taxonID	type	description	language	source
7CE30421DCC15A2F93C32F8ACA55333F.taxon	diagnosis	Diagnosis. The new genus differs from Labialithus Kamura, 2021 (see Kamura 2021: figs 9 F-J, 10 B, C) by the small PME with indistinct black pigment around the eye cup (vs large PME with clear pigment around the eye cup in Labialithus) (Figs 1 D, 4 C, 6 D, 11 D), the femora I with one dorsal spine (vs absent in Labialithus) and three prolateral spines (vs one in Labialithus) (Figs 1 F, 4 F, 6 F, 8 A, 11 F) and the metatarsi III-IV lacking ventral spines (vs usually with two pairs in Labialithus), the male scutum covering nearly 1 / 2 of abdomen (vs more than 2 / 3 in Labialithus) and by the palpal tibia with a dorsal apophysis (vs absent in Labialithus). It can be separated from Otacilia (see Wang et al. 2015: fig. 14 A; Liu et al. 2022: suppl. 2, figs 72, 74, 75, 77 - 79, 81, 82, 84, 85, 87, 88, 90, 91, 93 - 96, 98, 99, 101 - 105, 107 - 109, 111, 113, 114, 116 - 118, 120, 124, 137, 141) by the light abdomen lacking dark stripes (vs present in Otacilia) (Figs 1 A, 4 A, 6 A, 11 A), femora II lacking prolateral spine (in most specimens) or with one prolateral spine (in the few specimens) (vs 2 - 4 spines in Otacilia) (Figs 1 G, 4 G, 6 G, 8 C, 11 G), the palpal femur with a weakly protruded ventral apophysis (vs moderately or strongly protruded in Otacilia) (Figs 2, 3, 9, 10) and the small, short embolus (vs relatively large hook-shaped or spine-like embolus) (Figs 2, 3, 9, 10). Male of this genus can be easily distinguished from Phrurolithus (see Wang et al. 2015: fig. 15 C-E; Zamani and Marusik 2020: figs 4 A-C, E, F, 7 A-E) by the scutum covering nearly 1 / 2 of abdomen (vs nearly entire abdomen in Phrurolithus) (Figs 1 A, 6 A) and by the palpal tibia with a dorsal apophysis (vs absent Phrurolithus) (Figs 2 D, 3 H, 9 E, 10 I). Females of this genus can be separated from the genus Labialithus by the very small, widely separated copulatory openings without atrium (vs relatively large, slightly separated copulatory openings with distinct atrium) (Figs 5, 12). Furthermore, Edelithus spp. differ from some phrurolithid genera by the tarsal claws lacking tooth (Fig. 8 B, D, I), while present in Acrolithus and Aculithus Liu & Li, 2022 with three teeth, in Alboculus with two teeth, and in Grandilithus and Otacilia with four teeth (see Liu et al. 2020 a: fig. 5 J; Liu et al. 2022: figs 4 C, D, G, H, L, P, 38 D, E, H, K, O, 122 B, C, E, I, M), but in Phrurolithus only with degenerated and inconspicuous blunt teeth (Ramirez 2014: fig. 75 E).	en	Liu, Keke, Ying, Yuanhao, Li, Shuqiang (2022): One new genus and two new species of the spider family Phrurolithidae (Arachnida, Araneae) from Xishuangbanna Tropical Botanical Garden, Southwest China. ZooKeys 1117: 71-94, DOI: http://dx.doi.org/10.3897/zookeys.1117.89211, URL: http://dx.doi.org/10.3897/zookeys.1117.89211
7CE30421DCC15A2F93C32F8ACA55333F.taxon	etymology	Etymology. The name is a combination of the first three letters of " edentatus " (referring to the tarsal claws lacking tooth) and the latter half of Phrurolithus. The gender is masculine.	en	Liu, Keke, Ying, Yuanhao, Li, Shuqiang (2022): One new genus and two new species of the spider family Phrurolithidae (Arachnida, Araneae) from Xishuangbanna Tropical Botanical Garden, Southwest China. ZooKeys 1117: 71-94, DOI: http://dx.doi.org/10.3897/zookeys.1117.89211, URL: http://dx.doi.org/10.3897/zookeys.1117.89211
7CE30421DCC15A2F93C32F8ACA55333F.taxon	description	Description. Small, body length 1.0 - 2.5. Eyes (Figs 1 D, 4 C, 6 D, 7 A, 11 D): AER straight and PER procurved in dorsal view, AME clearly smaller than other eyes, PME with indistinct black pigment around eye cups, smaller than ALE and PLE, nearly separated by their diameter. Chelicera (Figs 1 D, 4 A, 6 D, 7 A, B, 11 D) with one frontal strong spine, three promarginal and two retromarginal teeth. Legs without annulations and stripes. Femora I-IV with one dorsal spine each (Figs 1 F, G, 4 F, G, 6 F, G, 8 A, C, 11 F, G), femur I with three prolateral spines, and femur II with one prolateral spine or none, tibiae I and II with six pairs of ventral spines; metatarsi I and II with tour pairs of ventral spines. Scutum (Figs 1 A, 6 A) covers nearly 1 / 2 of abdomen in males, but absent in females (Figs 4 A, 11 A). Male palp (Figs 2, 3, 9, 10): femur with a weak ventral extension; tibia with two well-developed apophyses, retrolateral apophysis very thick, as long as or shorter than tibia, dorsal apophysis hook-shaped, shorter than the retrolateral one; tegulum with a leaf-shaped subdistal apophysis and a blunt retrolateral apophysis; embolus short, shorter than subdistal tegular apophysis, with a round sperm pore, touching subdistal tegular apophysis. Epigyne (Figs 5, 12) with a pair of small copulatory openings, located posteriorly or subposteriorly; median septum absent or located posteriorly; bursae large, covering nearly 1 / 2 of epigynal plate, anteriorly located.	en	Liu, Keke, Ying, Yuanhao, Li, Shuqiang (2022): One new genus and two new species of the spider family Phrurolithidae (Arachnida, Araneae) from Xishuangbanna Tropical Botanical Garden, Southwest China. ZooKeys 1117: 71-94, DOI: http://dx.doi.org/10.3897/zookeys.1117.89211, URL: http://dx.doi.org/10.3897/zookeys.1117.89211
7CE30421DCC15A2F93C32F8ACA55333F.taxon	distribution	Distribution. China (Yunnan Province).	en	Liu, Keke, Ying, Yuanhao, Li, Shuqiang (2022): One new genus and two new species of the spider family Phrurolithidae (Arachnida, Araneae) from Xishuangbanna Tropical Botanical Garden, Southwest China. ZooKeys 1117: 71-94, DOI: http://dx.doi.org/10.3897/zookeys.1117.89211, URL: http://dx.doi.org/10.3897/zookeys.1117.89211
FA7670D1A2AE5DB0A1D403511C9F1D19.taxon	description	Figs 1, 2, 3, 4, 5	en	Liu, Keke, Ying, Yuanhao, Li, Shuqiang (2022): One new genus and two new species of the spider family Phrurolithidae (Arachnida, Araneae) from Xishuangbanna Tropical Botanical Garden, Southwest China. ZooKeys 1117: 71-94, DOI: http://dx.doi.org/10.3897/zookeys.1117.89211, URL: http://dx.doi.org/10.3897/zookeys.1117.89211
FA7670D1A2AE5DB0A1D403511C9F1D19.taxon	materials_examined	Material examined. Holotype ♂ (Phu- 147), 21 ° 54.607 ' N, 101 ° 17.005 ' E, elevation ca 633 m, XTBG, Menglun Township, Mengla County, Xishuangbanna, Yunnan Province, China, 4 - 11. IV. 2007, G. Zheng leg. Paratypes 1 ♂, 2 ♀, the same data as holotype; 1 ♀, 4 - 11. IV. 2007, other data as holotype (JSIII- 2 - 18); 1 ♀, 10 - 20. VI. 2007, other data as holotype (JSIII- 1 - 20); 1 ♀, 1 - 15. VIII. 2007, other data as holotype (JSIII- 3 - 23); 3 ♂, 16 - 31. III. 2007, other data as holotype (JSIII- 5 - 16); 1 ♀, 10 - 20. VI. 2007, other data as holotype (JSIII- 2 - 20); 1 ♀, 16 - 31. V. 2007, other data as holotype (JSIII- 1 - 20); 2 ♂, 1 - 15. IV. 2007, other data as holotype (JSIII- 5 - 17); 5 ♂, 1 ♀, 1 - 15. IV. 2007, other data as holotype (JSIII- 2 - 17); 2 ♂, 1 - 15. IV. 2007, other data as holotype (JSIII- 4 - 17); 3 ♂, 2 juveniles, 1 - 15. IV. 2007, other data as holotype (JSIII- 3 - 17); 1 ♀, 19 - 26. V. 2007, other data as holotype (JSIII- 2 - 17); 1 ♀, 16 - 31. VI. 2007, other data as holotype (JSIII- 5 - 22); 3 ♀, 16 - 31. IV. 2007, other data as holotype (JSIII- 5 - 18); 2 ♀, 4 - 11. V. 2007, other data as holotype (JSIII- 3 - 18); 1 ♀, 4 - 11. V. 2007, other data as holotype (JSIII- 1 - 19); 1 ♀, 19 - 26. V. 2007, other data as holotype (JSIII- 2 - 17); 3 ♀, 16 - 31. IV. 2007, other data as holotype (JSIII- 3 - 22); 1 ♀, 4 - 11. V. 2007, other data as holotype (JSIII- 1 - 18); 1 ♀, 19 - 26. IV. 2007, other data as holotype (JSIII- 3 - 17); 1 ♀, 1 - 15. V. 2007, other data as holotype (JSIII- 5 - 19); 1 ♀, 10 - 20. VI. 2007, other data as holotype (JSIII- 3 - 20); 1 ♂, 16 - 31. IV. 2007, other data as holotype (JSIII- 4 - 18); 1 ♀, 16 - 31. V. 2007, other data as holotype (JSIII- 3 - 20); 1 ♀, 19 - 26. IV. 2007, other data as holotype (JSIII- 4 - 17); 2 ♀, 19 - 26. V. 2007, other data as holotype (JSIII- 2 - 19); 6 ♂, 1 ♀, 16 - 31. IV. 2007, other data as holotype (JSIII- 1 - 18); 1 ♀, 19 - 26. V. 2007, other data as holotype (JSIII- 4 - 19); 6 ♂, 1 ♀, 16 - 31. III. 2007, other data as holotype (JSIII- 1 - 16); 3 ♂, 16 - 31. III. 2007, other data as holotype (JSIII- 1 - 16); 2 ♂, 16 - 31. III. 2007, other data as holotype (JSIII- 3 - 16); 1 ♀, 1 - 15. V. 2007, other data as holotype (JSIII- 2 - 19); 1 ♀, 19 - 25. XI. 2007, other data as holotype (JSIII- 3 - 03); 4 ♂, 2 ♀, 1 - 15. IV. 2007, other data as holotype (JSIII- 1 - 17); 2 ♂, 1 - 15. III. 2007, other data as holotype (JSIII- 3 - 15); 1 ♂, 16 - 31. IV. 2007, other data as holotype (JSIII- 3 - 18); 1 ♂, 1 ♀, 16 - 31. IV. 2007, other data as holotype (JSIII- 2 - 18); 2 ♀, 16 - 31. VI. 2007, 21 ° 55.428 ' N, 101 ° 16.441 ' E, elevation ca 598 m, other data as holotype (CZI- 3 - 22); 1 ♀, 16 - 31. VI. 2007, other data as holotype (CZI- 5 - 22); 1 ♀, 16 - 31. VI. 2007, other data as holotype (CZI- 2 - 22); 4 ♂, 16 - 31. VI. 2007, 21 ° 54.984 ' N, 101 ° 16.982 ' E, elevation ca 656 m, other data as holotype (JSIII- 5 - 18); 1 ♀, 4 - 11. V. 2007, other data as previous (JSII- 3 - 18); 1 ♀, 10 - 20. VI. 2007, other data as previous (JSII- 2 - 20); 1 ♀, 16 - 31. VI. 2007, other data as previous (JSIII- 4 - 18); 2 ♂, 1 - 15. III. 2007, other data as previous (JSII- 5 - 15); 1 ♀, 1 - 15. V. 2007, other data as previous (JSII- 2 - 19); 3 ♀, 4 - 11. IV. 2007, other data as previous (JSII- 2 - 16); 5 ♂, 19 - 26. III. 2007, other data as previous (JSII- 4 - 15); 7 ♂, 1 - 15. IV. 2007, other data as previous (JSII- 2 - 17); 2 ♀, 1 - 15. V. 2007, other data as previous (JSII- 5 - 19); 4 ♂, 16 - 31. III. 2007, other data as previous (JSII- 4 - 16); 2 ♂, 1 - 15. III. 2007, other data as previous (JSII- 1 - 15); 2 ♀, 19 - 26. V. 2007, other data as previous (JSII- 4 - 19); 2 ♂, 16 - 31. III. 2007, other data as previous (JSII- 5 - 16); 2 ♂, 1 - 15. IV. 2007, other data as previous (JSII- 4 - 17); 6 ♂, 2 ♀, 16 - 31. IV. 2007, other data as previous (JSII- 3 - 18); 3 ♂, 1 - 15. IV. 2007, other data as previous (JSII- 1 - 17); 2 ♀, 4 - 11. V. 2007, other data as previous (JSII- 2 - 18); 1 ♀, 16 - 31. IV. 2007, other data as previous (JSII- 5 - 22); 3 ♀, 4 - 11. V. 2007, other data as previous (JSII- 4 - 18); 1 ♀, 19 - 26. V. 2007, other data as previous (JSII- 1 - 19); 2 ♀, 1 - 15. V. 2007, other data as previous (JSII- 1 - 19); 2 ♀, 16 - 31. IV. 2007, other data as previous (JSII- 4 - 22); 6 ♂, 16 - 31. III. 2007, other data as previous (JSII- 1 - 16); 2 ♂, 1 ♀, 16 - 31. IV. 2007, other data as previous (JSII- 2 - 18); 4 ♂, 16 - 31. III. 2007, other data as previous (JSII- 3 - 16); 6 ♂, 1 - 15. IV. 2007, other data as previous (JSII- 3 - 17); 3 ♀, 19 - 26. IV. 2007, other data as previous (JSII- 4 - 17); 2 ♀, 4 - 16. IV. 2007, other data as previous (JSII- 4 - 16); 1 ♀, 10 - 20. VI. 2007, other data as previous (JSII- 4 - 20); 1 ♀, 16 - 31. V. 2007, other data as previous (JSII- 3 - 20); 3 ♂, 1 ♀, 1 - 15. IV. 2007, other data as previous (JSII- 5 - 17); 1 ♀, 16 - 31. V. 2007, other data as previous (JSII- 5 - 20); 1 ♀, 19 - 26. IV. 2007, other data as previous (JSII- 1 - 17); 1 ♀, 19 - 26. IV. 2007, other data as previous (JSII- 2 - 17); 5 ♂, 16 - 31. III. 2007, other data as previous (JSII- 2 - 16); 3 ♀, 1 - 15. VI. 2007, other data as previous (JSII- 5 - 21); 1 ♀, 1 - 15. VII. 2007, other data as previous (JSII- 5 - 23); 2 ♀, 1 - 15. VI. 2007, other data as previous (JSII- 3 - 21); 1 ♀, 1 - 15. VI. 2007, other data as previous (JSII- 2 - 21); 2 ♀, 1 - 15. VII. 2007, other data as previous (JSII- 2 - 23); 1 ♂, 16 - 31. III. 2007, 21 ° 54.718 ' N, 101 ° 16.940 ' E, elevation ca 645 m, other data as holotype (JSI- 4 - 16); 1 ♀, 19 - 26. IV. 2007, other data as previous (JSI- 3 - 17); 2 ♂, 1 - 15. III. 2007, other data as previous (JSI- 3 - 15); 1 ♂, 16 - 31. IV. 2007, other data as previous (JSI- 5 - 18); 4 ♂, 1 - 15. IV. 2007, other data as previous (JSI- 4 - 17); 4 ♀, 16 - 31. VII. 2007, other data as previous (JSI- 2 - 24); 2 ♂, 10 - 20. VI. 2007, other data as previous (JSI- 3 - 20); 2 ♀, 1 - 15. V. 2007, other data as previous (JSI- 2 - 19); 1 ♀, 1 - 15. IV. 2007, other data as previous (JSI- 4 - 21); 1 ♀, 10 - 20. IV. 2007, other data as previous (JSI- 1 - 20); 2 ♀, 1 - 15. VI. 2007, other data as previous (JSI- 2 - 21); 2 ♀, 1 - 15. VII. 2007, other data as previous (JSI- 2 - 23); 5 ♂, 16 - 31. III. 2007, other data as previous (JSI- 1 - 16); 1 ♂, 1 - 15. IV. 2007, other data as previous (JSI- 3 - 17); 2 ♀, 16 - 31. V. 2007, other data as previous (JSI- 5 - 20); 1 ♀, 16 - 24. X. 2007, other data as previous (JSI- 2 - 06); 3 ♂, 1 ♀, 16 - 31. V. 2007, other data as previous (JSI- 1 - 20); 1 ♀, 16 - 31. VII. 2007, other data as previous (JSI- 3 - 24); 1 ♀, 4 - 11. V. 2007, other data as previous (JSI- 2 - 18); 3 ♂, 1 - 15. IV. 2007, other data as previous (JSI- 5 - 17); 1 ♀, 16 - 31. VII. 2007, other data as previous (JSI- 5 - 24); 2 ♂, 2 ♀, 19 - 26. IV. 2007, other data as previous (JSI- 4 - 17); 1 ♀, 4 - 11. V. 2007, other data as previous (JSI- 3 - 18); 2 ♂, 1 - 15. III. 2007, other data as previous (JSI- 2 - 15); 1 ♂, 2 ♀, 16 - 31. V. 2007, other data as previous (JSI- 4 - 20); 1 ♀, 1 - 15. V. 2007, other data as previous (JSI- 5 - 19); 2 ♀, 4 - 11. IV. 2007, other data as previous (JSI- 1 - 16); 1 ♀, 19 - 26. IV. 2007, other data as previous (JSI- 2 - 17); 1 ♀, 19 - 26. V. 2007, other data as previous (JSI- 3 - 19); 1 ♂, 1 ♀, 16 - 31. V. 2007, other data as previous (JSI- 2 - 20); 1 ♀, 10 - 20. VI. 2007, other data as previous (JSI- 4 - 20); 1 ♀, 19 - 26. V. 2007, other data as previous (JSI- 2 - 19); 1 ♂, 1 ♀, 1 - 15. V. 2007, other data as previous (JSI- 1 - 19); 1 ♀, 4 - 11. IV. 2007, other data as previous (JSI- 2 - 16); 1 ♀, 10 - 20. VI. 2007, other data as previous (JSI- 2 - 20); 1 ♀, 16 - 31. IV. 2007, other data as previous (JSI- 4 - 18); 6 ♂, 1 ♀, 16 - 31. IV. 2007, other data as previous (JSI- 3 - 18); 5 ♂, 4 ♀, 16 - 31. IV. 2007, other data as previous (JSI- 2 - 18); 8 ♂, 16 - 31. III. 2007, other data as previous (JSI- 2 - 16); 4 ♂, 1 - 15. IV. 2007, other data as previous (JSI- 1 - 17); 5 ♂, 1 ♀, 16 - 31. III. 2007, other data as previous (JSI- 3 - 16); 10 ♂, 2 ♀, 1 - 15. IV. 2007, other data as previous (JSI- 2 - 17); 1 ♂, 16 - 31. V. 2007, other data as previous (JSI- 3 - 30); 1 ♀, 19 - 26. V. 2007, other data as previous (JSI- 4 - 19); 2 ♂, 2 ♀, 16 - 31. IV. 2007, other data as previous (JSI- 1 - 18).	en	Liu, Keke, Ying, Yuanhao, Li, Shuqiang (2022): One new genus and two new species of the spider family Phrurolithidae (Arachnida, Araneae) from Xishuangbanna Tropical Botanical Garden, Southwest China. ZooKeys 1117: 71-94, DOI: http://dx.doi.org/10.3897/zookeys.1117.89211, URL: http://dx.doi.org/10.3897/zookeys.1117.89211
FA7670D1A2AE5DB0A1D403511C9F1D19.taxon	etymology	Etymology. The specific name refers to a famous tea from Xishuangbanna, Pu'er tea, which is planted on the mountainsides of Xishuangbanna and has a long history in China; noun in apposition.	en	Liu, Keke, Ying, Yuanhao, Li, Shuqiang (2022): One new genus and two new species of the spider family Phrurolithidae (Arachnida, Araneae) from Xishuangbanna Tropical Botanical Garden, Southwest China. ZooKeys 1117: 71-94, DOI: http://dx.doi.org/10.3897/zookeys.1117.89211, URL: http://dx.doi.org/10.3897/zookeys.1117.89211
FA7670D1A2AE5DB0A1D403511C9F1D19.taxon	diagnosis	Diagnosis. The new species can be distinguished from E. shenmiguo sp. nov. (Figs 9, 10, 12) by the retrolateral tegular apophysis with bent apex (vs straight) and the very short embolus lacking spine-like tip (vs the relatively long embolus with a spine-like tip) in male palp (Figs 2, 3) and the triangular median septum (vs absent), the stout copulatory ducts (vs slender) and the C-shaped spermathecae (vs oval) in female epigyne (Fig. 5).	en	Liu, Keke, Ying, Yuanhao, Li, Shuqiang (2022): One new genus and two new species of the spider family Phrurolithidae (Arachnida, Araneae) from Xishuangbanna Tropical Botanical Garden, Southwest China. ZooKeys 1117: 71-94, DOI: http://dx.doi.org/10.3897/zookeys.1117.89211, URL: http://dx.doi.org/10.3897/zookeys.1117.89211
FA7670D1A2AE5DB0A1D403511C9F1D19.taxon	description	Description. Male (holotype). Habitus as in Fig. 1 A-C. Total length 1.95, carapace 0.99 long, 0.78 wide, abdomen 0.92 long, 0.65 wide. Eye sizes and interdistances (Fig. 1 A, D): AME 0.04, ALE 0.06, PME 0.05, PLE 0.06; AME-AME 0.03, AME-ALE 0.01, PME-PME 0.04, PME-PLE 0.04, AME-PME 0.05, AME-PLE 0.09, ALE-ALE 0.13, PLE-PLE 0.21, ALE-PLE 0.03; PME separated by slightly less than their diameters. MOA 0.14 long, frontal width 0.11, posterior width 0.13. Chelicerae (Fig. 1 B, D, E) with three promarginal (median largest, distal smallest) and two retromarginal teeth (distal larger). Endites (Fig. 1 B, E) slightly oblique, brush shaped, anterolateral area of endite with row of thick serrula and six long, thick setae. Labium wider than long, anteriorly with 10 - 12 setae. Sternum (Fig. 1 E), longer than wide, lateral margin thickened, with weak precoxal triangles and lacking intercoxal extensions, posteriorly triangular, blunt end. Legs (Fig. 1): measurements: I 3.29 (0.90, 0.35, 0.84, 0.76, 0.44); II 3.85 (0.73, 0.48, 0.97, 0.99, 0.68); III 2.53 (0.66, 0.32, 0.48, 0.60, 0.47); IV 3.74 (0.96, 0.37, 0.84, 0.95, 0.62); spination: femora I d 1, pv 111, II d 1, III d 1, IV d 1; tibiae I v 222222, II v 222221, metatarsi I v 2221, II v 2221. Scutum (Fig. 1 A) nearly covering 1 / 2 of abdomen. Colouration (Fig. 1 A-C). Carapace yellow, with radial, irregular light yellow-brown stripes submarginally and arc-shaped dark stripes around margin. AME, ALE and PLE with dark layer of black pigment around the eye cup, but PME absent. Chelicerae, endites, and labium yellow. Sternum yellow, mottled around margin. Legs yellow, without dark stripes. Abdomen yellow-brown, mottled, with dark brown net-shaped stripes; venter yellow. Palp (Figs 2, 3). Femoral apophysis weak, with shallow groove and one strong dorsal spine near distal femur. Retrolateral tibial apophysis large, thick, finger-like, longer than tibia. Dorsal tibial apophysis longer than 1 / 2 length of retrolateral tibial apophysis, with broad base and a small hook-shaped tip, subdistal part with a strong constriction. Sperm duct V-shaped, reaching subposterior part of tegulum. Distal tegular apophysis lamellate, membranous, touching the base of embolus, covered by subdistal tegular apophysis in ventral view. Subdistal tegular apophysis gramineous leaf-shaped, membranous, slightly less than 1 / 2 of tegular length. Embolus very short, horn-like, less than 1 / 3 length of subdistal tegular apophysis, covered by subdistal tegular apophysis. Sperm opening round, located in subapical part. Female. Habitus as in Fig. 4. Total length 2.21, carapace 0.92 long, 0.75 wide, abdomen 1.27 long, 0.83 wide. As in male, except as noted. Eye sizes and interdistances (Fig. 4 A, D): AME 0.04, ALE 0.07, PME 0.04, PLE 0.06, AME-AME 0.02, AME-ALE 0.01, PME-PME 0.06, PME-PLE 0.04, AME-PME 0.04, AME-PLE 0.09, ALE-ALE 0.12, PLE-PLE 0.20, ALE-PLE 0.03. MOA 0.12 long, frontal width 0.10, posterior width 0.13. Leg (Fig. 4 A, B) measurements: I 4.05 (1.07, 0.48, 1.04, 0.95, 0.51); II 2.61 (0.67, 0.35, 0.54, 0.60, 0.45); III 2.37 (0.63, 0.29, 0.45, 0.57, 0.43); IV 3.41 (0.89, 0.37, 0.74, 0.89, 1.060.52). Leg spination (Fig. 4): tibiae II v 22222, metatarsi I v 2222, II v 2222. Colouration (Fig. 4 A, B). Lighter than male. Epigyne (Fig. 5). Epigynal plate slightly longer than wide, subposterolaterally with pair of round copulatory openings, posteriorly with triangular median septum. Copulatory ducts short and thick, slghtly shorter than spermathecae. Bursae large round, touching, covering nearly 1 / 2 of epigynal plate. Glandular appendages short, transversal, directed laterally, less than the length of copulatory ducts. Connecting tubes very short, nearly as long as glandular appendages. Spermathecae nearly C-shaped, widely separated by median septum. Fertilization ducts short, located posteriorly on spermathecae, directed anterolaterally.	en	Liu, Keke, Ying, Yuanhao, Li, Shuqiang (2022): One new genus and two new species of the spider family Phrurolithidae (Arachnida, Araneae) from Xishuangbanna Tropical Botanical Garden, Southwest China. ZooKeys 1117: 71-94, DOI: http://dx.doi.org/10.3897/zookeys.1117.89211, URL: http://dx.doi.org/10.3897/zookeys.1117.89211
FA7670D1A2AE5DB0A1D403511C9F1D19.taxon	distribution	Distribution. Known only from the type locality in Yunnan Province, China.	en	Liu, Keke, Ying, Yuanhao, Li, Shuqiang (2022): One new genus and two new species of the spider family Phrurolithidae (Arachnida, Araneae) from Xishuangbanna Tropical Botanical Garden, Southwest China. ZooKeys 1117: 71-94, DOI: http://dx.doi.org/10.3897/zookeys.1117.89211, URL: http://dx.doi.org/10.3897/zookeys.1117.89211
98D606520B6F52BC9A7B159B69C2249F.taxon	description	Figs 6, 7, 8, 9, 10, 11, 12	en	Liu, Keke, Ying, Yuanhao, Li, Shuqiang (2022): One new genus and two new species of the spider family Phrurolithidae (Arachnida, Araneae) from Xishuangbanna Tropical Botanical Garden, Southwest China. ZooKeys 1117: 71-94, DOI: http://dx.doi.org/10.3897/zookeys.1117.89211, URL: http://dx.doi.org/10.3897/zookeys.1117.89211
98D606520B6F52BC9A7B159B69C2249F.taxon	etymology	Etymology. The specific name refers to the Chinese name of Synsepalum dulcificum (Schumach. & Thonn.) Daniell, 1852, Edelithus shenmiguo, which was introduced to XTBG from Ghana; noun in apposition.	en	Liu, Keke, Ying, Yuanhao, Li, Shuqiang (2022): One new genus and two new species of the spider family Phrurolithidae (Arachnida, Araneae) from Xishuangbanna Tropical Botanical Garden, Southwest China. ZooKeys 1117: 71-94, DOI: http://dx.doi.org/10.3897/zookeys.1117.89211, URL: http://dx.doi.org/10.3897/zookeys.1117.89211
98D606520B6F52BC9A7B159B69C2249F.taxon	diagnosis	Diagnosis. The new species can be distinguished from E. puer sp. nov. (Figs 2, 3, 5) by the ridge-shaped retrolateral tegular apophysis (vs bent) and the relatively long embolus with a spine-like tip (vs the very short embolus lacking spine-like tip) in male palp (Fig. 10 B, H), and the epigynal plate lacking median septum (vs present), the relatively long, thin copulatory duct (vs very short and thick) and the oval spermathecae (vs C-shaped) (Fig. 12) in female epigyne (Fig. 12).	en	Liu, Keke, Ying, Yuanhao, Li, Shuqiang (2022): One new genus and two new species of the spider family Phrurolithidae (Arachnida, Araneae) from Xishuangbanna Tropical Botanical Garden, Southwest China. ZooKeys 1117: 71-94, DOI: http://dx.doi.org/10.3897/zookeys.1117.89211, URL: http://dx.doi.org/10.3897/zookeys.1117.89211
98D606520B6F52BC9A7B159B69C2249F.taxon	description	Description. Male (holotype). Habitus as in Fig. 6 A-C. Total length 1.93, carapace 1.03 long, 0.82 wide, abdomen 1.00 long, 0.70 wide. Eye sizes and interdistances (Fig. 6 A, D): AME 0.04, ALE 0.06, PME 0.05, PLE 0.06, AME-AME 0.03, AME-ALE 0.01, PME-PME 0.05, PME-PLE 0.03, AME-PME 0.04, AME-PLE 0.09, ALE-ALE 0.12, PLE-PLE 0.22, ALE-PLE 0.03. MOA 0.13 long, frontal width 0.10, posterior width 0.14. Chelicerae (Fig. 7) with three promarginal (median largest, distal smallest) and two retromarginal teeth (distal larger); promarginal and retromarginal escort setae present, longer than fang; promarginal cheliceral whisker setae in a line; promarginal rake setae in three lines, comb-shaped; promarginal and retromarginal base of fang with two slit sensilla. Endites (Fig. 6 E, 7 B) slightly oblique, brush shaped, anterolateral area of endite with a row of thick serrula and a row of eight long and thick setae. Labium (Figs 6 E, 7 B) wider than long, anteriorly with 12 setae. Sternum (Fig. 6 E), longer than wide, laterally with weak precoxal triangles and lacking intercoxal extensions, posteriorly triangular, blunt end. Leg measurements (Figs 6, 8): I 3.29 (0.93, 0.38, 0.88, 0.73, 0.42); II 3.85 (0.76, 0.34, 0.59, 0.62, 0.44); III 2.53 (0.64, 0.28, 0.48, 0.61, 0.42); IV 3.74 (0.98, 0.36, 0.83, 0.92, 0. 54). Leg spination (Figs 6, 8): femora I d 1, pv 111, II d 1, III d 1, IV d 1; tibiae I v 222222, II v 222221; metatarsi I v 2221, II v 2221; metatarsi III and IV with conspicuous preening brushes, lyriform organs, and dorsal stoppers distally; tarsi with abundant scales, several long trichobothria dorsally, and several chemosensory setae on ventro-posterior tarsi and base of claws, slit sensillum located subdistally on dorsal part, oval, labium-shaped; inferior tarsal claw smooth without tooth, with a ventral scopula of tenent setae. Scutum (Fig. 6 A) nearly covering 1 / 2 of abdomen. Colouration (Fig. 6 A-E). Carapace yellow, with light yellow-brown spot in front of fovea, radial, irregular yellow-brown stripes submarginally and arc-shaped dark stripes around margin. AME, ALE and PLE with dark layer of black pigment around the eye cup, but PME absent. Chelicerae, endites, and labium yellow. Sternum yellow, mottled around margin. Legs yellow, without dark stripes. Abdomen yellow-brown, mottled, with three light yellow chevrons posteriorly and many yellow spots on surface; venter yellow. Palp (Figs 9, 10). Femoral apophysis weak, with shallow groove and one strong dorsal spine near distal femur. Retrolateral tibial apophysis large, thick, longer than tibia in retrolateral view, with blunt apex. Dorsal tibial apophysis shorter than retrolateral tibial apophysis, with a strong hook-shaped tip, submedial part with a strong constriction. Sperm duct U-shaped, reaching subposterior part of tegulum. Retrolateral tegular apophysis, arising from retrolateral tegulum, with two parts, one lamellate, transversely directed, touching the base of embolus, arising from retrolateral tegulum, the other ridge-like, anteriorly located in retrolateral view. Subdistal tegular apophysis fan-shaped, slightly less than 1 / 2 of tegular length. Embolus short, right-angled, with a spine-like tip, covered by subdistal tegular apophysis. Sperm pore round, located in the medial part of embolus, around the sharp turn, slightly less than the length of dorsal tibial apophysis. Female. Habitus as in Fig. 11 A-C. As in male, except as noted. Total length 2.20, carapace 0.99 long, 0.79 wide, abdomen 1.18 long, 0.92 wide. Eye sizes and interdistances (Fig. 11 D): AME 0.04, ALE 0.06, PME 0.04, PLE 0.06, AME-AME 0.01, AME-ALE 0.01, PME-PME 0.05, PME-PLE 0.04, AME-PME 0.04, AME-PLE 0.08, ALE-ALE 0.12, PLE-PLE 0.20, ALE-PLE 0.02. MOA 0.13 long, frontal width 0.10, posterior width 0.13. Leg measurements (Fig. 11): I 2.99 (0.77, 0.36, 0.79, 0.67, 0.40); II 2.60 (0.72, 0.34, 0.57, 0.56, 0.41); III 2.39 (0.62, 0.30, 0.46, 0.56, 0.45); IV 3.50 (0.91, 0.34, 0.78, 0.88, 0.59). Leg spination (Fig. 11): femora II lacking prolateral spine; tibiae I v 222221; metatarsi I v 2222. Colouration (Fig. 11 A-C). Lighter than male. Epigyne (Fig. 12). Epigynal plate longer than wide, posterolaterally with pair of slit-like copulatory openings. Copulatory ducts tube-shaped, longer than bursal diameter, submedially with a slight constriction. Bursae large oval, anteriorly located, slightly separated. Connecting tubes slender, less than length of copulatory ducts. Spermathecae oval, medially located, separated by half of their diameter. Spermathecal head parallel, posteromedially located, directed posteriorly, as long as spermathecal diameter, club-shaped. Fertilization ducts as long as spermathecal length, located at the center of spermathecae, directed laterally.	en	Liu, Keke, Ying, Yuanhao, Li, Shuqiang (2022): One new genus and two new species of the spider family Phrurolithidae (Arachnida, Araneae) from Xishuangbanna Tropical Botanical Garden, Southwest China. ZooKeys 1117: 71-94, DOI: http://dx.doi.org/10.3897/zookeys.1117.89211, URL: http://dx.doi.org/10.3897/zookeys.1117.89211
98D606520B6F52BC9A7B159B69C2249F.taxon	distribution	Distribution. Known only from the type locality in Yunnan Province, China.	en	Liu, Keke, Ying, Yuanhao, Li, Shuqiang (2022): One new genus and two new species of the spider family Phrurolithidae (Arachnida, Araneae) from Xishuangbanna Tropical Botanical Garden, Southwest China. ZooKeys 1117: 71-94, DOI: http://dx.doi.org/10.3897/zookeys.1117.89211, URL: http://dx.doi.org/10.3897/zookeys.1117.89211
