Pygmarrhopalites principalis skelicus, Vargovitsh, Robert S., 2009

Vargovitsh, Robert S., 2009, New Cave Arrhopalitidae (Collembola: Symphypleona) from the Crimea (Ukraine), Zootaxa 2047, pp. 1-47 : 36-41

publication ID

https://doi.org/ 10.5281/zenodo.186465

DOI

https://doi.org/10.5281/zenodo.5618668

persistent identifier

https://treatment.plazi.org/id/BA7487DE-EF5D-FF91-FF28-41AAFF7C08D0

treatment provided by

Plazi

scientific name

Pygmarrhopalites principalis skelicus
status

subsp. nov.

Pygmarrhopalites principalis skelicus ssp. nov.

Figs 144–171 View FIGURES 144 – 157 View FIGURES 158 – 162 View FIGURES 163 – 171 , Table 3

Diagnosis. Body with weak reddish-brownish spotted pigmentation, eyes pigmented; trichobothrium B somewhat out of AC (ABC=~160o) and AB<BC; mesothorax with thickened dorsal setae; posterior dorsal setae of great abdomen as long as hind claw and longer; antenna in females 2 times as long as head; Ant IV with 5–7 subsegments; head with 4 + 4 spine-like setae; all claws with inner tooth, mid and hind claw with tunica; empodia with apical filament overtopping tip of claw, fore and mid empodia with, and hind – without corner tooth; trochanter II with 5 setae; tenaculum with 2 setulae; manubrium with 7 + 7 setae; dens with 5 spines or spiny setae, Ie very strong and looks somewhat articulated, anteriorly with 3, 2, 1, 1 setae; tip of mucro broadened or rounded; small abdomen with rather strong but not broadened circumanal setae and axial seta ms1 not forked; appendices anales palmate.

Material examined. Holotype on slide (C-277-1): female, Ukraine, Crimea, Aj-Petri Massif, Skelskaya Cave, 14.viii.1998. Paratypes on slides: 8 males, 23 females, 5 juv., collected together with holotype. Holotype and 34 paratypes are preserved in SIZNAS, 2 paratypes in SNHML.

Other material (on slides). Aj-Petri Massif: female, Kaskadnaya Cave (- 100 m), 17.viii.1998; 2 males, female, 3 juv., same cave (- 100 m, - 150 m), 20.viii.1998; male, female, 8 juv., Drugaya Cave (- 27 m), 1.viii.2005; male, female, 200-4 Cave (- 23 m), 1.viii.2005; 2 females, juv., Kamnepadnaya Cave (- 105 m), 29.vii.2005; 2 females, Oreshek Cave (- 25 m), 28.vii.2005; male, Paniya Cave (- 17 m), 2.viii.2005; 5 females, Bakhchisarai Distr., Vil'ya-Burun Mt., Vilyaburunskaya Cave, traps, 19.vii.2004 – 17.vii.2006. A.G. Koval leg. Besides slides, part of material is preserved in alcohol.

Description. Female: body ( Fig. 144 View FIGURES 144 – 157 ) length 1–1.3 mm, dorsally with reddish-brownish pigmentation, sometimes unpigmented.

Head ( Fig. 145 View FIGURES 144 – 157 ): Eyes 1 + 1, more or less pigmented (with pigmented spots in alcohol and clear on slides). Clypeal area with axial seta in row a. Interantennal area with axial seta in row β. Frontal area with 3 axial setae in rows A, B and C. 8 setae of frontal area are weakly spine-like (in row C: 2 + 2; D: 2 + 2) ( Fig. 151 View FIGURES 144 – 157 ).

Antennae 1.9–2.1 times as long as head. Ant I: II: III: IV = 1: 2.1–2.5: 3.3–4.2: 8.3–10.2. Ant I with 7 setae; Ant II with 15 setae ( Fig. 158 View FIGURES 158 – 162 ). Ant III ( Fig. 159 View FIGURES 158 – 162 ): slightly thickened in subbasal – middle part, with 18 setae and 2 sense rods; seta Aai very small and curved; setae Api and Ape shorter and thinner than others. Ant IV ( Fig. 160 View FIGURES 158 – 162 ) usually distinctly subdivided into 5 (rarely 6 or 7) subsegments with 13(12) setal whorls. If 5 subsegments present, basal one is 1.6–1.8 times as long as apical one and 1–1.1 times as long as Ant III. Subsegmental formula: 1 + 3 + 1 = (A + M1–M2) + (M3–M5) + (B).

Foreleg: precoxae and coxa with 1, 0, 1 setae respectively ( Fig. 146 View FIGURES 144 – 157 ). Trochanter with 3 anterior and 1 posterior setae; femur with 12–13 setae ( Fig. 163 View FIGURES 163 – 171 ), seta a 4 turned perpendicularly to the longitudinal axis of the segment. Tibiotarsus ( Fig. 164 View FIGURES 163 – 171 ) with 3 setae FP and seta FSa; whorl I with 9 setae among which Ja is curved and spiny; each of whorls II–V with 8 setae. Claw without tunica, with inner tooth and 2 pairs of lateral teeth; empodium narrow, with corner tooth, apical filament exceeding claw ( Fig. 164 View FIGURES 163 – 171 ). Claw 4.0–4.6 times shorter than tibiotarsus.

Mid leg: precoxae 1, 2 and coxa with 1, 1, 3 setae respectively ( Fig. 146 View FIGURES 144 – 157 ). Trochanter with anterior trochanteral organ, 3 anterior and 1 posterior setae; femur with 14 setae ( Fig. 166 View FIGURES 163 – 171 ). Tibiotarsus ( Fig. 165 View FIGURES 163 – 171 ): 3 setae FP and seta FSa present; whorl I with 9 setae, each of whorls II–IV with 8 setae, whorl V with 7 setae. Claw with tunica, broader than in foreleg, with inner tooth and 2 pairs of lateral teeth; empodium broadened in basal half, with corner tooth and apical filament exceeding claw ( Fig. 165 View FIGURES 163 – 171 ). Claw 4.5–5 times shorter than tibiotarsus.

Hind leg: precoxae and coxa with 1, 1, 3 setae respectively ( Fig. 146 View FIGURES 144 – 157 ). Trochanter as in mid leg; femur with 14 setae: 2 posterior ones are very small ( Fig. 167 View FIGURES 163 – 171 ). Chaetotaxy of tibiotarsus as in mid leg. Claw with tunica, a little broader than mid claw, with inner tooth and 2 pairs of lateral teeth; empodium broader than in mid leg, without tooth, apical filament exceeding claw ( Fig. 168 View FIGURES 163 – 171 ). Claw 5.5–6.2 times shorter than tibiotarsus.

Length ratio of tibiotarsi I: II: III = 1: 1–1.1: 1.3.

Ventral tube with 2 small subapical setulae, smooth and long eversible sacks. Tenaculum ( Fig. 157 View FIGURES 144 – 157 ): rami 3-dentate, with basal appendage; anterior lobe with 2 apical setulae; tip of posterior lobe exceeding tip of anterior lobe.

Furca ( Fig. 171 View FIGURES 163 – 171 ): manubrium with 7 + 7 posterior setae. Dens: setae Ie, Ii, IIpe, IIIpi and IVpi are spinelike; outer spine Ie very strong, elongated and looks somewhat articulated ( Fig. 156 View FIGURES 144 – 157 ); setae Ipe, IIIpe–Vpe simple; 3, 2, 1, 1 setae on anterior side ( Fig. 171 View FIGURES 163 – 171 ; Table 3). Tip of mucro rounded, slightly broadened ( Fig. 162 View FIGURES 158 – 162 ). Dens 1.5–1.7 times as long as mucro.

Great abdomen ( Fig. 146 View FIGURES 144 – 157 ): mesothorax with spiny dorsal setae ( Fig. 150 View FIGURES 144 – 157 ), which are longer than other anterior setae ( Fig. 149 View FIGURES 144 – 157 ); posterior lateral complex with 6 setae; furca base complex with 9 setae; ventral complex with 3 setae; posterior dorsal complex with setae at least as long as hind claw ( Fig. 148 View FIGURES 144 – 157 ); the most posterior seta of dI-row ( Fig. 147 View FIGURES 144 – 157 ) is 1.5 times longer than hind claw and longer than axial seta ms1 of Abd VI ( Fig. 153 View FIGURES 144 – 157 ). Trichobothrial complex: AB a little shorter than BC; ABC form an angle about 160o. Single seta of p-row of Abd I is located below the level of trichobothrium B anteriorly to the trichobothrial complex (marked with arrow); seta b1 lies close to the line between trichobothria B and C; seta c1 of thichobothrial complex lies on the level of trichobothrium C or lower.

Fifth abdominal segment with trichobothrium D and 4 setae ( Fig. 146 View FIGURES 144 – 157 ).

Sixth abdominal segment ( Fig. 169 View FIGURES 163 – 171 ): circumanal setae strong but not much thickened ( Figs 152, 153 View FIGURES 144 – 157 ). Appendices anales inserted in papilla, turned towards genital opening and palmated in distal part ( Figs 154–155 View FIGURES 144 – 157 ); about 1.3 times shorter than hind claw.

Male: body length 0.65–0.9 mm. Antenna: head = 1.9–2.2. Ant I: II: III: IV = 1: 2.1–2.4: 3.7–3.9: 8.9–10.3. Ant IV subdivided into 7–8 subsegments; one or two basal subsegments separated by weak annulations ( Fig. 161 View FIGURES 158 – 162 ). Abd VI as in Fig. 170 View FIGURES 163 – 171 .

Bionomy and distribution. In most caves specimens were taken from water surface of small pools, from stalagmites and walls, and from the wooden substance. In Kaskadnaya Cave specimens were collected from litter penetrating into the cave from surface down to - 150 m vertical depth. Troglophile or “recent” troglobite. Subspecies is distributed only in Western biospeleological region, sometimes shares caves with P. tauricus sp. nov. and A. peculiaris sp. nov. and shows allopatric mode of distribution with close related variance of P. principalis from Chatyr-Dag and P. pseudoprincipalis sp. nov. from two massifs of Eastern biospeleological region ( Table 1 View TABLE 1 ).

Etymology. The new subspecies is named after type locality, Skelskaya Cave.

Variability. Ant IV in females normaly with 5, rarely 6 or even 7 subsegments, in males 7–8 subsegments. Whorl BM2 of Ant IV with 0 to 4 setae. Seta pi2 of fore femur present or absent.

Remarks. The new subspecies generally fits to Stach’s (1945) description of P. principalis (appendices anales, strong but not winged circumanal setae, foot complex, dens chaetotaxy and shape of mucro tip, antennae), although some important features (number and shape of cephalic spines, shape of axial seta ms1 on small abdomen) are not mentioned in original description. Subsequently these important features were described by Gisin (1947) but his figures of mucro and winged circumanal setae contradict with original description; besides, the size of animals from Stach’s and Gisin’s descriptions is quite different (adult female not less than 1 mm and 0.6–0.75 mm respectively). Until full redescription of P. principalis sensu Stach, 1945 (especially such critical features as bifurcated or not axial seta ms1 of small abdomen and number and shape of cephalic spines) we consider subspecies described above as belonging to this species but with different antenna/head ratio (antennae 2 times as long as head instead of 1.3–1.6 times) and female with normally 5 subsegments in Ant IV.

P. principalis skelicus ssp. nov. is also very close to described above P. pseudoprincipalis but differs from it in following features: 1) broadened tip of mucro; 2) longer antennae; 3) not thickened setae Ipe, IIIpe–Vpe of dens; 4) longer dorsal posterior setae of great abdomen and longer setae of a and m rows of Abd VI; 5) less palmated appendices anales; 6) somewhat greater ratio ‘dens: mucro’.

Specimens belonging to P. principalis were found also in caves of Chatyr-Dag Massif ( Table 1 View TABLE 1 ). However, intraspecific taxonomical position of population from Chatyr-Dag remains unclear: Ipe, IIIpe–Vpe setae of dens thickened as in P. pseudoprincipalis , but body proportions more close to P. principalis skelicus and mucronal apex more swollen than in last subspecies. It is possible that specimens from Chatyr-Dag represent an independent subspecies. The question of geographical variability and intraspecific taxonomical borders of conspecific Crimean populations of P. principalis and their relation to P. pseudoprincipalis requires additional study.

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