Literature DB >> 26692793

Contributions to the knowledge of oribatid mites of Indonesia. 1. The genus Allogalumna (Galumnidae) with descriptions of two new species (Acari, Oribatida).

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

Abstract

Two new species of oribatid mites of the genus Allogalumna (Oribatida, Galumnidae) are described from litter and soil materials of Sumatra, Indonesia. Allogalumna indonesiensis sp. n. is morphologically most similar to Allogalumna borhidii Balogh & Mahunka, 1979, Allogalumna quadrimaculata (Mahunka, 1988), Allogalumna rotundiceps Aoki, 1996 and Allogalumna plowmanae Balogh & Balogh, 1983; however, the new species differs by having densely ciliate bothridial heads, larger body size and absence of a median pore. Allogalumna paranovazealandica sp. n. is morphologically most similar to Allogalumna novazealandica Hammer, 1968; however, the new species differs by the shorter body length and barbed and curving postero-laterad bothridial setae. The genus Allogalumna is recorded for the first time in the Indonesian fauna.

Entities:  

Keywords:  Allogalumna; Indonesia; Oribatid mites; new record; new species

Year:  2015        PMID: 26692793      PMCID: PMC4668900          DOI: 10.3897/zookeys.529.6326

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


Introduction

At present, the oribatid mite fauna (, ) of Indonesia is poorly known (Sellnick 1925, 1930; Willmann 1929, 1932; Csiszár 1961; Balogh and Mahunka 1968; Mahunka 1977, 1989, 1990; Hammer 1979, 1981a, 1981b, 1982; Aoki et al. 1994; Niedbała 2007, 2008). This work is a part of a study on Indonesian oribatids and based on material which was collected in 2013 in the framework of the interdisciplinary project “Ecological and socioeconomic functions of tropical lowland rainforest transformation systems (Sumatra, Indonesia)”. Litter and soil samples were taken along a land use gradient including rainforest, jungle rubber, rubber and oil palm plantations in Jambi Province. For more details on the study region and experimental design see Barnes et al. (2014). This paper includes the data on taxa of Grandjean, 1936 (). During taxonomic identification, two new species of this genus were found. The main goal of the paper is to describe and illustrate these species under the names sp. n. and sp. n. is a genus that was proposed by Grandjean (1936) with Jacot, 1935 as type species. Based on updated generic diagnosis (Ermilov et al. 2013a), it comprises more than 40 species collectively having a cosmopolitan distribution; has not been reported before in the Indonesian fauna. An identification key to all known species of this genus was given by Akrami (2015), while additional keys to selective species were presented by Balogh and Balogh (2002) and Ermilov and Anichkin (2014).

Materials and methods

Exact collection locality and habitat are given in the respective “Material examined” section for each new 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. Formulae for leg setation are given in parentheses according to the sequence trochanter–femur–genu–tibia–tarsus (famulus included). Formulae 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”.

Descriptions

sp. n.

http://zoobank.org/2E8C0C04-C670-4191-AA46-3134623A5D09 Figs 1 , 2 , 3–4 , 5–9
Figure 1.

sp. n., adult: dorsal view. Scale bar 50 μm.

Figure 2.

sp. n., adult: ventral view (gnathosoma and legs not shown). Scale bar 50 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 50 μm.

Figures 5–9.

sp. n., adult: 5 bothridial seta 6 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: 282–298 × 215–232. Rostral, lamellar and interlamellar setae minute. Bothridial setae with unilaterally dilated, densely ciliate head. Anterior notogastral margin not developed. Four pairs of porose areas rounded. Median pore absent. Postanal porose area elongate oval.

Description.

Measurements. Body length: 282 (holotype: male), 282–298 (five paratypes: two females and three males); notogaster width: 215 (holotype), 215–232 (five paratypes). Without sexual dimorphism. Integument. Body color brown. Body surface, pteromorphs, subcapitular mentum, genital and anal plates, and legs smooth. Prodorsum (Figs 1, 3, 5). Rostrum broadly rounded. Sublamellar lines (S) distinct, curving backwards. Rostral (ro), lamellar (le) and interlamellar (in) setae minute (all 4), thin, smooth. Bothridial setae (bs) comparatively short (49–53), with unilaterally dilated, densely ciliate head. Exobothridial setae and their alveoli absent. Porose areas Ad elongate oval, transversally oriented (16–20 × 6–8). sp. n., adult: dorsal view. Scale bar 50 μm. sp. n., adult: ventral view (gnathosoma and legs not shown). Scale bar 50 μm. sp. n., adult: 3 anterior part of body, lateral view (gnathosoma and leg I not shown) 4 posterior view. Scale bar 50 μm. sp. n., adult: 5 bothridial seta 6 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. Four pairs of porose areas rounded, with distinct margins: Aa (16–18) usually slightly larger than A1, A2 and A3 (all 12–16). Setal alveoli la inserted posteriorly to Aa. Median pore absent in males and females. All lyrifissures (ia, im, ip, ih, ips) distinct, im located between setal alveoli lm and lp. Opisthonotal gland openings (gla) located laterally to A1. Gnathosoma (Fig. 6). Morphology of subcapitulum, palps and chelicerae typical for most (for example, see Engelbrecht 1969, 1972; Ermilov and Anichkin 2010, 2011; Ermilov et al. 2011, 2013b; Bayartogtokh and Akrami 2014). Subcapitulum size: 61–69 × 61–69. Subcapitular setae setiform, smooth, a (10–12) longer than m (6–8) and h (4), a thickest, h thinnest. Two pairs of adoral setae (or1, or2, 8) thin, indistinctly barbed. Palps (57) with typical setation: 0–2–1–3–9(+ω). Axillary sacculi (sac) distinct. Chelicerae (77) with two setiform, barbed setae; cha (28) longer than chb (16). 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. Four pairs of short (all 4), thin setae, setal formula: 1–0–1–2. Pedotecta II (Pd II) scale-like in lateral view, rounded distally in ventral view. Discidia (dis) sharply triangular. Circumpedal carinae (cp) distinct, directed slightly laterally to setae 3b. Anogenital region (Figs 2, 4, 7, 8). Six pairs of genital (g1, 8; g2–g6, 4), one pair of aggenital (ag, 4), two pairs of anal (an1, an2, 4) and three pairs of adanal (ad1–ad3, 4) setae thin, smooth. Two genital setae on anterior edge of each genital plate. Adanal setae ad3 inserted laterally to adanal lyrifissures (iad). Postanal porose area (Ap) elongate oval, transversally oriented (28–32 × 6–8). Legs (Fig. 9). Morphology of leg segments, setae and solenidia typical for most (for example, see Engelbrecht 1969, 1972; Ermilov and Anichkin 2010, 2011; Ermilov et al. 2011; Bayartogtokh and Akrami 2014). Tridactylous; 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 at about 2/3 length of segment.
Table 1.

Leg setation and solenidia of adult sp. n. (same data for sp. n.)

LegTrFeGeTiTa
Ivd, (l), bv’’(l), v’, ε(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. (same data for 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, Jungle rubber agroforest, research site HJ2 (project site number), 01°49'31.9"S, 103°17'39.2"E, 84 m a.s.l., from forest floor litter material. Two paratypes (female and male): Indonesia, Sumatra, Bukit Duabelas landscape, secondary rainforest, research site BF1, 01°59'42.5"S, 102°45'08.1"E, 83 m a.s.l., from forest floor litter material. Three paratypes (female and two males): Indonesia, Sumatra, Bukit Duabelas landscape, Jungle rubber agroforest, research site BJ5, 02°08'35.6"S, E 102°51'04.7"E, 51 m a.s.l., from upper soil layer (0–5 cm). All specimens were collected by Bernhard Klarner (15.XI.2013) and determined 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 deposited in the collection of the Senckenberg Museum, Görlitz, Germany; two paratypes are deposited in the collection of the Tyumen State University Museum of Zoology, Tyumen, Russia.

Etymology.

The specific name indonesiensis refers to the country of origin, Indonesia.

Remarks.

sp. n. is most similar to Balogh & Mahunka, 1979 from the Neotropical region (see Balogh and Mahunka 1979), (Mahunka, 1988) from Malaysia (see Mahunka 1988), Aoki, 1996 from Japan and Vietnam (see Aoki 1996) and Balogh & Balogh, 1983 from Australia (see Balogh and Balogh 1983) in having small body size, minute prodorsal setae, four pairs of rounded notogastral porose areas and bothridial setae with unilaterally dilated head. However, the new species differs from these species by having densely ciliate bothridial heads (versus slightly barbed in distal parts), larger body size (282–298 × 215–232 versus 243–264 × 193–202 in , 249 × 166 in , 212–219 × 155–160 in and 261 × 171 in ) and absence of a median pore (versus present in , and ). http://zoobank.org/5DB5344A-F409-47AF-AF3A-EBDBADD7F990 Figs 10 , 11 , 12–13 , 14–18
Figure 10.

sp. n., adult: dorsal view. Scale bar 50 μm.

Figure 11.

sp. n., adult: ventral view (gnathosoma and legs not shown). Scale bar 50 μm.

Figures 12–13.

sp. n., adult: 12 anterior part of body, lateral view (gnathosoma and leg I not shown) 13 posterior view. Scale bar 50 μm.

Figures 14–18.

sp. n., adult: 14 bothridial seta 15 subcapitulum, ventral view 16 genital plate, right 17 anal plate, left, and adanal setae 18 tibia of leg IV, left, antiaxial view. Scale bar 20 μm.

Body size: 282–298 × 199–215. Rostral, lamellar and interlamellar setae minute. Bothridial setae with unilaterally slightly dilated, elongated, barbed in medio-distal part head. Anterior notogastral margin not developed. Four pairs of porose areas rounded. Median pore present. Postanal porose area elongate oval. Measurements. Body length: 282 (holotype: female), 282–298 (seven paratypes: two females and five males); notogaster width: 215 (holotype), 199–215 (seven paratypes). Without sexual dimorphism. Integument. Body color brown. Body surface, pteromorphs, subcapitular mentum, genital and anal plates, and legs smooth. Prodorsum (Figs 10, 12, 14). Rostrum broadly rounded. Sublamellar lines distinct, curving backwards. Rostral, lamellar and interlamellar setae minute (all 4), thin, smooth. Bothridial setae long (77–86), with unilaterally slightly dilated, elongated, barbed in medio-distal part head, directed postero-laterad. Exobothridial setae and their alveoli absent. Porose areas Ad elongate oval, transversally oriented (12–16 × 6–8). sp. n., adult: dorsal view. Scale bar 50 μm. sp. n., adult: ventral view (gnathosoma and legs not shown). Scale bar 50 μm. sp. n., adult: 12 anterior part of body, lateral view (gnathosoma and leg I not shown) 13 posterior view. Scale bar 50 μm. sp. n., adult: 14 bothridial seta 15 subcapitulum, ventral view 16 genital plate, right 17 anal plate, left, and adanal setae 18 tibia of leg IV, left, antiaxial view. Scale bar 20 μm. Notogaster (Figs 10, 12, 13). Anterior notogastral margin not developed. Dorsophragmata of medium size, elongated longitudinally. Notogastral setae represented by 10 pairs of alveoli. Four pairs of porose areas rounded, with distinct margins: Aa (14–16) PageBreaklarger than A1, A2 and A3 (all 6–10). Setal alveoli la inserted posteriorly to Aa. Median pore present in males and females, located between A2. All lyrifissures distinct, im located between setal alveoli lm and lp. Opisthonotal gland openings located laterally to A1. Gnathosoma (Fig. 15). Morphology of subcapitulum, palps and chelicerae typical for most (for example, see Engelbrecht 1969, 1972; Ermilov and Anichkin 2010, 2011; Ermilov et al. 2011, 2013b; Bayartogtokh and Akrami 2014). Subcapitulum size: 73 × 61–65. Subcapitular setae setiform, smooth, a (12) longer PageBreakthan m (8) and h (4), a thickest, h thinnest. Two pairs of adoral setae (6–8) thin, indistinctly barbed. Palps (61) with typical setation: 0–2–1–3–9(+ω). Axillary sacculi (sac) distinct. Chelicerae (82) with two setiform, barbed setae; cha (28) longer than chb (16). Trägårdh’s organ long, tapered. Epimeral and lateral podosomal regions (Fig. 11). Anterior tectum of epimere I smooth. Apodemes 1, 2, sejugal and 3 well visible. Four pairs of short (all 4), thin setae, setal formula: 1–0–1–2. Pedotecta II scale-like in lateral view, rounded distally in ventral view. Discidia sharply triangular. Circumpedal carinae indistinctly developed, directed to setae 3b. Anogenital region (Figs 11, 13, 16, 17). Six pairs of genital (g1, 10; g2–g6, 4), one pair of aggenital (4), two pairs of anal (4) and three pairs of adanal (4) setae thin, smooth. Two genital setae on anterior edge of each genital plate. Adanal setae ad3 inserted laterally to adanal lyrifissures. Postanal porose area elongate oval, transversally oriented (20 × 6–8). Legs (Fig. 18). Morphology of leg segments, setae and solenidia typical for most (for example, see Engelbrecht 1969, 1972; Ermilov and Anichkin 2010, 2011; Ermilov et al. 2011; Bayartogtokh and Akrami 2014). Tridactylous; 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 c Solenidion φ of tibiae IV inserted dorsally at about 2/3 length of segment. Holotype (female): Indonesia, Sumatra, Bukit Duabelas landscape, Jungle rubber agroforest, research site BJ5, 02°08'35.6"S, E 102°51'04.7"E, 51 m a.s.l., from upper soil layer (0–5 cm). Four paratypes (female and three 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 upper soil layer (0–5 cm). Three paratypes (female and two males): Indonesia, Sumatra, Harapan landscape, secondary rainforest, research site HF4, S 02°11'15.2"S, 103°20'33.4"E, from upper soil layer (0–5 cm). All specimens were collected by Bernhard Klarner (15.XI.2013) and determined and collected to morphospecies level by Dorothee Sandmann. The holotype is deposited in LIPI (Indonesian Institute of Science) Cibinong, Indonesia; three paratypes are deposited in the collection of the Senckenberg Museum, Görlitz, Germany; four paratypes are deposited in the collection of the Tyumen State University Museum of Zoology, Tyumen, Russia. The specific name paranovazealandica refers to the morphological similarity of the new species to Hammer, 1968. sp. n. is most similar to Hammer, 1968 from New Zealand in having minute prodorsal setae, long bothridial setae with slightly dilated head, four pairs of rounded notogastral porose areas, median pore and elongated postanal porose area. However, the new species differs from the latter by the shorter body length (282–298 versus 400–410 in ) and barbed in medio-distal part and curving postero-laterad bothridial setae (versus smooth and straight, directed upwards-laterally in ).
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1.  Systematic placement of some taxa in the family Galumnidae (Acari, Oribatida).

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5.  Two new species of oribatid mites of the family Galumnidae (Acari, Oribatida) from Vietnam.

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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
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