, size of largest polygons much smaller than bases of chaetae. Abd.V and VI with rugosity ( Figs 13 View FIGURES 11 – 14 , 39 View FIGURES 34 – 41 ), profile of Abd.V concave (slightly varies, less in juvenile specimens). Ocelli 8+8, G and H smaller. PAO narrow, elliptical, not constricted, as long as 1.4–2.1 ocellus diameter and 0.4–0.7 as long as U3. Maxillary outer lobe with simple maxillary palp and 4 sublobal hairs 2 of which larger ( Fig. 2 View FIGURES 1 – 10 ). Maxillary head with unmodified lamellae. 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 4 guards ( Fig. 4 View FIGURES 1 – 10 ), with 3 proximal and 4 basomedian chaetae. Ventral side of head with 5+5 postlabial chaetae (more rarely with 6 or 4 on one side). Ant.1 with about 30 chaetae, 2 small basal microsens (bms), one each dorsally and ventrally, the dorsal microsens often as a pair, 3–4 ventral sens (s) in females ( Fig. 5 View FIGURES 1 – 10 ) and 5–8 in males ( Figs 6–7 View FIGURES 1 – 10 ); increased number of sens in males due to additional pair in more lateral position. Ant.2 with 3 (rarely 4) bms and 1 laterodistal s, Ant.3 without bms and with 5 distal s (including one lateral spine-like), guard sens of AO 1.5 times the length of inner ones ( Fig. 3 View FIGURES 1 – 10 ). Sens on Ant.4 weakly differentiated, subapical organite small.

Body with numerous and rather long chaetae. Dorsal axial chaetom of Th.II–Abd.IV variable: 9–11,8–9/7– 8,7–8,8–9,10–11. Common chaetae long and often curved, smooth ( Fig. 14 View FIGURES 11 – 14 ). Th.III with 1–2 ventral axial chaetae on each side of ventral line, Th.I and II without ventral chaetae. Macrochaetae differentiated, medial chaetae on Abd.V as long as 0.30–0.45 of tergal midline, often curved apically. Sens on tergites clearly differentiated, short. S-formula as 3,3/2,2,2,2,4 (s) and 1,1/1,1,1 (ms). Sens on Abd.I–III in front of p-row of

chaetae. Microsens on Abd. I–III in front of lateral sens ( Fig. 1 View FIGURES 1 – 10 ). On Abd.V sens arranged as one long pair in anterior position and one short pair in posterior position ( Figs 1 View FIGURES 1 – 10 , 13, 14 View FIGURES 11 – 14 ). Unguis simple, without inner or lateral teeth ( Fig. 10 View FIGURES 1 – 10 ). Tibiotarsi with many chaetae: 28–31 chaetae on Ti.1 and 2, and>32 on Ti.3. B-row of chaetae on Ti.1–2 complete (B4 and B5 present). Tibiotarsal tenent chaetae (1,2,2), blunt, sometimes very slightly clavate, 1.1–1.4 as long as U3. Femur 1 with 10–12 a -chaetae, 1 ae -chaeta, 4–5 e -chaetae, and 15–17 chaetae of pe-p-pi-i - group (after the notation of Huang & Potapov 2012). Ventral tube with 6–9 chaetae on each side, 8 – 10 posterior chaetae. Tenaculum with 3+3 teeth and one chaeta. Anterior furcal subcoxae with 20–29 chaetae, posterior subcoxae with 10–15 chaetae. Furca well developed. Anterior side of manubrium with a pair of distal chaetae ( Figs 8 View FIGURES 1 – 10 , 12 View FIGURES 11 – 14 ), posterior side with about 30+30 chaetae on main part and 6+6 chaetae on laterobasal lobes ( Fig. 11 View FIGURES 11 – 14 ). Dens stout, normally with 5 anterior chaetae arranged as 1,1,1,2, one of them always proximal, the others distal. Variants with arrangements as 1,1,1,1,2 and 1,1,1,3 also found ( Figs 8, 9 View FIGURES 1 – 10 , 12 View FIGURES 11 – 14 ). Posterior side of dens with clear humps and 7 (6–8) chaetae, arranged as 5–6 chaetae in proximal half, one at the middle and one distally. Mucro with 2 teeth, slightly lamellate. Ratio of manubrium: dens: mucro = 6.0–9.0: 4.0–6.0: 1.0.

Epitokous males. Reproductive males are absent in our collection so only preliminary description of their sexual dimorphism is possible so far. Subadult males show slightly broader antennae ( Fig. 16 View FIGURES 15 – 16 ) and slightly thicker macrochaetae on lateral parts of the body tergites and head than in females ( Fig. 15 View FIGURES 15 – 16 ). Males also have more sens on Ant.1.

Affinity. Among congeners the new species most closely resembles E. porcella (Mediterranean: Crete) by having a rugose swelling at the posterior margin of Abd.V ("rosette" of Ellis 1976), presence of ventral chaetae on metathorax, and similar sexual dimorphism. In the first description of porcella ( Ellis 1976) a ventral chaetotaxy of 0+0, 1+1, 0+0 was given for the three thoracic segments. We believe this was an error since such a combination has never been reported in Collembola . The new species differs by the presence of a distant proximal chaeta on anterior side of dens (encircled in Figs 8 and 9 View FIGURES 1 – 10 ), and an increased number of sens on Ant.1; both characters are unique for the new species. In both E. skarzynskii sp. nov. and E. porcella the sexual dimorphism affects the head and body spines, which are grouped together on lateral parts of body tergites in males. The shape of basal segments of the antennae is also affected (swollen in males). Strict comparison of the dimorphism between the two species is impossible since E. skarzynskii sp. nov. is described based on females and non reproductive males while E. porcella was collected in a reproducing population.

Distribution and ecology. Known only from the type locality. The species was observed in mass aggregations in oak leaf litter and on the ground. It was recorded only in January and February and was absent in June and September.

Name derivation. It is our pleasure to dedicate this species to our colleague, Dr. Dariusz Skarżyński, the leading expert on collembolans of the family Hypogastruridae .

MNHN

Museum National d'Histoire Naturelle

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