Literature DB >> 25901120

Chaeriluspseudoconchiformus sp. n. and an updated key of the chaerilid scorpions from China (Scorpiones, Chaerilidae).

Shijin Yin1, Yanning Qiu2, Zhaohui Pan3, Shaobin Li4, Zhiyong Di2.   

Abstract

A new species, Chaeriluspseudoconchiformus sp. n., is described from Xizang, China. The present new species is distinguished from its congeners by a body length of 32-40 mm, carapace with the anterior margin straight, chela with length/width ratio average of 3.3 in males (3.2-3.4, two adults), and 2.5 in females (2.3-2.6, nine adults), eight or nine (eight usually) rows of denticles on fixed and movable fingers of pedipalp chelae, five pectinal teeth in males and three or four in females. To date, the chaerilid species fauna of China consists of nine species. An updated identification key to Chaerilus from China is presented.

Entities:  

Keywords:  Chaerilidae; Chaerilus; China; Xizang; new species

Year:  2015        PMID: 25901120      PMCID: PMC4400404          DOI: 10.3897/zookeys.495.9016

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


Introduction

The small monotypic family, , has been reported containing one genus with 39 species (1/2015, http://www.ntnu.no/ub/scorpion-files/). The only genus is , which is found in southern and southeast Asia. In Xizang (Tibet), the chaerilid scorpions live under stones and fallen trees in humid habitats. Chaerilid scorpions have a unique type B trichobothrial arrangement (Vachon 1974; Soleglad and Fet 2001). Kovařík (2000) reported 18 species in this genus in his review. Kovařík (2012) published an identification key for the genus. Recently, new species were described (Kovařík et al. 2014; Lourenço and Pham 2014). Kovařík (2000) reported an old species and erected a new species of chaerilid from Xizang in his revision: (Pocock, 1890) and Kovařík, 2000. In fact, one locality of Pocock, 1899, Upper Rotung (Abor District), is also a territory belonging to Xizang (China). Therefore, Kovařík’s revision recorded three species for China (Di et al. 2009). Zhu et al. (2004) recorded one chaerilid species () found in China. Qi et al. (2005) described one new species ( Qi, Zhu & Lourenço, 2005) and redescribed (misidentification). Bastawade (2006) reported a new species from southeast Xizang: Bastawade, 2006. Zhu et al. (2008) redescribed and , and pointed out that as redescribed by Qi et al. (2005) was misidentified and erected it as a new species: Zhu, Han & Lourenço, 2008. Zhu et al. (2008) also suggested that distribution of in China was doubtful. Di and Zhu (2009) reported one new species: Di & Zhu, 2009. Di et al. (2009) reviewed the genus in China, registered seven species, and described the female of for the first time. Kovařík (2012) described a new species from Xizang: Kovařík, 2012. Di et al. (2014) reviewed the research history of the order from China, and recorded eight chaerilid species. To date, the chaerilid fauna of China consists of nine species including the new species described in this paper, sp. n.

Material and methods

Illustrations and measurements were made using a Motic K700 stereomicroscope with an Abbe drawing tube and an ocular micrometer. The photos were taken with a Canon (650D) camera. Measurements follow Sissom (1990) and are given in mm. Trichobothrial notations follow Vachon (1974) and morphological terminology mostly follows Hjelle (1990). Research materials have been deposited in the Specimen Room of University of Science and Technology of China, Hefei, China (USTC).

Taxonomy

Family Pocock, 1893 Genus Simon, 1877

sp. n.

http://zoobank.org/569B23FC-86FB-4E16-8487-047B100BF9DC Figs 1–4 , 5−25 , 26–35 , Tables 1 , 2
Figures 1–4.

sp. n., dorsal and ventral habitus: 1–2 Male holotype (Ar.−USTC−XZLZ1401) 3–4 Female paratype (Ar.−USTC−XZLZ1402). Scale bar = 10 mm.

Figures 5–25.

sp. n. Male holotype: 5 Carapace, dorsal aspect 6 Lateral eyes area 7–8 Chelicera, dorsal and ventral aspects 11 Tegument of the seventh sternite; 12 Sternum, genital operculum and pectines 14–15 Metasomal segment V, lateral and ventral aspects 16 Telson 18–19 Femur, dorsal and external aspects 20–22 Patella, dorsal, external and ventral aspects. Female paratype (Ar.−USTC−XZLZ1402): 9–10 Chelicera, dorsal and ventral aspects 17 Telson 23–24 Femur, dorsal and external aspects 25 Patella, dorsal aspect. Scale bars = 2 mm.

Figures 26–35.

sp. n. Male holotype: 28–30 Chela, dorsoexternal, ventral, and internal aspects 34 Movable finger of pedipalp. Female paratype (Ar.−USTC−XZLZ1402): 26–27 Patella, external and ventral aspects 31–33 Chela, dorsoexternal, ventral, and internal aspects 35 Movable finger of pedipalp. Scale bars = 2 mm.

Table 1.

Measurements (mm) of sp. n., male holotype (Ar.-USTC-XZLZ1401) and female paratype (Ar.-USTC-XZLZ1402). The information of from Kovařík (2012).

Chaerilus pseudoconchiformus sp. n.Chaerilus wrzecionkoi
Male holotypeFemale paratypeMale holotypeFemale paratype
Total length37.437.137.039.0
Carapace: -Length -Anterior width -Posterior width 4.5 2.4 5.0 4.4 2.7 5.3 4.3 4.4 4.5 5.1
Mesosomal segments: -Length 11.3 13.5
Metasomal segment I: -Length -Width -Depth 2.0 2.9 2.1 1.8 2.8 2.1 2.0 2.4 1.8 2.7
Metasomal segment II: -Length -Width -Depth 2.6 2.4 1.9 2.2 2.4 1.8 2.4 2.0 2.2 2.2
Metasomal segment III: -Length -Width -Depth 2.9 2.3 1.7 2.5 2.2 1.8 2.4 2.0 2.2 2.0
Metasomal segment IV: -Length -Width -Depth 3.3 2.1 1.6 3.0 2.0 1.6 2.7 1.9 2.7 1.8
Metasomal segment V: -Length -Width -Depth 5.4 1.9 1.5 4.9 1.8 1.5 4.7 1.8 4.4 1.6
Telson: -Length -Width -Depth 5.5 2.1 1.7 4.8 2.0 1.7 4.9 4.9
Pedipalp femur: -Length -Width -Depth 5.4 1.8 1.9 4.1 1.7 1.9 4.5 1.6 3.7 1.7
Pedipalp patella: -Length -Width -Depth 5.3 1.9 2.1 4.1 2.0 2.4 4.8 1.7 4.0 2.2
Chela: -Length -Width (manus) -Depth (manus) 10.2 3.2 3.1 9.0 3.6 3.1 9.0 3.5 8.3 3.5
Movable finger: -Length 5.2 5.2 5.0 4.5
Pectinal teeth (left/right)5/54/44/5?
Table 2.

Feature datasets of body length (BL, mm; segment by segment was measured and added in type specimens, while others were measured for overall length only), chela with length/width ratio (CR), number of granule rows of movable finger of pedipalp (RN), and number of pectinal teeth (PT) of (CO, Ar.-USTC-XZLZ1412), sp. n., and (TY, Ar.-USTC-XZBM1401−02).

SexBLCRRNPT
XZLZ140137.43.28/85/5
XZLZ140237.12.58/84/4
XZLZ140332.03.48/85/5
XZLZ140436.02.58/84/4
XZLZ140539.02.69/94/4
XZLZ140632.52.48/83/3
XZLZ140738.02.68/84/3
XZLZ140837.02.38/83/3
XZLZ140938.02.38/83/3
XZLZ141037.02.58/84/3
XZLZ141135.52.58/84/3
XZLZ1412(CO)32.01.97/74/4
XZBM1401(TY)44.02.88/83/3
XZBM1402(TY)39.02.68/83/3

Type material.

Holotype, male, China: Xizang, Nyingchi County (Linzhi County), VIII/2014, Zhiyong Di and Tao Li leg. (Ar.-USTC-XZLZ1401); paratypes: 1 adult male, 9 adult females, same data as holotype (Ar.-USTC-XZLZ1402−11) (kept in USTC).

Diagnosis.

The new species differs from its congeners by the following features: approximately 30−40 mm in total length (Table 2); carapace with the anterior margin straight; chela with length/width ratio: average of 3.3 in males, and 2.5 in females (Table 2); eight or nine (usually eight) rows of denticles on fixed and movable fingers of pedipalp chelae; five pectinal teeth in males and three or four in females. PageBreakPageBreakPageBreak sp. n. can be distinguished from the geographically and morphologically closely related species (Tables 2–3, and key). Morphologically closest are and . Both these species have similar body lengths, as well as similar numbers of denticle rows on fixed and movable fingers of the pedipalp chelae. They can be distinguished by the length/width ratio of the pedipalp chela: manus of pedipalp in male narrow and long, chela length/width ratio in male higher than 3 (average of 3.3 in two males, and 2.5 in nine females) in sp. n.; manus of pedipalp in male robust (Kovařík 2012: Fig. 68), chela length/width ratio in both sex adults lower than 2.6 in (Kovařík, 2012: 2); manus of pedipalp in both sex adults robust (Zhu et al. (2008): Figs 3, 17), chela length/width ratio in one male adult is 2.4 (paratype: Ar.–MHU–XZ0102), in two females (including the holotype) lower than 2.0 in . Furthermore, sp. n. has more slender pedipalps than (Table 1; Kovařík 2012: 13), in other words, the length ratio of pedipalp (LRP) is distinctly larger than the length ratio of total length (LRT) of sp. n. and : 1.14 (LRP), 1.01 (LRT) in male holotypes; 1.08 (LRP), 0.95 (LRT) in female allotypes of sp. n. and (Table 1).
Table 3.

The differences between chaerilids from China: , , , , sp. n., , , , and ; body length (BL, mm); carapace with the anterior margin (straight or curving, CA); chela with length/width ratio respectively in females and males (CR(F), CR(M)), dorsal secondary carinae of the chela (DS); rows number of denticles on fixed and movable fingers of chelae (RF); the tegument of the seventh sternite (SVII); holotype (H), paratype (P), new material (N).

conchiformus (H&N)dibangvalleycus (H&P)mainlingensis (H&P)pictus (H&P)pseudoconchiformus sp. n. (H&P)wrzecionkoi (H&P)tessellatus (H&P)tricostatus (N)tryznai (H, P&N)
BL32−4436−4240−4138−6632–3933−4135−5248−6030–44
CAstraightslightly curvingslightly depressedslightly curvingstraightstraightstraightstraightstraight
CR(F)1.8−1.9?2.4−2.82.42.3−2.62.42.22.2−2.42.6−2.9
CR(M)???2.53.2−3.42.6?3.7>3
DSpresentabsentabsentpresentpresentpresentpresentabsentpresent
RF87 or 8 *1713 or 148 or 98(9?) *21111or 128
SVIIweakly granular; with carinaegranular; with carinaeweakly granular; with carinae?granular; without carinaegranular; without carinaewith carinaegranular; with carinaegranular; without carinae

Nine rows of denticles on fixed and movable fingers of pedipalp chelae in the holotype (Bastawade 2006: Fig. 5). But the author thought that there are seven or eight rows in and 10−11 in (Bastawade 2006: 454).

Nine rows of denticles on movable fingers of pedipalp chelae in the holotype (Kovařík 2012: Fig. 64), but the author described eight rows in (Kovařík 2012: 11).

sp. n., dorsal and ventral habitus: 1–2 Male holotype (Ar.−USTC−XZLZ1401) 3–4 Female paratype (Ar.−USTC−XZLZ1402). Scale bar = 10 mm. sp. n. Male holotype: 5 Carapace, dorsal aspect 6 Lateral eyes area 7–8 Chelicera, dorsal and ventral aspects 11 Tegument of the seventh sternite; 12 Sternum, genital operculum and pectines 14–15 Metasomal segment V, lateral and ventral aspects 16 Telson 18–19 Femur, dorsal and external aspects 20–22 Patella, dorsal, external and ventral aspects. Female paratype (Ar.−USTC−XZLZ1402): 9–10 Chelicera, dorsal and ventral aspects 17 Telson 23–24 Femur, dorsal and external aspects 25 Patella, dorsal aspect. Scale bars = 2 mm. Measurements (mm) of sp. n., male holotype (Ar.-USTC-XZLZ1401) and female paratype (Ar.-USTC-XZLZ1402). The information of from Kovařík (2012). Feature datasets of body length (BL, mm; segment by segment was measured and added in type specimens, while others were measured for overall length only), chela with length/width ratio (CR), number of granule rows of movable finger of pedipalp (RN), and number of pectinal teeth (PT) of (CO, Ar.-USTC-XZLZ1412), sp. n., and (TY, Ar.-USTC-XZBM1401−02). The differences between chaerilids from China: , , , , sp. n., , , , and ; body length (BL, mm); carapace with the anterior margin (straight or curving, CA); chela with length/width ratio respectively in females and males (CR(F), CR(M)), dorsal secondary carinae of the chela (DS); rows number of denticles on fixed and movable fingers of chelae (RF); the tegument of the seventh sternite (SVII); holotype (H), paratype (P), new material (N). Nine rows of denticles on fixed and movable fingers of pedipalp chelae in the holotype (Bastawade 2006: Fig. 5). But the author thought that there are seven or eight rows in and 10−11 in (Bastawade 2006: 454). Nine rows of denticles on movable fingers of pedipalp chelae in the holotype (Kovařík 2012: Fig. 64), but the author described eight rows in (Kovařík 2012: 11).

Etymology.

The specific name refers to the geographically and morphologically most closely related species , adding the Greek prefix “pseudo−” as “pseudoconchiformus”, because the habitus of both sexes is very similar to that of .

Description.

Based on male holotype and female paratype. Coloration (Figs 1–4). Basically reddish brown. Carapace dark red-brown with black parts and yellowish stripes. Mesosomal tergites dark red-brown with yellowish stripes. Metasoma: all segments dark red-brown. Telson dark red-brown with reddish brown part; aculeus light red-brown. Chelicerae reddish brown with dark reticular pattern on dorsal surface. Pedipalps: femur, patella and chela dark red-brown with dark carinae. Legs dark red-brown and red-brown on distal segments. Sternum, genital operculum and sternites red-brown with some light parts. Pectines light yellow. Morphology. Carapace carinated, with the anterior margin straight; with dense granules of nearly equal size; lateral furrow moderately deep; large granules form 2 longitudinal lateral carinae (Fig. 5). Median ocular tubercle with granules. Lateral ocular tubercle small with a pair of lateral eyes and some granules (Fig. 6). Lateral eyes distinctly smaller than median eyes (Fig. 5). Mesosoma: Tergites uniform distributing with granules of larger and unequal size; tergites I to II without carinae, each of tergites III to VI bearing a pairs of obsolete granular carinae on posterior margin, tergite VII bearing two pairs of obsolete granular lateral carinae, but middle pair is represented only by ridges without expressed carinae; sternum pentagonal; genital operculum triangular; pectinal teeth count 5/5 in males and 3−4 in females, with fulcra well developed (Figs 12–13); sternites III to VI are smooth, sternite VII granular without carinae (Fig. 11). Metasoma: Length about 4.8 times as long as carapace in males and 4.4 in females; segment I always wider than long; segments I to V with 10-8-8-8-7 granular carinae; the ventromedian and ventrolateral carinae of segment V composed of strong, dentated granules, ventromedian carina posteriorly bifurcated as “Y” (Figs 14–15); all segments with sparse small granules. Vesicle is almost smooth; aculeus slightly curved (Figs 16–17). Chelicerae: Tibia surfaces smooth; thickly covered with numerous short, silky hairs, extending to ventral aspect of chelicerae and dorsal aspect of fixed fingers; ventral inner edges of movable finger with some minute teeth (2−3 obsolete teeth in two males and 3−9 well developed and obsolete teeth in nine females) (Figs 7–10). Pedipalp: Tegument granular. The femur has four carinae and the patella has five granular carinae (Figs 18–27). Chela with length/width ratio average of 3.3 in males (two adults) and 2.5 in females (nine adults), has seven granulated dorsointernal, except internal carina obsolete; entire tegument of chela manus densely covered with coarse granules, forming some indistinct reticular pattern (Figs 28–33); fingers straight, the cutting edge of movable finger with 8 or 9 (mainly 8) rows of denticles (Figs 34–35). Trichobothriotaxy of type B; orthobothriotaxic (Vachon 1974) (Figs 18–33). sp. n. Male holotype: 28–30 Chela, dorsoexternal, ventral, and internal aspects 34 Movable finger of pedipalp. Female paratype (Ar.−USTC−XZLZ1402): 26–27 Patella, external and ventral aspects 31–33 Chela, dorsoexternal, ventral, and internal aspects 35 Movable finger of pedipalp. Scale bars = 2 mm. Legs: Tibia without tibial spur. Basitarsus with two pedal spurs strongly developed. Tarsi with two rows of spiniform setae.

Variation.

Coloration and morphology in holotype and paratypes are very similar (feature datasets please see Table 2).

Habitat.

Found under the stones in mixed forest.

Distribution.

China (Xizang).
1Movable finger of pedipalp with 7–9 rows of granules2
Movable finger of pedipalp with 10–14 rows of granules7
2Chela length to width ratio in female adults 1.6–1.9Chaerilus conchiformus
Chela length to width ratio in female adults higher than 2.03
3Ventral side of seventh mesosomal segment with 2 pairs of granular carinae; carapace with anterior margin straight with a median notch4
Ventral side of seventh mesosomal segment with many granules but without carinae; carapace with anterior margin straight without median notch5
4Pedipalp femur shorter than carapace; 8–9 minute teeth on inner ventral margins of movable and immovable fingers respectively (Bastawade 2006: 451, fig. 5)Chaerilus dibangvalleycus
Pedipalp femur longer than carapace, 7–8 minute teeth on inner ventral margins of movable and immovable fingers respectively (Di and Zhu 2009: 101, fig. 11)Chaerilus mainlingensis
5Manus of pedipalp narrower and longer with the ventral margin not round in females (Zhu et al. 2008: fig. 47); chela length/width ratio in females is 2.6–2.9 (Kovařík 2000: table 1)Chaerilus tryznai
Manus of pedipalp robust in females with the ventral margin very round in females; chela length/width ratio in females is 2.3–2.66
6Chela length/width ratio in males average of 3.3 (3.2−3.4), and 2.5 in females (2.3−2.6), chelae of male and female with sexual dimorphismChaerilus pseudoconchiformus sp. n.
Chela length/width ratio about 2.6 in male, and about 2.4 in female, chelae of male and female without sexual dimorphism (Kovařík 2012: 13, figs 62, 76)Chaerilus wrzecionkoi
7Movable finger of pedipalp with 13–14 rows of granules; telson of male rather long and about 4.7 times longer than wide, with an obvious sexual dimorphism in both sexesChaerilus pictus
Movable finger of pedipalp with 11–12 rows of granules; telsons of male and female without sexual dimorphism8
8Carapace and tergites nearly smooth in adults (Zhu et al. 2008: 44, 47)Chaerilus tessellatus
Carapace and tergites with many big granules in adults (Di et al. 2009: 133, 136)Chaerilus tricostatus
  3 in total

1.  History of study, updated checklist, distribution and key of scorpions (Arachnida: Scorpiones) from China.

Authors:  Zhi-Yong Di; Zi-Zhong Yang; Shi-Jin Yin; Zhi-Jian Cao; Wen-Xin Li
Journal:  Dongwuxue Yanjiu       Date:  2014-01

2.  The genus Chaerilus Simon, 1877 in Vietnam (Scorpiones; Chaerilidae): a possible case of a vicariant species.

Authors:  Wilson R Lourenço; Dinh-Sac Pham
Journal:  C R Biol       Date:  2014-04-24       Impact factor: 1.583

3.  Notes on the scorpions (Arachnida, Scorpiones) from Xizang with the redescription of Scorpiops jendeki Kovařík, 2000 (Scorpiones, Euscorpiidae) from Yunnan (China).

Authors:  Zhiyong Di; Xiaobo Xu; Zhijian Cao; Yingliang Wu; Wenxin Li
Journal:  Zookeys       Date:  2013-05-17       Impact factor: 1.546

  3 in total

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