Research Article
Print
Research Article
Two new cave-dwelling species of the millipede genus Paracortina Wang & Zhang, 1993 from southern China (Diplopoda, Callipodida, Paracortinidae)
expand article infoWeixin Liu, Mingyi Tian
‡ South China Agricultural University, Guangzhou, China
Open Access

Abstract

Two new species of the millipede genus Paracortina Wang & Zhang, 1993 are described. Both are presumed troglophiles: P. zhangi sp. n. from a cave in Ceheng County, southwestern Guizhou Province and P. yinae sp. n. from a cave in Longlin County, western Guangxi Zhuang Autonomous Region. A distribution map and a key to all 12 Paracortina species are also provided.

Keywords

Paracortina , new species, taxonomy, cave-dwelling, China

Introduction

The family Paracortinidae was first established to comprise three genera: Paracortina Wang & Zhang, 1993, Relictus Wang & Zhang, 1993, Altum Wang & Zhang, 1993 (Wang and Zhang 1993). A fourth genus, Angulifemur Zhang, 1997, was added soon thereafter (Zhang 1997). All these genera are distributed in southern China only Yunnan and Sichuan provinces, as well as Tibet (Xizang Automomous Region).

The family has since been reviewed and shown to have Relictus and Altum as junior synonyms of Paracortina (Stoev and Geoffroy 2004). The genus Scotopetalum Shear, 2000, which only included a single species from Vietnam, has been synonymized with Paracortina (Stoev and Geoffroy 2004). Although Angulifemur Zhang, 1997, with two species still remains treated as an independent genus, it is likely to also represent only a junior synonym of Paracortina (Stoev et al. 2008). In 2004, the first troglomorphic species P. wangi Stoev was described from south Yunnan, but it was subsequently synonymized with A. unidigitis Zhang, 1997 (Stoev et al. 2008).

As a result, Angulifemur consists of two species only from Mengzi, Yunnan of China. Paracortina is the largest genus in the family Paracortinidae including ten species and ranging from Tibet, Sichuan and Yunnan in southwestern China in the north of its distribution to Thanh Hoa and Hoa Binh provinces of northern Vietnam in the south (Stoev et al. 2008, Stoev and Enghoff 2011).

A. tridigitis Zhang, 1997, from Mengzi City, Yunnan, China.

A. unidigitis Zhang, 1997, from Mengzi City, Yunnan, China.

P. carinata Wang & Zhang, 1993, from Shangrila County (=Zhongdian County), Yunnan, China.

P. chinensis Stoev & Geoffroy, 2004, from Zhenxiong County, Yunnan, China.

P. leptoclada Wang & Zhang, 1993, from Shangrila County, Yunnan, China.

P. multisegmentata Stoev & Geoffroy, 2004, from Ngoc-Lac and Loc Thinh, Thanh Hoa, Vietnam.

P. serrata Wang & Zhang, 1993, from Deqin County, Yunnan, China.

P. stimula Wang & Zhang, 1993, from Shangrila County, Yunnan, China.

P. thallina Wang & Zhang, 1993, from Batang County, Sichuan, and Shangrila County, Yunnan, China.

P. viriosa Wang & Zhang, 1993, from Shangrila County, Yunnan, and Mangkang County, Tibet, China.

P. voluta Wang & Zhang, 1993, from Yajiang County, Sichuan, China.

P. warreni Shear, 2000, from Hong Mat, Hoa Binh, Vietnam.

Of these, four species have been considered as troglophiles: A. tridigitis, A. unidigitis, P. chinensis, and P. warreni (Stoev and Geoffroy 2004, Stoev et al. 2008). The present paper records two new paracortinid millipedes found in two caves, one in Guizhou Province, the other in Guangxi Zhuang Autonomous Region, both in southern China.

Material and methods

All types are deposited in the zoological collection of the South China Agricultural University, Guangzhou, China (SCAU). All specimens used in this study were collected by hand in caves and preserved in 75% ethanol.

Observations and dissections were performed using a Leica DFC295 stereoscope. The line illustrations were executed with the help of a Leica MZ125 stereoscope and a camera lucida attached to the stereoscope. The photographs were taken with a Canon EOS 40D camera, further processed using Adobe Photoshop CS5 computer software. The distribution map was created using MapInfo Professional 12.0 software.

The terminology used in the text is after Wang and Zhang (1993) and Stoev (2004).

Taxonomic treatment

Paracortina zhangi Liu & Tian, sp. n.

Figs 1–6, 7, 8–10, 11–14, 15–18, 19–22

Material examined

Holotype: adult male (SCAU), China, Guizhou, Qianxinan Zizhizhou, Ceheng County, Rongdu Village, Cave Qiaoxia Dong, 24°03.008N, 105°43.147E, 964 m, 26.XII.2012, leg. Mingyi Tian, Weixin Liu, Feifei Sun & Haomin Yin. Paratypes. 1 male, 3 females, 10 juveniles (SCAU), same locality, together with holotype.

Description

Length of adults of both sexes 46–55 mm, width of midbody segments 2.6–3.0 mm, body with 55–58 pleurotergites + telson. Holotype 46 mm long, 2.6 mm wide on midbody segment, maximum width on 6th pleurotergite 3.5 mm, body with 57 pleurotergites + telson. Body coloration light yellow-brownish, anterior part of body slightly lighter. Metazonae slightly darker than prozonae, posterior margin of pleurotergites brownish to dark brown, more infuscate on anterior pleurotergites (Figs 17). Head yellowish, epicranial suture distinct, with a large, median, beak-shaped process located between antennae in males, below it densely and finely setose and granulate (Figs 1–2). Edges of genae, posterior margin of the head, and bases of antennae marbled light brown-yellowish. Labrum dark brown. Ocellaria composed of ca. 16–23, dark grey ocelli arranged in four irregular longitudinal rows (Fig. 2). Tömösváry’s organs about 2–3 times larger than an ocellus, placed between ocellaria and base of antenna. Antennae light yellow, rather long and slender, extending behind posterior edge of pleurotergite 6 in males or pleurotergite 3(4) in females when stretched backwards; antennomere length ratios: 2=3>4=5>6>1>7, antennomeres 5 and 6 with a small distodorsal field of fine setae (Fig. 16). Legs light yellow to yellow-brownish, tarsi much darker (Figs 17).

Figures 1–6. 

Paracortina zhangi sp. n. holotype 1 anterior body, subventral view 2 anterior body, sublateral view 3 midbody, ventral view 4 midbody, dorsal view 5 posterior body, ventral view 6 posterior body, dorsal view.

Figure 7. 

Paracortina zhangi sp. n. female paratype.

Collum much narrower than head, pleurotergite 6 in males strongly enlarged (Fig. 2). Prozonae delicately alveolate-areolate; fine longitudinal striations in front of stricture between prozonae and metazonae. Crests on collum normal, extended forwards from about midlength (Figs 1–2). All crests on the metazonae well-developed, forming 5+5 primary crests, 5+5 secondary crests, and 12–18 lower crests down to ventral pleurotergal edge (Figs 4, 6). 3rd primary crest strongly enlarged. Ozopores starting with pleurotergite 6, present until penultimate pleurotergite, placed on tip of 3rd primary crest (Figs 2, 4, 7). 2+2 primary and 3+3 secondary crests between poriferous crests. Pleurotergal setae 5+5, located at edges of primary crests; setal pattern as in Table 1. Axial line rather distinct (Figs 4, 6).

Table 1.

Chaetotaxy of P. zhangi sp. n. and P. yinae sp. n.

Anterior setae Posterior setae
Collum 5+5 -
Pleurotergites 2 to 4 5+5 -
Pleurotergite 5 d, a + a, d e, c, b + b, c, e
Pleurotergite 6 to penultimate - 5+5

Male leg-pairs 1 and 2 much shorter, leg-pair 3 slightly shorter than following legs (Figs 1–2). Midbody legs about 4 (male) or 3 times (female) as long as pleurotergite height. Prefemora to a lesser extent, postfemora and tibiae more strongly, but still finely micropapillate ventrally (Fig. 15). Tarsi 1–3 only 1-segmented, from leg 4 to ultimate pair 2-segmented in both sexes; male tarsal pads visible from leg-pairs 3 to 23. All legs ending with a rather slender, long and curved claw (Figs 1, 2, 15). Coxal sacs present from leg 3 to 23. Male coxa 2 with a small anterior process and a posterior gonopore, the latter placed on a small cone. Coxa 7 with a long, subfalcate and apically pointed posterior (f), and a rather strong, pear-shaped anterior process (t) (Fig. 8); f in situ protruding between the gonopods. Coxae of remaining legs normal. Epiproct simple, with about 10 tuberculations in irregular rows (Fig. 6). Hypoproct tripartite, medial sclerite largest, subrectangular, bearing two paramedian macrosetae; each lateral sclerite with a single macroseta. Anal valves smooth, each divided into a small triangle and a large sclerite, both with a pair of macrosetae. Spinnerets comparatively thin and long, ending with a long macroseta (Fig. 5).

Figures 8–10. 

Paracortina zhangi sp. n. male paratype 8 leg-pair 7, anterior view 9 gonopods, dorsal view 10 gonopods, subventral view.

Gonopods (Figs 9–10, 17–18) yellow-brown to brown basally, seminal groove and telopodite black brown. Coxa with a large, curved, arch-shaped, anterior process (a) and a rather slender process (b), the latter a little more than half the length of telopodite. Prefemur with a large, clavate process (c) densely covered with long macrosetae. Femoroidal stem long, slender, rather clearly curved, directed cephalad. Telopodite’s terminal part twisted, with a large median (l), and a small lateral lobe (h). Solenomere (s) bifid, parasolenomere (ps) much shorter; seminal groove ending on the longer branch.

Female. Pleurotergites 2 and 3 greatly enlarged. Leg-pairs 1 and 3 with tarsal pads (Figs 11–12). Coxa 3 with a rather small process (m). Prefemora 3 and 4 relatively stout and clearly enlarged (Fig. 12). Leg-pair 2 (Fig. 13) rather strongly reduced down to a pairs of stout, apically shallowly biramous remnants in adult female (Fig. 7), normal in younger ones. Cyphopods small, densely setose, hidden in membranous sacs, divided laterally in the middle (Fig. 14). Coxae 7 normal, without processes.

Figures 11–14. 

Paracortina zhangi sp. n. female paratype 11 leg-pair 1, anterior view 12 leg-pair 3, posterior view 13 leg-pair 2, anterior view 14 cyphopod, lateral view.

Figures 15–18. 

Paracortina zhangi sp. n. male paratype 15 midbody leg, anterior view 16 antenna, lateral view 17 right gonopod, mesal view 18 right gonopod, lateral view.

Etymology

The species is dedicated to the memory of Mr. Chongzhou Zhang for his contribution to the systematics of Diplopoda in China.

Remarks

This species is distinguished from its congeners by the presence of 5+5 primary crests, 5+5 secondary crests on the metazonae, two processes on coxa 7 in males, and in certain specific characters of the male gonopods, as well as in the small process on coxa 3, and reduced leg-pair 2 in females.

Distribution

China: Guizhou (Fig. 46).

The entrance of cave Qiaoxia Dong (Figs 19–22) is located under a bridge in the village of Rongdu. The cave is about 200 meters long, 10 meters wide and 5 meters high. It is rather polluted from sewage water and rubbish. Other animals living in this cave are the ubiquitous diplopod, Oxidus gracilis C. L. Koch, 1847 (Polydesmida, Paradoxosomatidae), some ground beetles, crickets (Fig. 19), glowworms (Fig. 20), and spiders, etc.

Figures 19–22. 

Cave Qiaoxia Dong 19–20 cave ceiling 21 cave deposits 22 P. zhangi sp. n. walking on a rock.

Paracortina yinae Liu & Tian, sp. n.

Figs 23–28, 29, 30–33, 34–37, 38–41, 42–45

Material examined

Holotype: adult male (SCAU), China, Guangxi, Baise City, Longlin County, Tianshengqiao Town, Yanchang Village, Cave I, 24.875732°N, 105.150143°E, 867 m, 12.VI.2014, leg. Mingyi Tian, Weixin Liu, Haomin Yin & Xiaozhu Luo. Paratypes. 2 males, 3 females, 2 juveniles (SCAU), same locality, together with holotype.

Description

Length of adult males 39–52 mm, of adult females 47–55 mm. Width of midbody segments in adult males 2.2–2.6 mm, in adult females 2.5–3.0 mm. Body with 53–61 pleurotergites + telson. Holotype 44.0 mm long, 2.5 mm wide on midbody segments, maximum width on 6th pleurotergite 2.5 mm, body with 54 pleurotergites + telson. Body coloration yellow-brownish. Metazonae slightly darker than prozonae, posterior margin of pleurotergites dark brown to brownish, more evidently so on the anterior pleurotergites (Figs 2329). Head brownish to chocolate brown, epicranial suture distinct, with a slightly smaller, median, beak-shaped process located between antennae in males, surface below the vertex and genae densely beset with brown granules and fine setae (Fig. 23). Genae, labrum, the edge between the dorsal and the frontal face of head marbled dark brown. Ocellaria composed of ca. 21–32, dark grey ocelli arranged in four irregular longitudinal rows. Tömösváry’s organs about 4 times larger than an ocellus, placed between ocellaria and base of antenna (Fig. 23). Antennae brownish, tip of each antennomere infuscate; very long, extending behind posterior edge of pleurotergite 6 (male) or 4 (female) when stretched backwards (Figs 23, 29), antennomere length ratios: 2=3>4=5>6>1>7, antennomeres 5 and 6 with a small distodorsal field of fine setae (Fig. 39). Legs yellow-brownish to dark brownish, distal parts of femora much darker.

Figures 23–28. 

Paracortina yinae sp. n. holotype 23 anterior body, subventral view 24 anterior body, subdorsal view 25 midbody, ventral view 26 midbody, sublateral view 27 posterior body, ventral view 28 posterior body, lateral view.

Figure 29. 

Paracortina yinae sp. n. female paratype.

Collum much narrower than head, with two paramedian spots covered with brown granules, pleurotergite 6 in males strongly enlarged. Prozonae delicately alveolate-areolate; fine longitudinal striations in front of stricture between pro- and metazonae. Two first primary crests on collum relatively large. All crests on the metazonae, ozopores site, pleurotergal setae, and axial line as in P. zhangi sp. n. (Figs 24, 26, 28); setal pattern as in Table 1.

Male leg-pairs 1 and 2 much shorter, leg-pair 3 slightly shorter than following legs (Fig. 23). Midbody legs about 4 (male) or 3 times (female) as long as pleurotergal height, only tibia finely micropapillate ventrally (Fig. 38). Tarsi 1–3 only 1-segmented, from 4 to ultimate pair 2-segmented; tarsal pads present from leg-pairs 3 to about 15. All legs ending with a rather slender, long and curved claw (Figs 1, 2, 15). Coxal sacs present from leg 3 to at least 25, but most abrased. Coxa 2 with a small anterior process and a posterior gonopore, the latter placed on a small cone. Coxa 6 with a small, pointed posterior process (e) (Fig. 30). Coxa 7 with a long, subfalcate and apically pointed posterior (f), and a very strong, rounded anterior process (t) (Fig. 31). Coxae of remaining legs normal. Epiproct simple, with 3+3 anterior and 8+8 posterior tuberculations in transverse rows. Hypoproct, anal valves and spinnerets as in P. zhangi sp. n. (Fig. 27).

Figures 30–33. 

Paracortina yinae sp. n. male paratype 30 leg-pair 6, anterior view 31 leg-pair 7, anterior view 32 gonopods, mesal view 33 gonopods, lateral view.

Gonopods (Figs 32–33, 40–41) yellow-brown to brown basally, seminal groove and telopodite black brown. Coxa with an anterior process (a) and a rather slender process (b), the latter about half the length of telopodite. Prefemur with a large, clavate process (c), densely covered with long macrosetae apically. Femoroidal stem long, slender, rather strongly curved, directed cephalad. Telopodite’s terminal part twisted, trifid, with a digitiform lateral (h), and a slender, apically pointed lobe (t). Solenomere (s) bifid, parasolenomere (ps) much shorter; seminal groove ending on the longer branch.

Female. A little larger than males, pleurotergites 2 and 3 strongly enlarged. Leg-pairs 1 and 3 with tarsal pads (Figs 34–35). Prefemur 3 evidently enlarged (Fig. 35). Leg-pair 2 (Fig. 36) rather strongly reduced down to a pairs of stout, apically deeply biramous remnants in adult females, normal in younger ones. Cyphopods small, densely setae, hidden in membranous sacs, partly extruded, laterally divided in the middle, the smaller part roundly concave apically (Figs 36–37). Coxae 6 and 7 normal, without processes.

Figures 34–37. 

Paracortina yinae sp. n. female paratype 34 leg 1, anterior view 35 leg 3, posterior view 36 leg-pair 2 and cyphopod, anterior view 37 cyphopod, lateral view.

Figures 38–41. 

Paracortina yinae sp. n. male paratype 38 midbody leg, anterior view 39 antenna, lateral view 40 right gonopod, mesal view 41 right gonopod, lateral view.

Etymology

The species is named in honour of Miss Haomin Yin, an active collector in our team.

Remarks

The new species differs from its congeners by the presence of small, pointed, posterior processes (e) on coxae 6 and two pairs of processes on coxae 7 in males, as well as in certain specific charaters of the male gonopods and reduced leg-pair 2 in females.

Distribution

China: Guangxi (Fig. 46).

Cave I (Figs 42–45) is situated at the foot of a karst mountain. It is a large cave, made up of a hall of several layers covered by numerous big rock boulders. We explored approximately 150 meters deep, but then had to withdraw because of a rushing underground river. Other animals also found in this cave are diplopods from the genera Glyphiulus (Spirostreptida, Cambalopsidae) and Eutrichodesmus (Polydesmida, Haplodesmidae), the blind trechine beetle Satotrechus longlinensis Deuve & Tian, 2011, and bats.

Figures 42–45. 

Cave I 42 location 43 entrance 44 cave walls 45 P. yinae sp. n. walking on a rock.

Figure 46. 

Distribution map of Paracortina in China. a P. voluta b P. thallina c P. viriosa d P. serrata e P. carinata f P. leptoclada g P. stimula h P. chinensis i P. zhangi sp. n. j P. yinae sp. n.

Key to species of the genus Paracortina

1 Gonopod prefemur with two processes covered with long macrosetae 2
Gonopod prefemur with only one process covered with long macrosetae 8
2 6+6 setae on pleurotergite 5 3
5+5 setae on pleurotergite 5 4
3 Head with a large median beak-shaped process located between antennae in males, 3+3 primary crests between poriferous crests P. thallina
Head without such a process, 5+5 primary crests between poriferous crests P. stimula
4 6+6 setae on pleurotergite 6 to penultimate 5
5+5 setae on pleurotergite 6 to penultimate 6
5 4+4 primary crests between poriferous crests; coxa 7 with two processes; gonopod prefemur with two processes clothed with dense long macrosetae apically P. leptoclada
3+3 primary crests between poriferous crests; coxa 7 without processes, gonopod prefemur’s nearby process smaller, with 8–9 strong macrosetae apically P. voluta
6 Coxa 7 with two processes; gonopod prefemur’s nearby process twisted, without setae P. serrata
Coxa 7 without process; gonopod prefemur’s nearby process apical with several apical setae 7
7 Collum with two large crests; gonopod telopodite’s terminal part trifid P. viriosa
Collum normal; gonopod telopodite’s terminal part bifid P. carinata
8 Body with 81–85 pleurotergites P. multisegmentata
Body with 50–65 pleurotergites 9
9 Gonopod coxa without any process P. warreni
Gonopod coxa with two processes 10
10 Gonopod coxa with a large, subtringular, ovoid anterior process (a) and a small tooth (b) P. chinensis
Gonopod coxa with a large, arch-shaped, anterior process (a) and a rather long and slender process (b) (Figs 17, 30) 11
11 Coxa 6 with a small, pointed, posterior process (e) (Fig. 30) P. yinae sp. n.
Coxa 6 normal, without process P. zhangi sp. n.

Acknowledgements

We express our cordial gratitude to two reviewers, Prof. Dr. Sergei I. Golovatch, Institute for Problems of Ecology and Evolution, Russian Academy of Sciences, Moscow, Russia, and Prof. Dr. Pavel Stoev, National Museum of Natural History, Sofia, Bulgaria, for their constructive suggestions and useful comments. Our thanks also go to members of our team in SCAU, for their various ways of assistance. This study was sponsored by the Specialized Research Fund for the Doctoral Program of Higher Education of China (Grant no. 20134404110026).

References

  • Deuve T, Tian MY (2011) Nouveaux Trechini et Tachyini des cavites souterraines de Chine meridionale (Coleoptera, Caraboidea). Nouvelle Revue d’Entomologie 27(2): 99–108.
  • Shear WA (2000) A new genus and species of callipodidan millipede from Vietnam (Callipodida, Schizopetalidae). Myriapodologica 6(11): 95–100.
  • Stoev P (2004) The first troglomorphic species of the millipede genus Paracortina Wang & Zhang, 1993 from south Yunnan, China (Diplopoda: Callipodida: Paracortinidae). Zootaxa 441: 1–8. doi: 10.2476/asjaa.53.93
  • Stoev P, Enghoff H (2011) A review of the millipede genus Sinocallipus Zhang, 1993 (Diplopoda, Callipodida, Sinocallipodidae), with notes on gonopods monotony vs. peripheral diversity in millipedes. ZooKeys 90: 13–34. doi: 10.3897/zookeys.90.1291
  • Stoev P, Geoffroy JJ (2004) Review of the millipede family Paracortinidae Wang & Zhang 1993 (Diplopoda: Callipodida). Acta Arachnologica 53(2): 93–103.
  • Stoev P, Sierwald P, Billey A (2008) An annotated world catalogue of the millipede order Callipodida (Arthropoda: Diplopoda). Zootaxa 1706: 1–50.
  • Wang DQ, Zhang CZ (1993) A new family of millipeds (Diplopoda: Callipodida) from southwestern China. Peking Natural History Museum 53: 395–390.
  • Zhang CZ (1997) Diplopoda from Yunnan Caves III. A new genus Angulifemur, including two new species of the cave-dwelling callipodid millipedes (Diplopoda, Callipodida, Paracortinidae). Thesis Compilation of Tianjin Natural History Museum 14: 1–5.
login to comment