Research Article |
Corresponding author: Yong-hong Xiao ( yonghongxiao01@126.com ) Academic editor: Yuri Marusik
© 2020 Ke-ke Liu, Hui-pu Luo, Xiang Xu, Zhiwu Chen, Yong-hong Xiao.
This is an open access article distributed under the terms of the CC0 Public Domain Dedication.
Citation:
Liu K-k, Luo H-p, Xu X, Chen Z, Xiao Y-h (2020) Description of two new species of Tonsilla Wang & Yin, 1992 with an updated key to species (Araneae, Agelenidae). ZooKeys 944: 31-46. https://doi.org/10.3897/zookeys.944.48575
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Two new species of Tonsilla Wang & Yin, 1992 are described from Jinggang Mountain National Nature Reserve, Jiangxi Province, China: T. jinggangensis K. Liu & X. Xu, sp. nov. (♀) and T. subyanlingensis K. Liu & X. Xu, sp. nov. (♂♀). The new species are illustrated, and their distributions are mapped. Detailed generic characters and an updated key to Tonsilla species are also given.
Jiangxi, Coelotinae, identification key, Jinggang Mountain, spider, taxonomy
At present, the Coelotinae, with approximately 770 species belonging to 33 genera, is the largest subfamily of Agelenidae. The number of species in this subfamily has increased in the last five years greatly due to more than 20 publications, so that now the Agelenidae is the tenth largest spider family (
Tonsilla Wang & Yin, 1992 is relatively small genus with 11 named species which are known exclusively from China. It is a relatively well-studied genus due to numerous publications (see
While studying the Agelindae from the Jinggang Mountain National Nature Reserve, Jiangxi Province, we found two new species belonging to Tonsilla, and the main goals of this paper are, therefore, to describe these new species, to provide a key to all species of the genus, and to discuss the affinities of Tonsillia.
Specimens were examined using a Zeiss Stereo Discovery V12 stereomicroscope with a Zoom Microscope System. Both the male palps and female copulatory organs were detached and examined in 75−80% ethanol under a Zeiss Axio Scope A1 compound microscope with a KUY NICE CCD. For SEM photographs, the specimens were dried on filter paper and photographed with the ZEISS EVO LS15 scanning electron microscopes under a low vacuum. The specimens were subsequently stored in 75% ethanol after SEM.
All measurements were made by using ImageView CM2000 software and in millimetres. Leg measurements are given as total length (femur, patella, tibia, metatarsus, tarsus). All the specimens are deposited in the Animal Specimen Museum, Life Science of College, Jinggangshan University (ASM-JGSU).
Terminology of the male and female copulatory organs follows
Eyes
ALE anterior lateral eye;
AME anterior median eye;
PLE posterior lateral eye;
PME posterior median eye;
Male palp
BLC basal lamella of conductor;
CF cymbial furrow;
Con conductor;
DAC dorsal apophysis of conductor;
Em embolus;
MA median apophysis;
PA patellar apophysis;
RTA retrolateral tibial apophysis;
VTA ventrolateral tibial apophysis;
Epygine
At atrium;
CD copulatory duct;
CO copulatory opening;
EH epigynal hood;
ET epigynal teeth;
FD fertilization duct;
SH spermathecal head;
Spe spermatheca;
Legs
fe femur;
mt metatarsus;
pa patella;
ta tarsus;
ti tibia.
Subfamily Coelotinae F.O. Pickard-Cambridge, 1893
Tonsilla
Tonsilla:
Tonsilla: Yin et al. 2012: 1029.
Tonsilla:
Tonsilla truculenta Wang & Yin, 1992.
Males of this genus can be easily distinguished from these of other genera of Coelotinae by the male palpal patella with a large strong apophysis, which is more than half of the patella length (Figs
Tonsilla jinggangensis sp. nov., female holotype A habitus, dorsal view B same, ventral view C epigyne, ventral view D vulva, dorsal view. Scale bars: 2 mm (A, B), 0.2 mm (C, D). Abbreviations: At – atrium, CD – copulatory duct, CO – copulatory opening, EH – epigynal hood, ET – epigynal teeth, FD – fertilization ducts, SH – spermathecal heads, Spe – spermathecae.
Body size
7.0–17.0 mm. The morphological appearance of this genus is similar to that of other coelotines. Carapace anteriorly narrowed to between 0.6 and 0.9 times its maximum width. PLE–PLE covered half width of anterior carapace. Chelicerae (Figs
Male palp
(Figs
Epigyne : atrium from large to small, heart-shaped, posteromedially located, broad and anteriorly located in T. defossa, with an arch-shaped or triangular septum arising antero-medially in T. truculenta Wang & Yin, 1992; copulatory openings located postero-laterally in the atrium; epigynal teeth tube-shaped or horn-like, flattened in T. subyanlingensis sp. nov., located antero-medially, separated by its length or less, or slightly fused basally; copulatory ducts sac-shaped, mostly rounded, tube-shaped in T. jinggangensis sp. nov., T. subyanlingensis sp. nov., and T. yanlingensis; spermathecae spherical or ovoid, duct-shaped in T. defossa, widely separated or close to each other; spermathecal heads arising anteriorly or posteriorly, from short or long; fertilization ducts arising from the posterior part of spermathecae.
The genus is known from subtropics in south China (Sichuan, Anhui, Guizhou, and Jiangxi provinces). Habitats of these spiders are not very diverse, usually found in woody debris, among tree roots on the ground, in humus, and under stones or tree bark.
T. defossa Xu & Li, 2006 (♂♀; Sichuan), T. distalis Zhang, Zhu & Wang, 2017 (♀; Guizhou), T. eburniformis Wang & Yin, 1992 (♀; Hubei), T. jinggangensis K. Liu & X. Xu, sp. nov. (♀; Jiangxi), T. lyrata (Wang, Yin, Peng & Xie, 1990) (♀; Hunan), T. makros Wang, 2003 (♂; Guizhou), T. mopanensis Zhang, Zhu & Wang, 2017 (♂♀; Guizhou), T. rostrum Jiang, Chen & Zhang, 2018 (♂♀; Guizhou), T. subyanlingensis K. Liu & X. Xu, sp. nov. (♂♀; Jiangxi), T. tautispina (Wang, Yin, Peng & Xie, 1990) (♀; Jiangxi), T. truculenta Wang & Yin, 1992 (♂♀; Hunan, Hubei, Guizhou, Sichuan), T. variegata (Wang, Yin, Peng & Xie, 1990) (♂♀; Anhui), and T. yanlingensis (♀; Hunan).
Males (males of T. distalis, T. eburniformis, T. jinggangensis sp. nov., T. lyrata, T. tautispina and T. yanlingensis are unknown)
1 | Cymbial furrow less than half of cymbial length (see |
2 |
– | Cymbial furrow more than half of the cymbial length (Fig. |
4 |
2 | Patellar apophysis shorter than patella (see |
3 |
– | Patellar apophysis as long or longer than patella (see |
6 |
3 | Ventrolateral tibial apophysis not extending beyond the distal end of tibia (see |
T. defossa |
– | Ventrolateral tibial apophysis extending beyond the distal end of tibia (Fig. |
4 |
4 | Retrolateral tibial apophysis large and strong, longer than half of tibia (Figs |
T. subyanlingensis sp. nov. |
– | Retrolateral tibial apophysis small, less than half length of tibia (see |
5 |
5 | Retrolateral tibial apophysis arising from the base of tibia (see |
T. makros |
– | Retrolateral tibial apophysis arising from the middle part of tibia (see |
6 |
6 | Conductor with posterior lobe (see |
T. truculenta |
– | Conductor without lobe (see |
7 |
7 | Tip of conductor bifurcated (see |
T. rostrum |
– | Tip of conductor not bifurcated (see |
7 |
8 | Tip of dorsal apophysis of conductor close to median apophysis of tegulum (see |
T. variegata |
– | Tip of dorsal apophysis of conductor separated with median apophysis of tegulum (see |
T. mopanensis |
Females (female of T. makros is unknown)
1 | Atrium located anteriorly | T. defossa |
– | Atrium located posteriorly or medially | 2 |
2 | Epigynal teeth basally fused | T. truculenta |
– | Epigynal teeth slightly separated | 3 |
3 | Spermathecal heads located antero-laterally | T. lyrata |
– | Spermathecal heads located medially or posteriorly | 4 |
4 | Spermathecae coiled | T. mopanensis |
– | Spermathecae sac-shaped, round or tube-shaped | 5 |
5 | Spermathecae separated by their width | T. distalis |
– | Spermathecae, separated by less than radius | 6 |
6 | Spermathecal heads extending from median to anterior vulva | T. eburniformis |
– | Spermathecal heads not extending median to anterior vulva | 7 |
7 | Copulatory ducts strongly expanded anteriorly | 8 |
– | Copulatory ducts not anteriorly expanded | 9 |
8 | Spermathecal heads arising from median part of spermatheca | T. variegata |
– | Spermathecal heads arising from postero-lateral part of spermathecae | T. tautispina |
9 | Spermathecae kidney-shaped, with a light constriction | T. rostrum |
– | Spermathecae oval or tube-shaped with strong constriction | 10 |
10 | Spermathecal heads very long, tapering anteriorly | T. jinggangensis sp. nov. |
– | Spermathecal heads relatively short, not tapering anteriorly | 11 |
11 | Copulatory ducts extending along the lateral part of spermathecae; sspermathecae close to each other | T. yanlingensis |
– | Copulatory ducts not extending along the lateral part of spermathecae; spermathecae, separated by less than each half width | T. subyanlingensis sp. nov. |
Holotype ♀; China: Jiangxi Province, Ji’an City, Jinggangshan County Level City, Luofu Town, Pingtou Village, Jinggang Mountain National Nature Reserve, Changguling Forest Farm; 26°38'28"N, 114°14'6"E, 583 m; 5.X.2014; Ke-ke Liu et al. leg.
The specific name refers to the type locality; adjective.
The female of this species is similar to that of T. yanlingensis but differs by the long horn-shaped epigynal teeth (vs short, bell-shaped in T. yanlingensis), the widened posterior part of atrium (vs narrowed in T. yanlingensis) and the slender spermathecal heads (vs relatively short and curved in T. yanlingensis) (Figs
Female. Habitus as in Figure
Carapace brown. Chelicerae red brown. Endites, labium, and sternum yellow-brown. Legs yellow-brown. Abdomen dark brown, dorsally with 2 pairs of yellow-brown spots from antero-median to middle and 4 yellow-brown chevron-like stripes in posterior half.
Epigyne
(Figs
Tonsilla jinggangensis sp. nov., female holotype A epigyne, ventral view B vulva, dorsal view. Scale bars: 0.5 mm. Abbreviations: At – atrium, CD – copulatory duct, CO – copulatory opening, EH – epigynal hood, ET – epigynal teeth, FD – fertilization ducts, SH – spermathecal heads, Spe – spermathecae.
Known only from the type locality in Jiangxi Province, China (Fig.
Although we have only the female of this species, we are convinced that it is not conspecific with T. makros a species known from Guizhou. The male of T. makros (6.20) is slightly larger than half of the female of T. jinggangensis sp. nov. (11.03). Tonsilla species seem to have a narrow distribution, except for T. truculenta from south China. Tonsilla jinggangensis sp. nov. and T. tautispina from Jiangxi are more similar to species from Hunan, such as T. lyrata and T. yanlingensis, than species from Guizhou (T. makros, T. mopanensis). Hence, the male palp of this species may have a stout patellar apophysis.
Holotype ♂; China: Jiangxi Province, Ji’an City, Jinggangshan County Level City, Ciping Town, Wuzhi Peak Scenic Spot; 26°31'59.07"N, 114°08'28.47"E, 735 m; 2.X.2018; Ke-ke Liu et al. leg. Paratypes: 2 ♀; same data as holotype; 1 ♀; same locality, Dajing Village; 26°33'50.4"N, 114°07'26.4"E, 930 m; 19.X.2014; Ke-ke Liu et al. leg.; 1 ♀; same locality; 26°34'12.89"N, 114°07'41.87"E, 950 m; 30.IX.2018; Ke-ke Liu et al. leg.; 1 ♀; same locality, Jingzhushan Scenic Spot; 26°31'33.37"N, 114°06'30.34"E, 786 m; 1.X.2018; Ke-ke Liu et al. leg.
The specific name refers to its similarity to T. yanlingensis (Zhang, Yin & Kim, 2000); adjective.
Females of the new species closely resemble T. yanlingensis by the heart-shaped, large atrium and wide epigynal teeth, but can be distinguished by the spermathecae separated by less than 1/5 of their width (vs touching each other in T. yanlingensis), long and broad copulatory ducts along with the spermathecae (vs very short in T. yanlingensis), the slightly procurved spermathecal heads located at posterior part of spermatheca (Figs
Male (Holotype). Habitus as in Figures
Tonsilla subyanlingensis sp. nov., male holotype A habitus, dorsal view B same, ventral view C palp, prolateral view D same, ventral view E same, retrolateral view. Scale bars: 2 mm (A, B), 1 mm (C–E). Abbreviations: BLC – basal lamella of conductor, CF – cymbial furrow, Con – conductor, DAC – dorsal apophysis of conductor, Em – embolus, ET – epigynal teeth, MA – median apophysis, RTA – retrolateral tibial apophysis, PA – patellar apophysis, VTA – ventrolateral tibial apophysis.
Carapace dark brown. Chelicerae dark brown. Endites and labium dark yellow-brown. Sternum and legs yellow-brown. Abdomen dark brown with 5 pairs of yellow-brown spots on posterior half.
Palp
(Figs
Female (Paratype). Habitus as in Figures
Tonsilla subyanlingensis sp. nov., female paratype A habitus, dorsal view B same, ventral view C epigyne, ventral view D vulva, dorsal view. Scale bars: 2 mm (A, B), 0.5 mm (C, D). Abbreviations: At – atrium, CD – copulatory duct, CO – copulatory opening, EH – epigynal hood, ET – epigynal teeth, FD – fertilization ducts, SH – spermathecal heads, Spe – spermathecae.
SEM images of Tonsilla subyanlingensis sp. nov., male holotype and female paratype A palp, prolateral view B same, ventral view C same, detail of conductors, ventral view D same, detail of embolus, ventral view E same, retrolateral view F same, detail of patellar apophysis, retrolateral tibial apophysis and lateral tibial apophysis, retrolateral view G same, detail of conductor dorsal apophysis, retrolateral view H epigyne, dorsal view I vulva, ventral view.
Lighter than male. Abdomen, dorsally with four indistinct yellow-brown chevron-like stripes on posterior half.
Epigyne
(Figs
Tonsilla subyanlingensis sp. nov., male holotype and female paratype A male palp, prolateral view B same, ventral view C same, retrolateral view D epigyne, ventral view E vulva, dorsal view. Scale bars: 1 mm. Abbreviations: At – atrium, BLC – basal lamella of conductor, CD – copulatory duct, CF – cymbial furrow, CO – copulatory opening, Con – conductor, DAC –dorsal apophysis of conductor, EH – epigynal hood, Em – embolus, ET – epigynal teeth, FD – fertilization ducts, MA – median apophysis, PA – patellar apophysis, RTA – retrolateral tibial apophysis, SH – spermathecal heads, Spe – spermathecae, VTA – ventrolateral tibial apophysis.
We are grateful to Wen Sun, Ze-yuan Meng, Lei Zhang, Jian-yun Wen, and Tian-ming Wang (all from Ji’an, China) for collecting the specimens. We also thank Nathalie Yonow (Swansea, Wales) for improving the English of the manuscript. Facundo Labarque, Alireza Zamani (Turku, Finland), Kadir B. Kunt (Turku, Finland), and Yuri Marusik (Magadan, Russia) made valuable comments on a previous draft of this manuscript. This study was supported by the Science and Technology Foundation of Jiangxi Provincial Department of Education (GJJ160753), the Natural Science Foundation of Jiangxi Province (20181BAB214008), and the Natural Science Foundation of China (31560592/31772423).