Research Article |
Corresponding author: Mikhail Potapov ( mpnk-abroad@yandex.ru ) Academic editor: Wanda M. Weiner
© 2019 Mikhail Potapov, Alexey Brinev, Xin Sun.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Potapov M, Brinev A, Sun X (2019) Isotomidae of Japan and Asiatic part of Russia. II. The genus Tetracanthella of the Far East. ZooKeys 855: 31-54. https://doi.org/10.3897/zookeys.855.33000
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The paper considers new and little-known species of the genus Tetracanthella distributed in the Far East of Russia and in Japan. Sensillar chaetotaxy and labial palp, two less known morphological characters for the genus, are discussed. Two new species T. annulata sp. nov. and T. tardoki sp. nov. are described; T. manschurica Kutyreva, 1980 and T czernovae Kutyreva, 1980 are redescribed. For the latter species a lectotype and paralectotypes are designated. Remarks are provided for T. sylvatica Yosii, 1939. A second undescribed species is recorded for Japan. New records for T. orientalis Martynova, 1977 and T. sibirica Deharveng, 1987 are listed.
α-taxonomy, Collembola, the Far East of Russia, Japan
Tetracanthella is a typically Holarctic genus and is one of largest in the family (
Abbreviation used
A, B, C, D, E papillae of labial palp following notation of
A.B. A. Brinev
A.F. A. Fjellberg
A.G A. Geras’kina
A.K. A. Kuprin
a1 medial mesochaetae on Abd.V
a2 medial macrochaetae on Abd.V
Abd. abdominal segments
Alt altitude
Ant. antennal segments
Ap unpaired chaetae in anterior part of head
B5, X
chaetae on tibiotarsus 3 following notation of
dA, dH diameter of ocellus A and H
eAS external pair of anal spines
M.P. M. Potapov
Md, Mdl, Ml macrochaetae in dorsal, dorso-lateral and lateral position
ms micro s-chaeta(e) or ms-chaeta(e)
MSPU Moscow State Pedagogical University
PAO postantennal organ
N.K. N. Kuznetsova
p1, p3 chaetae of p-row on tergites
PAO postantennal organ
p3
chaetae of p-row on head following notation of
pp
chaetae of pp-row on head following notation of
s in the text and figures, macro s-chaeta(e) or s-chaeta(e)
s’ male s-chaeta on Ant.3 in lateral position
Th. thoracic segments.
S-chaetae on tergites. In his monograph
Labial palp. The character is poorly studied for the genus but appears to be promising at least at level of species group. After
‘sylvatica’ group
Tetracanthella annulata sp. nov. (R)
Tetracanthella manschurica Kutyreva, 1980 (R)
Tetracanthella sylvatica Yosii, 1939 (J)
Tetracanthella sp. 1 (R)
‘stebaevae’ group
Tetracanthella czernovae Kutyreva, 1980 (R)
Tetracanthella sp. 2 (J)
‘ethelae’ group
Tetracanthella orientalis Martynova in
Tetracanthella tardoki sp. nov. (R)
‘wahlgreni’ group
Tetracanthella martynovae Potapov, 1997 (R)
Tetracanthella sibirica Deharveng, 1987 (R)
Holotype: subadult female, Russia, Far East, Primorye, Terneyski District, Sikhote-Alinski Reserve, Kabani station, 900 m alt., 45.14122°N, 135.87759°E, coniferous forest with Rhododendron fauriei, rotten wood, 8.08.2017, leg. N.K., A.G., A.K. Three paratypes: nearly the same place, 932 m alt., 45.13840°N, 135.88702°E, leg. N.K., A.G., A.K.; seven paratypes: Sikhote-Alinski Reserve, Blagodatny station, 95 m alt., 44.96670°N, 136.53410°E, oak forest, rotten wood, 7.08.2017, leg. N.K., A.G., A.K.
(all from the Far East of Russia): Primorski Krai: Shkotovski district, Livadiysky Range, Pidan Mt., rotten wood, ~800 m alt., 20.09.2004, leg. M.Potapov; ibidem, trail to Falaza Mt., ~600 m alt., mosses on rotten wood, 08.09.2018, leg. M.P., A.K.; Primorski Krai, Khasanski district, “Kedrovaya Pad “ Reserve, valley of Kedrovaya River, cedar litter of mixed forest, 29.09.2004, leg. M.P.; ibidem, 5 km of trail to Central shelter, valley mixed forest, rotten wood, 29.07.2016, leg. N.K., M.P.; ibidem, right bank of Kedrovaya River, 2nd Zolotisti Spring, coniferous litter, 14.07.2013, leg. S. Spiridonov; Primorski Krai, Lazovsky district, in mountains nearby Preobrazheniye, Sredni stream (tributary of Maralovaya (valley of Sokolovka River), mixed forest, rotten wood, 21.09.2011, leg. M.P.; Primorski Krai, Terneyski district, Ostraya Mt., litter, 02.06–04.06.2018, leg. A.K.; Sikhote-Alinski Reserve, Kabani station, 900 m alt., 45.14122°N, 135.87759°E, coniferous wood with Rhododendron fauriei, rotten wood, 8.08.2017, leg. N.K., A.G., A.K.; ibidem, 932 m alt., 45.13840°N, 135.88702°E; Sikhote-Alinski Reserve, Blagodatny station, oak wood, rotten wood, 7.08.2017. 95m alt., 44.96670°N, 136.53410°E; leg. N.K., A.G., A.K. Primorski Krai, Partyzanski district, Olkhovaya Mt., 540 m alt., 43.3058°N, 133.6679°E, rotten wood in mixed forest, 20.08.2018, leg. M.P., A.K.
Khabarovski Krai, Nanaiski District, Anyuiski National Park, Tormasu River, mixed forest, rotten wood, 204 m alt., 49.30332°N, 137.57004°E, 07.08.2018, leg. N.K., A.G., A.K.; ibidem, Anyuiski National Park, Anyui River, mixed forest, rotten wood, 205 m alt., 49.36350°N, 137.70227°E; Komsomolsk-Khabarovsk road, 270 km, cedarn-large-leaved valley forest, litter, 42 m alt., 048.93659°N, 136.33167°E, leg. N.K., A.G., A.K.; Khabarovski Krai, Komsomolski District, Komsomolski Reserve, foothills of Sergol Mt., aspen-oak forest, rotten wood, 259 m alt., 50.73823°N, 137.40182°E, 11.08.2018, leg. N.K., A.G., A.K.; ibidem, Komsomolski Reserve, Sergol Mt., mixed forest with cedar, rotten wood, 228 m alt., 50.73710°N, 137.39772°E, 11.08.2018, leg. N.K., A.G., A.K.; Komsomolski District, Komsomolsk–Khabarovsk road, 85 km, 1,5 km from Gorely Klyuch Stream, mixed forest, rotten wood, 50.21810°N, 137.33202°E, 12.08.2018, leg. N.K., A.G., A.K.
Amurskaya Region, Arkharinski district, Khinganski Reserve, 10 km E Uril, coniferous forest, litter, 07.10.2009, leg M.Babykina.
Coloration spotty, from dark to light grey. Coxa I without an external chaeta. Macrochaetotaxy: 2,2/2,2,2. Dens long, with clear crenulations, without anterior and normally with seven posterior chaetae.
Body length 0.9–1.5 mm. Body cylindrical, not narrowing (Fig.
8+8 ocelli, G and H reduced (dA : dH = 1.5–2.0). PAO 1.9–2.7 times as long as the diameter of ocellus A (Fig.
Axial chaetotaxy: 12–14,10/6,6,6,6 (without chaetae in Md-position on Abd.I–III and p1’ chaetae on Abd.IV) (Figs
Coxa I without an external chaeta. Tibiotarsi with 1,2,2 clavate dorsal tenent hairs (Fig.
Retinaculum with a chaeta and 4+4 teeth, basal tooth smaller. Anterior furcal subcoxa with 8–9 (rarely seven or ten) chaetae, posterior one with 5–6 (rarely four or seven) chaetae. Dorsal side of manubrium with 3+3 laterobasal chaetae and 11+11 (sometimes ten or 12 on one side) chaetae on main part (14+14 at whole), besides with a chaeta on each lateral side (Fig.
Anal spines parallel, large, on moderate papillae. Medial mesochaetae (a1) of Abd. V slightly in front of medial macrochaetae (a2). Arrangement of chaetae and spines on dorsum of Abd V as a2-a2/a1-a1 =2.1–2.3; a2-a2/a2-eAS = 1.7–1.8 (Fig.
The species is characterized by annulated posterior side of dens.
The species is widely distributed in southern areas of the Far East of Russia (Primorsky Krai, Khabarovsky Krai and Amurskaya District), both in flatland and in the mountains (Fig.
The new species belongs to ‘sylvatica’ group and differs from all species of the group by absence of chaetae on anterior side of dens. The disproportion of anterior and posterior number of chaetae on dens (0 vs. ~7), clear humps on posterior side of dens and grey coloration make T. annulata sp. nov. unmistakable in the area of its distribution.
Japan, Honshu, Kyoto, Kamigamo experimental forest in Kyoto University, 2011, leg. S. Fujii.
Tetracanthella sylvatica was described from Osaka (central Honshu) and was numerously recorded around here afterwards, particularly from Kamigamo Experimental Forest of Kyoto University (e.g.,
The remarks to chaetotaxy of the species were given by
In the alpine zone of Ezop Range (western part of Khabarovski Krai, leg. A.B.) we discovered a form which shares many essential characters with typical T. sylvatica from which it differs by larger body (~2 mm), 4+4 postlabial chaetae and absence of annulations on posterior side of dens.
(all from the Far East of Russia): Khabarovski Krai, Imeni Lazo district, upper flux of Katen River, Ko Mt., upper part of Ko Stream, ~970 м alt., 29.06.2018, soil in coniferous forest, A.B.; Khabarovski Krai, Vaninski district, ~14 km N Vysokogorny, upper flux of Mulinka River, closed spruce forest at pass, ~900 m alt., 29.09.2011, leg. M.P.; Primorski Krai, Partyzanski district, Olkhovaya Mt., 1380 m alt., 43.3375°N, 133.6615°E, spruce litter, 20.08.2018, leg. M.P., A.K.; Primorski Krai, Chuguevski district, Oblachnaya Mt., 1230 m alt., 43.6483°N, 134.1978°E, spruce litter, 19–20.09.2018, leg. A.K.; Primorski Krai, Chuguevski district (unprecise locality), spruce forest, 8.09.1973, leg. L. Kutyreva.
Body length 1.6–1.9 mm. Body thick, tubular, not narrowed (Fig.
8+8 ocelli, G and H smaller. PAO short, 1.1–1.6 as long as the diameter of ocellus A (Fig.
Chaetotaxy abundant (Figs
Coxa I without an external chaeta. Tibiotarsi with 1,2,2 long and clavate dorsal tenent hairs and without well developed ventral tenent hairs. Tibiotarsi with many additional chaetae on all legs, tibiotarsi I and II with 26–28 chaetae each, III with more than 30 chaetae (Fig.
Ventral tube with 3+3 laterodistal and four posterior chaetae. Retinaculum with 4+4 teeth and a chaeta. Anterior furcal subcoxa with 10–17 chaetae, posterior one with 3–4 chaetae (Fig.
Tetracanthella manschurica 26 furca, lateral view (Vaninski district) 27 position of macrochaetae and s-chaetae on corpus 28 PAO and ommatidia 29–31 dens, lateral view in specimen from Imeni Lazo district (29) and Vaninski district (30, 31) 32 furca, posterior view, juvenile specimen 33 furcal subcoxae 34 distal part of leg 3 35 mucro.
Tetracanthella manschurica occurs in the mountains of Sikhote-Alin Range (Fig.
Tetracanthella manschurica was described from Lazovski district of Primorski Krai. Afterwards, it was recorded once with few morphological remarks by
Population from the northern part of Sikhote-Alin Range (Vaninski district) show longer meso- and macrochaetae (Fig.
Lectotype and one paralectotype (females) designated and labeled as: Primorski Krai: Shkotovski district, NE part of Livadiysky Range, Krinichnaya (= Falaza) Mt., coniferous forest belt with Picea and Abies, litter under Abies nephrolepis, 12.10.1977, leg. L. Kutyreva
Body length 2.0 mm (for subadult female). Body thick, tubular. Coloration dark, antennae white. Reticulation thin, polygons smaller than mesochaeta socket (Fig.
8+8 ocelli, G and H smaller. Four prelabral chaetae. Outer maxillary lobe with four sublobal hairs and simple maxillary palp. Labium with complete set of guards [A(1)B(4)C(0)D(4)E(7)], three proximal and four basomedian chaetae. Postlabial chaetae 4+4. With 7–8 chaetae between medial line and pc3 on head (Fig.
Chaetotaxy abundant (Figs
Coxa I without an external chaeta. Tibiotarsi with 1,2,2 long and clavate dorsal tenent hairs. Ventral tenent hairs weakly developed. Tibiotarsi I, II, III with 21, 21, 25 chaetae, respectively. Empodial appendage 0.7–0.8 as long as inner edge of claw, with apical filament.
Ventral tube with 3+3 laterodistal and four posterior chaetae. Retinaculum with 4+4 teeth and a chaeta. Anterior furcal subcoxa with 8–9 chaetae, posterior one with four chaetae (Fig.
The species is known only from type locality, by two specimens.
Tetracanthella czernovae belongs to the ‘stebaevae’ group due to chaeta on coxa I missing and complete set of macrochaetae on tergites. The species however shares many essential characters, incl. appearance, with T. manschurica (‘sylvatica’ group). Tetracanthella czernovae was briefly redescribed by
One individual from central Honshu (Japan, Nagano Prefecture: Chino, leg. M.P. and N.K.) is close to T. czernovae but obviously represents a new species differing by absence of additional macrochaetae on body and presence of additional chaetae on Tibiotarsi I and II. It is the second species of the genus Tetracanthella occurring in Japan.
Holotype: female, Russia, Far East, Khabarovsky Krai, Nanaisky district, ~40 km S road Khabarovsk-Sov.Gavan, Tardoki-Yani Mt., ~2050 m alt., tundra on top, 16–26.06.2017, leg. A.B. 19 paratypes from the same place and nearby, 1800–1900 m alt.
(all from Tardoki-Yani Mt.): different open sites nearby type locality (moss and lichen on talus, mountain tundra, and mosses on rocks), 16–26.06.2017, leg. A.B.
Coxa I without an external chaeta. Macrochaetotaxy: 3(W),3(W)/2,3,3. Retinaculum and furca absent.
Body length 1.2–1.7 mm. Body slender, continuously narrowing (Fig.
8+8 ocelli, G and H reduced. PAO 2.5–3.3 as long as the diameter of ocellus A. Chaeta s’ of ant.III in males present. Two prelabral chaetae. Outer maxillary lobe with three sublobal hairs and simple maxillary palp. Labium with three proximal and four basomedian chaetae, labial palp with reduced set of guards [A(1)B(3)C(0)D(3)E(4)] (Fig.
Chaetotaxy scarce (Figs
Tetracanthella tardoki sp. nov. 42–43 dorsal chaetotaxy of thorax (42) and abdomen (43), dorsal view 44 tenacular, furcal and genital areas of female 45 distal part of leg 3. Abbreviations: fsc-a and fsc-p–anterior and posterior furcal subcoxae, man manubrial field, ta tenacular area.
Coxa I without an external chaeta. Tibiotarsi with 1,2,2 long and clavate dorsal tenent hairs and 3,3,1 enlarged ventral tenent hair (Fig.
Ventral tube with 3+3 lateral and four posterior chaetae.
Retinaculum and furca absent. Retinacular field with 3–5 chaetae. Anterior furcal subcoxa with three (rarely two or four) chaetae, posterior one with four chaetae. Manubrial field normally with eight chaetae (Fig.
The species is named after the type locality.
It is known only from the Tardoki-Yany mountain massive (central part of Sikhote-Alin Range) where it occurs in all samples from alpine sites which we have examined (Fig.
The new species belongs to the ‘ethelae’ group by absence of chaeta on coxa I, three sublobal hairs, two prelabral chaetae and other characters. Together with T. orientalis they are the only representatives of this Nearctic group in Palearctic. The two species share several apomorphic characteristics unknown in North American species: absence of furca, presence of the third macrochaetae in p-position on thorax, low number of axial chaetae, short empodium. Tetracanthella tardoki sp. nov. differs from T. orientalis by the presence of Md macrochaetae on Abd.II resulting in formula 2,3,3 (vs. 2,2,3) on abdomen.
Magadanskaya region: vicinities of Magadan, Snow Valley, 18.09.1974. It is the type locality of the species although the type specimens were not seen by us and are probably lost.
Chukotski AO: Anadyrski district, vicinities of Anadyr, Observatsii Cape, tundra, 27.06.1974, leg. E. Bondarenko, Anadyrski district, Ugolnaya Bay, tundra, leg. M. Chernyakhovski.
Kamchatka: Yuzhno-Kamchatski Reserve, Elizovski district (south), Kambalnoye Lake, pine elfin wood, 14.09.2005, leg. L. Lobkova; Elizovski district (north), Kronotski reserve, caldera of Uzon, moss-lichen tundra, 20.08.2005, leg. L. Lobkova; Kronotski reserve, Vachkazhets Volcano, 1000 ma lt., tundra, gopher burrow, leg. L. Lobkova; Bystrinski district, vicinities of Anavgai and Esso, 3–5.07.2012, tundra at lake (Ledum, Empetrum), leg. M.P.
Body length 1.2–1.6 mm. Body slender, continuously narrowing (Fig.
Tetracanthella tardoki sp. nov. (46) and T. orientalis (47–50) 46–47 position of macrochaetae and s-chaetae on corpus 48 tenacular and furcal areas 49–50 dorsal chaetotaxy of Abd.II–V (49), head and Th.II (50), dorsal view. Abbreviations: fsc-a and fsc-p anterior and posterior furcal subcoxae, man manubrial field, ta tentacular area.
Reticulation of cuticle in Tetracanthella of East Asia 51 T. annulata sp. nov., posterior edge of Abd.IV 52 T. sylvatica, ibidem 53 T. manschurica, posterior edge of Abd.IV, lateral part 54 T. czernovae, posterior edge of Abd.IV 55–56 T. tardoki sp. nov., posterior edge of head (55) and posterior edge of Abd.IV (56) 57 T. orientalis, posterior edge of head. Abbreviations: p1 and p2, chaetae of p-row, sm-f smooth field.
8+8 ocelli, G and H reduced (dA : dH = ~1.5). PAO 2.5–4.0 as long as the diameter of ocellus A. Chaeta s’ of ant.III in males present. Two prelabral chaetae. Outer maxillary lobe with three sublobal hairs and simple maxillary palp. Labium with three proximal and four basomedian chaetae, labial palp with reduced set of guards [A(1)B(3)C(0)D(3)E(4)] (as in Fig.
Chaetotaxy scarce (Figs
Legs as in T. tardoki sp. nov. Tibiotarsi I, II, III with 21, 21, 22 chaetae. Claw without teeth. Empodial appendage short, 0.2–0.3 as long as inner edge of claw. Ventral tube with 3+3 lateral and four posterior chaetae.
Retinaculum and furca absent. Retinacular field with 3–5 chaetae. Anterior furcal subcoxa with three (rarely four) chaetae, posterior one with four chaetae. Manubrial field with eight (rarely seven) chaetae (Fig.
Tetracanthella orientalis is widely distributed in northern part of the Far East of Russia (Fig.
See the remarks to T. tardoki sp. nov.
Tetracanthella arctica auct.
Tetracanthella cf. arctica auct.
Chukotski AO: Anadyrski district, vicinities of Anadyr (holotype and paratype), leg. E. Bondarenko; ibidem, Anadyrski district, vicinities of Shakhterski, Volchikha River, leg. E. Bondarenko; ibidem, Iul’tinski district, Shmidta Cape, leg. K. Gorodkov; ibidem, Iul’tinski district, Wrangel Island, Somnitel’naya Bay, leg. K. Gorodkov.
Yakutia, Bulunski Ulus, Bol’shoi Lyakhovski Isl. (Novosibirskiye Islands), mouth of Bol’shoi Etirikan River; ibidem, Bol’shoi Lyakhovski Isl., Shalourova Cape, leg. V. Bulavintsev.
USA, Alaska, Kotzebue, 66.90°N, 162.59°W, 04.IX.1976, trough, moss & Carex litter, leg. R. Greenberg; Alaska, North Slope, 10 ml NW Franklin Bruffs, moss in active polygon, 70.26°N, 161.89°W, 17.VIII.1976, leg.A.F.; Alaska, North Slope, Icy Cape, trough between polygons, moss and Carex sp., 28.VIII.1976, leg. P. Connors; Alaska, North Slope, Canning River Delta, 70.05°N, 145.50°W, 23.VII.1980, several sites with Dryas sp., moss and Carex sp., leg. S. MacLean; Alaska, Norton Bay, Inglutalik River, moist tundra, leg. A.F.; Alaska, Nunivak Island, Duchikthluk Bay, 59.86°N, 166.07°W, 19.IX.1976 tundra with Empetrum sp., Carex sp., Vaccinium sp., lichens, leg. P. Michelson; Alaska, Point Barrow, 71.31°N, 156.66°W, 30.VIII.1976, thick moss, some algae and lichens; ibidem, moss , Saxifraga sp., Cochlearia sp. on sandy stream bank, leg. A.F.; Alaska, Cape Thompson, Ogoturuk Creek Basin, 68.16°N, 165.35°W, 11.VIII.1980, moss in tussock tundra, leg. D. & B. Murrey; Alaska, Chevak in Yukon, Kuskokwin Delta, 61.51°N, 165.26°W, 09.VII.1976, mesic upland, moss and Betula nana, leg. T. Seasted; Alaska, Cape Krusenstern, rather dry site, lichens, 67.25°N, 163.50°W, 03.IX.1976, Vaccinium sp., leg. R. Greenberg.
Common in Asiatic and American parts of Arctic. In the Far East of Russia was recorded from Chukotka, in Wrangel Island, Anadyrskij, Uil’tinskij, Chaunskij and Chukotskij districts, as T. arctica Cassagnau, 1959 or T. cf. arctica in older publications (
The status of species is somewhat doubtful because morphological intergrading to T. arctica (
The species is distributed in central part of Russian sector of Arctic. From the Far East it is known only in Chaunski district (Chaun Bay) of Chukotka, as “cf. britannica” by
We would like to express our sincere thanks to Drs Vasily Alpatov, Marina Babykina, Anne Bedos, Elena Bondarenko, Yun Bu, Valery Bulavintsev, Huang Chen-Wang, Louis Deharveng, Arne Fjellberg, Saori Fujii, Anna Geraskina, Natalia Kuznetsova, Alexander Kuprin, Arkady Lelej, Taizo Nakamori, Oleg Novoselov, Andrey Ptashinsky, Seikoh Saitoh, Yulia Shveenkova, Olga Smirnova, Sophia Stebaeva, and Irina Volonikhina for kindly providing material on Collembola or for field assistance. Many thanks to Takuo Hishi and Keiko Niijima for providing some information from the Japanese literature. The authors are grateful to the management and staff of the Ussurisky Nature Reserve (Russia, Primorsky Krai), “Land of Leopard” National Park (Primorsky Krai), Sikhote-Alin Nature Reserve (Primorsky Krai), State Reserve of Laso (Primorsky Krai), “Zov tigra” National Park (Primorsky Krai), who provided the collecting permit and the favorable conditions for our field work. All the materials from North America were provided by Arne Fjellberg. We are also indebted to Louis Deharveng and two reviewers for their critical comments.
The study was partly supported by Chinese–Russia Research Cooperative Program of RFBR (project No. № 18-54-53032 GFEN) for M. Potapov and A. Brinev.