Literature DB >> 26692794

Contributions to the knowledge of oribatid mites of Indonesia. 2. The genus Pergalumna (Galumnidae) with description of a new species and key to known species in the Oriental region (Acari, Oribatida).

Sergey G Ermilov1, Dorothee Sandmann2, Bernhard Klarner2, Rahaju Widyastuti3, Stefan Scheu2.   

Abstract

A new species of oribatid mite of the genus Pergalumna (Oribatida, Galumnidae) is described from litter and soil materials in Sumatra, Indonesia. Pergalumna paraindistincta sp. n. is morphologically most similar to Pergalumna indistincta Ermilov & Anichkin, 2011, Pergalumna pertrichosa Mahunka, 1995 and Pergalumna sura Balogh, 1997; however, the new species differs from Pergalumna indistincta by the smaller body size, presence of long adanal setae ad 1, and large, single median pore in females and males; from Pergalumna pertrichosa by the smaller body size, presence of three pairs of notogastral porose areas, elongated A1 and minute anal setae; from Pergalumna sura by the presence of strong adanal setae ad 1, large, single median pore in females and males, and shorter bothridial setae. Furthermore, Pergalumna hawaiiensis hawaiiensis (Jacot, 1934) and Pergalumna panayensis Ermilov & Corpuz-Raros, 2015 are recorded for the first time in the Indonesian fauna. An identification key to the known species of Pergalumna in the Oriental region is given.

Entities:  

Keywords:  Indonesia; Oribatid mites; Oriental region; Pergalumna; key; new record; new species

Year:  2015        PMID: 26692794      PMCID: PMC4668901          DOI: 10.3897/zookeys.529.6421

Source DB:  PubMed          Journal:  Zookeys        ISSN: 1313-2970            Impact factor:   1.546


Introduction

This work is a part of a continuing study on the Indonesian fauna of oribatid mites, and it includes the data on the genus Grandjean, 1936 (, ). During taxonomic identification, four species were identified, including one new to science. The primary goal of the paper is to present data on the specific localities, notes on new records and overall known distributions of registered taxa and to describe the new species. is a genus that was proposed by Grandjean (1936) with Berlese, 1914 as type species. Based on an updated generic diagnosis (Ermilov et al. 2013b), it comprises more than 140 species (Subías 2004, updated 2015; Ermilov and Bayartogtokh 2015; Ermilov and Corpuz-Raros 2015) having collectively a cosmopolitan distribution (Subías 2004, updated 2015). The identification keys to selected species were given by Shaldybina (1975), Balogh and Balogh (1990, 2002), Weigmann (2006), and Ermilov et al. (2014b). The secondary goal of the paper is to provide an identification key to known species of in the Oriental region.

Materials and methods

Exact collection locality and habitat are given in the respective “Material examined” section for each species. Specimens were mounted in lactic acid on temporary cavity slides for measurement and illustration. The body length was measured in lateral view, from the tip of the rostrum to the posterior edge of the ventral plate. Notogastral width refers to the maximum width in dorsal aspect. Lengths of body setae were measured in lateral aspect. All body measurements are presented in micrometers. Formulas for leg setation are given in parentheses according to the sequence trochanter–femur–genu–tibia–tarsus (famulus included). Formulas for leg solenidia are given in square brackets according to the sequence genu–tibia–tarsus. General terminology used in this paper follows that of Grandjean (summarized by Norton and Behan-Pelletier 2009). Drawings were made with a camera lucida using a Carl Zeiss transmission light microscope “Axioskop-2 Plus”.

Description

sp. n.

http://zoobank.org/F1F876B8-867F-4EA9-851D-FB4186C05342 Figs 1 , 2 , 3–4 , 5–9
Figure 1.

sp. n., adult: dorsal view. Scale bar 100 μm.

Figure 2.

sp. n., adult: ventral view (gnathosoma and legs not shown). Scale bar 100 μm.

Figures 3–4.

sp. n., adult: 3 anterior part of body, lateral view (gnathosoma and leg I not shown) 4 posterior view. Scale bar 100 μm.

Figures 5–9.

sp. n., adult: 5 bothridial seta 6 anterior part of left half of subcapitulum, ventral view 7 genital plate, right 8 anal plate, left, and adanal setae 9 tibia of leg IV, right, antiaxial view. Scale bar 20 μm.

Diagnosis.

Body size: 415–481 × 298–365. Rostral, lamellar and interlamellar setae well developed, barbed. Bothridial setae long, setiform, ciliate. Anterior notogastral PageBreakmargin not developed. Three pairs of elongate oval porose areas on notogaster, Aa transversally oriented, located between la and lm, A1 longitudinally oriented. Median pore single, large. Adanal setae ad1 of medium size, straight, heavily barbed. Postanal porose area absent.

Description.

Measurements. Body length: 431 (holotype: male), 415–481 (10 paratypes: three females and seven males); notogaster width: 298 (holotype), 298–365 (10 paratypes). Without sexual dimorphism. Integument. Body color brown. Body surface microgranulate, visible under high magnification, ×1000 (diameter of granules less than 1). Prodorsum (Figs 1, 3, 5). Rostrum broadly rounded. Lamellar (L) and sublamellar (S) lines distinct, parallel, curving backwards. Rostral (ro, 41–49), lamellar (le, 69–77) and interlamellar (in, 86–90) setae setiform, barbed. Bothridial setae (bs, 114–127) PageBreaksetiform, densely ciliate in medio-distal parts. Exobothridial setae and their alveoli absent. Porose areas Ad narrowly elongate oval, transversally oriented (16–20 × 4). sp. n., adult: dorsal view. Scale bar 100 μm. sp. n., adult: ventral view (gnathosoma and legs not shown). Scale bar 100 μm. sp. n., adult: 3 anterior part of body, lateral view (gnathosoma and leg I not shown) 4 posterior view. Scale bar 100 μm. sp. n., adult: 5 bothridial seta 6 anterior part of left half of subcapitulum, ventral view 7 genital plate, right 8 anal plate, left, and adanal setae 9 tibia of leg IV, right, antiaxial view. Scale bar 20 μm. Notogaster (Figs 1, 3, 4). Anterior notogastral margin not developed. Dorsophragmata (D) of medium size, elongated longitudinally. Notogastral setae represented by 10 pairs of alveoli. Three pairs of porose areas: Aa clearly bordered, elongate oval, transversally oriented (28–32 × 8–12), A1 distinctly bordered only in anterior part, elongate oval to slightly elongate triangular, longitudinally oriented (57–68 × 12–16), A3 without clear borders, elongate oval (24–28 × 8–12). Areas Aa located between setal alveoli PageBreakla and lm, equal distanced from them. Median pore present in males and females, comparatively large (diameter 10–16). All lyrifissures (ia, im, ip, ih, ips) distinct, im located antero-laterally to A1. Opisthonotal gland openings (gla) located laterally to A1. Gnathosoma (Fig. 6). Morphology of subcapitulum, palps and chelicerae typical for (see Engelbrecht 1972; Ermilov and Anichkin 2011a, b). Subcapitulum size: 102–106 × 102–106. Subcapitular setae setiform, slightly barbed, m (14–16) shorter than a and h (both pairs 18–20); a thickest, m thinnest. Two pairs of adoral setae (or1, or2, 12–14) setiform, hook-like distally, barbed. Palps (90–94) with typical setation: 0–2–1–3–9(+ω). Axillary sacculi (sac) distinct. Chelicerae (164) with two setiform, barbed setae; cha (41) longer than chb (24). Trägårdh’s organ long, tapered. Epimeral and lateral podosomal regions (Fig. 2). Anterior tectum of epimere I smooth. Apodemes 1, 2, sejugal and 3 well visible. Six pairs of setae, setal formula: 1–0–2–3. Setae thin, slightly barbed, 1a, 3c and 4c (24) longer than 3b (10–14) and 4a and 4b (4); 1a thicker than others. Pedotecta II (Pd II) scale-like in lateral view, rounded distally in ventral view. Discidia (dis) sharply triangular. Circumpedal carinae (cp) slightly developed. Anogenital region (Figs 2, 4, 7, 8). Six pairs of genital (g1, g2, 12; g2–g6, 8), one pair of aggenital (ag, 8), two pairs of anal (an1, an2, 8) and two pairs of adanal setae (ad2, ad3, 8) thin, indistinctly barbed. One pair of adanal setae (ad1, 24–36) thickened, straight, heavily barbed, however, in three paratypes one seta of the ad1 pair is short, as ad2 and ad3 in morphology. Adanal setae ad3 inserted laterally to adanal lyrifissures (iad). Genital plates with two or three setae on anterior edge of each plate. Postanal porose area absent. Legs (Fig. 9). Morphology of leg segments, setae and solenidia typical for (see Engelbrecht 1972; Ermilov and Anichkin 2011a, b). Claws smooth. Formulas of leg setation and solenidia: I (1–4–3–4–20) [1-2-2], II (1–4–3–4–15) [1-1-2], III (1–2–1–3–15) [1-1-0], IV (1–2–2–3–12) [0-1-0]; homology of setae and solenidia indicated in Table 1. Solenidion φ of tibiae IV inserted dorsally in posterior part of segments.
Table 1.

Leg setation and solenidia of adult sp. n.

LegTrFeGeTiTa
Ivd, (l), bv’’(l), v’, σ(l), (v), φ1, φ2(ft), (tc), (it), (p), (u), (a), s, (pv), v’, (pl), l’’, ε, ω1, ω2
IIvd, (l), bv’’(l), v’, σ(l), (v), φ(ft), (tc), (it), (p), (u), (a), s, (pv), ω1, ω2
IIIvd, evl’, σl’, (v), φ(ft), (tc), (it), (p), (u), (a), s, (pv)
IVvd, evd, ll’, (v), φft’’, (tc), (p), (u), (a), s, (pv)

Note: Roman letters refer to normal setae, Greek letters to solenidia (except ε = famulus). Single prime (‘) marks setae on the anterior and double prime (“) setae on the posterior side of a given leg segment. Parentheses refer to a pair of setae. Tr, Fe, Ge, Ti, Ta.

– trochanter

– femur

– genu

– Tibia

– tarsus

Leg setation and solenidia of adult sp. n. Note: Roman letters refer to normal setae, Greek letters to solenidia (except ε = famulus). Single prime (‘) marks setae on the anterior and double prime (“) setae on the posterior side of a given leg segment. Parentheses refer to a pair of setae. Tr, Fe, Ge, Ti, Ta. – trochanter – femur – genu – Tibia – tarsus

Material examined.

Holotype (male): Indonesia, Sumatra, Harapan landscape, secondary rainforest, research site HF1, 02°09'09.9"S, 103°21'43.2"E, 76 m a.s.l., from forest floor litter material. Six paratypes (two females and four males): Indonesia, Sumatra, Harapan landscape, rubber plantation, research site HR2, 01°52'44.5"S, 103°16'28.4"E, 59 m a.s.l., from forest floor litter material. Four paratypes (one female and three males): Sumatra, Indonesia, Harapan landscape, jungle rubber agroforest, research site HJ1, 01°55'40.0"S, 103°15'33.8"E, 51 m a.s.l., from forest floor litter material. All specimens were collected by Bernhard Klarner (15.XI.2013) and identified and collected to morphospecies level by Dorothee Sandmann.

Type deposition.

The holotype is deposited in LIPI (Indonesian Institute of Science) Cibinong, Indonesia; three paratypes are in the collection of the Senckenberg Museum, Görlitz, Germany; seven paratypes are in the collection of the Tyumen State University Museum of Zoology, Tyumen, Russia.

Etymology.

The specific name paraindistincta refers to the morphological similarity of the new species to Ermilov & Anichkin, 2011.

Remarks.

sp. n. is morphologically most similar to Ermilov & Anichkin, 2011 from Vietnam (see Ermilov and Anichkin 2011b) and Balogh, 1997 from the Neotropical region (see Balogh 1997; Ermilov et al. 2014a) in having rounded rostrum, well-developed prodorsal setae, setiform and ciliate of bothridial setae, three pairs of notogastral porose areas, transversally oriented Aa and strongly elongated, longitudinally oriented A1, and the absence of anterior notogastral margin as well as postanal porose area. However, the new species differs from both by the presence of strong adanal setae ad1 (vs. minute in and ) and large, single median pore in females and males (vs. median pore absent in males and represented by several foveae in females in , and absent in females and males in ). Additionally, the new species is smaller than (415–481 × 298–365 vs. 547–614 × 381–415) and has shorter bothridial setae than . Furthermore, sp. n. is morphologically similar to Mahunka, 1995 from Borneo (see Mahunka 1995) in having a rounded rostrum, well developed prodorsal setae, setiform and ciliate bothridial setae, strong adanal setae ad1, a single median pore, and the absence of an anterior notogastral margin. However, the new species differs from the latter by the smaller body size (415–481 × 298–365 vs. 550–608 × 413–454 in ), presence of three pairs of notogastral porose areas with elongated A1 (vs. four pairs of porose areas with A1 rounded in ) and minute anal setae (vs. well developed in ).

Records

(Jacot, 1934) (see Jacot 1934a). Distribution: Pacific Islands. New record for Indonesia. Material examined. One specimen: Indonesia, Sumatra, Harapan landscape, Jungle rubber agroforest, research site HJ1, 01°55'40.0"S, 103°15'33.8"E, 51 m a.s.l., from upper soil layer (0–5 cm), 15.XI.2013 (B. Klarner). Three specimens: Indonesia, Sumatra, Bukit Duabelas landscape, rubber plantation, research site BR2, 02°05'06.8"S, 102°47'20.7"E, 95 m a.s.l., from upper soil layer (0–5 cm), 15.XI.2013 (B. Klarner). One specimen: Indonesia, Sumatra, Bukit Duabelas landscape, oil palm plantation, research site BO3, 02°04'15.2"S, 102°47'30.6"E, 71 m a.s.l., from upper soil layer (0–5 cm), 15.XI.2013 (B. Klarner). Ermilov & Corpuz-Raros, 2015 (see Ermilov and Corpuz-Raros 2015). Distribution: Philippines. New record for Indonesia. Material examined. One specimen: Indonesia, Sumatra, Harapan landscape, rubber plantation, research site HR2, 01°52'44.5"S, 103°16'28.4"E, 59 m a.s.l., from forest PageBreakfloor litter material, 15.XI.2013 (B. Klarner). One specimen: same data, but in upper soil layer (0–5 cm). One specimen: Indonesia, Sumatra, Bukit Duabelas landscape, jungle rubber agroforest, research site BJ4, 02°00'57.3"S, 102°45'12.3"E, 60 m a.s.l., from upper soil layer (0–5 cm), 15.XI.2013 (B. Klarner). (Canestrini, 1898) (see Mahunka 1992). Distribution: Oriental region. New record for Indonesia. Material examined. One specimen: Indonesia, Sumatra, Harapan landscape, jungle rubber agroforest, research site HJ2, 01°49'31.9’S’, 103°17'39.2"E, 84 m a.s.l., from forest floor litter material, 15.XI.2013 (B. Klarner). One specimen: Indonesia, Sumatra, Harapan landscape, jungle rubber, research site HJ4, 01°47'07.3"S, 103°16'36.9"E, 57 m a.s.l., from upper soil layer (0–5 cm), 15.XI.2013 (B. Klarner). One specimen: Indonesia, Sumatra, Bukit Duabelas landscape, secondary rainforest, research site BF2, 01° 58'55.1"S, 102°45'02.7"E, 77 m a.s.l., from upper soil layer (0–5 cm), 15.11.2013 (B. Klarner). Three specimens: Indonesia, Sumatra, Harapan landscape, jungle rubber agroforest, research site HJ2, 01°49'31.9"S, 03°17'39.2"E, 84 m a.s.l., from forest floor litter material, 15.XI.2013 (B. Klarner).

Key to known species of in the Oriental region

At present, 45 species/subspecies of are known in the Oriental region (Subías 2004, updated 2015; including present and personal data of the first author). (Willmann, 1931) from Java (see Willmann 1931), (Sellnick, 1925) from Sumatra (see Sellnick 1925) and Subías, 2004 from Taiwan (see Tseng 1984 as Tseng, 1984) are excluded from the key because these species have been poorly described. (Ewing, 1907) from the Holarctic and Oriental regions (see Ewing 1907; Jacot 1934b), (Willmann, 1931) from the Holarctic, Neotropical and Oriental regions and Polynesia (see Willmann 1931; Jacot 1934b; Hammer 1958, 1961, 1972), (Berlese, 1914) from the Ethiopian, Neotropical, Oriental and Palaearctic regions, and Hawaii and U.S.A. (see Weigmann 2006; Ermilov et al. 2013c), Tseng, 1984 from Taiwan (see Tseng 1984) and (Tseng, 1984) from Taiwan (see Tseng 1984) were not included because systematic placement of these species is not clear. We consider as a representative of the genus Heyden, 1826 (see Ermilov et al. 2013c). , and Tseng, 1984 have distinct notogastral setae, which are not traits for (see generic diagnosis in Ermilov et al. 2013b); these species are poorly described and redescribed; however, based on available data they should be considered as representatives of the genus Grandjean, 1936 or Balogh, 1960 (depending on presence or absence of lamellar lines). PageBreak has 14 pairs of notogastral setal alveoli, developed lamellae directed to insertions of lamellar setae and pteromorphs without setae (Tseng 1984); most likely this species is a representative of the subgenus Berlese, 1914 (, ), and it is morphologically most similar to Ermilov, Shtanchaeva & Subías, 2014 from Vietnam (see Ermilov et al. 2014d) and Willmann, 1956 from “Czechoslovakia” (see Willmann 1956) in having tubercles on pteromorphs and some other characters.
1Anterior margin of notogaster of specific structure, tuberculate2
Anterior margin of notogaster simple, smooth or not developed3
2Genital plates with several striae; notogastral porose areas of medium size, larger than diameter of bothridia; body size: 451–490 × 328–366Pergalumna margaritata Mahunka, 1989 (Mahunka 1989). Distribution: Vietnam
Genital plates with one pair of striae; notogastral porose areas small, similar to diameter of bothridia; body size: 402–447 × 281–315Pergalumna pseudomargaritata Mahunka, 1994 (see Mahunka 1994). Distribution: Thailand
3Anterior margin of notogaster distinctly developed, complete4
Anterior margin of notogaster not developed12
4Rostrum pointed5
Rostrum rounded7
5Four pairs of notogastral porose areas; Aa elongate triangular, transversally oriented; lateral parts of pteromorphs with strong ridges forming slightly visible reticulate pattern; body size: 517–670 × 397–525Pergalumna altera (Oudemans, 1915) (see Aoki 1961 as Pergalumna harunaensis Aoki 1961, 1975; Engelbrecht 1972; Weigmann 2006). Distribution: Semicosmopolitan
Three pairs of notogastral porose areas; Aa rounded; pteromorphs without strong ridges and reticulate pattern6
6Interlamellar setae long; posterior part of notogaster without furrows; body size: 664–830 × 498–630Pergalumna yurtaevi Ermilov & Anichkin, 2011 (see Ermilov and Anichkin 2011a; Ermilov et al. 2012a). Distribution: Vietnam
Interlamellar setae represented by alveoli; posterior part of notogaster with two parallel, longitudinal furrows; body size: 664–830 × 498–630Pergalumna asetosa Ermilov, Shtanchaeva, Kalúz & Subías, 2013 (see Ermilov et al. 2013a). Distribution: India
7Bothridial setae setiform; body size: 520–676 × 502Pergalumna foveolata Hammer, 1973 (see Hammer 1973; Bayartogtokh and Chatterjee 2010). Distribution: Australian, Neotropical and Oriental region
Bothridial setae with developed head8
8Interlamellar setae minute; body surface foveolate; body size: 222–235 × 177–190Pergalumna annulata Mahunka, 1995 (see Mahunka 1995). Distribution: Borneo
Interlamellar setae long; body surface not foveolate9
9Three pairs of notogastral porose areas; Aa rounded; body length: 820Pergalumna corniculata (Berlese, 1905) (see Berlese 1905; Mahunka 1992). Distribution: Java
Four pairs of notogastral porose areas; Aa elongated, transversally oriented10
10Notogastral porose areas Aa triangular; median pore present; body size: 623 × 533Pergalumna taprobanica Balogh, 1988 (see Balogh 1988). Distribution: Oriental region
Notogastral porose areas Aa elongate oval to boot-shaped11
11Bothridial setae fusiform, with well-developed head rounded distally; postanal porose area present; body size: 672 × 528Pergalumna andhraense Raju, Appalanaidu & Rao, 1981 (see Raju et al. 1981). Distribution: India
Bothridial setae lanceolate, with slightly developed head pointed distally; postanal porose area absent; body size: 830–898 × 630–680Pergalumna paraelongata Ermilov & Anichkin, 2012 (see Ermilov et al. 2012b). Distribution: Vietnam
12Rostrum trapezoid; anal setae comparatively long, longer than width of anal plate; body size: 1278–1311 × 976–1045Pergalumna paraclericata Ermilov, Chatterjee, Das & Bordoloi, 2014 (see Ermilov et al. 2014c). Distribution: India
Rostrum not trapezoid; anal setae comparatively short, shorter than width of anal plate13
13Rostrum pointed14
Rostrum rounded18
14Four pairs of notogastral porose areas; Aa located nearer to setal alveoli la than lm; body size: 730–780 × 564–597Pergalumna cattienica Ermilov & Anichkin, 2011 (see Ermilov and Anichkin 2011a). Distribution: Vietnam
Three pairs of notogastral porose areas; Aa located nearer to setal alveoli lm or distanced equal from la and lm15
15Interlamellar setae represented by alveoli; anterior part of prodorsum with two longitudinal ridges; notogastral porose areas Aa located nearer to setal alveoli lm than la; body size: 1162–1278 × 898–1012Pergalumna minipora Ermilov, Chatterjee, Das & Bordoloi, 2014 (see Ermilov et al. 2014c). Distribution: India
Interlamellar setae of medium size or long; prodorsum without ridges; notogastral porose areas Aa distanced equal from la and lm16
16Notogastral porose areas A1 elongated, longitudinally oriented; body surface foveolate; genital plates not striate; body size: 365–415 × 265–332Pergalumna paratsurusakii Ermilov, Shtanchaeva, Kalúz & Subías, 2013 (see Ermilov et al. 2013a). Distribution: India
Notogastral porose areas A1 rounded; body surface not foveolate; genital plates striate17
17Adanal setae ad1 and ad2 comparatively long, not shorter than width of anal plate; median pore absent; interlamellar setae longer than bothridial setae; body size: 597–680 × 431–498Pergalumna paracattienica Ermilov, Chatterjee, Das & Bordoloi, 2014 (see Ermilov et al. 2014c). Distribution: India
Adanal setae ad1 and ad2 minute; median pore present; interlamellar setae shorter than bothridial setae; body size: 498–531 × 381–398Pergalumna mahunkai Ermilov, Shtanchaeva, Kalúz & Subías, 2013 (see Ermilov et al. 2013a). Distribution: India
18Four pairs of notogastral porose areas19
Three pairs of notogastral porose areas22
19Interlamellar setae represented by alveoli; notogastral porose areas Aa located anteriorly to setal alveoli la; body length: 730Pergalumna corolevuensis Hammer, 1973 (see Hammer 1973). Distribution: Fiji and India
Interlamellar setae of medium size or long; notogastral porose areas Aa located between setal alveoli la and lm20
20Notogastral porose areas A1 located antero-medially to A2; interlamellar setae of medium size; body size: 745–842 × 567–640Pergalumna hauseri Mahunka, 1995 (see Mahunka 1995). Distribution: Borneo
Notogastral porose areas A1 located anteriorly to A2; interlamellar setae long21
21Adanal setae ad1 and ad2 similar in length; median pore absent; body size: 510–630 × 410–481Pergalumna pterinervis (Canestrini, 1898) (see Canestrini 1898; Berlese 1905, 1914; Mahunka 1992; including our data). Distribution: Oriental region
Adanal setae ad1 longer than ad2; median pore present; body size: 550–608 × 413–454Pergalumna pertrichosa Mahunka, 1995 (see Mahunka 1995). Distribution: Borneo
22Notogastral porose areas Aa located nearer to setal alveoli la than lm; bothridial setae clavate23
Notogastral porose areas Aa located nearer to setal alveoli lm than la or distanced equal from them; bothridial setae setiform or with slightly dilated, elongate head24
23Interlamellar setae minute, shorter than diameter of bothridia; body surface not foveolate; median pore represented by several foveae; body size: 262–282 × 192–209Pergalumna pseudosejugalis Ermilov & Anichkin, 2012 (see Ermilov and Anichkin 2012). Distribution: Vietnam
Interlamellar setae short, but longer than diameter of bothridia; body surface foveolate; median pore absent; body size: 246–275 × 186–212Pergalumna crassipora Mahunka, 1995 (see Mahunka 1995). Distribution: Borneo
24Notogastral porose areas Aa located nearer to setal alveoli lm than la25
Notogastral porose areas Aa distanced equal from la and lm30
25Notogastral porose areas minute, smaller than diameter of bothridia; body size: 527–612 × 390–428Pergalumna imadatei Aoki & Hu, 1993 (see Aoki and Hu 1993). Distribution: Oriental region
Notogastral porose areas well developed, larger than diameter of bothridia26
26Body surface slightly striate; median pore represented by several foveae; body size: 610–715 × 475–545Pergalumna hawaiiensis hawaiiensis (Jacot, 1934) (see Jacot 1934a; including our data)
Body surface not striate; median pore single or absent27
27Interlamellar setae minute, shorter than diameter of bothridia; body length: 720Pergalumna bimaculata Hammer, 1973 (see Hammer 1973). Distribution: Polynesia and Philippines
Interlamellar setae of medium size, longer than diameter of bothridia28
28Median pore present, large; body length: 720Pergalumna remota (Hammer, 1968) (see Hammer 1968). Distribution: New Zealand and India
Median pore absent29
29Bothridial setae densely ciliate; body size: 451–490 × 300–334Pergalumna kotschyi Mahunka, 1989 (see Mahunka 1989). Distribution: Vietnam
Bothridial setae smooth; body size: 398–453 × 275–340Pergalumna indivisa Mahunka, 1995 (see Mahunka 1995). Distribution: Borneo
30Bothridial setae with slightly dilated, elongated head31
Bothridial setae setiform33
31Body surface heavily tuberculate; body size: 385–425 × 285–331Pergalumna granulata Balogh & Mahunka, 1967 (see Balogh and Mahunka 1967). Distribution: Vietnam and Japan
Body surface not tuberculate32
32Body surface heavily granulate; body size: 302–356 × 237–262Pergalumna punctulata Balogh & Mahunka, 1967 (see Balogh and Mahunka 1967). Distribution: Vietnam
Body surface smooth; body size: 437–465 × 310–324Pergalumna intermedia intermedia Aoki, 1963 (see Aoki 1963, 1966). Distribution: Palaearctic and Oriental regions
33Notogastral porose areas A1 elongated, longitudinally oriented34
Notogastral porose areas A1 rounded to oval36
34Adanal setae ad1 long, not shorter than width of anal plate; median pore single; body size: 415–481 × 298–365Pergalumna paraindistincta sp. n. Distribution: Indonesia
Adanal setae ad1 minute; median pore absent or represented by several foveae35
35Postanal porose area absent; median more present in females; body size: 547–614 × 381–415Pergalumna indistincta Ermilov & Anichkin, 2011 (see Ermilov and Anichkin 2011b). Distribution: Vietnam
Postanal porose area present; median more absent in females; body size: 576 × 426Pergalumna magnipora capensis Engelbrecht, 1972 (see Engelbrecht 1972). Distribution: Southern Africa and India
36Body surface striate and short ridges; posterior part of notogaster with longitudinal concavity; body size: 408–485 × 298–352Pergalumna menglunensis Aoki & Hu, 1993 (see Aoki and Hu 1993). Distribution: southern China
Body not striate and without short ridges; posterior part of notogaster without concavity37
37Adanal setae ad1 and ad2 comparatively long, not shorter than width of anal plate; setae c developed on pteromorphs; body size: 514–597 × 365–431Pergalumna minituberculata Ermilov & Martens, 2014 (see Ermilov and Martens 2014). Distribution: Nepal
Adanal setae ad1 and ad2 shorter than width of anal plate; setae c represented by alveoli on pteromorphs38
38Interlamellar setae represented by alveoli; median pore present; body size: 863–1145 × 639–970Pergalumna panayensis Ermilov & Corpuz-Raros, 2015 (see Ermilov and Corpuz-Raros 2015)
Interlamellar setae of medium size or long; median pore absent39
39Bothridial setae densely ciliate40
Bothridial setae densely smooth41
40Notogastral porose areas amorphous, without distinct borders; genital plates not striate; body size: 332–377 × 245–276Pergalumna amorpha Mahunka, 2008 (see Mahunka 2008). Distribution: Thailand
Notogastral porose areas with distinct borders; genital plates striate; body size: 390–435 × 282–315Pergalumna intermedia retroversa Aoki & Hu, 1993 (see Aoki and Hu 1993). Distribution: southern China
41Interlamellar setae comparatively short, about 1/3 as long as their mutual distance; genital plates smooth; body size: 742–845 × 589–653Pergalumna magnipora capillaris Aoki, 1961 (see Aoki 1961). Distribution: Palaearctic and Oriental regions
Interlamellar setae of medium size, about 1/2 as long as their mutual distance; genital plates striate; body size: 822–840 × 618–650Pergalumna magnipora xishuangbanna Aoki & Hu, 1993 (see Aoki and Hu 1993). Distribution: southern China
  5 in total

1.  Systematic placement of some taxa in the family Galumnidae (Acari, Oribatida).

Authors:  Sergey G Ermilov; Badamdorj Bayartogtokh
Journal:  Zootaxa       Date:  2015-06-04       Impact factor: 1.091

2.  New taxa and new records of oribatid mites of the family Galumnidae (Acari: Oribatida) from Ecuador.

Authors:  Sergey G Ermilov; Josef Starý; Dorothee Sandmann; Franca Marian; Mark Maraun
Journal:  Zootaxa       Date:  2013       Impact factor: 1.091

3.  Three new species of the genus Pergalumna (Acari: Oribatida: Galumnidae) from India.

Authors:  Sergey G Ermilov; Umukusum Ya Shtanchaeva; Stanislav Kalúz; Luis S Subías
Journal:  Zootaxa       Date:  2013       Impact factor: 1.091

4.  Two new species of Pergalumna (Acari, Oribatida, Galumnidae) from Costa Rica, including a key to all species of the genus from the Neotropical region.

Authors:  Sergey G Ermilov; Olman Alvarado-Rodríguez; Axel P Retana-Salazar
Journal:  Zookeys       Date:  2014-08-15       Impact factor: 1.546

5.  Morphology of adult and juvenile instars of Galumna obvia (Acari, Oribatida, Galumnidae), with discussion of its taxonomic status.

Authors:  Sergey G Ermilov; Gerd Weigmann; Andrei V Tolstikov
Journal:  Zookeys       Date:  2013-11-29       Impact factor: 1.546

  5 in total
  1 in total

1.  Contributions to the knowledge of oribatid mites (Acari, Oribatida) of Indonesia. 3. The genus Galumna (Galumnidae) with description of a new subgenus and seven new species.

Authors:  Sergey G Ermilov; Dorothee Sandmann; Bernhard Klarner; Rahaju Widyastuti; Stefan Scheu
Journal:  Zookeys       Date:  2015-11-23       Impact factor: 1.546

  1 in total

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