ZooKeys 160: 47–57, doi: 10.3897/zookeys.160.2160
First record of the subgenus Damaeus (Paradamaeus) Bulanova-Zachvatkina (Oribatida, Damaeidae) from China, with description of a new species
Lixia Xie 1,†, Yi Yan 1,‡, Rong Huang 1,§, Maofa Yang 1,|
1 Institute of Entomology, Guizhou University; The Provincial Key Laboratory for Agricultural Pest Management of Mountainous Region, Guiyang, Guizhou,  P. R. China,  550025

Corresponding author: Maofa Yang (yangmaofa@sohu.com)

Academic editor: A. Bochkov

received 29 September 2011 | accepted 11 November 2011 | Published 29 December 2011


(C) 2011 Lixia Xie. This is an open access article distributed under the terms of the Creative Commons Attribution License 3.0 (CC-BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.


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Abstract

A new species Damaeus (Paradamaeus) yushuensis sp. n. is described from Three Rivers’ Headwaters National Natural Reserve, Qinghai province, China. This is the first record of this subgenus in China. A key is given to distinguish all species of the genus.

Keywords

Oribatida, Damaeus, Paradamaeus, new species, new record

Introduction

Bulanova-Zachvatkina (1957) proposed Paradamaeus to be a subgenus of Damaeus with Damaeus (Paradamaeus) clavipes Hermann, 1804 as type species, which is only single known species in the world. The diagnosis of this subgenus as given by Bulanova-Zachvatkina (1957): large body size; rugged prodorsum with distinct ridges; apophysis P well developed; interlamellar setae(in) much shorter than sensillus (ss); prodorsal tubercles Da, Ba and Bp present; spinae adnatae (s.a.) well developed; companion seta d lost on genu III; setation of genua 4-4-2-3.

We firstly recorded the species of Paradamaeus from Three Rivers’ Headwaters National Natural Reserve, Qinghai, China, which represented as new species, Damaeus (Paradamaeus) yushuensis. A key to the identification of all known species of Damaeus (Paradamaeus) is given.

Material and methods

Measurements and descriptions are based on specimens mounted in temporary cavity slides that were studied using a standard light microscope equipped with a drawing tube. In figures we used the following abbreviations: prodorsal and sejugal apophyses (Ba, Bp), lateral apophyses (Sa, Sp) and coxisternal apophyses (E2a, E2p, Va, Vp), spina adnatum (s.a.), discidium (di), prodorsal setae (ro, le, in, ex), bothridium (bo), sensillus (ss), notogastral or gastronotal setae (c-, l-, h-, p- series), adanal and anal setae (ad-, an- series), aggenital setae (ag), coxisternal setae (1a, 1b, 1c, 2a, 3a, 3b, 3c, 4a, 4b, 4c, 4d), opisthonotal gland opening (gla), lyrifissures or cupules (ia, im, ip, ian, iad, ips, ih).

Terminology generally follows Grandjean (1949, 1954b, 1960), Miko (2006) and Norton and Behan-Pelletier (2009). The unit of measurement is micrometre (μm). All type specimens and other material studied are kept in alcohol and deposited in the Institute of Entomology, Guizhou University, Guiyang, China (GUGC).

Taxonomy
Damaeus (Paradamaeus) clavipes (Hermann, 1804)
Notaspis clavipes: Hermann 1804; Grandjean 1936, 1954a; Hammen 1952; Sellnick 1960.
Oribata clavipes: Oudemans 1900; Kulczyński 1902; Sellnick 1928.
Belba clavipes: Willmann 1931; Grandjean 1935; Schweizer 1956.
Damaeus (Paradamaeus) clavipes: Bulanova-Zachvatkina 1957; Balogh and Balogh 1992; Pérez-Íñigo 1997; Subías 2004; Miko 2006.
Paradamaeus clavipes: Bulanova-Zachvatkina 1967, 1975; Schatz 1983; Siepel 1996.
Distribution.

China, Germany, Ireland, Southern Mediterranean, Faroe Islands, Norway, Latvia, Caucasus, Crimea, Ukraina, Czechoslovakia, Czech Republic, Belgium, Sweden, England, America, Finland, Azores Islands, France, Austria, Netherlands.

Keys to species of Damaeus (Paradamaeus)
1 With dorsosejugal tubercles Da, Dp; setae in short and thin; notogastral setae similar to one another Damaeus (Paradamaeus) clavipes
Without dorsosejugal tubercles Da, Dp; setae in long and thick; notogastral setae not similar to one another Damaeus (Paradamaeus) yushuensis sp. n. (Figs 1–6)
Material examined.

Holotype: male (in alcohol, QHYS-XLX-8-5), China, Three Rivers' Headwaters Natural Reserve Area of Yushu Tibetan Autonomous Prefecture, Qinghai province (32°33'48.65"N , 97°39'55.66"E), from soil under the Picea crassifolia, 3464M, 5 Aug., 2009, col. Lixia Xie. Paratypes: Three females (in alcohol, QHYS-XLX-8-5), same data as holotype; Two males (in alcohol, QHYS-XLX-8-6), same data as QHYS-XLX-8-5, from soil under the Kobresia pygmaea.

Diagnosis.

Propodolateral apophysis P distinct, with broader base and arched tip; setae ro slightly barbed, setae le heavily barbed, thick. Sensillus short, thick, heavily barbed and rod-like. Interlamellar setae long, rather thick and conspicuously barbed. Prodorsal tubercles Da, Dp absent, Ba well developed, Bp weakly developed. Spinae adnatae beak like, short, distinct, strongly curved inwards (about 30 µm in total), with broader base and quite sharp tip. Notogastral setae smooth, slender except c- series and p- series. Setae of c- series rather thick, with conspicuously barbed and frizzled tip, oriented forwards and the rest backwards.

Comparative length of notogastral setae: lp< lm= ps3< ps2< la= h3= h2= h1< ps1< c1<c2. Epimeral setae mostly smooth except 1b, 1c, 3b, 3c, 4d and hypostomal setae a, m, h. Seta 1a, 2a and 3a rather short. Epimeral setal formula: 3-1-3-4. Enantiophyses E2 and V present, E2p and Vp weakly developed, E2a and Va well developed. Parastigmatic tubercle Sa long, acuminate, with sharp tip; Sp small, triangular. Hypostomal setae a, h and m thin, slightly barbed. Legs rod-like and longer than body.

Figure 1.

Damaeus (Paradamaeus) yushuensis sp. n.– dorsal view (100μm)

Figure 2.

Damaeus (Paradamaeus) yushuensis sp. n. – Ventral view (100μm)

Figure 3.

Damaeus (Paradamaeus) yushuensis sp. n. – lateral view (100μm)

Description of adult.

Dimensions. Holotype: Body length 980; length of prodorsum: 420, width 280, height 370, setae: ss 175, in 100, le 150, ro 125, ex 75, distance between setae: ro-ro 110, in-in 125, le-le 125, in-le 105, le-ro 40; length of notogaster: 700, width 670, height 780; setae: c1 135, c2 175, la 110, lm 95, lp 90, h3 110, h2 110, h1 110, ps1 125, ps2 105, ps3 95; c1-c2 75, c2-c2 275, la-la 375, lm-lm 435; ventral region: genito-aggenital plate 225×220, ano-adanal plate 190×175. Paratypes: length of prodorsum: 415-425, width 275-285, height 365-375; length of notogaster: 695-705, width 665-670, height 775-780; ventral region: genito-aggenital plate 220×215, ano-adanal plate 185×170.

Integument. Surface of body and leg segments with filamentous cerotegument. Conspicuous microtubercles present on prodorsum and around leg acetabula, legs with dense fungal mycelic.

Prodorsum (Fig. 1). Triangular, propodolateral apophysis P distinct, with broader base and arched tip. Lamellar setae (le) and rostral setae (ro) both in dorsalaterad position, long, arched and tapered. Lamellar setae with obvious barbs, thick, being longer than slender, weakly barbed rostral pair. Bothridia well developed, funnel-like, with broad margin and pair of thick, heavily barbed sensillus. Interlamellar setae (in) long, thick and conspicuously barbed (specially in holotype). Exobothridial setae (ex) thick, with obvious barbs, frizzled. Comparative length of prodorsal setae: ex< in< ro< le< ss. Weakly developed transverseridge connected to the base of bothridium and directed to median end of prodorsum. Prodorsal tubercles Da absent, Ba distinct; Bp weakly developed, usually as tuberculate sclerotised ridge, in light microscope sometimes discernible only in lateral view.

Notogaster (Fig. 1). Circular viewed perpendicular to circumgastric scissure, length almost equivalent to wider. Spinae adnatae beak like, short, distinct, strongly curved inwards (about 30 µm in length), with broader base and quite sharp tip. Notogastral setae short, smooth, slender except c- series and p- series. Setae of c- series rather thick and long, with conspicuous barbed and frizzled tip, oriented forwards and the rest backwards. Comparative length of notogastral setae: lp< lm= ps3< ps2< la= h3= h2= h1< ps1< c1< c2. Pseudanal setae comparatively long, with obvious barbs, attenuate.

Ventral region. (Fig. 2). Epimere I with medial pit (cp). Epimeral setae mostly smooth except 1b, 1c, 3b, 3c, 4d; setae 1c, 3b, 3c, 4d long, with obvious barbs; Seta 1a, 2a and 3a rather short, lanciform. Epimeral setal formula: 3–1–3–4. Ano-genital setal formula: 6–1–2–3. Enantiophyses E2 and V present, E2a triangular with pointed tip; E2p weakly developed, usually as tuberculate sclerotised ridge. Ventrosejugal tubercle Va large, strong, represented by broad ridge; Vp represented by low, broadly curved ridge, with setae 3b Parastigmatic tubercle Sa long, acuminate, with broader base and heavily pointed tip; Sp small, triangular; Discidium (di) long, acuminate, with broader base and heavily pointed tip, directed posterolaterad.

Gnathosoma. Infracapitular mentum without noticeable microtubercles. Hypostomal setae a, m, h slender, weakly barbed. Chelicera rather strong, fixed and movable digits with four blunt teeth; setae cha with obvious barbsand chb smooth. Palpal setation: 0–2–1–3–8, including solenidion ω (Fig. 4M).

Legs. (Figs 5–6). Monodactylous, moderately long, leg I, III, IV longer than body, leg II shorter than body. Relative length of femur to tarsus of legs I to IV 1: 0.88: 1.01: 1.2. Leg IV 1.3 times ventral body length. Femur IV 1.4 times length of trochanter IV, proximal stalk 1.4 times length of bulb. Leg setae medium in length and thick, mostly with distinct short barbs on outer curvature. Setal formulas of legs as follows (from trochanter to tarsus, famulus and solenidia included): I: 1–7–4 (1)–4 (2)–20 (2); II: 1–6-4 (1)–4 (1)–18 (2); III: 2–4-3 (1)–3 (1)–16 (0); IV: 1–4-3 (1)–3 (1)–15 (0). Solenidia of genua I-II with companion seta d. Solenidia δ equivalent to seta d on genuaI, Solenidia δ shorter and thinner than seta d on genuaII. Solenidion φ1 on tibia I 3 times longer than φ2. Seta d absent from all tibiae, solenidia on all tibiae free, as usual for genus.

Figure 4.

Damaeus (Paradamaeus) yushuensis sp. n. A–H notogastral setae (100μm) I interlamellar seta(100μm) J s.a.–spina adnata(100μm) K Sa –anterior sejugal apophysis(100μm), Sp –posterior sejugal apophysis(100μm) L di –discidium(100μm) M Pe. –pedipalp(100μm).

Figure 5.

Damaeus (Paradamaeus) yushuensis sp. n. A femur, genu I (100μm) B tibia I (100μm) C tarsus I (100μm) D femur, genu II (100μm) E Tibia II (100μm) F tarsus II (100μm) G trochanter, femur III (100μm) H genu III (100μm) I tibia, tarsus III (100μm).

Figure 6.

Damaeus (Paradamaeus) yushuensis sp. n. A trochanter, femur IV (100μm) B genu IV (100μm) C tibia, tarsus IV (100μm).

Etymology.

The specific name is derived from the type locality, Yushu Tibetan Autonomous Prefecture, Qinghai province.

Remarks.

This new species is characterised by following characters: interlamellar setae (in) long, rather thick and conspicuously barbed; spinae adnatae beak like, short, distinct, strongly curved inwards; c-series rather thick, long with conspicuous barbed and frizzled tip, oriented forwards and the rest backwards, other notogastral setae smooth, slender and short, except p- series (see Table 1).

Table 1.

Comparison of two species belonging to the subgenus Paradamaeus

Morphological character Damaeus (Paradamaeus) clavipes Damaeus (Paradamaeus) yushuensis sp. n.
propodolateral apophysis P with angular tip with arched tip
Interlamellar setae (in) short, thin long, thick
Spinae adnatae (s.a.) slender, medium long, triangular with sharp tip beak like, short, quite sharp tip
Notogastral setae c1, c2 similar in length, slender unequal length, thick
Number of setae on Femora III–IV 5 4
Prodorsal tubercles Da, Dp present absent
Parastigmatic tubercle Sa small, indistinct large, acuminate, with broader base and heavily pointed tip
Acknowledgements

The authors are very grateful to Prof. Roy A. Norton (College of Environmental Science and Forestry, State University of New York, Syracuse) for his encouragement to our research and kind help. The authors are also grateful to Dr. Owen Seeman (Queensland Museum, South Brisbane, Australia) and Dr. Sergey G. Ermilov (Laboratory of Entomology, Center of Independent Examinations, Nizhniy Novgorod, Russia) for their help. We are very grateful to Qiongzhang Song, Fangling Xu, Zaihua Yang, Bin Li (Institute of Entomology, Guizhou University, Guiyang, Guizhou province, China) for making it possible to work by their collections.

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