Research Article |
Corresponding author: Yun Bu ( buy@sstm.org.cn ) Academic editor: Pavel Stoev
© 2020 Ya-Li Jin, 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:
Jin Y-L, Bu Y (2020) Two new species of the genus Symphylella (Symphyla, Scolopendrellidae) from East China. ZooKeys 1003: 1-18. https://doi.org/10.3897/zookeys.1003.60210
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Symphylella minuta sp. nov. and Symphylella communa sp. nov. from China are described and illustrated. Symphylella minuta sp. nov. is characterized by the delicate and minute body, a well-developed and thin central rod with a vestige of a transverse suture in the middle, eight setae on the first tergite, pointed processes on the tergites, and short cerci with sparse setae. Symphylella communa sp. nov. is characterized by the chaetotaxy of the first tergite with 4+4 setae, processes of the tergites somewhat longer or the same length with broad, most of lateromaginal setae long, anterolateral setae of tergites 2–4, 6, 7, 9, and 10 distinctly longer than other lateromarginal setae, approximately as long as the process of the same tergite, and cerci with numerous subequal and slightly curved setae. In addition, the chaetotaxic variation on the tergites, the distribution, the habitat, and the feeding habit of the genus Symphylella are discussed.
Chaetotaxy, morphology, Myriapoda, taxonomy
Symphyla is an ignored group of myriapods with about 200 species reported in the world and only six species are known from China (
Specimens were collected using Berlese-Tullgren funnels and preserved in 80% ethanol. They were mounted under slides using Hoyer’s solution and dried in an oven at 50 °C. Observations were performed under a phase contrast microscope (Leica DM 2500). Photographs were taken with a digital camera installed on the microscope (Leica DMC 4500). Line drawings were done using a drawing tube. All specimens are deposited in the collections of Shanghai Natural History Museum (SNHM), Shanghai, China.
Family Scolopendrellidae Bagnall, 1913
Symphylella isabellae (Grassi, 1886), described from Italy.
Symphylella minuta sp. nov. is characterized by the delicate and minute body, well-developed but thin central rod with a vestige of a transverse suture in the middle, eight setae on first tergite, pointed processes on tergites, and short cerci with sparse setae.
Holotype , female (slide no. JS-WX-SY2017020) (SNHM), China, Jiangsu Province, Wuxi City, Daji Mountain, extracted from soil samples of broad-leaf forest, alt. 5 m, 31°32'N, 120°12'E, 9-X-2017, coll. Y. Bu. Paratypes, 1 female (slide no. JS-WX-SY2017031) (SNHM), same data as holotype; 2 females (slides no. JS-WX-SY2020001, JS-WX-SY2020002) (SNHM), ibidem, 14-VII-2020, coll. Y. Bu; 3 females (slides no. SH-DJS-SY2015112, SH-DJS-SY2015114) (SNHM), China, Shanghai, Dajinshan Island, extracted from soil samples of broad-leaf forest, alt. 103 m, 30°41'N, 121°26'E, 22-IX-2015, coll. Y. Bu & Y. L. Jin; 3 females (slides no. ZJ-JLS-SY2019001, ZJ-JLS-SY2019002) (SNHM), China, Zhejiang, Lishui City, Suichang County, Jiulongshan National Nature Reserve, extracted from soil samples of broad-leaf forest, alt. 703 m, 28°13'N, 118°31'E, 27-V-2019, coll. Y. Bu & J. Y. Li. 1 female (slide no. ZJ-GTS-SY2012005) (SNHM), China, Zhejiang, Gutian Mountain, extracted from soil samples of broad-leaf forest, alt. 800 m, 29°15'N, 118°06'E, 11-IV-2012, coll. Y. Bu et al.; Non-type specimens: 7 juveniles with 8–10 pairs of legs, China, Shanghai, Dajinshan Island, extracted from soil samples of broad-leaf forest, alt. 103 m, 30°41'N, 121°26'E, 22-IX-2015, coll. Y. Bu & Y. L. Jin; 1 juvenile with 10 pairs of legs, China, Zhejiang, Lishui City, Suichang County, Jiulongshan National Nature Reserve, extracted from soil samples of broad-leaf forest, alt. 703 m, 28°13'N, 118°31'E, 27-V-2019, coll. Y. Bu & J. Y. Li; 3 juveniles with 9–10 pairs of legs, China, Zhejiang, Gutian Mountain, extracted from soil samples of broad-leaf forest, alt. 800 m, 29°15'N, 118°06'E, 11-IV-2012, coll. Y. Bu et al.; 1 juvenile with 10 pairs of legs, ibidem, 24-IV-2013; 1 juvenile with 10 pairs of legs, ibidem, 16-V-2012; 1 juvenile with 9 pairs of legs, ibidem, 19-VI-2012; 1 juvenile with 7 pairs of legs, ibidem, 15-VII-2012; 2 juveniles with 7 and 9 pairs of legs, ibidem, 14-X-2012; 2 juveniles with 9–10 pairs of legs, ibidem, 17-XI-2012, coll. Y. Bu et al.
Adult body 1.5 mm long in average (1.2–2.2 mm, n = 8), holotype 1.4 mm (Fig.
Head
length 150–170 μm, width 133–158 μm, with widest part somewhat behind the middle on a level with the points of articulation of mandibles. Central rod well developed but thin, with a vestige of a transverse suture in the middle. Anterior branches normally developed, without median branches. Dorsal side of head moderately covered with setae of different length, longest setae (18–25 μm) located most anterior on head, at least 3.0 times as long as central ones (4–6 μm). Cuticle of anterolateral part of head with rather coarse granules, around Tömösváry organ with moderate granules, other area with fine and faint granulation (Fig.
Symphylella minuta sp. nov. A habitus B left antenna, 1st–6th antennomeres, dorsal view C distal five antennomeres, dorsal view D distal five antennomeres, ventral view E distal five antennomeres, show lateral organs F head, right side, dorsal view G head, ventral view H first pair of legs (arrows indicate the reduced legs) and coxa of leg 2 I styli, and coxal sacs on base of 3rd leg (arrows indicate styli). Scale bars: 100 μm (A); 20 μm (B–I).
Tömösváry organ
globular, diameter 11–14 μm, about half of greatest diameter of third antennomere (24–27 μm), opening small and round (5–8 μm), with distinct vertical inner striate (Fig.
Mouthparts. Mandible with two fused lamellae and 12 teeth in total (Fig.
Antennae
with 14–19 antennomeres (holotype with 19 on left, 14 on right), length 320–380 μm (350 μm in holotype), about 0.2 of body length. First antennomere cylindrical, greatest diameter almost two times wider than long (23–27 μm, 14–16 μm), with three or four setae on inner side, longest inner seta 8–10 μm, outer side without seta. Second antennomere wider (22–29 μm) than long (16–19 μm), with six to eight setae evenly inserted around the antennal wall with interior setae (10–18 μm) slightly longer than exterior ones (6–7 μm). Chaetotaxy of third antennomere similar to preceding ones. Setae on proximal antennomeres longer than on distal ones. Proximal antennomeres with only primary whorl of setae, middle and subapical antennomeres with secondary whorl setae present. Three kinds of sensory organs observed on antenna: rudimentary spined sensory organs on dorsal side of middle antennomeres (Figs
Antennomeres | No. of primary whorl setae | No. of secondary whorl setae | Rudimentary spined sensory organs | Cavity-shaped organs on dorsal side | Bladder-shaped organs |
---|---|---|---|---|---|
1st | 4 | ||||
2nd | 7 | ||||
3rd | 7 | ||||
4th | 8 | 1 | |||
5th | 8 | ||||
6th | 8 | ||||
7th | 8 | 1 | |||
8th | 9 | 1 | |||
9th | 9 | 1 | |||
10th | 9 | 1 | |||
11th | 9 | 1 | |||
12th | 9 | 1 | |||
13th | 8 | 1 | 1 | ||
14th | 11 | 1 | 1 | 1 | |
15th | 10 | 4 | 1 | 1 | 2 |
16th | 12 | 4 | 1 | 5 | |
17th | 11 | 5 | 1 | 12 | |
18th | 5 | 2 | 9 |
Trunk
with 17 dorsal tergites. Tergites 2–13 and 15 each with one pair of sharp triangular processes. Length from base to tip of processes distinctly longer than its basal width except for the tergites 4, 7, 10 and 13, in which processes are almost as broad as long; basal distance between processes of tergites distinctly longer than their length from base to tip (Table
No. of tergites | lateromarginal | Central setae | Other setae |
---|---|---|---|
1st | 8* | ||
2nd | 4 (4) | 1 (1) | 4 (4) |
3rd | 4–5 (5) | 1–2 (1) | 9–10 (9) |
4th | 4 (4) | 1–3 (2) | 4–9 (4) |
5th | 4 (4) | 2 (2) | 4–5 (4) |
6th | 4–5 (5) | 2–3 (2) | 10–12 (10) |
7th | 4 (4) | 2–3 (2) | 4–5 (4) |
8th | 4 (4) | 2 (2) | 4–6 (4) |
9th | 5 (5) | 2 (2) | 10–12 (12) |
10th | 4 (4) | 2–3 (2) | 4–5 (4) |
11th | 4 (4) | 2 (2) | 4 (4) |
12th | 5 (5) | 2 (2) | 8–15 (14) |
13th | 4 (4) | 2–3 (3) | 4 (4) |
14th | 5–14 (5) | ||
15th | 4–5 (5) | 1–2 (2) | 6–10 (10) |
16th | 4–13 (4) | ||
17th | 6–17 (6) |
Tergites. Tergite 1 reduced, with eight short setae in a row. Tergite 2 complete, with two triangular posterior processes, four lateromarginal setae, one central seta, anterolateral setae 0.6–0.7 of length of process, longer than other lateromarginal ones, processes 1.1 or 1.2 times as long as broad, basal distance between processes 1.2–1.7 times as long as their length (Fig.
Symphylella minuta sp. nov. A 1st and 2nd tergites (als-anterolateral seta, as-apical seta, cs-central seta, ibs-inner basal seta, lms-lateromarginal seta) B 3rd tergite C 4th tergite D 5th tergite E 13th tergite F 14th tergite G 15th tergite H 16th tergite I styli and base of 4th leg (arrows indicate styli) J cerci, dorsal view. Scale bars: 20 μm.
Measurements of tergites and processes (mean ± se, in μm, n = 6) (holotype in brackets).
No. of tergites | Length | Width | Length of processes | Basal width of processes | Basal distance between processes |
---|---|---|---|---|---|
1st | 24 ± 3 (20) | 96 ± 8 (108) | |||
2nd | 37 ± 2 (40) | 100 ± 6 (108) | 21 ± 2 (23) | 18 ± 2 (21) | 31 ± 3 (28) |
3rd | 64 ± 5 (70) | 106 ± 1 (108) | 22 ± 1 (24) | 16 ± 4 (20) | 30 ± 3 (30) |
4th | 39 ± 5 (43) | 114 ± 5 (120) | 20 ± 2 (22) | 22 ± 3 (25) | 39 ± 1 (37) |
5th | 40 ± 2 (43) | 103 ± 4 (108) | 25 ± 3 (25) | 20 ± 1 (21) | 42 ± 1 (43) |
6th | 77 ± 6 (85) | 135 ± 11 (135) | 27 ± 2 (30) | 21 ± 3 (26) | 42 ± 4 (40) |
7th | 43 ± 4 (45) | 136 ± 11 (150) | 24 ± 2 (26) | 24 ± 2 (27) | 49 ± 4 (50) |
8th | 45 ± 4 (50) | 118 ± 11 (135) | 25 ± 4 (31) | 21 ± 2 (24) | 49 ± 4 (50) |
9th | 79 ± 8 (85) | 154 ± 10 (155) | 28 ± 2 (31) | 20 ± 3 (24) | 48 ± 6 (55) |
10th | 44 ± 6 (45) | 148 ± 19 (160) | 24 ± 2 (26) | 90 ± 3 (27) | 52 ± 3 (55) |
11th | 36 ± 5 (38) | 120 ± 4 (125) | 24 ± 4 (29) | 20 ± 2 (22) | 53 ± 1 (53) |
12th | 76 ± 8 (85) | 141 ± 6 (150) | 24 ± 1 (24) | 21 ± 5 (19) | 51 ± 5 (58) |
13th | 45 ± 4 (50) | 136 ± 13 (155) | 23 ± 3 (27) | 22 ± 3 (27) | 54 ± 4 (59) |
14th | 47 ± 5 (50) | 125 ± 24 (160) | |||
15th | 65 ± 7 (75) | 135 ± 11 (150) | 22 ± 2 (25) | 20 ± 3 (22) | 44 ± 8 (53) |
16th | 53 ± 7 (63) | 113 ± 8 (125) | |||
17th | 74 ± 3 (75) | 81 ± 7 (75) |
Legs.
First pair of legs reduced to two small hairy cupules, each with two long setae (Fig.
Coxal sacs
present at bases of legs 3–9, fully developed, each with three to five setae on surface (Fig.
Styli
present at base of legs 3–12, subconical (length 2–4 μm, width 2–3 μm), basal part with straight hairs; with a distal blunt apex (2–3 μm) (Figs
Sense calicles with smooth margin to pit, about same length as outer diameter. Sensory seta inserted in cup center, extremely long (90–100 μm).
Cerci
short and stout (Figs
The species name “minuta” refers to the delicate and minute body of the species.
China (Jiangsu, Shanghai, Zhejiang).
Symphylella minuta sp. nov. is similar to S. oligosetosa Scheller, 1971 from India and Sri Lanka in the shape of the central rod on head and the shape and chaetotaxy of the tergites. They can be distinguished by the chaetotaxy of the first tergite (eight setae in S. minuta sp. nov. vs six in S. oligosetosa), shape of the processes (pointed and with swollen ends in S. minuta sp. nov. vs strongly pointed and without swollen ends in S. oligosetosa), shape and chaetotaxy of cerci (short and stout, about 2.5 times as long as wide in S. minuta sp. nov. vs slender, 3.5–3.6 times as long as wide in S. oligosetosa). It is also similar to S. abbreviata Scheller, 1971 from Sri Lanka in the chaetotaxy of the tergites and shape of the processes, but can be easily separated by the chaetotaxy of the first tergite (with eight setae in S. minuta sp. nov. vs six setae in S. abbreviata), shape of the third tergite (without indentation in S. minuta sp. nov. vs with a distinct middle lateromarginal indentation in S. abbreviata), shape of cerci (tapering in S. minuta sp. nov. vs with outer side strongly bulging in S. abbreviata).
Symphylella communa sp. nov. is characterized by the chaetotaxy of the first tergite composed by 4+4 setae, processes of tergites somewhat longer or the same length with broad, most of lateralmaginal setae long, anterolateral setae of tergites 2–4, 6, 7, 9, and 10 distinctly longer than other lateromarginal setae, approximately as long as processes of the same tergite, cerci with numerous subequal and slightly curved setae.
Holotype , male (slide no. SH-DJS-SY2015048) (SNHM), China, Shanghai, Dajinshan Island, extracted from soil samples of broad-leaf forest, alt. 103 m, 30°41'N, 121°26'E, 30-VI-2015, coll. Y. Bu & Y. L. Jin. Paratypes, 1 male (slide no. SH-DJS-SY2015023) (SNHM), 10 females (slides no. SH-DJS-SY2015001, SH-DJS-SY2015018–SH-DJS-SY2015022, SH-DJS-SY2015024, SH-DJS-SY2015025, SH-DJS-SY2015048, SH-DJS-SY2015055) (SNHM), same data as holotype; 2 males (slides no. SH-DJS-SY2015099, SH-DJS-SY2015108) (SNHM), 1 female (slide no. SH-DJS-SY2015107) (SNHM), ibidem, 22-IX-2015; 4 males (slides no. SH-DJS-SY2015083, SH-DJS-SY2015124, SH-DJS-SY2015125) (SNHM), 5 females (slides no. SH-DJS-SY2015058, SH-DJS-SY2015059, SH-DJS-SY2015079, SH-DJS-SY2015122, SH-DJS-SY2015123) (SNHM), ibidem, extracted from soil samples of bamboo forest, 22-IX-2015, coll. Y. Bu & Y. L. Jin; 5 females (slides no. SH-DJS-SY2015117, SH-DJS-SY2015118, SH-DJS-SY2015120, SH-DJS-SY2015121) (SNHM), ibidem, extracted from soil samples of broad-leaf forest, 22-IX-2015, coll. Y. Bu & Y. L. Jin; 1 female (slide no. ZJ-GTS-SY2012018) (SNHM), 1 male (slide no. ZJ-GTS-SY2012009) (SNHM), Zhejiang, Gutian Mountain, extracted from soil samples of broad-leaf forest, alt. 800 m, 29°15'N, 118°06'E, 11-IV-2012, coll. Y. Bu et al.; 1 male (slide no. ZJ-GTS-SY2012021) (SNHM), ibidem, 16-V-2012; 1 female (slide no. ZJ-GTS-SY2012041) (SNHM), ibidem, 19-VI-2012; 1 female (slide no. ZJ-GTS-SY2012045) (SNHM), ibidem, 14-X-2012; 1 female (slide no. ZJ-GTS-SY2012054) (SNHM), ibidem, 17-XI-2012, coll. Y. Bu et al.; 4 females (slides no. JS-WX-SY2017012, JS-WX-SY2017017, JS-WX-SY2017018, JS-WX-SY2017033) (SNHM), 1 male (slide no. JS-WX-SY2017035) (SNHM), China, Jiangsu, Wuxi, Daji Mountain, extracted from soil samples of broad-leaf forest, alt. 5 m, 31°32'N, 120°12'E, 9-X-2017, coll. Y. Bu. Non-type specimens: 37 juveniles with 7–10 pairs of legs, same data as holotype; 6 juveniles with 7–10 pairs of legs, ibidem, 22-IX-2015; 32 juveniles with 7–10 pairs of legs, 22-IX-2015; 8 juveniles with 7–10 pairs of legs, 23-IX-2015, ibidem, extracted from soil samples of bamboo forest, 22-IX-2015, coll. Y. Bu & Y. L. Jin; 1 juvenile with 9 pairs of legs (slide no. ZJ-GTS-SY2012011), Zhejiang, Gutian Mountain, 11-IV-2012; 1 juvenile with 9 pairs of legs, ibidem, 19-VI-2012; 4 juveniles with 8 pairs of legs, ibidem, 15-VII-2012; 1 juvenile with 9 pairs of legs, ibidem, 19-IX-2012; 3 juveniles with 8 or 10 pairs of legs, ibidem, 14-X-2012; 3 juveniles with 8–10 pairs of legs, ibidem, 17-XI-2012; 6 juveniles with 8–9 pairs of legs, ibidem, 12-XII-2012; 1 juvenile with 8 pairs of legs, ibidem, 23-I-2013; 2 juveniles with 8 or 10 pairs of legs, ibidem, 27-III-2013; 1 juvenile with 10 pairs of legs, ibidem, 24-IV-2013, coll. Y. Bu et al.; 12 juveniles with 7–10 pairs of legs, Jiangsu, Wuxi, Daji Mountain, 9-X-2017, coll. Y. Bu.
Symphylella communa sp. nov. A habitus B left 2nd–5th antennomeres, dorsal view C distal five antennomeres, dorsal view D distal five antennomeres, show lateral organs E distal five antennomeres, ventral view F head, dorsal view G head, ventral view H first pair of legs (arrows indicate the reduced legs) I coxa of leg 2 J coxa of leg 3 (arrows indicate styli) K coxa of leg 4 and male genital plate (arrows indicate styli). Scale bars: 100 μm (A); 20 μm (B–K).
Adult body 2.2 mm long in average (1.7–3.1 mm, n = 40), holotype 2.1 mm (Fig.
Head
length 200–290 μm, width 200–350 μm, with widest part somewhat behind the middle on a level with the points of articulation of mandibles (Fig.
Tömösváry organ
globular (Fig.
Mouthparts. Mandible with two fused lamellae and 11 teeth in total (Fig.
Antennae
with 15–20 antennomeres, length 500–720 μm (550 μm in holotype), about one-quarter of body length. First antennomere shorter than second one, greatest diameter 1.2–1.7 times as wide as long (34–43 μm, 20–35 μm), with five to seven setae in one whorl, longest seta (20–21 μm) inserted at inner side and distinctly longer than outer ones (11–12 μm). Second antennomere wider (29–44 μm) than long (23–35 μm), with 6–10 setae evenly inserted around the antennal wall with interior setae (20–22 μm) slightly longer than exterior ones (13–15 μm). Chaetotaxy of third antennomere similar to preceding ones. Setae on proximal antennomeres longer and on distal antennomeres shorter. Proximal antennomeres with only primary whorl of setae (Fig.
Antennomeres | No. of primary whorl setae | No. of secondary whorl setae | Rudimentary spined sensory organs | Cavity-shaped organs on dorsal side | Bladder-shaped organs |
---|---|---|---|---|---|
1st | 6 | ||||
2nd | 8 | 1 | |||
3rd | 9 | 1 | |||
4th | 10 | 1 | 1 | ||
5th | 11 | 1 | |||
6th | 11 | 1 | |||
7th | 11 | 2 | 1 | ||
8th | 11 | 2 | 1 | 1 | 1 |
9th | 12 | 5 | 2 | 2 | |
10th | 13 | 6 | 1 | 2 | 3 |
11th | 14 | 6 | 1 | 1 | 2 |
12th | 14 | 5 | 1 | 6 | |
13th | 15 | 5 | 1 | 1 | 6 |
14th | 14 | 5 | 2 | 7 | |
15th | 13 | 1 | 8 | ||
16th | 12 | 1 | 1 | 7 | |
17th | 12 | 1 | 1 | 4 |
Trunk
with 17 dorsal tergites. Tergites 2–13, and 15 each with one pair of triangular processes. Length from base to tip of processes somewhat shorter than or the same as its basal width; basal distance between processes of tergites 4–13, and 15 longer than their length from base to tip (Table
No. of tergites | lateromarginal | Inserted seta | Central setae | Other setae |
---|---|---|---|---|
1st | 4+4/5 (4+4)* | |||
2nd | 5–7 (6) | 1–2 (1) | 2–5 (2) | 6–14 (8) |
3rd | 7–10 (8) | 1–3 (2) | 2–5 (2) | 14–27 (19) |
4th | 6–8 (6) | 1–2 (1) | 3–6 (4) | 7–18 (11) |
5th | 5–8 (6) | 1–3 (2) | 2–5 (2) | 8–18 (12) |
6th | 8–11 (8) | 1–3 (1) | 3–6 (5) | 21–36 (26) |
7th | 5–7 (6) | 0–2 (1) | 4–8 (5) | 7–20 (15) |
8th | 5–8 (6) | 1–3 (2) | 3–6 (4) | 8–20 (11) |
9th | 7–11 (8) | 1–3 (2) | 3–6 (4) | 21–36 (29) |
10th | 5–7 (6) | 0–2 (1) | 3–7 (4) | 6–19 (11) |
11th | 5–8 (6) | 0–3 (1) | 3–8 (4) | 6–18 (11) |
12th | 6–10 (6) | 1–2 (1) | 2–6 (4) | 9–33 (14) |
13th | 4–7 (5) | 0–2 (1) | 2–6 (5) | 2–15 (7) |
14th | 12–23 (18) | |||
15th | 5–8 (5) | 0–2 (1) | 1–4 (3) | 5–29 (14) |
16th | 10–16 (14) | |||
17th | 18–27 (19) |
Tergite. Tergite 1 reduced, with eight or nine unequal length setae in two groups (4+4 or 4+5) (Fig.
Symphylella communa sp. nov. A posterior of head and 1st tergite B 2nd tergite (als-anterolateral seta, as-apical seta, cs-central seta, is-inserted seta, ibs-inner basal seta, lms-lateromarginal seta) C 3rd tergite D 4th tergite, right side E 5th tergite F 14th tergite G 15th tergite H right cercus, dorsal view. Scale bars: 20 μm.
Measurements of tergites and processes (mean ± se, in μm, n = 22) (holotype in brackets).
No. of tergites | Length | Width | Length of processes | Basal width of processes | Basal distance between processes |
---|---|---|---|---|---|
1st | 33 ± 7 (25) | 175 ± 25 (150) | |||
2nd | 53 ± 4 (58) | 135 ± 4 (130) | 38 ± 6 (38) | 45 ± 7 (43) | 23 ± 5 (25) |
3rd | 89 ± 5 (95) | 178 ± 10 (168) | 41 ± 5 (38) | 48 ± 7 (40) | 33 ± 5 (40) |
4th | 61 ± 10 (50) | 192 ± 12 (178) | 36 ± 6 (25) | 56 ± 11 (43) | 54 ± 9 (65) |
5th | 69 ± 6 (75) | 185 ± 13 (180) | 43 ± 5 (45) | 51 ± 8 (53) | 55 ± 11 (48) |
6th | 117 ± 10 (125) | 234 ± 12 (225) | 49 ± 6 (45) | 54 ± 11 (45) | 59 ± 11 (53) |
7th | 67 ± 8 (75) | 236 ± 13 (232.5) | 40 ± 5 (45) | 59 ± 10 (63) | 79 ± 16 (68) |
8th | 72 ± 4 (75) | 194 ± 9 (200) | 46 ± 6 (45) | 54 ± 10 (50) | 70 ± 12 (65) |
9th | 121 ± 4 (120) | 258 ± 18 (240) | 52 ± 8 (50) | 61 ± 13 (50) | 63 ± 10 (58) |
10th | 70 ± 9 (75) | 239 ± 10 (230) | 38 ± 6 (33) | 60 ± 15 (55) | 81 ± 12 (75) |
11th | 83 ± 8 (75) | 219 ± 9 (213) | 43 ± 6 (40) | 54 ± 11 (43) | 73 ± 10 (75) |
12th | 111 ± 10 (100) | 258 ± 11 (250) | 42 ± 7 (40) | 57 ± 14 (50) | 68 ± 9 (70) |
13th | 71 ± 4 (70) | 233 ± 4 (230) | 30 ± 4 (30) | 58 ± 9 (50) | 72 ± 12 (70) |
14th | 75 ± 13 (70) | 198 ± 4 (195) | |||
15th | 82 ± 6 (75) | 218 ± 14 (208) | 31 ± 5 (25) | 54 ± 12 (38) | 58 ± 9 (58) |
16th | 75 ± 5 (70) | 171 ± 7 (163) | |||
17th | 111 ± 3 (113) | 157 ± 16 (145) |
Legs. First pair of legs reduced to two small, hairy cupules, each with at least one long setae (4–10 μm) (Fig.
Coxal sacs
present at bases of legs 3–9, fully developed, each with four or five setae on surface (Fig.
Styli
present at base of legs 3–12, subconical (length 6–10 μm, width 3–6 μm), basal part with dense straight hairs; distal quarter hairless and blunt (3–5 μm) (Figs
Sense calicles with smooth margin to pit. Sensory seta inserted in cup center, extremely long (120–180 μm).
Cerci
about 0.4–0.8 of head length and leg 12, 2.4–3.3 times as long as its greatest width (115–178 μm, 37–63 μm), moderately covered with subequal length setae (Figs
The species name “communa” is derived from “common” which refer to the common morphology and wide distribution of the species.
China (Jiangsu, Shanghai, Zhejiang).
Symphylella communa sp. nov. is most similar to S. asiatica Scheller, 1971 from India and Sri Lanka and S. macropora Jin & Bu, 2019 from Tibet in the shape of the central rod, tergites, processes, anterolateral setae, and leg 12. It differs from S. asiatica and S. macropora in the size of the opening of the Tömösváry organ (moderate in S. communa sp. nov. vs very small in S. asiatica, extremely large in S. macropora) and chaetotaxy of the first tergite (4+4 in S. communa sp. nov. and S. macropora vs 3+3 setae in S. asiatica). It is also affiliated to S. neotropica (Hansen, 1903) from Brazil in the shape of tergites and processes, but can be easily distinguished by the central rod (both the anterior and posterior parts are in the same width in S. communa sp. nov. vs the anterior part is distinctly narrow than the posterior part in S. neotropica).
The genus Symphylella is well defined by the presence of 17 tergites with 13 of them having triangular processes present on posterior margins, the first pair of legs replaced by two protuberances with a few setae inserted on, and short styli present on the base of legs 3–9. The shapes of the central rod, Tömösváry organ, tergites and their processes, and cerci, as well as the chaetotaxy of the tergites and cerci, are good characters for the species identification. The measurements of anterolateral setae on tergites are also taxonomically informative for the species definition. The number of lateromarginal setae, inserted setae, central setae, and other setae on tergites often show considerable variations among adult individuals. Asymmetrical setae are usually observed on tergites. In Symphylella communa sp. nov., most specimens with 4+4 setae on the first tergite while several specimens exhibits 4+5 and one specimens with 5+5 setae, and the same variation is also observed in S. macropora. The shape of the cerci is a relative stable character of the species, but the ratio of the length and width of the cercus may be affected by the mounting process of specimens. Therefore, caution is advised when identify the species of Symphylella, which should be based on multiple differential stable characters of fully mature specimens.
The members of the genus Symphylella are distributed in almost all faunal regions of the world: 17 species (34.7%) in Nearctic Region, 12 (24.5%) in Ethiopian Region, 11 (22.5%) in Oriental Region, 7 (14.3%) in Palaearctic Region, 6 (12.2%) in Australian Region, and two (4.1%) in Neotropical Region. Most of the species occur in Nearctic, Ethiopian, and Oriental regions. It seems they are more adaptable to the temperate climate. In China, Symphylella are often found with high density in the tropical and subtropical area. More species are expected to be discovered in East and South China in the future.
According to the previous studies, the species of the genus Symphylella are adapted to diverse habitats and a variety of biotopes: from litter and moss, soil and leaf litter in bamboo and broad-leaf forest, pineapple field, to the plantation of bananas and coco, lawn, botanical garden, tea plantation, orchards, and unoccupied sites. They can live on moist slopes of hills, along streams, in silty soil of agricultural lands, and in caves. They are also present under stone or bricks, in decaying vegetable matter, under bark, in heaps of rotten coconut shells, and under coco trunks on grassy ground (
Symphylella species are supposed to be phytophagous or saprophagous (
We cordially thank Dr Bi-Cheng Li, Professor Xin Ke, and Professor Yi-Ping Wang for their well organization of expeditions to Dajinshan Isalnd, Gutian Mountain, and Jiulongshan National Nature Reserve, respectively. Thanks are also given to Dr Jing-Yang Li for his help in the collection. We appreciate Professor José G. Palacios-Vargas (Mexico) for his linguistic corrections of the manuscript as well as his valuable advice. Special thanks are given to Dr Nikolaus Szucsich (Austria) and Dr Pavel Stoev (Bulgaria) for their valuable comments in review of the manuscript. This research was supported by the National Natural Science Foundation of China (no. 31772509) and the Basic Research Foundation of Shanghai Science and Technology Museum.