Morphology, molecular genetics, and acoustics reveal two new species of the genus Leptobrachella from northwestern Guizhou Province, China (Anura, Megophryidae)

Jian Wang; Yu-Long Li; Yao Li; Hong-Hui Chen; Ya-Jun Zeng; Jing-Min Shen; Ying-Yong Wang

doi:10.3897/zookeys.848.29181

Research Article

Morphology, molecular genetics, and acoustics reveal two new species of the genus Leptobrachella from northwestern Guizhou Province, China (Anura, Megophryidae)

Jian Wang^‡, Yu-Long Li^‡, Yao Li^‡, Hong-Hui Chen^‡, Ya-Jun Zeng^§, Jing-Min Shen^§, Ying-Yong Wang^‡

‡ Sun Yat-sen University, Guangzhou, China

§ Guizhou Academy of Forestry, Guizhou, China

Corresponding author: Ying-Yong Wang ( wangyy@mail.sysu.edu.cn )

Academic editor: Angelica Crottini

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: Wang J, Li Y-L, Li Y, Chen H-H, Zeng Y-J, Shen J-M, Wang Y-Y (2019) Morphology, molecular genetics, and acoustics reveal two new species of the genus Leptobrachella from northwestern Guizhou Province, China (Anura, Megophryidae). ZooKeys 848: 119-154. https://doi.org/10.3897/zookeys.848.29181

ZooBank: urn:lsid:zoobank.org:pub:F688F9C1-BD6E-4986-BD3E-9C219C4DF585

Abstract

Two new species of the genus Leptobrachella Smith, 1925, L. bijie J. Wang, Y.L. Li, Y. Li, H.H. Chen & Y.Y. Wang, sp. nov. and L. purpuraventra J. Wang, Y.L. Li, Y. Li, H.H. Chen & Y.Y. Wang, sp. nov., were described from northwestern Guizhou Province, China based on a combination of acoustic, molecular, and morphological data. The new discoveries bring the total number of this genus to 73, with 16 congeners recorded in China, and represent the second and third species of the genus reported from Guizhou Province.

Keywords

Acoustics, Leptobrachella bijie sp. nov., L. purpuraventra sp. nov., molecular phylogeny, morphology, taxonomy

Introduction

The Asian leaf litter toad genus Leptobrachella Smith, 1925 currently contains seventy-one species, widely distributed from southern China west to northeastern India and Myanmar, through mainland Indochina to peninsular Malaysia and the island of Borneo (Eto et al. 2018; Frost 2017; Nguyen et al. 2018; Rowley et al. 2016, 2017; Yang et al. 2016; Yuan et al. 2017). Currently, 14 species of this genus are known from China, i.e., L. alpinus from Yunnan and Guangxi provinces, L. laui from southern Guangdong Province including Hong Kong, L. liui from Fujian, Jiangxi, Guangdong, Guangxi, Hunan and Guizhou provinces, L. mangshanensis from southern Hunan Province, L. oshanensis from Gansu, Sichuan, Chongqing, Guizhou and Hubei provinces, L. cf. pelodytoides (which may be a population of L. eos (Ohler et al. 2011)), L. purpura, L. tengchongensis, L. ventripuntatus and L. yingjiangensis from Yunnan Province, L. wuhuangmontis from southern Guangxi Province, L. yunkaiensis from western GuangdongProvince, and L. sungi and L. maoershanensis from Guangxi Province (Hou et al. 2018; Sung et al. 2014; Wang et al. 2018; Yang et al. 2016; Yuan et al. 2017, Yang et al. 2018).

During recent field surveys in northwestern Guizhou Province of China in 2018, a number of specimens were collected from Zhaozishan Nature Reserve and Wujing Nature Reserve in Qixingguan District of Bijie City, respectively (Figure 1), which can be morphologically assigned to the genus Leptobrachella, based on the following characters: (1) small or moderate size, snout-vent length not greater than 60.0 mm, (2) rounded finger tips, the presence of an elevated inner palmar tubercle not continuous to the thumb, (3) presence of macroglands on body including supra-axillary, pectoral, femoral and ventrolateral glands, (4) vomerine teeth absent, (5) tubercles on eyelids present, and (6) anterior tip of snout with whitish vertical bar (Dubois 1983; Matsui 1997, 2006; Lathrop et al. 1998; Delorme et al. 2006; Das et al. 2010). Subsequent 16S rRNA sequences from these specimens revealed that these collections represent two distinct evolving lineages. Combine of morphological characters, acoustic data, and molecular divergences; they are described herein as two new species.

Figure 1.

Collection localities of the two new Leptobrachella species: 1 Jinjiazhai Village in Wujing Nature Reserve, the type locality of L. purpuraventra sp. nov. 2a Baimashan Forest Station in Zhaozishan Nature Reserve, the other collection site of L. purpuraventra sp. nov. 2b Qingshan Village in Zhaozishan Nature Reserve, the type locality of L. bijie sp. nov.

Material and methods

Sampling

For molecular analyses, a total of 71 sequences (23 muscle tissues were sequenced and 48 sequences downloaded from GenBank) from 32 species of the genus Leptobrachella were used, including two undescribed species from China, i.e., the populations from Zhaozishan Nature Reserve and Wujing Nature Reserve of Guizhou Province. And four sequences were downloaded from GenBank as outgroups (see Table 1; Pelobates syriacus, P. varaldii, Leptobrachium cf. chapaense, and Megophrys major).

Table 1.

Download as

CSV

XLSX

Localities and voucher data for all specimens used in this study.

ID	Species	Locality	voucher No.	GenBank No.
ID	Species	Locality	voucher No.	16S rRNA
1	Leptobrachella purpuraventra sp. nov.	China: Wujing Nature Reserve, Bijie City, Guizhou	SYS a007081	MK414517
2	Leptobrachella purpuraventra sp. nov.	China: Wujing Nature Reserve, Bijie City, Guizhou	SYS a007277/CIB 110003	MK414518
3	Leptobrachella purpuraventra sp. nov.	China: Wujing Nature Reserve, Bijie City, Guizhou	SYS a007278	MK414519
4	Leptobrachella purpuraventra sp. nov.	China: Wujing Nature Reserve, Bijie City, Guizhou	SYS a007279	MK414520
5	Leptobrachella purpuraventra sp. nov.	China: Wujing Nature Reserve, Bijie City, Guizhou	SYS a007280	MK414521
6	Leptobrachella purpuraventra sp. nov.	China: Wujing Nature Reserve, Bijie City, Guizhou	SYS a007282	MK414522
7	Leptobrachella purpuraventra sp. nov.	China: Wujing Nature Reserve, Bijie City, Guizhou	SYS a007283	MK414523
8	Leptobrachella purpuraventra sp. nov.	China: Wujing Nature Reserve, Bijie City, Guizhou	SYS a007284	MK414524
9	Leptobrachella purpuraventra sp. nov.	China: Zhaozishan Nature Reserve, Bijie City, Guizhou	SYS a007300	MK414525
10	Leptobrachella purpuraventra sp. nov.	China: Zhaozishan Nature Reserve, Bijie City, Guizhou	SYS a007301	MK414526
11	Leptobrachella purpuraventra sp. nov.	China: Zhaozishan Nature Reserve, Bijie City, Guizhou	SYS a007302	MK414527
12	Leptobrachella purpuraventra sp. nov.	China: Zhaozishan Nature Reserve, Bijie City, Guizhou	SYS a007303	MK414528
13	Leptobrachella purpuraventra sp. nov.	China: Zhaozishan Nature Reserve, Bijie City, Guizhou	SYS a007304	MK414529
14	Leptobrachella purpuraventra sp. nov.	China: Zhaozishan Nature Reserve, Bijie City, Guizhou	SYS a007305	MK414530
15	Leptobrachella purpuraventra sp. nov.	China: Zhaozishan Nature Reserve, Bijie City, Guizhou	SYS a007306	MK414531
16	Leptobrachella bijie sp. nov.	China: Zhaozishan Nature Reserve, Bijie City, Guizhou	SYS a007313/CIB 110002	MK414532
17	Leptobrachella bijie sp. nov.	China: Zhaozishan Nature Reserve, Bijie City, Guizhou	SYS a007314	MK414533
18	Leptobrachella bijie sp. nov.	China: Zhaozishan Nature Reserve, Bijie City, Guizhou	SYS a007315	MK414534
19	Leptobrachella bijie sp. nov.	China: Zhaozishan Nature Reserve, Bijie City, Guizhou	SYS a007316	MK414535
20	Leptobrachella bijie sp. nov.	China: Zhaozishan Nature Reserve, Bijie City, Guizhou	SYS a007317	MK414536
21	Leptobrachella bijie sp. nov.	China: Zhaozishan Nature Reserve, Bijie City, Guizhou	SYS a007318	MK414537
22	Leptobrachella bijie sp. nov.	China: Zhaozishan Nature Reserve, Bijie City, Guizhou	SYS a007319	MK414538
23	Leptobrachella bijie sp. nov.	China: Zhaozishan Nature Reserve, Bijie City, Guizhou	SYS a007320	MK414539
24	Leptobrachella aerea	Vietnam: Quang Binh	RH60165	JN848437
25	Leptobrachella applebyi	Vietnam: Kon Tum	AMS R 173778	KR018108
26	Leptobrachella applebyi	Vietnam: Kon Tum	AMS R 173635	KU530189
27	Leptobrachella bidoupensis	Vietnam: Lam Dong	AMS R 173133	HQ902880
28	Leptobrachella bidoupensis	Vietnam: Lam Dong	NCSM 77321	HQ902883
29	Leptobrachella bourreti	Vietnam: Lao Cai	AMS R 177673	KR018124
30	Leptobrachella eos	Lao: Phongsaly	MNHN: 2004.0278	JN848450
31	Leptobrachella firthi	Vietnam: Kon Tum	AMS R 176524	JQ739206
32	Leptobrachella fritinniens	Malaysia: Borneo	KUHE55371	AB847557
33	Leptobrachella gracilis	Malaysia: Borneo	KUHE55624	AB847560
34	Leptobrachella hamidi	Malaysia: Borneo	KUHE17545	AB969286
35	Leptobrachella heteropus	Malaysia: Peninsula	KUHE15487	AB530453
36	Leptobrachella isos	Vietnam: Gia Lai	VNMN A 2015.4 / AMS R 176480	KT824769
37	Leptobrachella laui	China: San zhoutian, Shenzhen	SYS a002540	MH055904
38	Leptobrachella laui	China: Mt. Wutong, Shenzhen	SYS a003477	MH605576
39	Leptobrachella liui	China: Mt. Wuyi, Fujian	SYS a002478	MH605573
40	Leptobrachella liui	China: Mt. Huanggang, Jiangxi	SYS a001620	KM014549
41	Leptobrachella mangshanensis	China: Mangshan, Hunan	MSZTC201702	MG132197
42	Leptobrachella mangshanensis	China: Mangshan, Hunan	MSZTC201703	MG132198
43	Leptobrachella marmorata	Malaysia: Borneo	KUHE53227	AB969289
44	Leptobrachella maura	Malaysia: Borneo	SP21450	AB847559
45	Leptobrachella macrops	Vietnam: Phu Yen Prov.	ZMMU-A5823	MG787993
46	Leptobrachella maoershanensis	China: Maoershan, Guangxi	KIZ019386	KY986931
47	Leptobrachella melica	Cambodia: Ratanakiri	MVZ258198	HM133600
48	Leptobrachella minima	Thailand: Chiangmai	/	JN848369
49	Leptobrachella nyx	/	ROM26828	MH055818
50	Leptobrachella oshanensis	China: Sichuan	SYSa001830	KM014810
51	Leptobrachella pallida	Vietnam: Lam Dong	UNS00511	KU530190
52	Leptobrachella picta	Malaysia: Borneo	UNIMAS 8705	KJ831295
53	Leptobrachella pluvialis	Vietnam: Lao Cai	MNHN:1999.5675	JN848391
54	Leptobrachella pururus	China: Yingjiang, Yunnan	SYS a006530	MG520354
55	Leptobrachella pyrrhops	Vietnam: Lam Dong	ZMMU A-5208	KP017575
56	Leptobrachella pyrrhops	Vietnam: Lam Dong	ZMMU A-4873 (ABV-00213)	KP017576
57	Leptobrachella sabahmontana	Malaysia: Borneo	BORNEENSIS 12632	AB847551
58	Leptobrachella tengchongensis	China: Tengchong County, Yunnan	SYS a004596	KU589208
59	Leptobrachella tengchongensis	China: Tengchong County, Yunnan	SYS a004598	KU589209
60	Leptobrachella ventripunctata	Laos: Phongsaly	MNHN 2005.0116	JN848410
61	Leptobrachella ventripunctata	China: Zhushihe, Xishuangbanna, Yunnan	SYS a001768	KM014811
62	Leptobrachella yingjiangensis	China: Yingjiang, Yunnan	SYS a006533	MG520350
63	Leptobrachella yunkaiensis	China: Dawuling Forest Station, Maoming City, Guangdong	SYS a004663	MH605584
64	Leptobrachella yunkaiensis	China: Dawuling Forest Station, Maoming City, Guangdong	SYS a004664 / CIB107272	MH605585
65	Leptobrachella wuhuangmontis	China: Mt. Wuhuang, Pubei County, Guangxi	SYS a003485	MH605577
66	Leptobrachella wuhuangmontis	China: Mt. Wuhuang, Pubei County, Guangxi	SYS a003486	MH605578
67	Leptobrachella zhangyapingi	Thailand: Chiang Mai	KJ-2013	JX069979
68	Leptobrachium cf. chapaense	Vietnam: Lao Cai	AMS R 171623	KR018126
69	Pelobates syriacus	/	MVZ234658	AY236807
70	Pelobates varaldii	/	/	AY236808
71	Megophrys major	Vietnam: Kon Tum	AMS R173870	KY476333

All specimens were fixed in 10 % buffered formalin and later transferred to 70 % ethanol for preservation, and deposited at the Museum of Biology, Sun Yat-sen University (SYS) and Chengdu Institute of Biology, the Chinese Academy of Sciences (CIB), China; tissue samples were preserved in 95% ethanol for molecular studies.

DNA Extraction, PCR and sequencing

DNA was extracted from muscle tissue using a DNA extraction kit from Tiangen Biotech (Beijing) Co., Ltd. The mitochondrial gene 16S ribosomal RNA gene (16S rRNA) fragment from each sample was sequenced. Fragments were ampliﬁed using primer pairs L3975 (5’-CGCCTGTTTACCAAAAACAT-3’) and H4551 (5’-CCGGTCTGAACTCAGATCACGT-3’) (Simon et al. 1994). PCR ampliﬁcations were performed in a 20 μl reaction volume with the following cycling conditions: an initial denaturing step at 95 °C for five min; 35 cycles of denaturing at 95 °C for 40 s, annealing at 53 °C for 40 s and extending at 72 °C for one min; and a ﬁnal extending step of 72 °C for 10 min. PCR products were puriﬁed with spin columns. The purified products were sequenced with both forward and reverse primers using BigDye Terminator Cycle Sequencing Kit according to the guidelines of the manufacturer. The products were sequenced on an ABI Prism 3730 automated DNA sequencer in Shanghai Majorbio Bio-pharm Technology Co., Ltd.. All sequences have been deposited in GenBank (Table 1).

Phylogenetic analyses

Sequences were first aligned in Clustal X 2.0 (Thompson et al. 1997), with default. The alignment was then checked and manually revised, if necessary. Trimmed with the gaps were partially deleted in MEGA 6.06 (Tamura et al. 2013), while within high variable regions, all gaps were removed.We ran Jmodeltest v2.1.2 (Darriba et al. 2012) with Akaike and Bayesian information criteria on the alignment, resulting the best-fitting nucleotide substitution models of GTR + I + G. Phylogenetic trees were constructed using maximum likelihood (ML) implemented in RaxmlGUI 1.3 (Silvestro and Michalak 2012), and Bayesian inference (BI) using MrBayes 3.2.4 (Ronquist et al. 2012). For ML analysis, the maximum likelihood tree inferred from 1000 replicates was used to represent the evolutionary history of the taxa analyzed. Branches corresponding to partitions reproduced in less than 60% of bootstrap replicates were collapsed. For BI analysis, two independent runs with four Markov Chain Monte Carlo simulations were performed for ten million iterations and sampled every 1000 iterations. The first 25% of samples were discarded as burn-in. Convergence of the Markov Chain Monte Carlo simulations was assessed with PSRF ≤0.01 and ESS (effective sample size) value > 200 using Tracer 1.4 (http://tree.bio.ed.ac.uk/software/tracer/). Pairwise distances were also calculated in MEGA 6.06 based on uncorrected p-distance (Tamura et al. 2013).

Morphometrics

Measurements followed Fei et al. (2009) and Rowley et al. (2013), and were taken with a digital caliper to the nearest 0.1 mm. These measurements were as follows:

SVL snout-vent length (from tip of snout to vent);

HDL head length (from tip of snout to rear of jaws);

HDW head width (head width at commissure of jaws);

SNT snout length (from tip of snout to anterior corner of eye);

EYE eye diameter (diameter of exposed portion of eyeball);

IOD interorbital distance (minimum distance between upper eyelids);

IND internasal distance (distance between nares);

TMP tympanum diameter (horizontal diameter of tympanum);

TEY tympanum-eye distance (distance from anterior edge of tympanum to posterior corner of eye);

TIB tibia length (distance from knee to heel);

ML manus length (distance from tip of third digit to proximal edge of inner palmar tubercle);

LAHL length of lower arm and hand (distance from tip of the third finger to elbow);

PL pes length (distance from tip of fourth toe to proximal edge of the inner metatarsal tubercle);

HLL hindlimb length (distance from tip of fourth toe to vent).

Sex was determined by direct observation of calling in life, the presence of internal vocal sac openings, and the presence of eggs in abdomen seen via external inspection. Comparative morphological data of Leptobrachella species were obtained from examination of museum specimens (see Appendix 1) and from the references listed in Table 2. Due to the high likelihood of undiagnosed diversity within the genus (Rowley et al. 2016; Yang et al. 2016), where available, we rely on examination of topotypic material and/or original species descriptions.

Table 2.

Download as

CSV

XLSX

References for morphological characters for congeners of the genus Leptobrachella.

ID	Leptobrachella species	Literature obtained
1	L. aereus (Rowley, Stuart, Richards, Phimmachak & Sivongxay, 2010)	Rowley et al. 2010c
2	L. alpinus (Fei, Ye & Li, 1990)	Fei et al. 2009
3	L. applebyi (Rowley and Cao, 2009)	Rowley and Cao 2009
4	L. arayai (Matsui, 1997)	Matsui 1997
5	L. ardens (Rowley, Tran, Le, Dau, Peloso, Nguyen, Hoang, Nguyen & Ziegler, 2016)	Rowley et al. 2016
6	L. baluensis Smith, 1931	Dring 1983; Eto et al. 2016
7	L. bidoupensis (Rowley, Le, Tran & Hoang, 2011)	Rowley et al. 2011
8	L. bondangensis Eto, Matsui, Hamidy, Munir & Iskandar, 2018	Eto et al. 2018
9	L. botsfordi (Rowley, Dau & Nguyen, 2013)	Rowley et al. 2013
10	L. bourreti (Dubois, 1983)	Ohler et al. 2011
11	L. brevicrus Dring, 1983	Dring 1983; Eto et al. 2015
12	L. crocea (Rowley, Hoang, Le, Dau & Cao, 2010)	Rowley et al. 2010a
13	L. dringi (Dubois, 1987)	Inger et al. 1995; Matsui and Dehling 2012
14	L. eos (Ohler, Wollenberg, Grosjean, Hendrix, Vences, Ziegler & Dubois, 2011)	Ohler et al. 2011
15	L. firthi (Rowley, Hoang, Dau, Le & Cao, 2012)	Rowley et al. 2012
16	L. fritinniens (Dehling and Matsui, 2013)	Dehling and Matsui 2013
17	L. fusca Eto, Matsui, Hamidy, Munir & Iskandar, 2018	Eto et al. 2018
18	L. fuliginosa (Matsui, 2006)	Matsui 2006
19	L. gracilis (Günther, 1872)	Günther 1872; Dehling 2012b
20	L. hamidi (Matsui, 1997)	Matsui 1997
21	L. heteropus (Boulenger, 1900)	Boulenger 1900
22	L. isos (Rowley, Stuart, Neang, Hoang, Dau, Nguyen & Emmett, 2015)	Rowley et al. 2015a
23	L. itiokai Eto, Matsui & Nishikawa, 2016	Eto et al. 2016
24	L. juliandringi Eto, Matsui & Nishikawa, 2015	Eto et al. 2015
25	L. kajangensis (Grismer, Grismer & Youmans, 2004)	Grismer et al. 2004
26	L. kalonensis (Rowley, Tran, Le, Dau, Peloso, Nguyen, Hoang, Nguyen & Ziegler, 2016)	Rowley et al. 2016
27	L. kecil (Matsui, Belabut, Ahmad & Yong, 2009)	Matsui et al. 2009
28	L. khasiorum (Das, Tron, Rangad & Hooroo, 2010)	Das et al. 2010
29	L. lateralis (Anderson, 1871)	Anderson 1871; Humtsoe et al. 2008
30	L. laui (Sung, Yang & Wang, 2014)	Sung et al. 2014
31	L. liui (Fei and Ye, 1990)	Fei et al. 2009; Sung et al. 2014
32	L. macrops (Duong, Do, Ngo, Nguyen & Poyarkov, 2018)	Duong et al. 2018
33	L. maculosa (Rowley, Tran, Le, Dau, Peloso, Nguyen, Hoang, Nguyen & Ziegler, 2016)	Rowley et al. 2016
34	L. mangshanensis (Hou, Zhang, Hu, Li, Shi, Chen, Mo & Wang, 2018)	Hou et al. 2018
35	L. maoershanensis (Yuan, Sun, Chen, Rowley & Che, 2017)	Yuan et al. 2017
36	L. marmorata (Matsui, Zainudin and Nishikawa, 2014)	Matsui et al. 2014b
37	L. maura (Inger, Lakim, Biun and Yambun, 1997)	Inger et al. 1997
38	L. melanoleuca (Matsui, 2006)	Matsui 2006
39	L. melica (Rowley, Stuart, Neang & Emmett, 2010)	Rowley et al. 2010b
40	L. minima (Taylor, 1962)	Taylor 1962; Ohler et al. 2011
41	L. mjobergi Smith, 1925	Eto et al. 2015
42	L. nahangensis (Lathrop, Murphy, Orlov & Ho, 1998)	Lathrop et al. 1998
43	L. natunae (Günther, 1895)	Günther 1895
44	L. nokrekensis (Mathew and Sen, 2010)	Mathew and Sen 2010
45	L. nyx (Ohler, Wollenberg, Grosjean, Hendrix, Vences, Ziegler & Dubois, 2011)	Ohler et al. 2011
46	L. oshanensis (Liu, 1950)	Fei et al. 2009
47	L. pallida (Rowley, Tran, Le, Dau, Peloso, Nguyen, Hoang, Nguyen & Ziegler, 2016)	Rowley et al. 2016
48	L. palmata Inger and Stuebing, 1992	Inger and Stuebing 1992
49	L. parva Dring, 1983	Dring 1983
50	L. pelodytoides (Boulenger, 1893)	Boulenger 1893; Ohler et al. 2011
51	L. petrops (Rowley, Dau, Hoang, Le, Cutajar & Nguyen, 2017)	Rowley et al. 2017
52	L. pictua (Malkmus, 1992)	Malkmus 1992
53	L. platycephala (Dehling, 2012)	Dehling 2012a
54	L. pluvialis (Ohler, Marquis, Swan & Grosjean, 2000)	Ohler et al. 2000, 2011
55	L. puhoatensis (Rowley, Dau & Cao, 2017)	Rowley et al. 2016
56	L. purpura (Yang, Zeng & Wang, 2018)	Yang et al. 2018
57	L. pyrrhops (Poyarkov, Rowley, Gogoleva, Vassilieva, Galoyan & Orlov, 2015)	Poyarkov et al. 2015
58	L. rowleyae (Nguyen, Poyarkov, Le, Vo, Ninh, Duong, Murphy & Sang, 2018)	Nguyen et al. 2018
59	L. sabahmontana (Matsui, Nishikawa & Yambun, 2014)	Matsui et al. 2014a
60	L. serasanae Dring, 1983	Dring 1983
61	L. sola (Matsui, 2006)	Matsui 2006
62	L. sungi (Lathrop, Murphy, Orlov & Ho, 1998)	Lathrop et al. 1998
63	L. tadungensis (Rowley, Tran, Le, Dau, Peloso, Nguyen, Hoang, Nguyen & Ziegler, 2016)	Rowley et al. 2016
64	L. tamdil (Sengupta, Sailo, Lalremsanga, Das & Das, 2010)	Sengupta et al. 2010
65	L. tengchongensis (Yang, Wang, Chen & Rao, 2016)	Yang et al. 2016
66	L. tuberosa (Inger, Orlov & Darevsky, 1999)	Inger et al.1999
67	L. ventripunctata (Fei, Ye & Li, 1990)	Fei et al. 2009
68	L. wuhuangmontis Wang, Yang and Wang, 2018	Wang et al. 2018
69	L. yingjiangensis (Yang, Zeng & Wang, 2018)	Yang et al. 2018
70	L. yunkaiensis Wang, Li, Lyu and Wang, 2018	Wang et al. 2018
71	L. zhangyapingi (Jiang, Yan, Suwannapoom, Chomdej & Che, 2013)	Jiang et al. 2013

Acoustic analyses

We compared the advertisement calls from three localities. One was in Wujing Nature Reserve and two were in Zhaozishan Nature Reserve. Advertisement calls were recorded between 20:00–24:00 h on 2–6 July 2018, using a Sony PCM-D100 digital sound recorder held within 20 cm of the calling individuals. The ambient temperature of the type locality was obtained using a Volt TP-2200 Humidity & Temperature Logger. The sound files in wave format were sampled at 44.1 kHz with sampling depth 24 bits. Praat 6.0.27 (Boersma 2001) was used to obtain the oscillograms, sonograms and power spectrums (window length = 0.005s). Raven pro 1.5 software (Bioacoustics Research Program 2013) was used to quantify the acoustic properties (window size = 256 points, fast Fourier transform, Hanning window). The measurements taken were as follows:

Call Duration: the time between onset of the first pulse and offset of the last pulse in a call;

IQR (Inter-quartile Range): Duration of the difference between the 1^st and 3^rd quartile times which divides the selection into four time intervals containing equal energy in the selection;

Dominant Frequency: the frequency at which max power occurs within the selection;

IQR (Inter-Quartile Range): Bandwidth of the difference between the 1^st and 3^rd quartile frequencies which divides the selection into four frequency intervals containing equal energy in the selection;

fNote Pulses: the number of pulses for the first note in a call;

sNote Pulses: the number of pulses for the second note in a call;

Note Rise Time: the time between onset of the first pulse and pulse of max amplitude;

Note Interval: the interval between the first note and the second note in a call;

fNote Duration: the duration of the first note in a call;

sNote Duration: the duration of the second note in a call.

Mean and standard deviation (SD) were calculated. We used median and interquartile range instead of mean and SD when calculating the undivided properties, like fNote Pulses and sNote Pulses. To identify different groups on acoustic properties, a hierarchical clustering using Mahalanobis distance was conducted (Mahalanobis 1936). The dendrogram was constructed based on Ward’s method (Ward Jr 1963). All statistical analyses were conducted in R 3.3.2 (R Core Team 2016).

Results

Molecular results

Bayesian inference (BI) and maximum likelihood (ML) phylogenetic trees were constructed based on DNA sequences of the mitochondrial 16S rRNA gene with a total length of 481-bp. The two analyses resulted in essentially identical topologies (Figure 2) which clustered the population of Leptobrachella from Jinjiazhai Village (JV) from Wujing Nature Reserve and those from Baimashan Forest Station (BFS) of Zhaozishan Nature Reserve together with very high node supporting values (0.97 in BI and 100% in ML) and represented a separately evolving lineage (Clade A). The population from Qingshan Village (QV) of Zhaozishan Nature Reserve (Clade B) was a sister taxon to Clade A with high node support values (0.99 in BI and 82% in ML). There was almost no genetic divergence between the two populations in Clade A even though the specimens were collected in two different sites with a straight-line distance at approximately 65 kilometers, and the smallest genetic divergence among individuals in Clade B was only 0.3%. The pairwise genetic divergence between Clade A and Clade B was 3.9–4.2%, and between Clade A and all other species of the genus Leptobrachella for which comparable sequences were included was 3.2% (between Clade A and L. bourreti), and between Clade B and all other species was 5.2–5.6% (between Clade B and L. purpura). However, these values were larger than or equal to observed pairwise genetic distances between recognized species (2.2% between L. liui and L. mangshanensis; 3.2% between L. eos and L. purpura) (Table 3).

Figure 2.

Bayesian inference tree of Leptobrachella species and out-groups derived from partial DNA sequences of the mitochondrial 16S r RNA gene. Numbers before slashes indicate Bayesian posterior probabilities (>0.6 retained) and numbers after slashes are bootstrap support for maximum likelihood (1000 replicates) analyses (>60 retained). The symbol “–” represents bootstrap value below 0.60/60%.

Table 3.

Download as

CSV

XLSX

Uncorrected p-distances among Leptobrachella species based on 16S rRNA fragment (4 parts).

Species & ID No.	(1)–(15)	(16)–(23)	(24)	(25)–(26)	(27)–(28)	(29)	(30)	(31)	(32)
Leptobrachella purpuraventra sp. nov. (1)–(15)	0
Leptobrachella bijie sp. nov. (16)–(23)	3.9–4.2	0.0–0.3
Leptobrachella aerea (24)	9.7	10.5–10.9	-
Leptobrachella applebyi (25)–(26)	13.5	14.7–15.1	14.7	0
Leptobrachella bidoupensis (27)–(28)	17	17.8–18.2	15.9	10.6	0
Leptobrachella bourreti (29)	3.2	5.6–5.9	10.9	14.6	17.4	-
Leptobrachella eos (30)	5.6	7.3–7.7	12	14.7	15.4	4.2	-
Leptobrachella firthi (31)	14.6	14.2–14.6	13.1	16.6	18.7	13.5	13.8	-
Leptobrachella fritinniens (32)	18.9	19.3–19.7	16.1	18.9	16.5	18.5	17.2	18.5	-
Leptobrachella gracilis (33)	22	23.3–23.8	20.7	18.1	21.8	21.5	22.8	24.1	13.1
Leptobrachella hamidi (34)	18.6	20.8–21.2	17.4	14.9	18.1	19.4	16.5	19	8.7
Leptobrachella heteropus (35)	21	23.2–23.7	18.1	17	18.9	21.5	21.4	22.6	19.6
Leptobrachella isos (36)	13.5	15.1–15.5	13.5	16.2	14.6	12	13.5	12.8	18.9
Leptobrachella laui (37)–(38)	11.3	10.9–11.2	11.3	16.7	17.4	10.9	10.2	14.7	18.9
Leptobrachella liui (39)–(40)	8.3	9.0–9.4	9.4	15.4	14.6	8.7	8	13.1	17.7
Leptobrachella mangshanensis (41)–(42)	9.7	10.5–10.8	10.5	16.2	15.7	10.1	9.4	15.1	19.3
Leptobrachella marmorata (43)	15.7	17.7–18.1	15.7	13	17.7	16.1	14.9	17.3	9.4
Leptobrachella maura (44)	16.5	17.0–17.4	17	17	17.7	18.2	17.4	18.5	10.8
Leptobrachella macrops (45)	15.4	17.9–18.3	14.2	12	9.8	15.8	15	17.8	16.9
Leptobrachella maoershanensis (46)	9.8	12.8–13.2	8.7	16.2	14.6	10.9	10.9	17.1	18.9
Leptobrachella melica (47)	11.9	14.3–14.7	11.7	6.3	10.3	13.8	15.1	16.6	16.9
Leptobrachella minima (48)	11.2	11.2–11.6	6.2	15	17	11.2	12	14.2	18.5
Leptobrachella nyx (49)	9	10.8–11.2	5.9	13.5	15	9.4	9.7	11.6	18.1
Leptobrachella oshanensis (50)	4.9	5.6–5.9	10.5	14.2	18.6	3.9	5.9	13.4	18.1
Leptobrachella pallida (51)	16.1	17.3–17.8	14.7	11.2	6.6	17.7	14.9	19	16.1
Leptobrachella picta (52)	18.5	19.7–20.2	17.3	16.1	17.7	18.1	17.2	17.3	5.6
Leptobrachella pluvialis (53)	9.7	11.9–12.3	5.2	14.6	15.4	10.1	11.2	14.2	18.4
Leptobrachella purpura (54)	4.3	5.2–5.6	10.1	13.9	14.6	3.9	3.2	13	16
Leptobrachella ventripunctata (60)–(61)	10.4–10.8	10.8–12.3	5.6	16.2–16.6	17.9–18.3	11.6–12.7	11.9–13.1	11.6–11.9	16.9–17.6
Leptobrachella yingjiangensis (62)	10.9	12.0–12.4	12.4	15.6	13.9	10.9	9.4	16.2	18.1
Leptobrachella yunkaiensis (63)–(64)	10.5–10.8	12.0–12.7	11.7–12	17.5	16.5–16.9	10.1–10.5	10.1–10.5	16.2	20.2–20.6
Leptobrachella wuhuangmontis (65)–(66)	13.1	14.3–14.7	8	16	15.4	11.2	12	13.9	19
Leptobrachella zhangyapingi (67)	11.7	12.0–12.4	10.3	15.5	16.2	11.3	10.1	13.1	19.8
Part 2
Species & ID No.	(33)	(34)	(35)	(36)	(37)–(38)	(39)–(40)	(41)–(42)	(43)	(44)
Leptobrachella gracilis (33)	-
Leptobrachella hamidi (34)	12.8	-
Leptobrachella heteropus (35)	21.8	18.5	-
Leptobrachella isos (36)	23.3	17.7	22.3	-
Leptobrachella laui (37)–(38)	22.4	18.6	22.8	15.5	0
Leptobrachella liui (39)–(40)	24.9	19.5	21.5	13.2	0.6	0
Leptobrachella mangshanensis (41)–(42)	24.7	21.3	22.7	14.3	5.6	2.2	0
Leptobrachella marmorata (43)	12.4	5.3	18.4	17.7	17.3	16.1	17.7	-
Leptobrachella maura (44)	12	10.2	19.5	16.5	19.5	174	19.5	9.4	-
Leptobrachella macrops (45)	20.7	16.5	21.4	15.4	16.6	14.6	14.9	14.9	17
Leptobrachella maoershanensis (46)	24.3	20.4	21.9	15.1	7.7	6.3	6.2	17.7	19.5
Leptobrachella melica (47)	14.9	16.6	17.7	16.7	17.6	16.7	17.9	13.4	15
Leptobrachella minima (48)	21.5	19.5	19.4	14.3	9.8	9.4	9.7	16.9	17.8
Leptobrachella nyx (49)	23.7	17.3	18.1	13.1	9.8	8.3	9.7	15.7	17.3
Leptobrachella oshanensis (50)	20.2	19.4	22.8	12.7	8.7	8.3	9	17.3	17.7
Leptobrachella pallida (51)	19.7	16.9	20.5	18.3	15.4	15.3	15.7	15.3	16.5
Part 3
Species & ID No.	(45)	(46)	(47)	(48)	(49)	(50)	(51)	(52)	(53)
Leptobrachella macrops (45)	-
Leptobrachella maoershanensis (46)	15	-
Leptobrachella melica (47)	11.3	16.3	-
Leptobrachella minima (48)	16.1	9.4	14.6	-
Leptobrachella nyx (49)	16.1	8.1	12.8	8	-
Leptobrachella oshanensis (50)	16.6	11.3	14.2	9.4	9.7	-
Leptobrachella pallida (51)	9	15.4	12.1	15	15.8	16.1	-
Leptobrachella picta (52)	16.5	19.3	16.1	18	18.1	18.4	16.9	-
Leptobrachella pluvialis (53)	16.1	7.3	14.7	7.2	5.9	10.5	14.6	18.4	-
Leptobrachella purpura (54)	14.6	10.1	14.3	11.6	9.4	5.6	14.5	17.3	9.7
Leptobrachella pyrrhops (55)–(56)	8.3–8.7	14.9–15.3	12.4–12.8	16.1–16.5	15.7–16.1	16.5–16.9	7.6–8.0	16.9–17.3	15.7–16.1
Leptobrachella sabahmontana (57)	15.3	19.9	13.7	16.9	18.9	17.3	14.9	5.2	19.3
Leptobrachella tengchongensis (58)–(59)	15.8	10.9	13.9	9.4	9.7	8.7	15.8	16.4	10.8
Leptobrachella ventripunctata (60)–(61)	17.8–18.1	9.4–9.8	15.1–15.4	6.2–7.2	6.2–6.6	10.9–12.0	16.6–17.0	17.6–18.4	6.9–7.2
Part 4
Species & ID No.	(54)	(55)–(56)	(57)	(58)–(59)	(60)–(61)	(62)	(63)–(64)	(65)–(66)	(67)
Leptobrachella purpura (54)	-
Leptobrachella pyrrhops (55)–(56)	15.7–16.5	0.3
Leptobrachella sabahmontana (57)	16.9	16.1–16.4	-
Leptobrachella tengchongensis (58)–(59)	8.7	16.1–16.5	16.5	0
Leptobrachella ventripunctata (60)–(61)	10.8–11.9	16.1–16.2	16.5–16.6	16.5–17.3	9.4–10.5	0.9
Leptobrachella yingjiangensis (62)	9.4	13.9–14.3	18.6	9.1	12.7	13.1	-
Leptobrachella yunkaiensis (63)–(64)	10.1–10.5	16.2–16.5	16.6–17.0	21.1–21.5	12.4–12.7	11.6–11.9	0.3
Leptobrachella wuhuangmontis (65)–(66)	12.4	16.2	16.6	19	13.9	9.8	10.9–15.6	0
Leptobrachella zhangyapingi (67)	9.4	18.2	18.7	19	9.5	10.9	11.3	12.4	-

Acoustic results

Calling from nine male individuals were measured, respectively. They were recorded in Jinjiazhai Village (two males), Baimashan Forest Station (three males), and Qingshan Village (four males) at an ambient temperature approximately of 18.8 °C, 19.3 °C, and 18.6 °C, respectively. The result of hierarchical clustering analysis was consistent with the molecular result (Figure 3). Nine calling males were clustered into two clades based on acoustic properties of advertisement calls. All JV males and BFS males were clustered into Clade A, and all the QV males were clustered into Clade B. In Clade A, there were some differences in the advertisement calls between JV and BFS in Clade B. Measurements of the advertisement calls of the three localities are listed in Table 4.

Figure 3.

Hierarchical clustering of advertisement calls of Leptobrachella purpuraventra sp. nov. from BFS Baimashan Forest Station in Zhaozishan Nature Reserve and JV Jinjiazhai Village in Wujing Nature Reserve, respectively; and L. bijie sp. nov. from QV Qingshan Village in Zhaozishan Nature Reserve.

Table 4.

Download as

CSV

XLSX

Measurements (mean ± standard deviation) of 11 acoustic properties for Leptobrachella species in this study.

Locality

Individuals

Call Type

Call Duration (ms)

Call Interval (ms)

IQR Duration (ms)

Dominant Frequency (Hz)

IQR Bandwidth (Hz)

fNote Pulses*

sNote Pulses*

Note Rise Time (ms)

Note Interval (ms)

fNote Duration (ms)

sNote Duration (ms)

Leptobrachella purpuraventra sp. nov.

A (n=20)

111.6±3.0

119.1±8.0

30.8±27.3

4806.2±135.7

361.7±53.0

4±0

6±1

87.2±2.4

58.2±3.5

27.8±3.4

25.6±2.8

B (n=14)

189.9±13.6

193.6±36.3

41.4±20.6

4835.7±196.6

319.9±148.9

4±1

20±2

69.3±9.6

42.6±11.2

24.7±5.6

122.5±11.4

A (n=24)

110.7±5.0

128.5±13.7

57.8±23.1

4679.9±65.6

236.9±85.2

4±0

85.8±3.3

51.6±4.7

32.4±4.8

26.7±3.8

B (n=18)

188±10.9

196.2±39.3

54.1±24.0

4679.9±66.0

306.2±73.7

3±0.75

19.5±1

57.3±30.1

43.1±9.1

25.3±5.9

119.7±7.4

BFS

A (n=20)

93.7±6.1

102.6±13.2

41.3±23.4

4823.4±0.0

180.9±38.5

3±0

4±1

70.5±3.1

45.0±4.2

24.5±2.8

24.2±6.0

B (n=21)

192.2±13.0

174.5±51.1

50.4±20.1

4675.8±61.7

328.1±51.8

2±0

17±1

55.6±9.2

37.5±8.6

16.9±4.5

137.7±8.8

A (n=20)

90.3±2.0

90.8±5.6

47.2±9.9

4823.4±0.0

344.5±0.0

3±0

4±0.25

69.4±2.0

39.4±2.2

28.2±1.1

22.8±2.4

B (n=25)

191.8±11.9

174.5±51.1

60.6±16.6

4823.4±0.0

186.1±47.7

3±1

16±2

63.9±4.1

40.4±6.7

22.1±6.2

129.4±11.6

A (n=20)

91.7±2.2

117.2±31.2

52.5±9.7

4720.1±86.6

198.1±63.1

3±0

4±0

67.4±3.4

40.3±4.7

25.2±3.7

26.2±3.4

B (n=11)

144.8±31.5

217.8±64.9

27.2±7.1

4745.1±89.9

219.3±80.4

2±0.5

13±3.5

53.5±6.7

33.5±8.0

18.3±6.4

93.3±25.9

Summary

A (n=104)

100.0±10.4

112.3±21.3

46.3±22.0

4767.1±97.3

263.4±92.8

3±1

4±1

76.4±9.1

47.1±8.1

27.8±4.4

25.2±4.1

B (n=89)

185.0±21.7

182.7±47.9

49.7±21.4

4751.8±115.6

269.0±100.4

3±1

17±3

60.2±15.7

39.8±9.0

21.4±6.5

123.8±18.3

Leptobrachella bijie sp. nov.

A (n=26)

103.1±2.3

109.0±3.3

28.0±31.1

5068.6±86.8

344.5±0.0

2±0

3±0

87.8±2.1

70.1±7.8

16.4±7.2

16.6±0.8

B (n=21)

221.0±14.0

235.6±45.1

38.1±20.5

5036.7±92.9

278.9±85.7

2±0

17±2

82.2±3.9

63.0±5.2

17.7±5.3

140.4±12.8

A (n=25)

98.8±6.4

122.2±23.4

19.5±18.9

4823.4±0.0

172.3±0.0

3±1

4±1

76.4±3.7

55.9±4.9

19.3±4.6

23.5±6.5

B (n=20)

206.8±10.1

245.2±79.4

56.6±20

4780.4±76.5

206.7±70.7

2±1

20±3

68.4±10.2

48.6±9.3

18.4±5.7

139.7±9.9

A (n=22)

102.6±7.5

112.9±8.2

71.4±15.4

4909.6±88.2

172.3±0.0

3±0

4±1

85.3±5.2

61.3±5.9

22.5±1.6

18.9±3.2

B (n=28)

253.0±19.0

225.6±61.1

71.5±34.9

4835.7±45.2

319.9±61.4

2±0.25

23±2.25

69.7±11.4

51.7±12.6

16.5±7.3

184.9±19.0

A (n=33)

99.4±3.2

101.9±6.4

34.4±29.1

4823.4±0

302.8±74.9

2±1

83.0±2.9.0

60.1±6.6

21.7±6.6

17.7±1.9

B (n=25)

264.0±12.5

166.5±44.5

64.6±23.5

4823.4±70.3

227.4±82.0

2±1

23±2

83.6±7.2

61.1±7.8

21.2±6.1

181.7±11.6

Summary

A (n=106)

100.8±5.4

110.7±14.5

37.0±31.0

4901.4±116.8

255.2±86.4

3±1

3±2

83.1±5.4

61.8±8.2

20.0±6.0

19.0±4.5

B (n=94)

239.0±27.0

216.3±65.4

59.0±28.7

4865.6±117.7

262.1±86.5

2±1

21.5±4

75.9±11.1

56.1±11.0

18.4±6.4

164.5±25.8

All advertisement calls contain two notes, each of which consists of repeated pulses (Figure 4). Clade A had more fNote pulses in second type of advertisement calls than those of Clade B (3 ± 1 vs. 2 ± 1), more sNote pulses in first type of advertisement calls (4 ± 1 vs. 3 ± 1), and less sNote pulses in the second type of advertisement calls (17 ± 3 vs. 21.5 ± 4). Accordingly, the sNote duration of Clade A was greater than those of Clade B (164.5 ± 25.8 vs. 123.8 ± 18.3 ms). Compared with individuals in Clade A, those from Clade B had little difference in the first type of advertisement calls, but had relatively short call duration (185.0 ± 21.7 vs. 239.0 ± 27.0 ms) and call interval (182.7 ± 47.9 vs. 216.3 ± 65.4 ms) in the second type. The dominant frequency of Clade A was higher than those of Clade B in both the first type of advertisement calls (4901.4 ± 116.8 vs. 4767.1 ± 97.3 Hz) and the second type (4865.6 ± 117.7 vs. 4751.8 ± 115.6 Hz).

Figure 4.

Different call types (A the first call type B the second call type.) of Leptobrachella purpuraventra sp. nov. from BFS Baimashan Forest Station in Zhaozishan Nature Reserve and JV Jinjiazhai Village in Wujing Nature Reserve, respectively; and different call types of L. bijie sp. nov. from QV Qingshan Village in Zhaozishan Nature Reserve. (Window length: 0.005 s).

Combining morphological, molecular genetics, and acoustic evidence, we herein describe these specimens as two new species.

Taxonomy accounts

Leptobrachella bijie J. Wang, Y.L. Li, Y. Li, H.H. Chen & Y.Y. Wang, sp. nov.

http://zoobank.org/550E8562-0EC9-40C4-A6B3-FFAC35B25444

Figure 5

Holotype

SYS a007316, adult male, collected by Jian Wang (JW hereafter) and Yulong Li (YLL hereafter) on 6 July 2018 from Qingshan Village (27°39'24"N, 105°23'14"E; 1670 m a.s.l.) in Zhaozishan Nature Reserve, Linkou Town, Qixingguan District, Bijie City, Guizhou Province, China.

Paratypes

Seven adult males, SYS a007313/CIB 110002, SYS a007314–7315, 7317–7320, collected by Honghiu Chen (HHC hereafter), Yongyou Zhao (YYZ hereafter) and Jiahe Li (JHL), the same collection data as the holotype.

Diagnosis

(1) small size (SVL 29.0–30.4 mm in eight adult males), (2) dorsal skin shagreened, some of the granules forming longitudinal short skin ridges, (3) iris bicolored, coppery orange on upper half and silver on lower half, (4) tympanum distinctly discernible, slightly concave, distinct black supratympanic line present, (5) internasal distance equal to interorbital distance, (6) supra-axillary, femoral, pectoral and ventrolateral glands distinctly visible, (7) absence of webbing and lateral fringes on fingers, toes with rudimentary webbing and narrow lateral fringes, (8) longitudinal ridges under toes not interrupted at the articulations, (9) relative finger lengths I = II = IV < III, relative toe length I < II < V = III < IV, (10) heels just meeting, tibia-tarsal articulation reaches the region between middle of eye to anterior corner of eye, (11) dorsal surface shagreened and granular, lacking enlarge tubercles or warts, some of the granules forming short longitudinal folds, (12) dorsum greyish-brown grounding, with small light orange granules, distinct darker brown markings scattered with irregular light orange pigmentations, (13) flanks with several dark blotches, longitudinally in two rows, (14) ventral surface white, with distinct nebulous greyish speckling on chest and ventrolateral flanks, (15) dorsal limbs including fingers and toes with dark bars, and (16) dense tiny conical spines present on surface of chest in males during breeding season.

Figure 5.

General aspect in life: A–D SYS a007316, the male holotype of Leptobrachella bijie sp. nov. E the male paratype SYS a007313 F the male paratype SYS a007317.

Comparisons

Comparative morphological data of Leptobrachella bijie sp. nov. and 45 recognized Leptobrachella species occurring north of the Isthmus of Kra were listed in Table 5.

Compared with the 26 known congeners of the genus Leptobrachella occurring south of the Isthmus of Kra, by the presence of supra-axillary and ventrolateral glands, L. bijie sp. nov. can be easily distinguished from L. arayai, L. dringi, L. fritinniens, L. gracilis, L. hamidi, L. heteropus, L. kajangensis, L. kecil, L. marmorata, L. melanoleuca, L. maura, L. picta, L. platycephala, L. sabahmontana, and L. sola, all of which lacking supra-axillary and ventrolateral glands; and by the significantly larger body size, SVL 29.0–30.4 mm in males, L. bijie sp. nov. differs from the smaller L. baluensis (14.9–15.9 mm in males), L. brevicrus (17.1–17.8 mm in males), L. bondangensis (17.8 mm in male), L. fusca (16.3 mm in male), L. itiokai (15.2–16.7 mm in males), L. juliandringi (17.0–17.2 mm in males), L. mjobergi (15.7–19.0 mm in males), L. natunae (17.6 mm in one adult male), L. parva (15.0–16.9 mm in males), L. palmata (14.4–16.8 mm in males), L. serasanae (16.9 mm in female), and Dring’s (1983) Leptobrachella sp. 3 “baluensis” (15.0–16.0 mm in males).

Table 5.

Download as

CSV

XLSX

Selected diagnostic characters for species described herein and species in the genus Leptobrachella occurring north of the Isthmus of Kra (modified from Rowley et al. 2017; Yuan et al. 2017; Yang et al. 2018; Wang et al. 2018).

Species	Male SVL (mm)	Black spots on flanks	Toes webbing	Fringes on toes	Ventral coloration	Dorsal skin texture
L. bijie sp. nov.	29.0–30.4	Yes	Rudimentary	Narrow	White with distinct nebulous greyish speckling on chest and ventrolateral flanks	Shagreened and granular
L. purpuraventra sp. nov.	27.3–29.8	Yes	Rudimentary	Narrow	Grey purple with distinct nebulous greyish speckling on chest and ventrolateral flanks	Shagreened and granular
L. aerea	25.1–28.9	No	Rudimentary	Wide	Near immaculate creamy white, brown specking on margins	Finely tuberculate
L. alpinus	24.0–26.4	Yes	Rudimentary	Wide in males	Creamy-white with dark spots	Relatively smooth, some with small warts
L. applebyi	19.6–22.3	Yes	Rudimentary	No	Reddish brown with white speckling	Smooth
L. ardens	21.3–24.7	Yes	No	No	Reddish brown with white speckling	Smooth- finely shagreened
L. bidoupensis	18.5–25.4	Yes	Rudimentary	Weak	Reddish brown with white speckling	Smooth
L. botsfordi	29.1–32.6	No	Rudimentary	Narrow	Reddish brown with white speckling	Shagreened
L. bourreti	28.0–36.2	Yes	Rudimentary	Weak	Creamy white	Relatively smooth, some with small warts
L. crocea	22.2–27.3	No	Rudimentary	No	Bright orange	Highly tuberculate
L. eos	33.1–34.7	No	Rudimentary	Wide	Creamy white	Shagreened
L. firthi	26.4–29.2	No	Rudimentary	Wide in males	Creamy white	Shagreened with fine tubercles
L. fuliginosa	28.2–30.0	Yes	Rudimentary	Weak	White with brown dusting	Nearly smooth, few tubercles
L. isos	23.7–27.9	No	Rudimentary	Wide in males	Creamy white with white dusting on margins	Mostly smooth, females more tuberculate
L. kalonensis	25.8–30.6	Yes	No	No	Pale, speckled brown	Smooth
L. khasiorum	24.5–27.3	Yes	Rudimentary	Wide	Creamy white	Isolated, scattered tubercles
L. lateralis	26.9–28.3	Yes	Rudimentary	No	Creamy white	Roughly granular
L. laui	24.8–26.7	Yes	Rudimentary	Wide	Creamy white with dark brown dusting on margins	Round granular tubercles
L. liui	23.0-28.7	Yes	Rudimentary	Wide	Creamy white with dark brown spots on chest and margins	Round granular tubercles with glandular folds
L. macrops	28.0–29.3	Yes	Rudimentary	No	Greyish-violet with white speckling	Roughly granular with larger tubercles
L. maculosa	24.2–26.6	Yes	No	No	Brown, less white speckling	Mostly smooth
L. maoershanensis	25.2–30.4	Yes	Rudimentary	Narrow	Creamy white chest and belly with irregular black spots	Longitudinal folds
L. mangshanensis	22.22–27.76	Yes	Rudimentary	Weak	White speckles on throat and belly	Nearly smooth
L. melica	19.5–22.7	Yes	Rudimentary	No	Reddish brown with white speckling	Smooth
L. minima	25.7–31.4	Yes	Rudimentary	No	Creamy white	Smooth
L. nahangensis	40.8	Yes	Rudimentary	No	Creamy white with light specking on throat and chest	Smooth
L. nokrekensis	26.0–33.0	Yes	Rudimentary	unknown	Creamy white	Tubercles and longitudinal folds
L. nyx	26.7–32.6	Yes	Rudimentary	No	Creamy white with white with brown margins	Rounded tubercles
L. oshanensis	26.6–30.7	Yes	No	No	Whitish with no markings or only small, light grey spots	Smooth with few glandular ridges
L. pallida	24.5–27.7	No	No	No	Reddish brown with white speckling	Tuberculate
L. pelodytoides	27.5–32.3	Yes	Wide	Narrow	Whitish	Small, smooth warts
L. petrops	23.6–27.6	No	No	Narrow	Immaculate creamy white	Highly tuberculate
L. pluvialis	21.3–22.3	Yes	Rudimentary	No	Dirty white with dark brown marbling	Smooth, flattened tubercles on flanks
L. puhoatensis	24.2–28.1	Yes	Rudimentary	Narrow	Reddish brown with white dusting	Longitudinal skin ridges
L. purpura	25.0–27.5	Yes	Rudimentary	Wide	Dull white with indistinct grey dusting	Shagreen with small tubercles
L. pyrrhops	30.8–34.3	Yes	Rudimentary	No	Reddish brown with white speckling	Slightly shagreened
L. rowleyae	23.4–25.4	Yes	No	No	Pinkish milk-white to light brown chest and belly with numerous white speckles	Smooth with numerous tiny tubercles
L. sungi	48.3–52.7	No or small	Wide	Weak	White	Granular
L. tadungensis	23.3–28.2	Yes	No	No	Reddish brown with white speckling	Smooth
L. tamdil	32.3	Yes	Wide	Wide	White	Weakly tuberculate
L. tengchongensis	23.9–26.0	Yes	Rudimentary	Narrow	White with dark brown blotches	Shagreened with small tubercles
L. tuberosa	24.4–29.5	No	Rudimentary	No	White with small grey spots/streaks	Highly tuberculate
L. ventripunctata	25.5–28.0	Yes	Rudimentary	No	Chest and belly with dark brown spots	Longitudinal skin ridges
L. wuhuangmontis	25.6–30.0	Yes	Rudimentary	Narrow	Greyish white mixed by tiny white and black dots	Rough, scattered with dense conical tubercles
L. yingjiangensis	25.7–27.6	Yes	Rudimentary	Wide	Creamy white with dark brown flecks on chest and margins	Shagreened with small tubercles
L. yunkaiensis	25.9–29.3	Yes	Rudimentary	Wide	Belly pink with distinct or indistinct speckling	Shagreened with short skin ridges and raised warts
L. zhangyapingi	45.8–52.5	No	Rudimentary	Wide	Creamy-white with white with brown margins	Mostly smooth with distinct tubercles

For the remaining 45 members of the genus Leptobrachella, having SVL of 29.0–30.4 mm in males, L. bijie sp. nov. differs from the larger L. eos (33.1–34.7 mm in males), L. nahangensis (40.8 mm in male), L. sungi (48.3–52.7 mm in males), L. tamdil (32.3 mm in male), and L. zhangyapingi (45.8–52.5 mm in males); and from the smaller L. alpinus (24.0–26.4 mm in males), L. applebyi (19.6–22.3 mm in males), L. ardens (21.3–24.7 mm in males), L. bidoupensis (18.5–25.4 mm in males), L. crocea (22.2–27.3 mm in males), L. isos (23.7–27.9 mm in males), L. khasiorum (24.5–27.3 mm in males), L. lateralis (26.9–28.3 mm in males), L. laui (24.8–26.7 mm in males), L. maculosa (24.2–26.6 mm in males), L. melica (19.5–22.7 mm in males), L. pallida (24.5–27.7 mm in males), L. petrops (23.6–27.6 mm in males), L. pluvialis (21.3–22.3 mm in males), L. puhoatensis (24.2–28.1 mm in males), L. purpura (25.0–27.5 mm in males), L. rowleyae (23.4–25.4 mm in males), L. tadungensis (23.3–28.2 mm in males), L. tengchongensis (23.9–26.0 mm in males), L. ventripunctata (25.5–28.0 mm in males), and L. yingjiangensis (25.7–27.6 mm in males).

In having black spots on flanks, the new species differs from L. aerea, L. botsfordi, L. firthi, and L. tuberosa, all of which lacking distinct black spots on the flanks; by having rudimentary webbing on toes, the new species differs from L. kalonensis and L. oshanensis, both of which lacking webbing on toes, and from L. pelodytoides, which bears wide webbing on toes; by having narrow lateral fringes on toes, the new species differs from L. aerea, L. firthi, L. liui, and L. yunkaiensis, all of which having wide lateral fringes on toes, from L. bourreti and L. fuliginosa, both of which having weak lateral fringes on toes, and from L. kalonensis, L. macrops, L. minima, L. nyx, L. oshanensis, L. pyrrhops, and L. tuberosa, all of which lacking lateral fringes on toes; by having dorsal surface shagreened and granular, lacking enlarge tubercles or warts, the new species differs from L. bourreti (dorsum smooth with small warts), L. fuliginosa (dorsum smooth with fine tubercles), L. liui (dorsum with round tubercles), L. macrops (dorsum roughly granular with large tubercles), L. maoershanensis (dorsum shagreened with tubercles), L. minima (dorsum smooth), L. nyx (dorsum with round tubercles), L. pelodytoides (dorsum with small, smooth warts), L. tuberosa (dorsum hingly tuberculate), L. yunkaiensis (dorsum with raised warts), and L. wuhuangmontis (dorsum rough with conical tubercles); by having ventral surface white with distinct nebulous greyish speckling on chest and flanks, the new species differs from L. botsfordi and L. pyrrhops, (ventral reddish brown with white speckling), L. maoershanensis (belly with irregular black spots); by having tiny spines on surface of chest in males during breeding season, the new species differs from all male specimens collected in breeding season of L. liui, L. oshanensis, L. yunkaiensis, and L. wuhuangmontis, all of which are lacking such spines.

Description of holotype

Adult male. Body size small, SVL in 29.3 mm. Head length slightly larger than head width, HDL/HDW 1.03; snout slightly protruding, projecting slightly beyond margin of the lower jaw; nostril closer to snout than eye; canthus rostralis gently rounded; loreal region slightly concave; interorbital space flat, internarial distance equal to interorbital distance, IND/IOD 1.00; pineal ocellus absent; vertical pupil; snout length larger than eye diameter, SNT/EYE 1.11; tympanum distinct, rounded, and slightly concave, diameter smaller than that of the eye and larger than tympanum-eye distance, TMP/EYE 0.53 and TEY/TMP 0.47; upper margin of tympanum incontact with supratympanic ridge; distinct black supratympanic line present; vomerine teeth absent; vocal sac openings slit-like, paired, located posterolaterally on floor of mouth in close proximity to the margins of the mandible; tongue deeply notched behind; supratympanic ridge distinct, extending from posterior corner of eye to supra-axillary gland.

Tips of fingers rounded, slightly swollen; relative finger lengths I = II = IV < III; nuptial pad absent; subarticular tubercles absent; a large, rounded inner palmar tubercle distinctly separated from small, round outer palmar tubercle; absence of webbing and lateral fringes on fingers. Tips of toes like fingers; relative toe length I < II < V = III < IV; subarticular tubercles absent; distinct dermal ridges present under the 3^rd to 5^th toes, not interrupted; large, oval inner metatarsal tubercle present, outer metatarsal tubercle absent; toes webbing rudimentary; narrow lateral fringes present on all toes. Tibia 47% of snout-vent length; tibiotarsal articulation reaches to middle of eye; heels just meeting each other when thighs are appressed at right angles with respect to body.

Dorsal surface shagreened and granular, lacking enlarge tubercles or warts, some of the granules forming short longitudinal folds; ventral skin smooth; dense tiny conical spines present on surface of chest; pectoral gland and femoral gland oval; pectoral glands greater than tips of fingers and femoral glands; femoral gland situated on posteroventral surface of thigh, closer to knee than to vent; supra-axillary gland raised. Ventrolateral gland distinctly visible, forming an incomplete line.

Measurements of holotype (in mm)

SVL 29.2, HDL 10.0, HDW 9.7, SNT 4.0, EYE 3.6, IOD 3.0, IND 3.0, TMP 1.9, TEY 0.9, TIB 13. 8, ML 7.8, PL 13.2, LAHL 14.1, HLL 43.3.

Coloration of holotype in life

Dorsum greyish-brown grounding, with small reddish granules, distinct darker brown markings and rounded spots and scattered with irregular light orange pigmentation. A dark brown inverted triangular pattern between anterior corner of eyes, in connected to the dark brown W-shaped marking on interorbital region, and the W-shaped marking in connected to the other W-shaped marking between axillae. Tympanum brown. Small light orange granules present on dorsum of body and limb; a dark brown vertical bar under the eye; transverse dark brown bars on dorsal surface of limbs; distinct dark brown blotches on flanks from groin to axilla, longitudinally in two rows; elbow and upper arms with dark bars and distinct coppery orange coloration; fingers and toes with distinct dark bars.

Ventral surface of throat, chest, and belly white, presence of distinct nebulous greyish speckling on chest and ventrolateral flanks; ventral surface of limbs grey purple. Supra-axillary gland coppery orange; femoral, pectoral and ventrolateral glands greyish white. Iris bicolored, coppery orange on upper half and silver on lower half.

Coloration of holotype in preservative

Dorsum of body and limbs dark brown; transverse bars on limbs become more distinct; dark brown patterns, markings and spots on back become indistinct, orange pigmentations become greyish white. Ventral surface of body and limbs greyish white, nebulous speckling on chest and flanks balck brown. Supra-axillary, femoral, pectoral and ventrolateral glands greyish white.

Variations

Measurements and body proportions were listed in Table 6. All paratypes match the overall characters of the holotype except that: coloration of tympanum brown in the holotype SYS a007316 (vs. black in paratypes SYS a007313/CIB 110002 (Figure 5E), SYS a007315, 7317 (Figure 5F)); heels just meeting, tibia-tarsal articulation reaching the middle of eye in the holotype (vs. heels slightly overlapping in paratypes SYS a007315, 7317, 7319–7320; tibia-tarsal articulation reaching the anterior corner of eye in paratypes SYS a007315, 7317, 7319); W-shaped marking on interorbital region in connected to the other W-shaped marking between axillae in the holotype (vs. such markings not in connected with each other in paratypes SYS a007313/CIB 110002, SYS a007320); a dark brown inverted triangular pattern between anterior corner of eyes in the holotype (vs. a V-shaped pattern between anterior corner of eyes instead in paratype SYS a007317, 7320); relatively larger black spots on flanks (vs. black spots distinctly small in paratypes SYS a007313/CIB 110002, SYS a007317).

Table 6.

Download as

CSV

XLSX

Measurements (minimum–maximum (mean ± SD); in mm), and body proportions of Leptobrachella bijie sp. nov. from Qingshan Village of Zhaozishan Nature Reserve.

SEX	Males (n = 8)
SVL	29.0–30.4 (29.7 ± 0.6)	HLL	43.0–45.5 (43.7 ± 0.8)
HDL	10.0–10.6 (10.2 ± 0.2)	HDL/HDW	1.02–1.05 (1.04 ± 0.01)
HDW	9.5–10.2 (9.8 ± 0.3)	HDL/SVL	0.33–0.35 (0.34 ± 0.01)
SNT	4.0–4.7 (4.3 ± 0.3)	SNT/HDL	0.40–0.44 (0.42 ± 0.02)
EYE	3.6–4.1 (3.8 ± 0.2)	SNT/EYE	1.11–1.15 (1.13 ± 0.02)
IOD	2.8–3.4 (3.1 ± 0.2)	EYE/TMP	1.85–1.95 (1.89 ± 0.04)
IND	2.8–3.4 (3.1 ± 0.2)	IND/IOD	1
TMP	1.9–2.2 (2.0 ± 0.1)	TMP/EYE	0.51–0.54 (0.53 ± 0.01)
TEY	0.9–1.1 (1.0 ± 0.1)	TEY/TMP	0.45–0.53 (0.48 ± 0.02)
TIB	13.5–14.4 (13.8 ± 0.3)	TIB/SVL	0.45–0.47 (0.47 ± 0.01)
ML	7.4–8.3 (7.8 ± 0.3)	LAHL/SVL	0.47–0.49 (0.48 ± 0.01)
PL	13.0–13.8 (13.3 ± 0.2)	HLL/SVL	1.45–1.50 (1.47 ± 0.02)
LAHL	14.0–14.8 (14.3 ± 0.3)	TIB/HLL	0.31–0.32 (0.31 ± 0.01)

Etymology

The specific epithet bijie is in reference to the type locality, Qingshan Village in Bijie City of Guizohu Province, China. For the common name, we suggest “Bijie Leaf Litter Toad”, and for the Chinese name “Bi Jie Zhang Tu Chan (毕节掌突蟾)”.

Distribution and habits

Currently, Leptobrachella bijie sp. nov. is known only from its type locality Qingshan Village in Zhaozishan Nature Reserve, Linkou County, Qixingguan District, Bijie City, Guizhou Province, China (Figure 1). The new species was found along a clear-water rocky stream (ca. 2 m in width and ca. 20–30 cm in depth; 1670–1750 m a.s.l.) in karst landforms. The stream was surrounded by broad-leaved forest at an altitude below 1700 m, and by coniferous forest at an altitude above 1700 m (Figure 6, 1700 m a.s.l.). On 6 July 2018 at 22:00–23:30 P.M., a large number of males were found calling on leaves of plants (Figure 10A), and some were found calling perching on the rocks or under rocks by the side of the stream.

Figure 6.

The habitat of Leptobrachella bijie sp. nov. in Qingshan Village of Zhaozishan Nature Reserve in Guizhou Province.

Leptobrachella purpuraventra J. Wang, Y.L. Li, Y. Li, H.H. Chen & Y.Y. Wang, sp. nov.

http://zoobank.org/0B2C4A25-981B-4AE9-900D-60CAB4E7A560

Figure 7

Holotype

SYS a007284, adult male, collected by JW on 2 July 2018 from Jinjiazhai Village (27°7'5.92"N, 105°19'28.47"E; 1890 m a.s.l.) in Wujing Nature Reserve, Chahe Town, Qixingguan District, Bijie City, Guizhou Province, China.

Paratypes

A single adult female, SYS a007278 and seven adult males, SYS a007277/CIB 110003, 7279–7284, collected by JW, YLL, YYZ, HHC, JHL and Yingyong Wang (YYW hereafter), the same collection data as the holotype; besides, another three adult females, SYS a007304–7306, and four adult males, SYS a007300–7303, collected by JW, YLL, YYZ, HHC, JHL and YYW on 4 July 2018 from Baimashan Forest Station (27°41'25"N, 105°27'16"E; 1600 m a.s.l.) of Zhaozishan Nature Reserve, Shengji Town, Qixingguan District, Bijie City, Guizhou Province, China.

Diagnosis

(1) small size (SVL 27.3–29.8 mm in males, 33.0–35.3 mm in females), (2) dorsal skin shagreened, some of the granules forming longitudinal short skin ridges, (3) iris bicolored, coppery orange on upper half and silver on lower half, (4) tympanum distinctly discernible, slightly concave, distinct black supratympanic line present, (5) internasal distance smaller than interorbital distance, IND/IOD ratio 1.03–1.10, (6) supra-axillary, femoral, pectoral and ventrolateral glands distinctly visible, (7) absence of webbing and lateral fringes on fingers, toes with rudimentary webbing and narrow lateral fringes, (8) longitudinal ridges under toes not interrupted at the articulations, (9) heels just meeting or slightly overlapping, tibia-tarsal articulation reaching to the middle of eye, (10) relative finger lengths I = II = IV < III, relative toe length I < II < V < III < IV, (11) dorsal surface shagreened and granular, lacking enlarge tubercles or warts, some of the granules forming short longitudinal folds, (12) dorsum purple brown to dark purple brown or grey purple grounding, with small light orange granules, distinct darker brown markings scattered with irregular light orange pigmentations, (13) flanks with several dark blotches, longitudinally in two rows, (14) ventral surface grey purple, with distinct or indistinct nebulous greyish speckling on chest and ventrolateral flanks, without black spots (seldom present), (15) dorsal limbs including fingers and toes with dark bars, those on forearms indistinct, and (16) dense tiny conical spines present on surface of chest extending to anterior region of abdomen in males, and absent in females during breeding season.

Figure 7.

General aspect in life: A–D SYS a007284, the male holotype of Leptobrachella purpuraventra sp. nov. E the male paratype SYS a007300 F the male paratype SYS a007283.

Comparisons

Comparative morphological data of Leptobrachella purpuraventra sp. nov., L. bijie sp. nov., and 45 recognized Leptobrachella species occurring north of the Isthmus of Kra were listed in Table 5.

In the phylogenetic trees (Figure 2), Leptobrachella purpuraventra sp. nov. is a sister taxon to L. bijie sp. nov. with a high support value (99% in BI, 0.82 in ML), and it can be distinguished from the later by a genetic divergence (p=3.9–4.2%). Morphologically, it differs from the later by the coloration of dorsum and ventral, dorsum purple brown to dark purple brown or grey purple grounding, ventral grey purple grounding (vs. dorsum greyish-brown grounding, ventral white grounding); dark bars on dorsal limbs indistinct (vs. distinctly visible); dark bars on dorsal surface of tibia and tarsus much broader, especially those on dorsal skin of tarsus (vs. relatively narrow dark bars on dorsal surface of tibia and tarsus); internasal distance smaller than interorbital distance, IND/IOD ratio 1.03–1.10 (vs. internasal distance equal to interorbital distance, IND/IOD ratio 1.00); larger TEY value, TEY/TMP ratio 0.60–0.76 (vs. TEY/TMP ratio 0.45–0.53); dense tiny conical spines present on surface of chest extending to anterior region of abdomen (vs. such spines less developed, present on surface of chest, not extending to anterior region of abdomen); lateral fringes on toes narrow but more developed and distinct (vs. less developed); length of toe V < III (length of toe V = III).

Compared with the 26 known congeners of the genus Leptobrachella occurring south of the Isthmus of Kra, by the presence of supra-axillary and ventrolateral glands, L. purpuraventra sp. nov. can be easily distinguished from L. arayai, L. dringi, L. fritinniens, L. gracilis, L. hamidi, L. heteropus, L. kajangensis, L. kecil, L. marmorata, L. melanoleuca, L. maura, L. picta, L. platycephala, L. sabahmontana, and L. sola, all of which lacking supra-axillary and ventrolateral glands; and by the significantly larger body size, SVL 27.3–29.8 mm in males, 33.0–35.3 mm in females, L. purpuraventra sp. nov. differs from the smaller L. baluensis (14.9–15.9 mm in males), L. bondangensis (17.8 mm in male), L. brevicrus (17.1–17.8 mm in males), L. fusca (16.3 mm in male), L. itiokai (15.2–16.7 mm in males), L. juliandringi (17.0–17.2 mm in males and 18.9–19.1 mm in females), L. mjobergi (15.7–19.0 mm in males), L. natunae (17.6 mm in male), L. parva (15.0–16.9 mm in males and 17.8 mm in female), L. palmata (14.4–16.8 mm in males), L. serasanae (16.9 mm in female), and Dring’s (1983) Leptobrachella sp. 3 “baluensis” (15.0–16.0 mm in males).

For the remaining 45 members of the genus Leptobrachella, in having SVL 27.3–29.8 mm in males and 33.0–35.3 mm in females, L. purpuraventra sp. nov. differs from the larger L. bourreti (42.0–45.0 mm in females), L. eos (33.1–34.7 mm in males and 40.7 in female), L. lateralis (36.6 mm in females), L. nahangensis (40.8 mm in male), L. nyx (37.0–41.0 mm in females), L. sungi (48.3–52.7 mm in males and 56.7–58.9 mm in females), L. tamdil (32.3 mm in male), and L. zhangyapingi (45.8–52.5 mm in males); and from the smaller L. alpinus (24.0–26.4 mm in males), L. applebyi (19.6–22.3 mm in males and 21.7–26.4 mm in females), L. ardens (21.3–24.7 mm in males, 24.5 mm in female), L. bidoupensis (18.5–25.4 mm in males), L. kalonensis (28.9–30.6 mm in females), L. maculosa (27.0 mm in female), L. maoershanensis (29.1 mm in female), L. mangshanensis (30.2 mm in female), L. melica (19.5–22.7 mm in males), L. pluvialis (21.3–22.3 mm in males), L. rowleyae (23.4–25.4 mm in males), L. tadungensis (32.1 mm in female), and L. tengchongensis (23.9–26.0 mm in males).

In having black spots on flanks, the new species differs from L. aerea, L. botsfordi, L. crorea, L. firthi, L. isos, L. pallida, L. petrops, and L. tuberosa, all of which lacking black spots on flanks; by having rudimentary webbing on toes, the new species differs from L. oshanensis, L. pallida and L. petrops, all of which lacking webbing on toes, and from L. pelodytoides, which bears wide webbing on toes; by having narrow lateral fringes on toes, the new species differs from L. aerea, L. firthi, L. isos, L. khasiorum, L. laui, L. liui, L. purpura, L. yunkaiensis, and L. yingjiangensis, all of which having wide lateral frings on toes, from L. fuliginosa, which having weak lateral fringes on toes, and from L. crocea, L. macrops, L. minima, L. oshanensis, L. pallida, L. pyrrhops, L. tuberosa, and L. ventripunctata, all of which lacking lateral fringes on toes; by having dorsal surface shagreened and granular, lacking enlarge tubercles or warts, the new species differs from L. fuliginosa (dorsum smooth with fine tubercles), L. laui (dorsum with round granular tubercle, lacking skin ridges), L. liui (dorsum with round tubercles), L. macrops (dorsum roughly granular with large tubercles), L. minima (dorsum smooth), L. pelodytoides (dorsum with small, smooth warts), L. tuberosa (dorsum highly tuberculate), L. yunkaiensis (dorsum with raised warts), and L. wuhuangmontis (dorsum rough with conical tubercles); by having ventral surface grey purple with distinct nebulous greyish speckling on chest and ventrolateral flanks, the new species differs from L. botsfordi and L. pyrrhops, (ventral reddish brown with white speckling), L. khasiorum (ventral creamy white), L. macrops (ventral Greyish-violet with white speckling), L. nokrekensis (ventral creamy white), L. puhoatensis (ventral reddish brown with white dusting), L. purpura (ventral dull white with indistinct grey dusting), L. tuberosa (ventral white with small grey spots/streaks), L. ventripunctata (chest and belly with large dark brown spots), L. wuhuangmontis (ventral greyish white), L. yunkaiensis (belly pink with speckling), and L. yingjiangensis (ventral creamy white); by having tiny spines on surface of chest extending to anterior region of abdomen in males during breeding season, the new species differs from all male specimens collected in breeding season of L. liui, L. oshanensis, L. yunkaiensis and L. wuhuangmontis, all of which lacking such spines.

Description of holotype

Adult male. Body size small, SVL in 29.6 mm. Head length slightly larger than head width, HDL/HDW 1.05; snout slightly protruding, projecting slightly beyond margin of the lower jaw; nostril closer to snout than eye; canthus rostralis gently rounded; loreal region slightly concave; interorbital space flat, internarial distance larger than interorbital distance, IND/IOD 1.09; pineal ocellus absent; vertical pupil; snout length larger than eye diameter, SNT/EYE 1.14; tympanum distinct, rounded, and slightly concave, diameter smaller than that of the eye and larger than tympanum-eye distance, TMP/EYE 0.54 and TEY/TMP 0.68; upper margin of tympanum incontact with supratympanic ridge; distinct black supratympanic line present; vomerine teeth absent; vocal sac openings slit-like, paired, located posterolaterally on floor of mouth in close proximity to the margins of the mandible; tongue deeply notched behind; supratympanic ridge distinct, extending from posterior corner of eye to supra-axillary gland.

Tips of fingers rounded, slightly swollen; relative finger lengths I = II = IV < III; nuptial pad absent; subarticular tubercles absent; a large, rounded inner palmar tubercle distinctly separated from small, round outer palmar tubercle; absence of webbing and lateral fringes on fingers. Tips of toes like fingers; relative toe length I < II < V < III < IV; subarticular tubercles absent; distinct dermal ridges present under the 3^rd to 5^th toes, not interrupted; large, oval inner metatarsal tubercle present, outer metatarsal tubercle absent; toes webbing rudimentary; narrow lateral fringes present on all toes. Tibia 45% of snout-vent length; tibiotarsal articulation reaches to middle of eye; heels just meeting each other when thighs are appressed at right angles with respect to body.

Dorsal surface shagreened and granular, lacking enlarge tubercles or warts, some of the granules forming short longitudinal folds; ventral skin smooth; dense tiny conical spines present on surface of chest and extending to anterior region of abdomen; pectoral gland and femoral gland oval; pectoral glands greater than tips of fingers and femoral glands; femoral gland situated on posteroventral surface of thigh, closer to knee than to vent; supra-axillary gland raised. Ventrolateral gland distinctly visible, forming an incomplete line.

Measurements of holotype (in mm)

SVL 29.6, HDL 10.2, HDW 9.7, SNT 4.0, EYE 3.5, IOD 3.2, IND 3.5, TMP 1.9, TEY 1.3, TIB 13. 3, ML 7.7, PL 12.7, LAHL 13.8, HLL 42.7.

Coloration of holotype in life

Dorsum dark purple brown grounding, with small light orange granules, distinct darker brown markings and rounded spots and scattered with irregular light orange pigmentations. A dark brown V-shaped pattern between anterior corner of eyes, in connected to the dark brown W-shaped marking on interorbital region, and the W-shaped marking in connected to the other W-shaped marking between axillae. Tympanum brown. A dark brown vertical bar under the eye; transverse dark brown bars on dorsal surface of limbs; distinct dark brown blotches on flanks from groin to axilla, longitudinally in two rows; elbow and upper arms with dark bars and distinct coppery orange coloration; fingers and toes with distinct dark bars.

Ventral surface grey purple, with distinct nebulous greyish speckling scattered with white spots on chest and ventrolateral flanks. Supra-axillary gland coppery orange with dark brown speckling; femoral, pectoral and ventrolateral glands greyish white. Iris bicolored, coppery orange on upper half and silver on lower half.

Coloration of holotype in preservative

Variations

Measurements and body proportions were listed in Table 7. All paratypes match the overall characters of the holotype except that: coloration of dorsum dark purple brown in the holotype SYS a007284 (vs. grey purple brown in paratypes SYS a007300 (Figure 7E), 7303, 7305 (Figure 8C), 7306; purple brown in paratypes SYS a007278 (Figure 8E), 7279, 7282, 7283 (Figure 7F), 7304 (Figure 8A)); heels just meeting (vs. heels slightly overlapping in paratypes SYS a007300, 7302); W-shaped marking on interorbital region in connected to the other W-shaped marking between axillae in the holotype (vs. such markings not in connected with each other in paratypes SYS a007278, 7282); a V-shaped pattern between anterior corner of eyes in the holotype (vs. a dark brown inverted triangular pattern between anterior corner of eyes instead in the paratype SYS a007300); relatively smaller black spots on flanks (vs. black spots distinctly large in paratypes SYS a007300–7301, 7304, 7306); ventral surface without black spots in the holotype (vs. presence of irregular black spots in paratype SYS a007278 (Figure 8F)).

Table 7.

Download as

CSV

XLSX

Measurements (minimum–maximum (mean ± SD); in mm), and body proportions of Leptobrachella purpuraventra sp. nov.: population A from Wujing Nature Reserve in Bijie City, population B from Baimashan Forest Station of Zhaozishan Nature Reserve.

Population	A		B		A + B
SEX	Males	Female	Males	Females	Males	Females
SEX	(n = 7)	(n = 1)	(n = 4)	(n = 3)	(n = 11)	(n = 4)
SVL	27.3–29.6	35.3	28.3–29.8	33.0–34.5	27.3–29.8	33.0–35.3
SVL	(28.6 ± 0.7)	35.3	(29.3 ± 0.6)	(33.5 ± 0.7)	(28.9 ± 0.8)	(34.0 ± 1.0)
HDL	9.6–10.2	12	9.7–10.3	11.0–11.7	9.6–10.3	11.0–12.0
HDL	(9.9 ± 0.2)	12	(10.1 ± 0.2)	(11.3 ± 0.3)	(10.0 ± 0.2)	(11.5 ± 0.4)
HDW	9.3–9.7	11.5	9.6–9.8	10.5–11.3	9.3–9.8	10.5–11.5
HDW	(9.5 ± 0.1)	11.5	(9.8 ± 0.1)	(10.9 ± 0.3)	(9.6 ± 0.2)	(11.1 ± 0.4)
SNT	3.5–4.0	4.6	3.8–4.1	4.2–4.4	3.5–4.1	4.2–4.6
SNT	(3.8 ± 0.1)	4.6	(4.0 ± 0.1)	(4.3 ± 0.1)	(3.8 ± 0.2)	(4.4 ± 0.1)
EYE	3.1–3.5	3.8	3.3–3.6	3.7–3.9	3.1–3.6	3.7–3.9
EYE	(3.3 ± 0.2)	3.8	(3.5 ± 0.1)	(3.8 ± 0.1)	(3.4 ± 0.2)	(3.8 ± 0.1)
IOD	2.6–3.2	3.5	3.0–3.2	3.2–3.3	2.6–3.2	3.2–3.5
IOD	(2.9 ± 0.2)	3.5	(3.1 ± 0.1)	(3.2 ± 0.1)	(2.9 ± 0.2)	(3.3 ± 0.1)
IND	2.7–3.5	3.6	3.2–3.3	3.3–3.5	2.7–3.5	3.3–3.6
IND	(3.0 ± 0.3)	3.6	(3.0 ± 0.1)	(3.4 ± 0.1)	(3.1 ± 0.2)	(3.5 ± 0.1)
TMP	1.7–1.9	2.1	1.8–1.9	2.0–2.1	1.7–1.9	2.0–2.1
TMP	(1.8 ± 0.1)	2.1	(1.8 ± 0.1)	(2.0 ± 0.1)	(1.8 ± 0.1)	(2.1 ± 0.1)
TEY	1.2–1.3	1.3	1.1–1.2	1.2–1.3	1.1–1.3	1.2–1.3
TEY	(1.3 ± 0.1)	1.3	(1.1 ± 0.1)	(1.2 ± 0.1)	(1.2 ± 0.1)	(1.3 ± 0.1)
TIB	12.5–13.3	15.5	13.2–14.0	14.6–15.4	12.5–14.0	14.6–15.5
TIB	(12.8 ± 0.3)	15.5	(13.6 ± 0.4)	(15.0 ± 0.3)	(13.1 ± 0.5)	(15.2 ± 0.4)
ML	7.0–7.7	7.8	7.5–7.6	7.7–8.0	7.0–7.7	7.7–8.0
ML	(7.3 ± 0.2)	7.8	(7.5 ± 0.1)	(7.9 ± 0.1)	(7.4 ± 0.2)	(7.9 ± 0.1)
PL	12.1–12.7	14.8	12.6–13.2	13.7–14.7	12.1–13.2	13.7–14.8
PL	(12.4 ± 0.2)	14.8	(13.0 ± 0.2)	(14.2 ± 0.4)	(12.6 ± 0.4)	(14.4 ± 0.4)
LAHL	12.6–13.8	15.5	13.4–14.0	14.7–15.7	12.6–14.0	14.7–15.7
LAHL	(13.2 ± 0.4)	15.5	(13.6 ± 0.2)	(15.1 ± 0.4)	(13.3 ± 0.4)	(15.2 ± 0.4)
HLL	39.0–42.7	47.8	40.1–44.6	46.0–47.3	39.0–44.6	46.0–47.8
HLL	(40.4 ± 1.4)	47.8	(43.2 ± 1.8)	(46.8 ± 0.6)	(41.4 ± 2.1)	(47.0 ± 0.7)
HDL/HDW	1.01–1.05	1.04	1.01–1.06	1.04–1.05	1.01–1.06	1.04–1.05
HDL/HDW	(1.04 ± 0.01)	1.04	(1.04 ± 0.02)	(1.04 ± 0.01)	(1.04 ± 0.02)	(1.04 ± 0.01)
HDL/SVL	0.33–0.35	0.34	0.34–0.35	0.33–0.34	0.33–0.35	0.33–0.34
HDL/SVL	(0.34 ± 0.02)	0.34	(0.34 ± 0.01)	(0.34 ± 0.01)	(0.34 ± 0.01)	(0.34 ± 0.01)
SNT/HDL	0.36–0.39	0.38	0.39–0.40	0.38	0.36–0.40	0.38
SNT/HDL	(0.38 ± 0.01)	0.38	(0.39 ± 0.01)	0.38	(0.39 ± 0.01)	0.38
SNT/EYE	1.12–1.19	1.21	1.11–1.15	1.11–1.16	1.11–1.19	1.11–1.21
SNT/EYE	(1.14 ± 0.02)	1.21	(1.14 ± 0.02)	(1.13 ± 0.02)	(1.14 ± 0.02)	(1.15 ± 0.04)
EYE/TMP	1.82–1.89	1.81	1.83–1.94	1.85–1.90	1.82–1.94	1.81–1.90
EYE/TMP	(1.86 ± 0.03)	1.81	(1.89 ± 0.04)	(1.87 ± 0.02)	(1.87 ± 0.04)	(1.85 ± 0.03)
TMP/EYE	0.53–0.55	0.55	0.51–0.55	0.53–0.54	0.51–0.55	0.53–0.55
TMP/EYE	(0.54 ± 0.01)	0.55	(0.53 ± 0.01)	(0.53 ± 0.01)	(0.53 ± 0.01)	(0.54 ± 0.01)
IND/IOD	1.03–1.09	1.03	1.03–1.10	1.03–1.06	1.03–1.10	1.03–1.06
IND/IOD	(1.06 ± 0.02)	1.03	(1.07 ± 0.03)	(1.05 ± 0.01)	(1.07 ± 0.03)	(1.05 ± 0.02)
TEY/TMP	0.67–0.76	0.62	0.61–0.67	0.60–0.62	0.61–0.76	0.60–0.62
TEY/TMP	(0.71 ± 0.03)	0.62	(0.64 ± 0.02)	(0.61 ± 0.01)	(0.68 ± 0.04)	(0.61 ± 0.01)
TIB/SVL	0.44–0.46	0.44	0.45–0.47	0.44–0.46	0.44–0.47	0.44–0.46
TIB/SVL	(0.45 ± 0.01)	0.44	(0.47 ± 0.01)	(0.45 ± 0.01)	(0.45 ± 0.01)	(0.45 ± 0.01)
LAHL/SVL	0.45–0.47	0.44	0.45–0.47	0.44–0.46	0.45–0.47	0.44–0.46
LAHL/SVL	(0.46 ± 0.01)	0.44	(0.46 ± 0.01)	(0.45 ± 0.01)	(0.46 ± 0.01)	(0.45 ± 0.01)
HLL/SVL	1.36–1.46	1.35	1.42–1.51	1.37–1.42	1.36–1.51	1.35–1.42
HLL/SVL	(1.41 ± 0.03)	1.35	(1.47 ± 0.04)	(1.39 ± 0.02)	(1.43 ± 0.05)	(1.38 ± 0.02)
TIB/HLL	0.31–0.32	0.32	0.31–0.33	0.32–0.33	0.31–0.33	0.32–0.33
TIB/HLL	(0.31 ± 0.01)	0.32	(0.32 ± 0.01)	(0.32 ± 0.01)	(0.32 ± 0.01)	(0.32 ± 0.01)

Figure 8.

General aspect in life of the female paratypes of Leptobrachella purpuraventra sp. nov. A, B SYS a007304 C, D SYS a007305 E, F SYS a007278.

Etymology

The specific epithet pupura is given as a noun in apposition and means “purple color”, and ventra, is given as a noun in apposition and means “ventral”, in reference to the purple coloration of ventral of the new species. For the common name, we suggest “Purple-bellied Leaf Litter Toad”, and for the Chinese name “Zi Fu Zhang Tu Chan (紫腹掌突蟾)”.

Distribution and habits

Currently, Leptobrachella purpuraventra sp. nov. is known from its type locality Jinjiazhai Village in Wujing Nature Reserve, Chahe County, and Baimashan Forest Station in Zhaozishan Nature Reserve, both in Qixingguan District, Bijie City, Guizhou Province, China (Figure 1). The new species was found along a clear-water rocky stream (ca. 3 m in width and ca. 10–20 cm in depth) surrounded by a broad-leaved forest in karst landforms (Figure 9, 1600–1900 m a.s.l.). From 2 July to 4 July in 2018 at 21:00–23:50 P.M., a large number of males were found calling on leaves of plants (Figure 10B), and some were found calling perching on the rocks or under rocks by the side of the stream.

Figure 9.

The habitat of Leptobrachella purpuraventra sp. nov. in Baimashan Forest Station of Zhaozishan Nature Reserve in Guizhou Province.

Figure 10.

General aspect observed in the field of A Leptobrachella bijie sp. nov. and B L. purpuraventra sp. nov., showing a single vocal sac and different skin colors of the two new species.

Discussion

The discoveries of Leptobrachella bijie sp. nov. and L. purpuraventra sp. nov. bring the total number of this genus to 73, with 16 of them recorded in China (Fei et al. 2012; Frost 2017; Wang et al. 2018). Before the descriptions of the two new species from northwestern Guizhou Province in this study, only L. oshanensis was recorded in northeastern and southern Guizhou Province, which further highlights the underestimated of the species diversity of the genus. Further investigation of the genus in adjacent regions is required.

Studies of the taxonomy and phylogeny of Leptobrachella were difficult to perform because of the morphological conservativeness of the species (for example, the two new species appeared very similar morphologically in the field (Figure 10)), which likely to hinder our understanding of these cryptic species (Ohler et al. 2010; Sung et al. 2014; Wang et al. 2018).

Leptobrachella bijie sp. nov. and L. purpuraventra sp. nov. were both found in Zhaozishan Nature Reserve, only approximately seven kilometers apart, straight-line distance, but they possessed a significant genetic divergence (p=3.9–4.2%). This compares to the two populations of L. purpuraventra sp. nov. from Zhaozishan Nature Reserve and Wujing Nature Reserve, which were approximately 65 kilometers apart, but displayed almost no genetic divergence. Without phylogenetic, morphological, and acoustic analyses, it would be difficult to determine the taxonomic status of these two species. Thus, specimen, acoustic data, and tissue sample collection play important roles in discovering the high species diversity of the genus Leptobrachella.

Leptobrachella bijie sp. nov. and L. purpuraventra sp. nov. were found along clear-water rocky streams, and such environments are very limited in the karst landforms. At present, little is known about the ecology and behavior of the two new species, however, the known habitat of the two new species is under threat of degradation, particularly as a result of grazing. Thus, further research on the true distribution, population size and trends, and conservation actions required, are urgently needed.

Acknowledgements

We would like to thank Mr Yong-You Zhao and Jia-He Li for their help in the field work. This work was supported by the Project of the specimen platform of China (2005DKA21403-JK), teaching specimen sub-platform to Y.Y. Wang.

References

Anderson J (1871) A list of the reptilian accession to the Indian Museum, Calcutta from 1865 to 1870, with a description of some new species. Journal of the Asiatic Society of Bengal 40: 12–39.

Boulenger GA (1893) Concluding report on the reptiles and batrachians obtained in Burma by Signor L. Fea dealing with the collection made in Pegu and the Karin Hills in 1887–88. Annali del Museo Civico di Storia Naturale di Genova 13: 304–347.

Boulenger GA (1900) Descriptions of new batrachians and reptiles from the Larut Hills, Perak. Annals and Magazine of Natural History 6: 186–194. https://doi.org/10.1080/00222930008678356

Boersma P (2001) PRAAT, a system for doing phonetics by computer. Glot International 5: 341–345. https://doi.org/10.1097/AUD.0b013e31821473f7

Bioacoustics Research Program (2013) Raven Pro: Interactive sound analysis software. Version 1.5. http://www.birds.cornell.edu/raven

Chen JM, Poyarkov NJ, Suwannapoom C, Lathrop A, Wu YH, Zhou WW, Yuan ZY, Jin JQ, Chen HM, Liu HQ, Nguyen TQ, Nguyen SN, Duong TV, Eto K, Nishikawa K, Matsui M, Orlov NL, Stuart BL, Brown RM, Rowley J, Murphy RW, Wang YY, Che J (2018) Large-scale phylogenetic analyses provide insights into unrecognized diversity and historical biogeography of Asian leaf-litter frogs, genus Leptolalax (Anura: Megophryidae). Molecular Phylogenetics and Evolution 124: 162–171. https://doi.org/10.1016/j.ympev.2018.02.020

Darriba D, Taboada GL, Doallo R, Posada D (2012) jModelTest 2: more models, new heuristics and parallel computing. Nature methods 9: 772. https://doi.org/10.1038/nmeth.2109

Das I, Tron RKL, Rangad D, Hooroo RN (2010) A new species of Leptolalax (Anura: Megophryidae) from the sacred groves of Mawphlang, Meghalaya, north-eastern India. Zootaxa 2339: 44–56. https://doi.org/10.11646/zootaxa.2339.1.2

Dehling JM, Matsui M (2013) A new species of Leptolalax (Anura: Megophryidae) from Gunung Mulu National Park, Sarawak, East Malaysia (Borneo). Zootaxa 3670(1): 33–44.

Dehling JM (2012a) Eine neue Art der Gattung Leptolalax (Anura: Megophryidae) vom Gunung Benom, Westmalaysia/A new species of the genus Leptolalax (Anura: Megophryidae) from Gunung Benom, Peninsular Malaysia. Sauria 34: 9–21.

Dehling JM (2012b) Redescription of Leptolalax gracilis (Günther, 1872) from Borneo and taxonomic status of two populations of Leptolalax (Anura: Megophryidae) from Peninsular Malaysia. Zootaxa 3328: 20–34. https://doi.org/10.11646/zootaxa.3328.1.2

Delorme M, Dubois A, Grosjean S, Ohler A (2006) Une nouvelle ergotaxinomie des Megophryidae (Amphibia, Anura). Alytes 24: 6–21. https://doi.org/10.1163/156853883X00012

Dring J (1983) Frogs of the genus Leptobrachella (Pelobatidae). Amphibia-Reptillia 4: 89–102. https://doi.org/10.1163/156853883X00012

Dubois A (1983) Note preliminaire sur le genre Leptolalax Dubois, 1980 (Amphibiens, Anoures), avec diagnose d’une espece novelle du Vietnam. Alytes 2: 147–153.

Eto K, Matsui M, Nishikawa K (2015) Description of a new species of the genus Leptobrachella (Amphibia, Anura, Megophryidae) from Borneo. Current Herpetology 34(2): 128–139. https://doi.org/10.5358/hsj.34.128

Eto K, Matsui M, Nishikawa K (2016) A new highland species of dwarf litter frog genus Leptobrachella (Amphibia, Anura, Megophryidae) from Sarawak. Raffles Bulletin of Zoology 64: 194–203.

Eto K, Matsui M, Hamidy A, Munir M, Iskandar DT (2018) Two new species of the genus Leptobrachella (Amphibia: Anura: Megophryidae) from Kalimantan, Indonesia. Current Herpetology 37(2): 95–105. https://doi.org/10.5358/hsj.37.95

Fei L, Hu SQ, Ye CY, Huang YZ (2009) Fauna Sinica. Amphibia Vol. 2 Anura. Science Press, Beijing, 957 pp. [In Chinese]

Fei L, Ye CY, Jiang JP (2012) Colored atlas of Chinese amphibians and their distributions. Sichuan Publishing House of Science & Technology, Chengdu, 619 pp. [In Chinese]

Frost DR (2017) Amphibian Species of the World: an Online Reference. Version 6.0. Electronic Database. American Museum of Natural History, New York, USA. http://research.amnh.org/herpetology/amphibia/index.html [accessed 7 October 2017]

Grismer LL, Grismer JL, Youmans TM (2004) A new species of Leptolalax (Anura: Megophryidae) from Pulau Tioman, West Malaysia. Asiatic Herpetological Research 10: 8–11.

Günther A (1872) On the reptiles and amphibians of Borneo. Proceedings of the Scientific Meetings of the Zoological Society of London 1872: 586–600.

Günther A (1985) The reptiles and batrachians of the Natuna Islands. Novitates Zoologicae 2: 499–502.

Humtsoe LN, Bordoloi S, Ohler A, Dubois A (2008) Rediscovery of a long known species, Ixalus lateralis Anderson, 1871. Zootaxa 1921: 24–34.

Hou YM, Zhang MF, Hu F, Li SY, Shi SC, Chen J, Mo XY, Wang B (2018) A new species of the genus Leptolalax (Anura, Megophryidae) from Hunan, China. Zootaxa 4444(3): 247–266. https://doi.org/10.11646/zootaxa.4444.3.2

Inger RF, Lakim M, Biun A, Yambun P (1997) A new species of Leptolalax (Anura: Megophryidae) from Borneo. Asiatic Herpetological Research 7: 48–50. https://doi.org/10.5962/bhl.part.18855

Inger RF, Orlov N, Darevsky I (1999) Frogs of Vietnam: a report on new collections. Fieldiana Zoology 92: 1–46.

Inger RF, Stuebing RB, Tan FL (1995) New species and new records of anurans from Borneo. Raffles Bulletin of Zoology 43: 115–132.

Jiang K, Yan F, Suwannapoom C, Chomdej S, Che J (2013) A new species of the genus Leptolalax (Anura: Megophryidae) from northern Thailand. Asian Herpetological Research 4(2): 100–108. https://doi.org/10.3724/SP.J.1245.2013.00100

Lathrop A, Murphy RW, Orlov N, Ho CT (1998) Two new species of Leptolalax (Anura: Megophryidae) from northern Vietnam. Amphibia-Reptilia 19: 253–267. https://doi.org/10.1163/156853898X00160

Mahalanobis PC (1936) On the generalised distance in statistics. Proceedings of the National Institute of Sciences of India 2(1): 49–55.

Malkmus R (1992) Leptolalax pictus sp. nov. (Anura: Pelobatidae) vom Mount Kinabalu/Nord-Borneo. Sauria 14: 3–6.

Mahony S, Foley NM, Biju S, Teeling EC (2017) Evolutionary history of the Asian Horned Frogs (Megophryinae): integrative approaches to timetree dating in the absence of a fossil record. Molecular Biology and Evolution 34(3): 744–771. https://doi.org/10.1093/molbev/msw267

Matsui M (1997) Call characteristics of Malaysian Leptolalax with a description of two new species (Anura: Pelobatidae). Copeia: 158–165. https://doi.org/10.2307/1447851

Matsui M (2006) Three new species of Leptolalax from Thailand (Amphibia, Anura, Megophryidae). Zoological Science 23(9): 821–830. https://doi.org/10.2108/zsj.23.821

Matsui M, Dehling JM (2012) Notes on an enigmatic Bornean megophryid, Leptolalax dringi Dubois, 1987 (Amphibia: Anura). Zootaxa 3317: 49–58. https://doi.org/10.11646/zootaxa.3317.1.4

Matsui M, Belabut DM, Ahmad N, Yong HS (2009) A new species of Leptolalax (Amphibia, Anura, Megophryidae) from Peninsular Malaysia. Zoological Science 26(3): 243–247. https://doi.org/10.2108/zsj.26.243

Matsui M, Nishikawa K, Yambun P (2014a) A new Leptolalax from the mountains of Sabah, Borneo (Amphibia, Anura, Megophryidae). Zootaxa 3753(3): 440–452. https://doi.org/10.11646/zootaxa.3753.5.3

Matsui M, Zainudin R, Nishikawa K (2014b) A New Species of Leptolalax from Sarawak, Western Borneo (Anura: Megophryidae). Zoological Science 31(11): 773–779. https://doi.org/10.2108/zs140137

Mathew R, Sen N (2010 “2009”) Description of a new species of Leptobrachium Tschudi, 1838 (Amphibia: Anura: Megophryidae) from Meghalaya, India. Records of the Zoological Survey of India 109: 91–108.

Nguyen TQ, Schmitz A, Nguyen TT, Orlov NL, Böhme W, Ziegler T (2011) Review of the Genus Sphenomorphus Fitzinger, 1843 (Squamata: Sauria: Scincidae) in Vietnam, with Description of a New Species from Northern Vietnam and Southern China and the First Record of Sphenomorphus mimicus Taylor, 1962 from Vietnam. Journal of Herpetology 45(2): 145–154. https://doi.org/10.1670/09-068.1

Ohler A, Marquis O, Swan S, Grosjean S (2000) Amphibian biodiversity of Hoang Lien Nature Reserve (Lao Cai Province, northern Vietnam) with description of two new species. Herpetozoa 13(1/2): 71–87.

Ohler A, Wollenberg KC, Grosjean S, Hendrix R, Vences M, Ziegler T, Dubois A (2011) Sorting out Lalos: description of new species and additional taxonomic data on megophryid frogs from northern Indochina (genus Leptolalax, Megophryidae, Anura). Zootaxa 3147: 1–83. https://doi.org/10.11646/zootaxa.3147.1.1

Poyarkov NJ, Rowley JJ, Gogoleva SI, Vassilieva AB, Galoyan EA, Orlov NL (2015) A new species of Leptolalax (Anura: Megophryidae) from the western Langbian Plateau, southern Vietnam. Zootaxa 3931(2): 221–252. https://doi.org/10.11646/zootaxa.3931.2.3

R Core Team (2016) R: A language and environment for statistical computing. https://www.r-project.org/

Ronquist F, Teslenko M, Van Der Mark P, Ayres DL, Darling A, Höhna S, Larget B, Liu L, Suchard MA, Huelsenbeck JP (2012) MrBayes 3.2: efficient Bayesian phylogenetic inference and model choicem across a large model space. Systematic Biology 61: 539–542. https://doi.org/10.1093/sysbio/sys029

Rowley JJ, Cao TT (2009) A new species of Leptolalax (Anura: Megophryidae) from central Vietnam. Zootaxa 2198: 51–60.

Rowley JJ, Dau VQ, Nguyen TT (2013) A new species of Leptolalax (Anura: Megophryidae) from the highest mountain in Indochina. Zootaxa 3737(4): 415–428. https://doi.org/10.11646/zootaxa.3737.4.5

Rowley JJ, Dau VQ, Hoang HD, Le DTT, Cutajar TP, Nguyen TT (2017) A new species of Leptolalax (Anura: Megophryidae) from northern Vietnam. Zootaxa 4243: 544–564. https://doi.org/10.11646/zootaxa.4243.3.7

Rowley JJ, Tran DTA, Le DTT, Dau VQ, Peloso PLV, Nguyen TQ, Hoang HD, Nguyen TT, Ziegler T (2016) Five new, microendemic Asian Leaf-litter Frogs (Leptolalax) from the southern Annamite mountains, Vietnam. Zootaxa 4085: 63–102. https://doi.org/10.11646/zootaxa.4085.1.3

Rowley JJ, Hoang DH, Le TTD Dau QV, Cao TT (2010a) A new species of Leptolalax (Anura: Megophryidae) from Vietnam and further information on Leptolalax tuberosus. Zootaxa 2660: 33–45.

Rowley JJ, Le DTT, Tran DTA, Hoang DH (2011) A new species of Leptobrachella (Anura: Megophryidae) from southern Vietnam. Zootaxa 2796: 15–28. https://doi.org/10.11646/zootaxa.2796.1.2

Rowley JJ, Stuart BL, Neang T, Emmett DA (2010b) A new species of Leptolalax (Anura: Megophryidae) from northeastern Cambodia. Zootaxa 2567: 57–68. https://doi.org/10.11646/zootaxa.2567.1.3

Rowley JJ, Stuart BL, Richards SJ, Phimmachak S, Sivongxay N (2010c) A new species of Leptolalax (Anura: Megophryidae) from Laos. Zootaxa 2681: 35–46. https://doi.org/10.11646/zootaxa.2681.1.3

Rowley JJ, Hoang HD, Dau VQ, Le TTD Cao TT (2012) A new species of Leptolalax (Anura: Megophryidae) from central Vietnam. Zootaxa 3321: 56–68. https://doi.org/10.11646/zootaxa.3321.1.4

Rowley JJ, Stuart BL, Neang T, Hoang HD, Dau VQ, Nguyen TT, Emmett DA (2015a) A new species of Leptolalax (Anura: Megophryidae) from Vietnam and Cambodia. Zootaxa 4039: 401–417. https://doi.org/10.11646/zootaxa.4039.3.1

Rowley JJL, Tran DTA, Frankham GJ, Dekker AH, Le DTT, Nguyen TQ, Dau VQ, Hoang HD (2015b) Undiagnosed Cryptic Diversity in Small, Microendemic Frogs (Leptolalax) from the Central Highlands of Vietnam. PLoS ONE 10(5): e0128382. https://doi.org/10.1371/journal.pone.0128382

Sengupta S, Sailo S, Lalremsanga HT, Das A, Das I (2010) A new species of Leptolalax (Anura: Megophryidae) from Mizoram, north-eastern India. Zootaxa 2406: 56–68. https://doi.org/10.11646/zootaxa.2406.1.3

Silvestro D, Michalak I (2012) raxmlGUI: a graphical front-end for RAxML. Organisms Diversity & Evolution 12: 335–337. https://doi.org/10.1007/s13127-011-0056-0

Simon C, Frati F, Beckenbach A, Crespi B, Liu H, Flook P (1994) Evolution, weighting, and phylogenetic utility of mitochondrial gene sequences and a compilation of conserved polymerase chain reaction primers. Annals of the Entomological Society of America 87: 651–701. https://doi.org/10.1093/aesa/87.6.651

Sung YH, Yang JH, Wang YY (2014) A new species of Leptolalax (Anura: Megophryidae) from southern China. Asian Herpetological Research 5(2): 80–90. https://doi.org/10.3724/SP.J.1245.2014.00080

Taylor EH (1962) The amphibian fauna of Thailand. University of Kansas Science Bulletin 43: 265–599. https://doi.org/10.5962/bhl.part.13347

Tamura K, Stecher G, Peterson D, Filipski A, Kumar S (2013) MEGA6: Molecular Evolutionary Genetics Analysis version 6.0. Molecular Biology and Evolution 30: 2725–2729. https://doi.org/10.1093/molbev/mst197

Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG (1997) The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Research 25: 4876–4882. https://doi.org/10.1093/nar/25.24.4876

Nguyen LT, Poyarkov NJ, Le DTT, Vo BD, Phan HT, Duong TV, Murphy RW, Nguyen SN (2018) A new species of Leptolalax (Anura: Megophryidae) from Son Tra Peninsula, central Vietnam. Zootaxa 4388: 1–21. https://doi.org/10.11646/zootaxa.4388.1.1

Ward Jr JH (1963) Hierarchical grouping to optimize an objective function. Journal of the American statistical association 58: 236–244. https://doi.org/10.1080/01621459.1963.10500845

Wang YY, Yang JH, Liu Y (2013) New Distribution Records for Sphenomorphus tonkinensis (Lacertilia: Scincidae) with Notes on Its Variation and Diagnostic Characters. Asian Herpetological Research 4(2): 147–150. https://doi.org/10.3724/SP.J.1245.2013.00147

Yang JH, Wang YY, Chen GL, Rao DQ (2016) A new species of the genus Leptolalax (Anura: Megophryidae) from Mt. Gaoligongshan of western Yunnan Province, China. Zootaxa 4088: 379–394. https://doi.org/10.11646/zootaxa.4088.3.4

Yang JH, Zeng ZC, Wang YY (2018) Description of two new sympatric species of the genus Leptolalax (Anura: Megophryidae) from western Yunnan of China. PeerJ 6(e4586): 1–32. https://doi.org/10.7717/peerj.4586

Yuan ZY, Sun RD, Chen JM, Rowley JJ, Wu ZJ, Hou SB, Wang SN, Che J (2017) A new species of the genus Leptolalax (Anura: Megophryidae) from Guangxi, China. Zootaxa 4300: 551–570. https://doi.org/10.11646/zootaxa.4300.4.5

Appendix 1

Specimens examined

Leptobrachella alpinus (n = 6): China: Yunnan Province: Jingdong County: Mt. Wuliang: CIB 24353 (Holotype), CIB 24354; SYS a 003927.

Leptobrachella laui (n = 26): China: Hong Kong: SYS a002057 (Holotype), SYS a002058; China: Guangdong Province: Shenzhen City: SYSa 001505–1507, 1515–1521, 3471–3472, 5644–5645.

Leptobrachella liui (n = 18): China: Fujian Province: Mt. Wuyi: CIB 24355 (Holotype), CIB 24356, SYS a001571–1578, 1595–1599, 2478–2479, 5925–5826.

Leptobrachella oshanensis (n = 2): China: Sichuan Province: Meishan City: Mt. Emei: SYS a001829–1830.

Leptobrachella tengchongensis (n = 6): China: Yunnan Province: Baoshan City: Mt. Gaoligong: SYS a004600 (Holotype), 4596–4599, 4601–4602.

Leptobrachella wuhuangmontis (n = 12): China: Guangxi Province: Pubei County: Mt. Wuhuang: SYS a003500/CIB107274, SYS a000578, 0580–0581, 3485–3489, 3499, 3504–3506.

Leptobrachella yunkaiensis (n = 8): China: Guangdong Province: Maoming City: Dawuling Forest Station: SYS a004664/CIB107272, SYS a004663, 4665–4669, 4690.