Research Article |
Corresponding author: Yun Bu ( buy@sstm.org.cn ) Academic editor: Pavel Stoev
© 2020 Yun Bu.
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:
Bu Y (2020) Study on the Pauropoda (Myriapoda) from Tibet, China – Part II: New species and new record of the genus Samarangopus. ZooKeys 927: 53-64. https://doi.org/10.3897/zookeys.927.50100
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The pauropod family Eurypauropodidae Ryder, 1879 is recorded from Tibet, China for the first time. In this study, a new species Samarangopus zhongi sp. nov. is described and illustrated from Motuo County, southeastern Tibet of China. It is distinguished from other species in this genus by having one pair of spiniform appendages on the sternum of the last trunk segment, 28–34 marginal protuberances on tergite I, the distal quarter of bothriotricha T3 golf-club-shaped, and the leaf-shaped seta st on tergum of pygidium. In addition, Samarangopus canalis Scheller, 2009 is newly recorded from China.
appendages, Eurypauropodidae, Motuo County, pauropod, taxonomy
Four species of pauropods were recognized in Tibet: Sphaeropauropus sp. belonging to the family Sphaeropauropodidae Silvestri, 1930 (
The family Eurypauropodidae Ryder, 1879 is currently comprised of more than 60 species (
The purposes of this study are 1) to record the occurrence of family Eurypauropodidae Ryder, 1879 in Tibet; 2) to describe a new species of the genus Samarangopus Verhoeff, 1934; 3) to record the presence of Samarangopus canalis Scheller, 2009 in southeastern Tibet for the first time.
All pauropods were collected using a Tullgren’s funnel. The specimens were sorted under a stereomicroscope and preserved in 80% alcohol. They were mounted on slides using Hoyer’s solution and dried in an oven at 50 °C. Observations were performed under a phase contrast microscope (Leica DM 2500). Photos were taken using a digital camera (Leica DMC 4500). Line drawings were made using a drawing tube. All specimens were deposited in the collection maintained by the Shanghai Natural History Museum (SNHM).
Abbreviations used in the descriptions follow
Family Eurypauropodidae Ryder, 1879
Samarangopus jacobsoni (Silvestri, 1930).
Fourth antennal segment with 3 well developed setae; globulus of sternal antennal branch g short-stalked; all legs 5-segmented; empodia with 1 anterior accessory claw (
Palaearctic, Ethiopian, Oriental, and Australian regions.
Holotype , male adult with 9 pairs of legs (slide no. XZ-PA2015004) (SNHM), China, Tibet, Motuo county, Dexing town, extracted from soil samples in a broad-leaf forest, alt. 1100 m, 29°40'N, 95°26'E, 3-XI-2015, coll. Y. Bu. Paratypes, 5 male adults with 9 pairs of legs (slides no. XZ-PA2015001, XZ-PA2015006, XZ-PA2015052, XZ-PA2015056, XZ-PA2015057) (SNHM), 3 female adults, with 9 pairs of legs (slides no. XZ-PA2015005, XZ-PA2015024, XZ-PA2015054) (SNHM), same data as holotype. Other material, 1 juvenile, with 6 pairs of legs (slides no. XZ-PA2015051) (SNHM), same data as holotype.
Samarangopus zhongi sp. nov. is characterized by one pair of spiniform appendage on sternum of last trunk segment, 28–34 marginal protuberances on tergite I, the distal quarter of bothriotricha T3 golf-club-shaped, and the leaf-shaped seta st on tergum of pygidium.
Adult body length (0.62–) 0.69 (–0.75) mm (n = 9); body yellow to brown (Figs
Head
(Figs
Antennae
(Figs
Trunk. Setae of collum segment similar, furcate, branches tapering, pointed; main branch striate; secondary branch rudimentary, glabrous; both setae length 10 (–11) μm (Fig.
Samarangopus zhongi sp. nov. (holotype) A collum segment, sternal view B sternum of the last trunk segment, show spiniform appendages C tergum of pygidum D sternum of pygidum and anal plate E tarsus of leg 1 F tarsus of leg 9 G femur of leg 1 with appendage H male genital papillae. Scale bars: 20 μm.
Bothriotricha. All with thin axes and short almost erect pubescence, T1, T2, T4, and T5 with distal part curled (Fig.
Legs. All legs 5-segmented. Setae on coxa and trochanter of leg 9 similar to each other, thin, furcate, striate, with glabrous base, length of secondary branch 0.7 (–0.8) of primary one (Figs
Samarangopus zhongi sp. nov. (holotype) A habitus, sternal view B anal plate C right antenna, sternal view D anterior margin of tergite I E head, tergal view F leg 1, arrow shows appendage on femur G setae on coxa and trochanter of leg 1 H tarsus of leg 9 I last trunk segment, arrows show one pair of appendages, sternal view J setae on coxa and trochanter of leg 9 K male genital papillae and coxa of leg 2 L right side margin of tergite IV and T3. Scale bars: 100 μm (A); 20 μm (B–L).
Genital papillae
(Figs
Pygidium. Tergum (Fig.
Sternum
(Fig.
Anal plate
(Figs
The new species is dedicated in honor of the late Professor Zhong Yang (1964–2017) who was an eminent botanist from Fudan University and Tibet University, for his great contribution to the knowledge of flora and biodiversity of Tibet. This study is also to express my great gratitude to his help.
Known only from the type locality.
Samarangopus zhongi sp. nov. can be easily distinguished from all other congeners by the presence of the one pair of spiniform appendages on the sternal side of last trunk segment. It is most similar to S. campanulatus Scheller, 2004 from Vietnam in the shape of anal plate, the chaetotaxy of pygidium and the protuberances on the body. It can be distinguished from S. campanulatus by: the spiniform appendages on the sternum of last trunk segment (present in S. zhongi sp. nov. vs absent in S. campanulatus), shape of bothriotricha T3 (distal quarter golf-club-shaped, densely pubescent in S. zhongi sp. nov. vs distal 2/5 part clavate, end-swelling in S. campanulatus), shape of seta st on tergum of pygidium (leaf-shaped in S. zhongi sp. nov. vs lanceolate in S. campanulatus), the shape of proximal seta on tarsus 9 (striated in S. zhongi sp. nov. vs glabrous in S. campanulatus), and the shape of appendage on the femur of leg 1 (broad triangular in S. zhongi sp. nov. vs blunt cylindrical in S. campanulatus) . The shape of posterior appendage on anal plate of the new species is also similar to S. tuberosus Scheller, 2007 from Singapore and S. cylindratus Scheller, 2009 from Indonesia. The new species differs from S. tuberosus in the shape of setae b2 on pygidium (slender and pointed in S. zhongi sp. nov. vs large and lanceolate in S. tuberosus). It differs from S. cylindratus in the shape of appendages of the collum segment (barrel-shaped in S. zhongi sp. nov. vs cylindrical and large in S. cylindratus).
1 male adult with 9 pairs of legs (slide no. XZ-PA2015053) (SNHM), 1 female adult with 9 pairs of legs (slide no. XZ-PA2015055) (SNHM), China, Tibet, Motuo county, Dexing town, extracted from soil samples of broad-leaf forest, Alt. 1100 m, 29°40'N, 95°26'E, 3-XI-2015, coll. Y. Bu.
Samarangopus canalis Scheller, 2009 is characterized by the peculiar shape of distal part of male genital papillae which forming an anteriorly open furrow and the ovoid posterior appendages of the anal plate.
Length 0.90 mm (n = 2), yellow to brown in color (Fig.
Antennae
(Fig.
Trunk. Setae of collum segment similar, furcate, branches tapering, pointed; main branch cylindrical, annulated, blunt, secondary branch 0.3 of the length of primary branch, glabrous (Fig.
Bothriotricha. All with thin axes, glabrous proximal parts, distally with minute pubescence, T1, T2, T4 and T5 curled distally, T3 shorter than others, with thicker axis and terminated by an ovoid swelling (Fig.
Genital papillae
(Fig.
Legs. All legs 5-segmented. Setae on coxa and trochanter of leg 9 similar to each other, thin, furcate, densely annulated, length of secondary branch 0.7–0.8 of primary one (Fig.
Samarangopus canalis Scheller, 2009 (Chinese specimens) A habitus, tergal view B left antenna, tergal view C collum segment, sternal view D male genital papillae E right margin of tergite IV, show T3 F right anterolateral corner of tergite II, tergal view G posteriomedian margin of Tergite I H leg 1 I setae on coxa and trochanter of leg 9. Scale bars: 100 μm (A); 20 μm (B–I).
Pygidium. Tergum. Posterior margin with two narrow, digitiform posterior directed processes protruding from between setae a2 and a3. Setae glabrous, a1 straight, a2 clavate, short, a3 slender and long; st long and leaf-shaped, 10–11 μm. Two semicircle plates close to st with dense pubescence. Lengths of setae: a1= 5 μm, a2 =6–8 μm, a3 = 15 μm. Distance a1–a1=7–9 μm, a1–a2=5–7 μm, a2–a3=4–5 μm, st–st=10 μm.
Sternum. Posterior margin between b1 almost straight. Setae thin, tapering, pointed, distal part of b1 annulated, b2 and b3 striated. Lengths of setae: b1= 32 μm, b2=23–25 μm, b3= 11–13 μm. Distances b1–b1= 28–30 μm, b2–b2= 50–53 μm, b1–b2= 21–23 μm, b3–b3= 23–25 μm. b1 1.1 times as long as interdistance, b2 1.0–1.2 of distance b1 –b2, b3 0.55 of interdistance.
Anal plate. 1.2 times as long as broad; lateral margins straight anteriorly, concave posteriorly; distal part of plate cleft by narrow U-shaped incision, depth 0.3–0.4 of the length of plate, incision forming two posterior branches with subparallel sides, each with two appendages: a submedian short, straight, glabrous one and a thin folioform stalked appendage protruding backward. Folioform appendage about 0.6 of length of plate. Plate glabrous, distal appendages with somewhat granular surface.
China (Tibet), Indonesia (Sulawesi).
Samarangopus canalis was originally described and only known from Sulawesi Island, Indonesia (
I express my cordial gratitude to Dr Tian-Meng Liu, who was a doctoral student of Professor Zhong Yang, for his well organization of expedition in Tibet in November 2015. I appreciate Dr Shan Li and Professor José G. Palacios-Vargas (Mexico) for their linguistic improvement of this manuscript as well as the valuable advice. I give my special thank to the two anonymous reviewers for their comments for improving the manuscript. I also wish to thank Dr Gang Yang and Mr Zheng-Wei Wang for their generous help during the collection and Dr Chang-Yuan Qian for sharing some references. This research is supported by the National Natural Science Foundation of China (no. 31772509) and the Natural Science Foundation of Shanghai (no. 17ZR1418700).