1✉ Institute of Environmental and Agricultural Biology (X-BIO), Tyumen State University, Tyumen, Russia.
2023 - Volume: 63 Issue: 2 pages: 491-521
https://doi.org/10.24349/7fyj-me9uThe family Tydeidae is a diverse group of mites distributed worldwide and currently includes about 31 genera and more than 300 species (Silva et al. 2016; Kaźmierski et al. 2018; André 2021; Khaustov 2022). Most tydeid mites are fungivorous, however some species are predators of small arthropods, phytophagous and scavengers (Walter et al. 2009). The scientific history of tydeid mites and current state of knowledge in taxonomy are discussed in Kaźmierski (1998), Silva et al. (2016) and André (2021). The tydeid mites of Asian Russia are almost completely unstudied with only two papers describing three new species of Lorryia sensu Kaźmierski, 1989 (Kaźmierski 2008) and a new genus and species, Andrelorryia hajiqanbari Khaustov, 2022 (Khaustov 2022). In addition, Kaźmierski (2000) reported Lorryia woolleyi and L. maga from Tuva Republic in Russia.
This study provides a review of Tydeidae collected in Tyumen and Kurgan Regions of Western Siberia, Russia.
Mites were extracted from various samples (soil, litter, bark of trees, etc.) using Berlese funnels. All mites were mounted in Hoyer's medium. Mite morphology was studied using a Carl Zeiss AxioImager A2 compound microscope with phase contrast and differential interference contrast (DIC) illumination. Notation applied to the body and leg setae follow the system of Grandjean, overviewed by Kethley (1990) and André (1981b), respectively; palpal setation follows André (1981a). The diagnosis of the genus Lorryia follows Kaźmierski (1989). Photomicrographs were taken with an AxioCam ICc5 digital camera. For SEM microscopy several alcohol-preserved mites were dried in a JFD 320 freeze drying device (JEOL, Japan), dusted with gold and scanned with a JEOL–JSM-6510LV and TESCAN Mira3 LMU SEM microscopes. All measurements are given in micrometers (μm) for the holotype and for five paratypes (in parentheses).
Additional materials examined for the comparison with collected species:
Type species: Lorryia superba Oudemans, 1925, by original designation.
ZOOBANK: A6FED4F0-35C4-4A9E-8701-1B58A77292CF
(Figs 1–8)
Female — (Figs 1–3, 5–7, 8A–C). Body ovate (Figs 5A, 7). Length of idiosoma 355 (315–360), maximum width 270 (235–270).
Idiosomal dorsum – (Figs 1A, 5, 7A, 8A). Dorsal ornamentation type ''Lorryia''; reticulation forms discrete areas divided by striated integument as illustrated on Figs 1A, 5A and 7A; reticulation meshes irregular in shape (Figs 5C, 8A); cross-ties ''Y''-shaped, rarely ''X''-shaped, frames of meshes with rare ''I''-shaped costulae oriented longitudinally (Fig. 5D). Dorsal hysterosomal setae subequal in length and shape, curved, weakly blunt-tipped and weakly barbed (Fig. 5D); setae vi, ve and sce with more attenuate tips than hysterosomal setae; trichobothria smooth, whip-like, about three times longer than other dorsal setae. Only cupuli ia hardly discernible inside polygonal cells, other cupuli not evident. Lengths of setae: vi 17 (16–18), ve 20 (20–21), sci 65 (60–70), sce 23 (21–23), c1 21 (20–22), c2 22 (21–23), d 23 (21–23), e 21 (20–23), f1 23 (22–24), f2 23 (22–24), h1 23 (20–23), h2 23 (22–24), ps1 20 (19–21).
Idiosomal venter – (Figs 1B, 6A, B, 7B, 8B, C). Ventral surface mostly striated; striae between setae 3a and 4a more or less ''V''-shaped (Fig. 8B); some striae mesad bases of setae g2–g4 without tubercles (Fig. 6A). Coxal organ small, ovate (Fig. 6B). Ventral setae smooth and pointed, except ps1 with same shape as dorsal setae; in female holotype seta ps1 unpaired (Fig. 7B). Six pairs of genital setae (Fig. 6A). Two pairs of round genital papillae clearly visible inside progenital chamber (Fig. 8C).
Gnathosoma – (Figs 2, 6C). Gnathosoma usually completely covered by idiosoma. Cheliceral stylets 16 (16–17), longer than palptarsus 10 (10–11) and combined length of palptarsus and eupathidiun (p) 14 (14–15). Palpal terminal eupathidium very short, thick in basal part and slightly narrowed distally, with rounded tip; seta d bifurcates distally; seta acm blunt-tipped. All palpal setae smooth. Subcapitulum (Figs 2B, 6C) with smooth and pointed subcapitular setae (sc1, sc2) and two pairs of short smooth and pointed adoral setae (or1, or2). Gnathosomal supracoxal setae ep rod-like.
Legs – (Figs 3, 6D). Empodia with small empodial hooks; tarsal claws serrate (Fig. 6D). Leg I (Figs 3A, 6D). Setae (p), (tc) and ft″ of tarsus eupathid-like, smooth and longitudinally striated (Fig. 6D); setae d of femur, (l) of genu and d of tibia similar to dorsal idiosomal setae, other setae pointed and weakly barbed. Solenidion ω 8 (7–8) baculiform; famulus k on tibia multibranched distally. Leg supracoxal seta (el) rod-like, located dorsally near trochanter. Leg II (Fig. 3B). Setae d of femur, (l) of genu, d and v′ of tibia similar to dorsal idiosomal setae, other leg setae pointed and weakly barbed. Solenidion ω 5 (4–5) baculiform. Leg III (Fig. 3C). Setae d of femur, l′ of genu and d of tibia similar to dorsal idiosomal setae, other leg setae pointed and weakly barbed. Leg IV (Fig. 3D). Setae l′ of genu and d of tibia similar to dorsal idiosomal setae, other leg setae pointed and weakly barbed.
Male — Similar to female and differs only in having longitudinal slit-like genital opening and four pairs of short and barbed eugenital setae (Figs 4, 8D). Two pairs of round genital papillae clearly visible inside progenital chamber (Fig. 8D).
Larva, protonymph, deutonymph and tritonymph unknown.
Female holotype, slide ZISP T-Tyd-002, Russia, Tyumen Region, city of Tyumen, 57°09′N 65°27′E, in moss on bark of birch Betula pendula, 07 May 2014, collected by A.A. Khaustov; paratypes: 3 females, 5 males, same data; 31 female, 1 male, same locality and habitat, 12 May 2019; 1 female, 6 males, Russia, Tyumen Region, Tyumen District, vicinity of Malinovka village, 57°05′N 65°03′E, in moss on bark of aspen Populus tremula L., collected by A.A. Khaustov.
The holotype, one female and one male paratype are deposited in the acarological collection of Zoological Institute of RAS, Saint Petersburg, Russia; other paratypes are deposited in the collection of the Tyumen State University Museum of Zoology, Tyumen, Russia.
The name of the new species refers to its geographical distribution in Siberia.
The new species closely resembles L. catenulata (Thor, 1931) and L. polita Kuznetsov, 1975a in having ornamentation type ''Lorryia'' with discrete areas separated by striate cuticle and in having a very short palptarsus. The new species differs from both L. catenulata and L. polita in having irregular reticulate meshes (vs. regular, similar in shape in L. catenulata and L. polita), cross-ties ''Y'' or ''X''-shaped, with their ends and ''I''-shaped costulae directed along frames of meshes (vs. cross-ties ''Y''-shaped, their ends and ''I''-shaped costulae directed transversely from frames of meshes in L. catenulata and L. polita), and in having more blunted dorsal idiosomal setae (pointed in L. catenulata and L. polita).
ZOOBANK: 74E8D1C2-F2C9-4E8A-98E5-1D1D70B3382C
(Figs 9–13)
Male — (Figs 9–12, 13F). Body ovate (Fig. 12). Length of idiosoma 355 (335–355), maximum width 235 (225–235).
Idiosomal dorsum – (Figs 9A, 12, 13A). Dorsal ornamentation type ''mountains'' on hysterosomal dorsum and reticulated on prodorsum; reticulation without distinct discrete areas; with transverse depressions anteriad setae f1 and h1. Striae between ''mountains'' with semioval lobes. Dorsal hysterosomal setae subequal in length and shape, curved, distinctly blunt-tipped and weakly barbed (Fig. 13A); trichobothria smooth, whip-like, about two times longer than other dorsal setae. Cupuli well visible, ovoid in shape. Lengths of setae: vi 28 (26–28), ve 28 (26–28), sci 62 (56–62), sce 32 (31–35), c1 31 (30–34), c2 32 (32–34), d 33 (33–36), e 35 (32–35), f1 34 (34–35), f2 35 (33–36), h1 33 (31–34), h2 33 (33–36), ps1 27 (27–28).
Idiosomal venter – (Figs 9B, 13F). Ventral surface mostly striated; striae between setae 3a and 4a ''V''-shaped (Fig. 13B). Coxal organ small, ovate (Fig. 13C). Ventral setae smooth and pointed, except ps1 with same shape as dorsal setae. Six pairs of genital setae, four pairs of eugenital setae. Two pairs of round genital papillae clearly visible inside progenital chamber (Fig. 13F).
Gnathosoma – (Figs 10, 13C). Gnathosoma usually completely covered by idiosoma. Cheliceral stylets 22 (22–23) with short, posteriorly diffuse basal part and long narrow distal part (Fig. 13C), subequal in length with palptarsus 22 (22–23) and shorter than combined length of palptarsus and eupathidium (p) 29 (29–30). Palpal terminal eupathidium with ''T''-shaped projection distally; seta d unusually deeply bifurcated from its base, one of its projections weakly blunt-tipped and with subterminal barbs; seta acm blunt-tipped. All palpal setae smooth. Subcapitulum (Fig. 13C) with smooth and pointed subcapitular setae (sc1, sc2) and two pairs of short smooth and pointed adoral setae (or1, or2). Gnathosomal supracoxal setae ep rod-like.
Legs – (Fig. 11). Empodia with empodial hooks; tarsal claws serrate. Leg I (Fig. 11A). Setae (p), (tc) and ft″ of tarsus eupathid-like, smooth; setae d of femur, (l) of genu and d of tibia similar to dorsal idiosomal setae, other setae pointed and weakly barbed. Solenidion ω 9 (8–9) baculiform; famulus k on tibia multibranched distally. Leg supracoxal seta (el) rod-like, located dorsally near trochanter. Leg II (Fig. 11B). Setae d of femur, (l) of genu, and d of tibia similar to dorsal idiosomal setae, other leg setae pointed and weakly barbed. Solenidion ω 5 (5) baculiform. Leg III (Fig. 11C). Setae d of femur, l′ of genu and d of tibia similar to dorsal idiosomal setae; seta v′ of trochanter blunt-tipped, other leg setae pointed and weakly barbed. Leg IV (Fig. 11D). Setae l′ of genu and d of tibia similar to dorsal idiosomal setae, other leg setae pointed and weakly barbed.
Female — Similar to male and differs only in having different shape of genital aperture (Fig. 13D) and lacking eugenital setae. Two pairs of round genital papillae clearly visible inside progenital chamber (Fig. 13E).
Larva, protonymph, deutonymph and tritonymph unknown.
Male holotype, slide ZISP T-Tyd-003, Russia, Kurgan Region, Petuknovsky District, vicinity of lake Medvezh'ye, 55°10′N 67°55′E, soil in steppe, 14 October 2022, collected by A.A. Khaustov; paratypes: 7 females, 4 males, same data.
The holotype, four female and one male paratypes are deposited in the acarological collection of Zoological Institute of RAS, Saint Petersburg, Russia; other paratypes are deposited in the collection of the Tyumen State University Museum of Zoology, Tyumen, Russia.
The name of the new species is derived from Latin speciosus meaning beautiful and refers to the very impressive ornamentation of dorsal idiosoma.
The new species strongly resembles L. danhidalgoi Kazmierski, 1998 in having ornamentation type ''mountains'' and lacking discrete reticulate areas on idiosomal dorsum. The new species differs from L. danhidalgoi in having distinctly blunt-tipped dorsal idiosomal setae (vs. pointed in L. danhidalgoi), ''O''-shaped coxal organ (vs. ''8''-shaped in L. danhidalgoi), and in having unusual seta d of palptarsus divided from its base (vs. seta d of palptarsus divided only distally in L. danhidalgoi).
Lorryia evansi Baker, 1968a, 992, Fig. 16.
Brachytydeus evansi: Silva et al. 2016, 14.
(Figs 14–19)
Female — (Figs 14–18, 19A, B). Body ovate (Figs 14A, 17A, 18). Length of idiosoma 255–310, maximum width 185–215.
Idiosomal dorsum – (Figs 14A, 17A–D, 18, 19A). Dorsal ornamentation type ''Lorryia''; reticulation forms discrete areas divided by striated integument as illustrated on Figs 14A, 17A and 18; reticulation meshes regular in shape (Figs 17A–D); cross-ties triangular, rarely quadrangular in shape, frames of meshes with rare ''I''-shaped transversely aligned costulae. Dorsal hysterosomal setae subequal in length and shape, slightly curved, blunt-tipped, smooth or with very small serration on dorsal surface of setae; setae h1, h2 and ps1 slightly thicker and more blunt than other dorsal setae; trichobothria smooth, weakly blunt-tipped (sometimes pointed), about two times longer than other dorsal setae. All cupuli ovoid. Lengths of setae: vi 27–30, ve 30–34, sci 45–59, sce 32–34, c1 29–34, c2 31–36, d 28–32, e 31–34, f1 31–33, f2 30–34, h1 28–32, h2 31–33, ps1 22–28.
Idiosomal venter – (Figs 14B, 19B). Ventral surface mostly striated; striae between setae 3a and 4a longitudinally parallel (Fig. 19B). Coxal organ ''8''-shaped. Ventral setae smooth and pointed, except ps1 which of the same shape as dorsal setae. Six pairs of genital setae. Genital papillae not evident.
Gnathosoma – (Figs 15, 17E). Gnathosoma usually completely covered by idiosoma or distal part of chelicerae visible from above. Cheliceral stylets 18–20 subequal in length with palptarsus 17–19 and shorter than combined length of palptarsus and eupathidiun (p) 25–27. Palpal terminal eupathidium with ''T''-shaped tip; seta d bifurcates distally; seta acm blunt-tipped. All palpal setae smooth. Subcapitulum (Fig. 17E) with smooth and pointed subcapitular setae (sc1, sc2) and two pairs of short smooth and pointed adoral setae (or1, or2). Gnathosomal supracoxal setae ep rod-like.
Legs – (Figs 16, 17F). Empodia with small empodial hooks; tarsal claws serrate (Fig. 17F). Leg I (Figs 16A, 17F). Setae (p), (tc) and ft″ of tarsus eupathid-like, smooth and longitudinally striated (Fig. 17F); setae d of femur, (l) of genu and d of tibia similar to dorsal idiosomal setae, other setae pointed and weakly barbed. Solenidion ω 8 baculiform; famulus k on tibia multibranched distally. Leg supracoxal seta (el) rod-like, located dorsally near trochanter. Leg II (Fig. 16B). Setae d of femur, (l) of genu, and d of tibia similar to dorsal idiosomal setae, other leg setae pointed and weakly barbed. Solenidion ω 3–4 baculiform. Leg III (Fig. 16C). Setae d of femur, l′ of genu and d of tibia similar to dorsal idiosomal setae, other leg setae pointed and weakly barbed. Leg IV (Fig. 16D). Setae l′ of genu and d of tibia similar to dorsal idiosomal setae, other leg setae pointed and weakly barbed.
Male similar to female and differs only in having longitudinal slit-like genital opening (Fig. 19C) and four pairs of short and barbed eugenital setae.
Larva, protonymph, deutonymph and tritonymph unknown.
Sixteen females, 3 males, Russia, Tyumen Region, vicinity of Uspenka village, 57°03′N 65°03′E, in rotting bark of unknown tree, 07 May 2019, collected by A.A. Khaustov.
Lorryia evansi was described from quarantine in USA (New York) on cut flowers imported from the Netherlands (Baker 1968a). This species is very similar to L. polygonata Kulczyck1, 1992 described from Ukraine. According to keys provided by Kaźmierski (1998) and Silva et al. (2016), L. evansi differs from L. polygonata only by smooth or rough dorsal idiosomal setae, while in L. polygonata dorsal idiosomal setae clearly serrated. I examined several specimens of L. polygonata collected by me on apple bark in Ukraine. In fact, the dorsal setae in L. polygonata are smooth or rough, not clearly serrated. In the original description of L. polygonata the author also mentioned that most of the setae are smooth or just have few very small barbs apically. However, L. polygonata can be distinguished from L. evansi by distinctly thicker setae f2, h1, h2, and ps1; setae f2 clearly thicker and more blunt than f2 (Fig. 19D); in contrast to subequal in width and shape of setae f1 and f2 in L. evansi (Fig. 19A).
Retetydeus catenulatus Thor, 1931, 91
Lorryia catenulata: Baker 1968a, 1001
Tydeus catenulata: Momen and Lundqvist 1995, 43
Brachytydeus catenulata: Silva et al. 2016, 12
Brachytydeus catenulatus: André 2021
(Figs 20, 21A, B)
This species originally was described from Norway (Thor 1931). Baker (1968a) redescribed it based on specimens from Ireland. Kaźmierski (1980) redescribed it based on materials from Poland. Kuznetsov and Petrov (1984) recorded this species in Latvia. According to Kuznetsov and Petrov (1984) this species also was recorded in European Russia (Voronezh Region), Georgia and Ukraine. Momen and Lundqvist (1995) reported it from Sweden. Kaźmierski et al. (2018) noted that this species prefers such habitats as moss covering shady rocks in dark needle forests.
Kuznetsov and Petrov (1984) provided an illustration of L. catenulata which, in fact, repeat the illustration of L. polita Kuznetsov, 1975a, a closely related species described from Georgia. Most likely, they consider L. polita as a suspected junior synonym of L. catenulata. According to the key of Kaźmierski (1998) L. polita can be distinguished from L. catenulata in having separate reticulated area A[c2]0[e1] between setae c2 and e. In fact, in the original description of Thor (1931) this area is clearly depicted as well as in redescription of Baker (1968a). My specimens from Western Siberia fully correspond to the description of Thor (1931), especially in having an anterior invagination (poorly developed in some specimens) in the reticulate area A[c2]0[e1] (Figs 20A, 22A). For the separation or possible synonymy of L. polita, I examined the holotype of this species (Figs. 21C, D, 22C, D). Both species are very similar, however, the reticulate area A[c2]0[e1] in L. polita is hardly discernible on the left side and is clearly separated from area Ac2 on the right side of the holotype (Fig. 22D). Therefore, the use of this character for the separation of L. polita and L. catenulata is problematic. The study of palpal setae revealed some minor differences between L. polita and L. catenulata. In L. catenulata seta ba of the palptarsus is very short and blunt-tipped, distinctly shorter than seta acm and seta v is pointed (Fig. 21A, B); in L. polita seta ba is unusually long and thin, pointed, subequal in length with acm, and seta v is clearly blunt-tipped (Fig 21C, D). There are no differences in the shape of dorsal idiosomal setae and structure of reticulate areas on the idiosoma. In L. catenulata, the dorsal idiosomal setae are weakly barbed and pointed (Fig. 20C, D), and in L. polita the dorsal idiosomal setae not so strongly barbed as in the original description. Another character, which could be used for the separation of L. polita from L. catenulata, is the shape of striae between ventral setae 3a and 4a. In L. catenulata striae form a ''V''-shaped ornament (Fig. 22B), while in L. polita striae are parallel (Fig. 22C).
Fifteen females, 6 males, Russia, Tyumen Region, city of Tyumen, 57°09′N 65°27′E, in moss on soil in the mixed forest, 23 June 2019, collected by A.A. Khaustov.
Tydeus reticulatus Oudemans, 1928, 380
Tydeus reticulata: Baker 1947, 227
Lorryia reticulata: Oudemans 1929, 481
Brachytydeus reticulata: Silva et al. 2016, 23
Brachytydeus reticulatus: André 2021
Lorryia bedfordiensis: synonymy by Kaźmierski (1998), 300
Lorryia polaris: synonymy by Kaźmierski (1998), 300
This is one of the most widespread species of Tydeidae and probably cosmopolitan (Kaźmierski 1998). In Russia, it was recorded in European part (Kuznetsov and Petrov 1984).
Mondin et al. (2016) consider L. reticulata as suspected junior synonym of L. superba (type species of Lorryia) and Kaźmierski et al. (2018) consider L. reticulata as a junior synonym of L. superba. However, André (2005) described the history of L. superba and noted that type specimen of this species is lost. Therefore, the synonymy of L. reticulata and L. superba still not clear.
One female, 1 male, 5 TN, Russia, Tyumen Region, vicinity of Uspenka village, 57°03′N 65°03′E, in rotting bark of spruce, 08 May 2019, collected by A.A. Khaustov; 2 females, Russia, Tyumen Region, Tyumen District, city of Tyumen, 57°09′N 65°27′E, in rotting bark of dead spruce, 15 June 2019, collected by A.A. Khaustov; 2 females, same locality and date, in tree hole of birch.
Tydeus argutus Kuznetsov and Petrov, 1979, 131
This species was described from Latvia (Kuznetsov and Petrov 1979; 1984). Unfortunately, this species was not mentioned in the catalogue of Tydeidae (Silva et al. 2016) and in the latest online database (André 2021). It was originally placed in the genus Tydeus, but according to modern taxonomy of Tydeidae it should be placed in the genus Lorryia sensu Kaźmierski (1989).
This is the first record of L. argutus from Russia.
Two females, 3 males, Russia, Tyumen Region, vicinity of Uspenka village, 57°03′N 65°03′E, in moss on soil, 02 October 2017, collected by A.A. Khaustov.
Tydeus obstinatus Livshitz, 1973, 49
Lorryia obstinata: Kaźmierski 1998, 336
Brachytydeus obstinata: Silva et al. 2016, 20
Brachytydeus obstinatus: André 2021
This species was described from Crimea (Kuznetsov and Livshitz 1973a). It was also recorded from Latvia and Lithuania (Kuznetsov and Petrov 1984), Poland (Kaźmierski et al. 2018), Iran (Sadeghi et al. 2012), Sweden (Momen and Lundqvist 2005).
One female, Russia, Tyumen Region, vicinity of Uspenka village, 57°03′N 65°03′E, in rotting grass on the field, 18 October 2017, collected by A.A. Khaustov; 1 female, Russia, Tyumen Region, Berdyuzhsky District, vicinity of lake Solenoe, 55°42′35.0″N 68°42′49.0″E, soil in steppe, 20 June 2020, collected by A.A. Khaustov.
Lorryia arkadiensis Panou and Emmanouel, 1995a, 217
Brachytydeus arkadiensis: Silva et al. 2016, 10
This species was described from Greece (Panou and Emmanouel 1995a). It was also recorded from Poland (Kaźmierski 1998; Laniecki et al. 2021).
This is the first record of L. arkadiensis in Russia.
Seven females, 3 males, Russia, Tyumen Region, vicinity of Uspenka village, 57°03′N 65°03′E, in moss on the edge of the pine forest, 6 May 2019, collected by A.A. Khaustov; 3 females, Russia, Tyumen Region, city of Tyumen, 57°09′N 65°27′E, in soil, 04 May 2019, collected by A.A. Khaustov.
Tydeus filiformis Momen and Lundqvist, 1996, 89
Lorryia fusiformis: Kaźmierski 1998, 327
Brachytydeus fusiformis: Kaźmierski 2009, 80.
This species was described from Sweden (Momen and Lundqvist 1996). It was also recorded and redescribed from Poland (Kaźmierski 2009).
This is the first record of L. fusiformis in Russia.
Three females, Russia, Tyumen Region, vicinity of Uspenka village, 57°03′N 65°03′E, on bark of pine, 24 June 2019, collected by A.A. Khaustov; 3 females, same locality, on bark of spruce, 2 May 2019.
Brachytydeus szeptyckii Kaźmierski, 2009, 80
This species was described from Poland (Kaźmierski 2009).
It was originally placed in the genus Brachytydeus, but according to modern taxonomy of Tydeidae it should be placed in the genus Lorryia sensu Kaźmierski (1989).
This is the first record of L. szeptyckii from Russia.
Two females, 4 males, Russia, Kurgan Region, Zverinogolovskiy District, vicinity of settlement Zverinogolovskoe, 54°26′28.7″N 64°51′21.9″E, in grassy soil, 20 September 2019, collected by A.A. Khaustov.
Tydeus serpettae Momen and Lundqvist, 2005, 233
Brachytydeus serpettae: Silva et al. 2016, 25
This species was described from Sweden (Momen and Lundqvist 2005). It was originally placed in the genus Tydeus, but according to modern taxonomy of Tydeidae it should be placed in the genus Lorryia sensu Kaźmierski (1989).
This is the first record of L. serpettae from Russia.
Three females, 2 males, Russia, Tyumen Region, city of Tyumen, 57°09′N 65°27′E, on bark of apple tree, 12 May 2019, collected by A.A. Khaustov.
Lorryia grandiinsignia Kaźmierski, 1991, 339
Brachytydeus grandiinsignia: Silva et al. 2016, 16
Brachytydeus grandiinsignius: André 2021
This species was described from Poland (Kaźmierski 1991).
This is the first record of L. grandiinsignia from Russia.
Two females, Russia, Kurgan Region, Zverinogolovskiy District, vicinity of settlement Zverinogolovskoe, 54°26′28.7″N 64°51′21.9″E, in grassy soil, 20 September 2019, collected by A.A. Khaustov.
Tydeus (Eotydeus) mirabilis Kuznetsov, 1973a, 1578
Eotydeus mirabilis: André 1980, 113
Lorryia mirabilis: Kaźmierski 1989, 301
Lorryia mirabila: Kaźmierski 1998, 336
Brachytydeus mirabila: Silva et al. 2016, 19
Eotydeus mirabilis: André 2021
Tydeus unguis Karg, 1975: synonymy by Kaźmierski 1998, 336
This species was described from Crimea (Kuznetsov 1973a). It was also recorded from Poland (Błoszyk et al. 1994), Germany and Sweden (as Tydeus unguis) (Karg 1975; Momen and Lundqvist 1996).
Two females, Russia, Tyumen Region, vicinity of lake Kuchak, 57°21′N 66°02′E, in moss, 04 July 2014, collected by A.A. Khaustov.
Lorryia subularoides Kaźmierski, 1989, 293
Brachytydeus subularoides: Silva et al. 2016, 26
This species was described from Poland and Czech Republic (Kaźmierski 1989). It was also recorded from Iran (Darbemamieh et al. 2021).
This is the first record of L. subularoides in Russia.
Two females, Russia, Tyumen Region, vicinity of Uspenka village, 57°03′N 65°03′E, in rotting log, 02 May 2019, collected by A.A. Khaustov.
Tydeus paravarsoviensis Momen and Lundqvist, 1996, 86
Lorryia paravarsoviensis: Kaźmierski 1998, 326
Brachytydeus paravarsoviensis: Silva et al. 2016, 22
This species was described from Sweden (Momen and Lundqvist 1996).
This is the first record of L. paravarsoviensis in Russia.
Two females, Russia, Tyumen Region, vicinity of lake Kuchak, 57°21′N 66°02′E, n rotting log, 31 May 2014, collected by A.A. Khaustov; 3 females, Russia, Tyumen Region, city of Tyumen, 57°09′N 65°27′E, in forest litter, 09 June 2019, collected by A.A. Khaustov.
Paralorryia maga Kuznetsov, 1973, 604
Venilia maga: Kuznetsov 1979, 1413
Tydeus maga: Momen and Lundqvist 1995, 53
Lorryia maga: Kaźmierski 1998, 334
Kuznetsovia maga: Kammerer 2006, 269
Brachytydeus maga: Silva et al. 2016, 18
Brachytydeus magus: André 2021
This species was described from Crimea (Kuznetsov and Livshitz 1973b). It was also recorded in Sweden (Momen and Lundqvist 1995), Poland (Laniecki et al. 2021), Iran (Akbari et al. 2015) and Siberia (Kaźmierski 2000). Ueckermann et al. (2019) redescribed this species based on materials from Turkey.
One female, Russia, Tyumen Region, vicinity of lake Kuchak, 57°21′N 66°02′E, moss on soil in pine forest, 31 May 2014, collected by A.A. Khaustov; 2 females, 2 males, 2 TN, Russia, Kurgan Region, Petuknovsky District, vicinity of lake Medvezh'ye, 55°10′N 67°55′E, soil in steppe, 14 October 2022, collected by A.A. Khaustov.
Paralorryia opifera Kuznetsov, 1973, 16
Lorryia opifera: Kaźmierski 1998, 333
Brachytydeus opifera: Silva et al. 2016, 21
Brachytydeus opiferus: André 2021
This species was described from Crimea (Kuznetsov and Livshitz 1973c). It was also recorded in Poland (Kaźmierski 2000; Laniecki et al. 2021).
Two males, Russia, Tyumen Region, vicinity of Uspenka village, 57°03′N 65°03′E, in soil, 08 May 2019, collected by A.A. Khaustov.
Paralorryia livshitzi Kuznetsov, 1974, 1092
Lorryia livshitzi: Kaźmierski 1998, 333
Brachytydeus livshitzi: Silva et al. 2016, 17
This species was described from Lipetsk region of Russia (Kuznetsov 1974). It was also recorded from Poland (Kaźmierski 2000), Iran (Akbari et al. 2015) and Turkey (Ueckermann et al. 2019).
Two females, Russia, Kurgan Region, Petuknovsky District, vicinity of lake Medvezh'ye, 55°10′N 67°55′E, soil in steppe, 14 October 2022, collected by A.A. Khaustov; 1 female, Russia, city of Tyumen, 57°09′N 65°33′E, moss on bark of poplar, 13 April 2020, collected by A.A. Khaustov.
Paralorryia woolleyi Baker, 1968b, 1103
Lorryia woolleyi: Kaźmierski 1998, 332
Brachytydeus woolleyi: Silva et al. 2016, 15
This species was described from the USA (Baker 1968b). It was also recorded in Poland, Bulgaria, Russia (including Siberia) (Kaźmierski 2000; Kaźmierski et al. 2018), and Iran (Akbari et al. 2015).
Nineteen females, Russia, city of Tyumen, 57°09′N 65°33′E, moss on bark of poplar, 13 April 2020, collected by A.A. Khaustov.
Type species: Calotydeus croceus (Linnaeus) sensu Oudemans, 1928, by original designation
Pseudolorryia edwardbakeri Kaźmierski, 1989
Calotydeus edwardbakeri: André 2005, 995
This species was described from Poland (Kaźmierski 1989).
This is the first record of C. edwardbakeri in Russia.
Two females, 1 TN, Russia, Tyumen Region, vicinity of Uspenka village, 57°03′N 65°03′E, in soil, 02 October 2017, collected by A.A. Khaustov; 4 females, same locality, on the bark of pine, 26 May 2019.
Type species: Tydides ulter Kuznetsov, 1975, by original designation
Tydides ulter Kuznetsov, 1975b, 1255
Kuznetsovtydides ulter: André 2021, 1030
This species was described from Crimea (Kuznetsov 1975b). It was also recorded in Poland, Slovakia and Hungary (Kaźmierski 2000).
Three male, Russia, Kurgan Region, Zverinogolovskiy District, vicinity of settlement Zverinogolovskoe, 54°26′N 64°51′E, in grassy soil, 20 September 2019, collected by A.A. Khaustov.
Type species: Lorryia armaghensis Baker, 1968a, by original designation
Lorryia delicata Kuznetsov, 1971, 1745
Metalorryia delicata: Panou and Emmanouel 1995b, 211
Lorryia cristata Karg, 1975, synonymy by Kaźmierski 1998, 346
This species was described from Georgia (Kuznetsov 1971). It was also recorded in Germany (as Lorryia cristata) (Karg 1975), Greece (Panou and Emmanouel 1995b), and Poland (Kaźmierski 1998).
This is the first record of M. delicata in Russia.
One female, Russia, Tyumen Region, Berdyuzhsky District, vicinity of lake Solenoe, 55°42′35.0″N 68°42′49.0″E, soil in steppe, 20 June 2020, collected by A.A. Khaustov.
Type species: Neoapolorryia aegyptica El-Bagoury and Momen, 1990, by original designation
Lorryia regia Kuznetsov, 1973b, 773
Neoapolorryia regia: Kaźmierski 1998, 351
This species was described from Crimea (Kuznetsov 1973b). It was also recorded in Poland (Kaźmierski 1998).
One female, 1 TN, Russia, Kurgan Region, Petuknovsky District, vicinity of lake Medvezh'ye, 55°10′N 67°55′E, soil in steppe, 14 October 2022, collected by A.A. Khaustov.
Type species: Nudilorryia paraferula Kaźmierski, 1996, by original designation
Nudilorryia obsequens Kaźmierski, 1996, 207
This species was described from Germany (Kaźmierski 1996).
This is the first record of N. obsequens in Russia.
Three females, Russia, Tyumen Region, vicinity of lake Kuchak, 57°21′N 66°02′E, in nest of Formica rufa, 04 July 2014, collected by A.A. Khaustov.
Type species: Lorryia cumbrensis Baker, 1944, by original designation
Homeotydeus formosa Andre, 1984
Paralorryia formosa: Kaźmierski 1989, 292
This species was described from Belgium (André 1984).
This is the first record of P. formosa in Russia.
One female, Russia, city of Tyumen, 57°09′N 65°27′E, bark of dead birch, 31 May 2020, collected by A.A. Khaustov; 1 female, 1 male, Russia, Tyumen Region, Nizhnetavdinskiy District, vicinity of Tyunevo village, 57°22′N 65°41′E, on bark of linden Tilia cordata,31 May 2020, collected by A.A. Khaustov.
Paralorryia formosa (André) is very similar morphologically to Paralorryia formosa Livshitz, 1972. In the original description of P. formosa Livshitz the leg chaetotaxy is not described and its taxonomic position is not clear. I examined the holotype of P. formosa Livshitz and found that, besides striation type ''Paralorryia'', it differs from P. formosa (André) in having two setae on femur III and according to the modern system of Tydeidae P. formosa Livshitz should be placed in the genus Nudilorryia Kaźmierski, 1996, i. e. Nudilorryia formosa (Livshitz, 1972) n. comb.
Type species: Tydeus spathulatus Oudemans, 1928, designated by ICZN (2008)
For synonymy, see André (2021)
This species was described from Italy (André 2005). It was also reported from Hungary (Tempfli et al. 2015).
This is the first record of T. spathulatus in Russia.
One male, Russia, Tyumen Region, Tyumen District, vicinity of Malinovka village, 57°05′N 65°03′E, in moss on bark of aspen Populus tremula, collected by A.A. Khaustov.
Tydeus nieuwkerkeni André, 2005, 993
This species was described from the Netherlands (André 2005).
This is the first record of T. nieuwkerkeni in Russia.
Two females, Russia, Tyumen Region, vicinity of lake Kuchak, 57°21′N 66°02′E, on undetermined plant, 31 July 2018, collected by A.A. Khaustov.
The present research revealed a diverse fauna of Tydeidae in Western Siberia. However, there are many still undescribed and unidentified species in my collection, which will be described and reported later. Most of these new species were collected in the Altai Mountains.
During this study, I found well-developed genital papillae in adults of several species of Tydeidae, including Lorryia sibiriensis n. sp., L. speciosa n. sp., L. polita and L. catenulata. According to André (1981a) genital papillae (acetabula) in adults of Tydeidae are present, but hardly discernible. Moreover, I have never seen illustrations of the genital papillae in adults of Tydeidae in any publication. The presence of well-developed genital papillae potentially could be used in taxonomy of Tydeidae, probably in separation of species groups, etc. However, more detailed research of previously described species is necessary.
This research was supported by the cooperative agreement No. FEWZ-2021-0004 from the Russian Ministry of Science and Higher Education.