Research Article |
Corresponding author: Weixin Liu ( da2000wei@163.com ) Academic editor: Pavel Stoev
© 2017 Weixin Liu, Sergei Golovatch, Mingyi Tian.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Liu W, Golovatch S, Tian M (2017) Three new cavernicolous species of the millipede genus Trichopeltis Pocock, 1894 from southern China (Diplopoda, Polydesmida, Cryptodesmidae). ZooKeys 710: 1-14. https://doi.org/10.3897/zookeys.710.20025
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Three new species of Trichopeltis are described from caves in southern China: T. bellus sp. n., T. intricatus sp. n., and T. reflexus sp. n., all presumed troglobites. The former two come from Yunnan Province, the latter one from Hunan Province. An updated key to all eleven currently known species of Trichopeltis is provided.
Trichopeltis , new species, key, troglobite, southern China
The Cryptodesmidae is a relatively small millipede family that globally encompasses approximately 40 genera and 130 species. It is distributed from Mexico to Argentina in the Americas, occurring also in tropical Africa and tropical to subtropical Asia to Papua New Guinea and Japan in the East (
At present, the Indo-Malayan genus Trichopeltis Pocock, 1894 is composed of eight species: T. bicolor (Pocock, 1894), the type species from Sumatra, Indonesia; T. cavernicola Golovatch, 2016 and T. muratovi Golovatch & VandenSpiegel, 2017, both from Laos; T. doriae Pocock, 1895 and T. feae Pocock, 1895, both from Myanmar; T. kometis (Attems, 1938) (= T. deharvengi Golovatch, Geoffroy, Mauriès & VandenSpiegel, 2010) from Vietnam, Laos and Cambodia; T. latellai Golovatch, Geoffroy, Mauriès & VandenSpiegel, 2010 from Guizhou Province, China; and T. watsoni Pocock, 1895 from Myanmar and Darjeeling District, India. Trichopeltis latellai is also the only genus and species of Cryptodesmidae reported so far from China (
Rather recently, Trichopeltis has been reviewed and a key provided to five of its species (
All specimens used in this study were collected by hand from caves in southern China and are preserved in 95% ethanol. The type material is deposited in the zoological collection of the South China Agricultural University, Guangzhou, China (
Observations and dissections were performed using a Leica S8 APO stereo microscope. The line drawings were prepared with a Zeiss Imager Axioskop40 microscope and a camera lucida attached for the scope. Photographs were taken with a Canon EOS 40D camera, then focus-stacked with Z-stack software, or Keyence VHX-5000 digital microscope, and further edited using Adobe Photoshop CS5 and Illustrator CC software.
The terminology used here follows that of Golovatch et al. (2012) and
Holotype ♂ (
2 ♀ juv. (
To emphasize the very pretty appearance of this species; adjective.
Differs from other species of the genus by the unusually elongate and densely setose gonopodal coxa. Superficially similar to T. intricatus sp. n., but distinguished from the latter in the longer tergal setae (Fig.
Length of holotype ca. 16 mm, width of midbody pro- and metazonae 1.5 and 4.5 mm, respectively. Coloration in alcohol uniformly light yellow. Adults with 20 segments (Fig.
Head: vertex densely pilose and microgranulate, clypeus clearly smooth (Fig.
Trichopeltis bellus sp. n., ♂ holotype. A collum and segments 2–3, dorsal view B head and segments 1–4, ventral view C cross-section of segment 8, caudal view D segment 7, ventral views E–F segments 17–19 and telson, dorsal and ventral views, respectively. Abbreviations: an = antenna; co = collum; ga = gonopod aperture; ml = marginal lobules; ts = tergal seta; tu = tubercles.
Collum fan-shaped (Fig.
Mid-dorsal regions on segments 2–16 with five more or less regular, transverse rows of similarly small, setigerous tubercles, 6–8 + 6–8 per row (Fig.
Paraterga very strongly developed (Figs
Integument clearly microgranulate throughout (Fig.
Epiproct tip sharp, with four spinnerets apically (Fig.
Pleurosternal carinae clearly present on segment 2 alone. Sterna modestly setose, cross-impressions moderate, clearly broadened between ♂ coxae 6, 7 and 9 (Figs
Legs very long and slender, unmodified, produced beyond paratergal lateral margin (Figs
Gonopods (Fig.
Based on the unpigmented body and long legs, this species is probably a troglobite.
Holotype ♂ (
To emphasize the complex gonopods; adjective.
Differs from all congeners except T. bellus sp. n. by the unusually densely setose gonopodal coxa, and from all species by the particularly complex gonopod which shows a number of peculiar processes and lobules (Fig.
Length of holotype ca. 10 mm, width of midbody pro- and metazonae 1.5 and 2.5 mm, respectively. Coloration in alcohol nearly pallid. Body with 20 segments (Fig.
Head sparsely pilose. Antennae very short and clavate, reaching behind segment 2 when stretched dorsally; in length, antennomere 6 > 3 > 4 = 5 = 2 = 7 = 1 (Fig.
Collum fan-shaped, inverted subtrapeziform, incompletely covering the head from above, with five irregular transverse rows of small, round, setigerous tubercles (Fig.
Mid-dorsal regions on segments 2–16 with five regular, transverse rows of about 15+15 similarly small, setigerous tubercles extending onto paraterga, in frontal and caudal rows smaller than others (Fig.
Paraterga 3–5 with 4–5 small, dentiform, lateral and 5–6 much larger, squarish, caudal lobules. Similarly, paraterga 2 and 6–16 with 6 lateral, 6–7 caudal lobules.
Tergal setae simple, very short and mostly abraded (Fig.
Epiproct short, conical (Fig.
Gonopod aperture subcordiform (Figs
Legs short and robust (Figs
Gonopods (Fig.
Based on the pallid body, this species may be a troglobite.
Holotype ♂ (
1 ♂, 3 ♀ (
To emphasize that most of the paraterga are upturned.
Differs from all congeners except T. cavernicola Golovatch, 2016 by the clearly upturned paraterga, and from all congeners by the shapes of the various lobes which are all confined to the distal third of the gonopodal telopodite. Among congeners, only T. latellai Golovatch, Geoffroy, Mauriès & VandenSpiegel, 2010, from two caves in Guizhou Province (
Length of both sexes ca. 10 mm, width of midbody pro- and metazonae 0.8 and 2.5 (♂) or 1.0 and 2.5 mm (♀), respectively. Coloration in alcohol nearly pallid. Body with 20 segments (Fig.
Collum with 3–4 irregular transverse rows of small and sharpened tubercles. Marginal lobules on collum: 13+13 small, setigerous, nearly sharp anteriorly and 3+3 similarly small, dentiform laterally (Fig.
Mid-dorsal regions on segments 2–16 with two regular, transverse rows of 3+3 and 4+4 tubercles similar to those on collum (Fig.
Paraterga very strongly developed (Figs
Tergal setae simple and short, mostly abraded (Fig.
Epiproct short, conical (Fig.
Pleurosternal carinae poorly-developed, but present on segments 2 and 3.
Sterna clearly broadened only between ♂ coxae 9. Gonopod aperture suboval (Fig.
Legs short, but slender, about 1.2 times as long as midbody height (Figs
Gonopods (Fig.
Based on the pallid body and slender legs, this seems to be a troglobite.
(modified after
1 | Tegument unpigmented, pallid to light yellowish; cavernicolous species | 2 |
– | Tegument clearly pigmented, red- or grey-brown to blackish; epigean species | 6 |
2 | Central parts of metaterga with 2–4 irregular transverse rows of setigerous tubercles; gonopodal coxa as usual, at most with only few setae | 3 |
– | Central parts of metaterga with 5–6 irregular transverse rows of setigerous tubercles; gonopodal coxa unusually densely setose on lateral side (Figs |
5 |
3 | Paraterga declivous; tergal setae very long, about half as long as body diameter; gonopodal telopodite clearly twisted; Guizhou, China | T. latellai |
– | Paraterga clearly upturned; tergal setae much shorter; gonopodal telopodite untwisted, seminal groove running entirely on mesal side | 4 |
4 | Central parts of metaterga with 3–4 irregular transverse rows of setigerous tubercles; gonopodal telopodite with a pulvillus subapically; Laos | T. cavernicola |
– | Central parts of metaterga with 2–3 rather regular transverse rows of setigerous tubercles (Fig. |
T. reflexus sp. n. |
5 | Tergal setae very long (Figs |
T. bellus sp. n. |
– | Tergal setae very short (Figs |
T. intricatus sp. n. |
6 | Central parts of metaterga with 4–6 irregular transverse rows of setigerous tubercles | 7 |
– | Central parts of metaterga with 2–3 irregular transverse rows of setigerous tubercles | 10 |
7 | Gonopodal telopodite clearly 3-branched, solenomere long and slender; Myanmar | T. doriae |
– | Gonopodal telopodite without long branches, only more or less deeply notched apically; solenomere rudimentary, barely visible | 8 |
8 | Central parts of metaterga with 4–5 rather regular transverse rows of setigerous tubercles; gonopodal telopodite with a conspicuous accessory seminal chamber and a pulvillus, but devoid of denticles laterally or mesally; Laos | T. muratovi |
– | Central parts of metaterga with 5–6 rather regular transverse rows of setigerous tubercles; gonopodal telopodite without accessory seminal chamber, but with a pulvillus, also abundantly denticulate either laterally or mesally | 9 |
9 | Body ca. 12 mm long and 3.0 mm wide; gonopodal telopodite abundantly denticulate on lateral face. Vietnam, Laos and Cambodia and possibly endemic to the Indochina Peninsula | T. kometis |
– | Body ca. 16 mm long and 4.8 mm wide; gonopodal telopodite abundantly denticulate on mesal face. Sumatra, Indonesia | T. bicolor |
10 | Frontal margin of paraterga abundantly lobulated. Solenomere lobe-shaped, tip nearly pointed | T. feae |
– | Frontal margin of paraterga entire, not lobulated. Solenomere axe-shaped, tip pointed | T. watsoni |
The family Cryptodesmidae was hitherto known to encompass three presumed troglobiont species: Peridontodesmella alba Schubart, 1957, from Brazil (
Almost all of southern China is blanketed by Earth’s most extensive karsts (
At present, most of the species of Trichopeltis, including both epigean and cavernicolous taxa, occur in Indo-Burma and Indochina. With the description of the above three new taxa, and with further explorations of southern China karst region, the southern part of the country will certainly become an important hotspot of Trichopeltis diversity. Due to a rapid discovery of new species, the previous key (
We are particularly grateful to the caving team of the South China Agricultural University, Guangzhou, China, for their assistance in the field. We also thank three reviewers and the academic editor Dr. Pavel Stoev for their corrections and useful suggestions that improved our manuscript. This study was sponsored by the Specialized Research Fund for the Doctoral Program of Higher Education of China (Grant no. 20134404110026).