AnimaliaNot EvaluatedacceptedspeciesAccepted
Megalothorax sanctistephani

Megalothorax sanctistephani

Christian, 1998

GBIF:255061943

0year

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Descriptions(3)

Ecology of Megalothorax sanctistephani Megalothorax sanctistephani has been found from three special localities. First, the catacombs of the cathedral St. Stephan in Vienna (Christian 1998). Second, the underground galleries under the Jardin des Plantes (botanical garden) in Paris; and third, near an old greenhouse in the botanical garden of Kaliningrad, under furniture debris. Whether the botanical garden or subterranean habitat is the key factor is unclear. In Vienna and Paris, it seems clear that the soil was poor in organic material. In Paris, M. sanctistephani had no direct competition from other springtails. In Kaliningrad it was found twice: once alone, and in a second sample coexisting with M. minimus. Megalothorax sanctistephani as never been found in natural caves, and its morphology is typical of soil species, without any of the usual troglobiontic modification (such as increased body size, elongated claws and enlarged sensorial organs of the antenna). Since European troglophilous Neelidae have received some attention (Deharveng 1978, Deharveng & Beruete 1993, Kováč & Papáč 2010, Papáč & Kováč 2013, Papáč et. al 2016, Papáč et. al 2019) we estimate that M. sanctistephani is at least uncommon there, if not really absent. The known ecological niche of M. sanctistephani can thus be described as follows: poor soil with low to no competition in frost-dampened urban habitat. Its natural habitat is likely comparable. It may have been overlooked in Europe due to a cryptic habitat (such as Mesovoid Shallow Substratum, e. g. Pipan & Culver 2019) or perhaps the species was imported with plants from tropical regions.
Panina, Ksenia, Potapov, Mikhail, Rumak, Daria, Schneider, Clément (2025): Investigation on the origin of the “ nose ” in the genus Megalothorax Willem, 1900 (Neelidae, Collembola) by the means of integrative taxonomy. Zootaxa 5590 (2): 209-230, DOI: 10.11646/zootaxa.5590.2.3, URL: https://doi.org/10.11646/zootaxa.5590.2.3
Redescription. General aspect. Habitus and segmentation typical of the genus (Fig. 10 A, B). Body length around 0.2 – 0.34 mm (biggest Russian individual found: 0.26 mm). Specimens whitish in alcohol. Body chaetotaxy sparse including chaetae, s-chaetae, trichobothria (Fig. 12 C), neosminthuroid chaetae, wax-rods and inner sensilla within sensory fields 2 – 6. Body chaetae ordinary, without any remarkable development (Figs 5 A, 6, 10 A, B). Integument. Secondary granulation made of the usual dorsal rough granules (e. g. Fig. 11 C – F). Integumentary channels extending laterally and dorsally in anterior and posterior parts of head, anterior canal branching (detailed topology on Fig. 5 A, also see Fig. 10 A – E). Channels connection with linea ventralis could be compared to a roundabout. Sensory fields and wax rods (Figs 5 A, 6, 8 B, C, 10 A – E, 11 C – F). Same configuration as in the genus, but with a novel sensory field (sf 7) associated with wrc 7, being a depression devoid of secondary grain, without inner sensilla (s) (Fig. 11 D, E). All s are flame-shaped (Figs 10 A, 11 C, F). The size of the sensilla increases from anterior to posterior sf: sf 2 has the smallest s, sf 6 has the largest s. Mouthparts. Labrum as typical for the genus (Fig. 5 B). Chaetae a 1 and a 2 forked, with one tooth. Labium with 4 + 4 proximal chaetae (Fig. 5 C). Basomedian fields with 3 + 3 chaetae, basolateral fields with 1 + 1 chaetae on tubercle (Fig. 5 A). Labial palp (Fig 5 C), as common for the genus (A, B, C, D, E, b 1, b 2, d 1, d 2, 2 e, H, h 1, h 2). Oral fold with two chaetae (Fig. 5 A). Maxillary outer lobe with two sublobal hairs (Fig. 5 D). Maxillary head without strong modification (Fig. 5 E, F). Mandibula ordinary (Fig. 5 G). Head chaetotaxy (Fig. 5 A). Dorsal anterior area with 9 + 9 chaetae and only one unpaired chaeta, a 0 missing and replaced with a “ nose ”: an oval papilla with an axial groove, like a coffee bean (Figs 5 A, 10 C, D). Clypeal-labral formula: 2, 2, 5, 4, 5 / 5, 4. Lateral anterior area with 1 + 1 chaetae (one missing in pr. a row). Dorsal posterior area with 12 + 12 chaetae. Ventral side with three pairs of postlabial chaetae. Trend for posterior chaetae to be longer and stronger than anterior chaetae. Antennal chaetotaxy (Figs 7 A – C, 10 E, F, 11 A). Ant. I and II with one and four chaetae, respectively. Ant. III with six chaetae and two long S-chaetae (S 1 and S 4). Striations of Ant III sensory organ short sensilla (S 2 and S 3) distinguishable in light microscopy. Ant. IV with five chaetae (X-chaeta missing) and 10 long S-chaetae. Sensory organ with s-chaetae Sx, Sy, Or, a, sa. Organite (Or) short, seems apically flared. Diagram of the chaetotaxy of the antenna in Fig. 7 C. Summary on antennal chaetotaxy provided in Table 1. Th. II — Abd. VI chaetotaxy (Figs 6, 8 B, C, 10 A – B, 12 A – C). Th. II with 12 + 12 chaetae, 1 + 1 tubular and curved s 1 - sensilla (Figs 6 A, 8 B). Th. III with 10 + 10 chaetae, 6 + 6 free wax-rods (wrc 1 – 6). Chaetae p 4 far from wrc 2. Chaeta a 5 smaller than a 6. Abd I – V terga with 19 + 19 ordinary chaetae. Chaeta ζ 4 absent. Globular s-chaeta s 3 present (Fig. 12 B), smaller than s 2 (Figs 11 F, 12 A), equidistant from chaetae γ 1 and δ 1 and in lateral position to γ 1 and δ 1. Chaetae of body subequal, slightly thickened. Abd VI chaetotaxy: nine dorsal chaetae as usual; one chaeta on each anal valve (av); mature specimens have 7 + 7 ventral chaetae (Fig. 9 A). Males have additionally two axial pairs of swollen chaetae with blunt apex, the outer pair of chaetae being larger than the most axial ones (Fig. 9 B). Genital plate. Female with 2 + 2 chaetae as usual (Fig. 9 A), male with 8 + 9 chaetae (observed on the only preparation, Fig. 9 B). Abd. IV sternum and furca (Fig. 9 A). Abd. IV sternum with 2 + 2 neosminthuroid chaetae, 2 + 2 chaetae and 1 + 1 tegumentary lobe. Manubrium with 2 + 2 posterior chaetae. Proximal subsegment of dens with a posterior chaeta; distal subsegment posteriorly with two basal spines and one median chaeta. Anterior side of dens with five apical spines, spines without elongated apex. Mucro narrowing in the distal ⅖, with all three lamellae entirely smooth. Legs chaetotaxy typical of the genus (Table 2), consisting of ordinary chaetae of variable size (Figs 8 A – C). Claws. Claw III bulkier than claw I and II. Claws subequal in unguis length (with a trend as unguis I> unguis II> unguis III). Unguis basal and posterior auxiliary lamellae (la, lp and Bp) well developed (Figs 8 A – C). Unguiculus 0.5 – 0.6 as long as unguis. Tenaculum and ventral tube. Tenaculum with 3 + 3 hook-like teeth (Fig. 9 C). Ventral tube bulky with two apical pairs of chaetae.
Panina, Ksenia, Potapov, Mikhail, Rumak, Daria, Schneider, Clément (2025): Investigation on the origin of the “ nose ” in the genus Megalothorax Willem, 1900 (Neelidae, Collembola) by the means of integrative taxonomy. Zootaxa 5590 (2): 209-230, DOI: 10.11646/zootaxa.5590.2.3, URL: https://doi.org/10.11646/zootaxa.5590.2.3
Type material. Holotype: female on slide, Austria, Vienna, catacombs of St. Stephan’s cathedral [48.2084 ° N, 16.3732 ° E]; gravelly substrate mixed with human bone fragments (see Christian 1998); 30.09.1996 – 12.01.1997; leg. E. Christian; NMW (COLLEMBOLA Inv. Nr. 130 to 134). Four paratypes (sex undetermined), same data as for the holotype. Other material. Three females, four males and one juvenile on slides, France, Paris, underground tunnels of the Jardin des Plantes (botanical garden) [48.8450 ° N, 2.3605 ° E]; silty substrate without visible organic debris; 17.03.2011; leg. C. Schneider; MNHN (EA 040126 – 131, 133, 135). Five females, one juvenile and two sex undetermined on slides; Kaliningrad; Botanic garden Immanuel Kant Baltic Federal University [54.7365 ° N, 20.5156 ° E]; soil in an old greenhouse; leg. D. Levochko; 09.08.2023 and 04.02.2024. One female on slides, Russia, Saint-Petersburg, Peter the Great Botanical Garden [59.9731 ° N, 30.3272 ° E]; fern curtain; leg. N. Kuznetsova and M. Potapov; 25.04.2024. Obtained molecular data. France. One individual sequenced for the partial 28 S rDNA (d 1, d 1), COI mtDNA and 16 S mtDNA [PQ 900094, PQ 900415, PQ 900095], same collection data as above RUSSIA. One individual sequenced for near-complete n-rDNA operon sequence [PQ 900093], same collection data as above.
Panina, Ksenia, Potapov, Mikhail, Rumak, Daria, Schneider, Clément (2025): Investigation on the origin of the “ nose ” in the genus Megalothorax Willem, 1900 (Neelidae, Collembola) by the means of integrative taxonomy. Zootaxa 5590 (2): 209-230, DOI: 10.11646/zootaxa.5590.2.3, URL: https://doi.org/10.11646/zootaxa.5590.2.3

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FIGURE 6. Megalothorax sanctistephani Christian, 1998: trunk tergites chaetotaxy, dorsal view. Position of trichobothria marked with “τ".

Imageimage/png© Panina, Ksenia;Potapov, Mikhail;Rumak, Daria;Schneider, ClémentPanina, Ksenia;Potapov, Mikhail;Rumak, Daria;Schneider, Clément

FIGURE 7. Megalothorax sanctistephani Christian, 1998: A, antenna, anterior view; B, antenna, posterior view; C, diagram of the chaetotaxy of the antenna.

Imageimage/png© Panina, Ksenia;Potapov, Mikhail;Rumak, Daria;Schneider, ClémentPanina, Ksenia;Potapov, Mikhail;Rumak, Daria;Schneider, Clément

FIGURE 8. Megalothorax sanctistephani Christian, 1998: A, leg 1; B, leg 2; C, leg 3.

Imageimage/png© Panina, Ksenia;Potapov, Mikhail;Rumak, Daria;Schneider, ClémentPanina, Ksenia;Potapov, Mikhail;Rumak, Daria;Schneider, Clément

FIGURE 9. Megalothorax sanctistephani Christian, 1998: А, Abd. IV sternum, female genital plate and furca, posterior view; B, Abd VI sternum with sensilla and male genital plate; C, retinaculum.

Imageimage/png© Panina, Ksenia;Potapov, Mikhail;Rumak, Daria;Schneider, ClémentPanina, Ksenia;Potapov, Mikhail;Rumak, Daria;Schneider, Clément

FIGURE 10. Megalothorax sanctistephani Christian, 1998: A, habitus, lateral view; B, habitus, dorsal view; С, head, lateral view; D, cuticular process (“nose”): an oval papilla with an axial groove, like a coffee bean; E, antenna, anterior view; F, sensilla of Ant. IV, anterior view.

Imageimage/png© Panina, Ksenia;Potapov, Mikhail;Rumak, Daria;Schneider, ClémentPanina, Ksenia;Potapov, Mikhail;Rumak, Daria;Schneider, Clément

FIGURE 11. Megalothorax sanctistephani Christian, 1998: A, sensilla of Ant. IV, anterior view; B, sensilla of Ant. III, anterior view; С, sensory field 3 on thorax II; D & E, novel sensory field (sf 7) associated with wrc 7; F, sensory field 6 on abdomen.

Imageimage/png© Panina, Ksenia;Potapov, Mikhail;Rumak, Daria;Schneider, ClémentPanina, Ksenia;Potapov, Mikhail;Rumak, Daria;Schneider, Clément

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Investigation on the origin of the “ nose ” in the genus Megalothorax Willem, 1900 (Neelidae, Collembola) by the means of integrative taxonomy

checklist

This dataset contains the digitized treatments in Plazi based on the original journal article Panina, Ksenia, Potapov, Mikhail, Rumak, Daria, Schneider, Clément (2025): Investigation on the origin of the “ nose ” in the genus Megalothorax Willem, 1900 (Neelidae, Collembola) by the means of integrative taxonomy. Zootaxa 5590 (2): 209-230, DOI: 10.11646/zootaxa.5590.2.3, URL: https://doi.org/10.11646/zootaxa.5590.2.3

Abstract

Megalothorax Willem, 1900 is a genus of Collembola that comprises 36 species to date. For a long time, its diversity was overlooked, but recent integrative taxonomic works allowed us to understand better their seemingly cryptic diversity. Among the oddities of the genus are the so-called “nosed” species, i.e. species equipped with a frontal cuticular process, an unusual trait for Collembola.

In this work, we describe a new “nosed” species from the north of European part of Russia and redescribe the first known “nosed” species: Megalothorax sanctistephani Christian, 1998. This species is known only from peculiar places: initially the catacombs of a cathedral in Vienna, and our new findings in underground tunnel in Paris and Botanical Garden of Kaliningrad. We also used long-read sequencing to obtain new DNA data for “nosed” species of Collembola. We investigated the evolution of the “nose” using molecular and morphological phylogeny approaches.

This evolution remained unclear, as molecular and morphological data are conflicting on this specific point. The “nose” may have been acquired a single time, then lost secondarily in some species; or have been acquired independently several times.

Panina K, Potapov M, Rumak D, Schneider C, plazi (2025). Investigation on the origin of the “ nose ” in the genus Megalothorax Willem, 1900 (Neelidae, Collembola) by the means of integrative taxonomy. Plazi.org taxonomic treatments database. Checklist dataset https://doi.org/10.15468/ywcpd2 accessed via GBIF.org on 2026-06-14.

CC0Published 2/21/2025View dataset
GBIF Usage Key
255061943
Dataset Key
10f9f8f0-805d-4078-bc8f-412874df2cc3
Origin
source
Backbone Key
10408702
Taxon ID
752287812A4CF97B2EFB8CFAFEE9AF77.taxon
Last Crawled
6/8/2026
Last Interpreted
6/8/2026