Tuesday, April 28, 2020

[Mollusca • 2020] Alvania pizzinii • Revision of the Recent Alvania scabra (Philippi, 1844) Complex (Gastropoda, Rissoidae) from the Mediterranean Sea with the Description of A New Species


 Alvania pizzinii  Amati, Smriglio & Oliverio

in Amati, Appolloni, ... et Oliverio, 2020. 

Abstract
Herein we revise several Recent Mediterranean species of the rissoid genus Alvania Risso, 1826: Alvania scabra (Philippi, 1844), Alvania sculptilis (Monterosato, 1877), Alvania sororcula Granata-Grillo, 1877, Alvania lucinae Oberling, 1970, Alvania josefoi Oliver & Templado, 2009 and Alvania scuderii Villari, 2017. They represent a rather homogeneous group of morphologically similar species, referred to as the Alvania scabra complex, which includes also some other species from the northeastern Atlantic. We designate a neotype for Rissoa scabra Philippi, 1844 and a lectotype for Rissoa oranica Pallary, 1900 to stabilize the use of the names. Alvania oranica (Pallary, 1900) is confirmed as a synonym of Alvania scabra (Philippi, 1844), and Alvania asperella (Granata-Grillo, 1877) is proposed as a synonym of Alvania sororcula (Granata-Grillo, 1877) [new synonymy]. Finally, we describe one new Mediterranean species: Alvania pizzinii Amati, Smriglio & Oliverio n. sp. from Levanzo Is., Sicily.

Keywords: Mollusca, Gastropoda; Rissoidae; Mediterranean Sea; Alvania; new species; taxonomy



Bruno Amati, Massimo Appolloni, Andrea Di Giulio, Danilo Scuderi, Carlo Smriglio and Marco Oliverio. 2020. Revision of the Recent Alvania scabra (Philippi, 1844) Complex (Mollusca, Gastropoda, Rissoidae) from the Mediterranean Sea with the Description of A New Species. Zootaxa. 4767(3); 415–458. DOI: 10.11646/zootaxa.4767.3.3

Monday, April 27, 2020

[Herpetology • 2020] Cnemaspis tubaensis • A New Species of Cnemaspis Strauch 1887 (Squamata: Gekkonidae) from the Langkawi Archipelago, Kedah, Peninsular Malaysia


 Cnemaspis tubaensis
Quah, Wood, Anuar & Muin, 2020

 Tuba Island Rock Gecko  ||  DOI: 10.11646/zootaxa.4767.1.6  

Abstract
A new, diminutive species of Rock Gecko Cnemaspis tubaensis sp. nov. of the C. kumpoli group, is described from Tuba Island, Langkawi Archipelago, Kedah, Peninsular Malaysia and is differentiated from all other species in the kumpoli group by having a unique combination of morphological and color pattern characteristics, including a maximum SVL of 37.0 mm; 10 or 11 supralabials; eight or nine infralabials; 15–18 semi-linearly arranged paravertebral tubercles; lateral caudal furrow present; lateral caudal tubercles on the anterior portion of the tail; caudal tubercles not encircling tail; five or six precloacal pores; 28 or 29 subdigital lamellae on the fourth toe; smooth ventrals; smooth subcaudals with an enlarged median row of scales; subcaudal region light-grey and speckled with yellow; absence of light-colored ocelli on the shoulder; no yellow postscapular band; dorsum light-brown with sage-green blotches and black spots; flanks with scattered yellow spots; absence of black gular markings in both sexes; and 13.0–22.0% uncorrected pairwise sequence divergences in the NADH dehydrogenase subunit 2 gene (ND2). Cnemaspis tubaensis sp. nov. is the fourth species of Cnemaspis to be described from the Langkawi Archipelago and underscores the underestimated biodiversity of the islands which is in need of more thorough herpetological inventories.

Keywords: Reptilia, Integrative taxonomy, phylogeny, molecular systematics, karst, island, conservation, herpetology, reptile, amphibian, discovery 


Cnemaspis tubaensis sp. nov.  
(A) Dorsal and (B) ventral views of the male holotype (USMHC 2541). 
(C) Dorsal view of the male paratype (USMHC 2527).

Cnemaspis tubaensis sp. nov. 
 Tuba Island Rock Gecko

Distribution. Cnemaspis tubaensis sp. nov. is only known from the northeastern corner of Tuba Island, Langkawi Archipelago, Kedah on the karst towers where the Gua Wang Buluh Cave is located. It may be wider ranging on the island where other karst outcrops occur. 

Etymology. The specific epithet tubaensis is in reference to the type locality of this species on Tuba Island of the Langkawi Archipelago, Kedah, Peninsular Malaysia (Fig. 1). 


Evan S.H. Quah, Perry L. Jr. Wood, M.S. Shahrul Anuar and Mohd Abdul Muin. 2020. A New Species of Cnemaspis Strauch 1887 (Squamata: Gekkonidae) from the Langkawi Archipelago, Kedah, Peninsular Malaysia with An Updated Checklist of the Herpetofauna of Tuba Island. Zootaxa. 4767(1); 138–160. DOI: 10.11646/zootaxa.4767.1.6 

[Herpetology • 2020] Platypelis ranjomena • Genetic Variability and Partial Integrative Revision of Platypelis Frogs (Microhylidae) with Red Flash Marks from eastern Madagascar


 Platypelis ranjomena
Glaw, Scherz, Rakotoarison, Crottini, Raselimanana, Andreone, Köhler & Vences, 2020


Abstract 
We studied the genetic variability of Platypelis species (Anura: Microhylidae) with red fash marks from Madagascar based on mitochondrial (16S rRNA) and nuclear (RAG1) genes. Our molecular phylogenetic results suggest that the red colour evolved independently in the Platypelis barbouri complex and P. milloti and confrm the validity of a long-known but still undescribed new species from eastern Madagascar. Platypelis ranjomena sp. nov. is distinctly coloured with dark red to purple patches at the base of the forelimbs, in the inguinal region, and on the ventral parts of the hind limbs. It differs from most other arboreal cophylines by this red colour and from its sister species P. barbouri by smooth dorsal skin texture, iris colour, bioacoustics (much longer note duration in advertisement calls), and genetics (strong differences in mitochondrial and nuclear markers). The new species is widespread at low elevations along the east coast from Marojejy in the north to Manombo in the south. However, genetic evidence indicates substantial intraspecifc variability among populations, suggesting that the taxonomy of P. ranjomena and the other species in this complex is still incompletely resolved. An individual of P. barbouri from Mahasoa shared a nuclear allele with P. ranjomena, and its call was to some degree intermediate between these species, suggesting a possible case of hybridization in an area that we hypothesize could be a contact zone between the two species. Individuals from Madagascar’s northeast hitherto assigned to P. barbouri represent a lineage that is sister to the clade of P. barbouri + P. ranjomena. It is herein identifed as a new candidate species (Platypelis sp. Ca11), which occurs in syntopy with P. ranjomena. 

Key words Amphibia; Anura; colouration; Cophylinae; Madagascar; molecular genetics; new species; Platypelis ranjomena; systematics.


Fig. 3.  Platypelis ranjomena sp. nov. in life in dorsolateral (left) and ventral (right) views:
(a, b) adult male holotype ZSM 407/2010 from Ambodivoangy; (c, d) adult male paratype ZSM 406/2010 from Ambodivoangy; (e, f) adult male paratype ZFMK 59908 from Marojejy; (g, h) adult male specimen ZSM 2421/2007 from Manombo, provisionally assigned to this species.


Platypelis ranjomena sp. nov.

Diagnosis: A medium-sized arboreal cophyline frog, SVL 24.1–28.8 mm, tips of fngers and toes well expanded, third toe slightly shorter than ffth, hind limbs relatively short (tibiotarsal articulation reaching the tympanum), vomerine teeth absent (not recognisable when examining the oral cavity), tympanum small and poorly recognisable, dorsal skin smooth, belly reddish and yellowish with intensely dark red areas in the axilla, inguinal region, and on ventral parts of shanks. 
....

Etymology: The specifc epithet is derived from the Malagasy words ‘ranjo’ (= leg) and ‘mena’ (= red). It is used as a noun in the nominative singular, standing in apposition to the generic name.

Distribution: The distribution based on genetically confrmed locality records is shown in Figure 2 and indicates that the species is widespread in the lowlands of eastern and north-eastern Madagascar. Additional unconfrmed locality records based on photographs and non-sequenced voucher specimens include the coast of Masoala (near ‘Eco-Lodge chez Arol’, ..., ca. 21 m a.s.l.), Ambodiriana (...), and near Analalava (..., ca. 30 m a.s.l.) close to Foulpointe (= Mahavelona). The Manombo population deserves further study as it may represent a deep conspecifc lineage or (less likely) a more divergent form. 

Fig. 7.  Platypelis ranjomena sp. nov. in situ in Ambodivoangy, the type locality.
 (a) Individual of Platypelis ranjomena sp. nov. in life, as discovered in leaf axil of a banana-like plant at the type locality; (b) same leaf axil showing three adult individuals of Platypelis ranjomena sp. nov. together with freshly laid eggs; (c) semi-open habitat within rainforest in Ambodivoangy.

Available names: Several junior synonyms in the genus Platypelis must be excluded as available names for P. ranjomena. Platyhyla verrucosa Mocquard, 1901 and Platyhyla voeltzkowi Boettger, 1913 (both junior synonyms of P. grandis according to Noble & Parker, 1926) are larger, have a granular dorsal skin and completely lack any red ventral colour; Cophyla tuberculata Ahl, 1929, considered a further synonym of P. grandis based on the comparison of juveniles (Blommers-Schlösser & Blanc, 1991), has granular skin and differs in colour pattern (Ahl, 1929); Paracophyla tuberculata Millot & Guibé, 1951, currently considered a junior synonym of P. barbouri (Blommers-Schlösser & Blanc, 1991), has a similar dorsal pattern to P. ranjomena (see Guibé, 1978: Fig. 348) and no vomerine teeth but is very small (SVL 17 mm) and has distinct dorsal tubercles, which are absent in P. ranjomena. The holotype of Platypelis barbouri is a gravid female of 20 mm SVL with large ovary eggs of 1.5 mm diameter and rugose skin (Noble, 1940) and thus smaller and more rough-skinned than P. ranjomena. 

New candidate species: (Platypelis sp. Ca11) Our genetic analysis revealed a deep new lineage in this species group that was not previously recognised (Fig. 1): specimens hitherto assigned to P. barbouri from Marojejy closely resemble that species and in fact represent a lineage that is sister to the P. barbouri + P. ranjomena clade, herein named P. sp. Ca11 (Fig. 8). This lineage also occurs in Ambolokopatrika, and at Ambodivoangy in syntopy with P. ranjomena (Figs 1–2). We are confident that the assignment of the name P. barbouri should be attributed to the southern lineage, as the type locality of Fanovana Forest is located close to Andasibe in central eastern Madagascar. This therefore represents a new candidate species that should be taxonomically investigated in the future; we have here refrained from doing so, as insufficient material was available to us for examination.


Frank Glaw, Mark D. Scherz, Andolalao Rakotoarison, Angelica Crottini, Achille P. Raselimanana, Franco Andreone, Jörn Köhler and Miguel Vences. 2020. Genetic Variability and Partial Integrative Revision of Platypelis frogs (Microhylidae) with Red Flash Marks from eastern Madagascar. Vertebrate Zoology. 70(2); 141–156. DOI: 10.26049/VZ70-2-2020-04

     

[Ichthyology • 2020] Gymnothorax elaineheemstrae • A Taxonomic Revision of Gymnothorax undulatus (Anguilliformes: Muraenidae) in the Western Indian Ocean, with Description of A New Species


 Gymnothorax elaineheemstrae 
Sithole, Smith, Mwale & Gouws, 2020


Abstract
The taxonomic status of the widely distributed Indo-Pacific undulated moray eel, Gymnothorax undulatus, is revised using morphological and genetics features. Ninety-seven specimens previously identified as G. undulatus were examined and their mitochondrial COI and 16S rRNA genes were analysed. The multivariate analysis of eight morphometric characters resulted in separation with little to no overlap among some geographic regions. These groupings explained more than 90% of the total variation, with 86.6% overall classification. Two color morphs were identified, and the South African population was described as new species, Gymnothorax elaineheemstrae n. sp., distinct from G. undulatus in having mottled and faintly reticulated color pattern, 134–136 total vertebrae and further confirmed by the genetic analysis of COI and 16S rRNA with > 0.1 genetic distance. The morphological and genetics results indicate that G. undulatus, previously treated as a single species, consists of more than one species.

Keywords: Pisces, Taxonomy, morphometric, paraphyletic, genetic distance, Gymnothorax elaineheemstrae n. sp.


Yonela Sithole, David G. Smith, Monica Mwale and Gavin Gouws. 2020. A Taxonomic Revision of Gymnothorax undulatus (Anguilliformes: Muraenidae) in the Western Indian Ocean, with Description of A New Species. Zootaxa. 4767(1); 161–181. DOI: 10.11646/zootaxa.4767.1.7

[PaleoMammalogy • 2020] Chlamyphractus dimartinoi • A New Fairy Armadillo (Cingulata, Chlamyphorinae) from the upper Miocene of Argentina: First Fossil Record of the most Enigmatic Xenarthra


Right hemimandibles of fossil and extant chlamyphorines.
 A-C, Chlamyphractus dimartinoigen. et sp. nov., MMH-CH-87-7-100.  D-F, Chlamyphorus truncatus, CD-UNNE 1048.  G-I, Calyptophractus retusus, CML 03080. 

Chlamyphractus dimartinoi
Barasoain, Tomassini, Zurita,  Montalvo & Superina, 2020

 Reconstruction by P. Cuaranta.

ABSTRACT
Recent molecular analyses suggest that the evolutionary history of Cingulata (Xenarthra) could be more complex than believed previously. An ancient divergence was proposed for armadillos, recognizing two large monophyletic groups: Dasypodidae (including Dasypodinae) and Chlamyphoridae (including Euphractinae, Tolypeutinae, and Chlamyphorinae). Extant Chlamyphorinae (fairy armadillos) are among the most bizarre, elusive, and unknown mammals of the world. Here, we report the first accurate fossil record of this enigmatic xenarthran from the upper Miocene of the Argentine Pampas in southern South America, which represents a new genus and species (Chlamyphractus dimartinoi, gen. et sp. nov.). The phylogenetic analysis reflects the monophyly of the chlamyphorines. It is well supported by several unambiguous synapomorphies and includes the new fossil taxon as a sister group of the two extant species. This new taxon represents the most basal lineage among Chlamyphorinae and increases its diversity. The morphology of the forelimb suggests that it would have been a good digger, although, unlike extant species, it would not have had ‘fully’ subterranean habits.

FIGURE 2. Right hemimandibles of fossil and extant chlamyphorines.
A-C, Chlamyphractus dimartinoi, gen. et sp. nov., MMH-CH-87-7-100: A, labial view showing the angle between the horizontal and the vertical rami; B, lingual view; C, occlusal view.
 D-F, Chlamyphorus truncatus, CD-UNNE 1048: D, labial view showing the angle between the horizontal and the vertical rami; E, lingual view; F, occlusal view.
G-I, Calyptophractus retusus, CML 03080: G, labial view showing the angle between the horizontal and the vertical rami; H, lingual view; I, occlusal view.

SYSTEMATIC PALEONTOLOGY
Magnorder XENARTHRA Cope, 1889
Order CINGULATA Illiger, 1811

Family CHLAMYPHORIDAE Pocock, 1924
Subfamily CHLAMYPHORINAE Bonaparte, 1850

CHLAMYPHRACTUS, gen. nov.

Etymology— Chlamyphractus, from the Ancient Greek, Chlamy (alternative form of Chlamydo, meaning cloak, mantle) and phractus (derived from phraktos, meaning fortified, armored). It is a combination of names, considering the morphological resemblance to both extant genera of fairy armadillos (Chlamyphorus and Calyptophractus).

CHLAMYPHRACTUS DIMARTINOI, sp. nov.

Etymology— dimartinoi, in tribute to the late Vicente Di Martino, who carried out field work in the Arroyo Chasicó locality for many years and collected the specimen studied herein.


FIGURE 6. Rump plates of fossil and extant chlamyphorines.
A-C, Chlamyphractus dimartinoi, gen. et sp. nov., MMH-CH-87-7-100. Note the last band of fixed osteoderms fused to the rump plate. The features of these osteoderms are similar to the other isolated fixed osteoderms. A, posterior view; B, dorsal view; C, small fragments (lower margin?).
D, E, Chlamyphorus truncatus: D, bony surface, UNS-CTS1; E, surface covered by the keratinous coat, CD-UNNE 1048.
F, G, Calyptophractus retusus: F, bony surface, MACN 36874; G, surface covered by the keratinous coat, MACN 4110.

FIGURE 10. Reconstruction of Chlamyphractus dimartinoi, gen. et sp. nov., from the upper Miocene of the Argentine Pampas.
 drawn by P. Cuaranta.


Daniel Barasoain, Rodrigo L. Tomassini, Alfredo E. Zurita,Claudia I. Montalvo and Mariella Superina. 2020. A New Fairy Armadillo (Cingulata, Chlamyphorinae) from the upper Miocene of Argentina: First Fossil Record of the most Enigmatic Xenarthra. Journal of Vertebrate Paleontology. 39(5)e1716778. DOI 10.1080/02724634.2019.1716778

9 millones de años: Identifican el primer fósil de “pichiciego” similar a los “topos” y descubierto en la laguna de Chasicó en los ´70

Saturday, April 25, 2020

[Herpetology • 2020] How Little is Known about “the Little Brown Frogs”: Description of Three New Species of the Genus Leptobrachella (Anura: Megophryidae) from Yunnan Province, China


Leptobrachella niveimontis Chen, Poyarkov, Yuan & Che
Mt. Daxue Leaf Litter Toad | 雪山掌突蟾    

in Chen, Xu, Poyarkov, Wang, ... et Che, 2020. 

Abstract
Asian leaf-litter toads of the genus Leptobrachella represent a great anuran diversification in Asia. Previous studies have suggested that the diversity of this genus is still underestimated. During herpetological surveys from 2013 to 2018, a series of Leptobrachella specimens were collected from the international border areas in the southern and western parts of Yunnan Province, China. Subsequent analyses based on morphological and molecular data revealed three distinct and previously unknown lineages, which we formally describe as three new species herein. Among them, we describe a new species that occurs at the highest known elevation for Leptobrachella in China. Four species of Leptobrachella, including two new species, are found in the same reserve. Furthermore, our results suggest that the population from Longchuan County, Yunnan, may represent an additional new species of Leptobrachella, although we tentatively assigned it to Leptobrachella cf. yingjiangensis due to the small sample size examined. Lastly, we provide the first description of females of L. yingjiangensis. Our results further highlight that both micro-endemism and sympatric distributions of species are common patterns in Leptobrachella, that contribute to taxonomic and conservation challenges in these frogs. We provide an identification key for Leptobrachella known to occur in Yunnan. Given the lack of knowledge on species diversity of Leptobrachella along international border areas, we recommend that future studies include trans-boundary collaborative surveys.
Keywords: Biodiversity hotspot, Conservation, Cryptic diversity, Micro-endemism, National border,  Speciation, Taxonomy

Figure  1.  Sampling localities of Leptobrachella used in this study
A: Jinzhuzhai Village, Yingjiang, Yunnan, China; B: Gongdong, Longchuan, Yunnan, China; C: Daxueshan Nature Reserve, Lincang, Yunnan, China; D: Daweishan, Pingbian, Yunnan, China; E: Xiaoqiaogou Nature Reserve, Wenshan, Yunnan, China.


Figure  2.  Bayesian phylogram of Leptobrachella inferred from 16S mtDNA gene fragments
“*” denotes high support by Bayesian posterior probabilities (BPP>0.95) and bootstrap support values (BS>70%); “-” represents low support values. Scale bar represents 0.1 nucleotide substitutions per site. Outgroup taxa not shown. Photos showing species of Leptobrachella newly collected from Yunnan. Numbers in brackets after species names correspond to Samples IDs in Supplementary Table S1.

Figure  3.  Holotype of Leptobrachella niveimontis sp. nov. (KIZ028277) in life
A: Dorsolateral view; B: Ventral view; C: Left hand in dorsal view; D: Left foot in dorsal view; E: Lateral view; F: Cloacal area view.

Figure  5.  Paratypes of Leptobrachella niveimontis sp. nov. in life
A: KIZ015734; B: KIZ015743.

     

Leptobrachella niveimontis sp. nov. Chen, Poyarkov, Yuan & Che

Diagnosis: Leptobrachella niveimontis sp. nov. can be distinguished from its congeners by the following combination of morphological characters: (1) body size small (SVL 22.5–23.6 mm in four adult males, 28.5–28.7 mm in two females); (2) tympanum distinct, upper half black; (3) skin on dorsum scattered with fine reddish tubercles; (4) ventral sides marbled with distinct irregular black speckling on bluish-white background; (5) black blotches distinct, scattered on dorsum and flanks; (6) ventrolateral glands distinct, forming continuous white line; (7) finger webbing and fringes absent; (8) toe webbing rudimentary, toe lateral fringes narrow; (9) longitudinal ridges distinct under toes; (10) supratympanic ridges distinct, with reddish-brown pigmentation; (11) numerous rounded whitish speckles present on cloacal region; (12) pectoral gland white, larger than femoral gland; (13) iris distinctly bicolored, typically bright orange red in upper half, fading to silver white in lower half.


Etymology: The specific epithet “niveimontis” is a toponymic adjective derived from the Latin words “niveus” for “snowy”, and “montanus” meaning “related to mountains”, given in reference to the type locality of the new species, Mt. Daxue (literally “Great Snowy Mountain”) of Yunnan Province, China, and also in reference to the ecology of the new species, inhabiting high elevations in low temperature climate zones. 
For the common name, we recommend “Mt. Daxue Leaf Litter Toad” (English) and “Xue Shan Zhang Tu Chan” (雪山掌突蟾) (Chinese).

Figure  6.  Breeding habitat of Leptobrachella niveimontis sp. nov. near Wumulong Ganhe Protection Station, Daxueshan Nature Reserve, Yunnan Province, China.

Distribution and habits: Leptobrachella niveimontis sp. nov. is presently known only from its type locality, near Wumulong Ganhe Protection Station of Daxueshan Nature Reserve in Yongde County, Lincang, Yunnan Province, China. The new species was found along small creeks or rocky streams in well-preserved montane evergreen broadleaf forest at elevations between 2 569 m and 2 601 m a.s.l. (Figure 6). Leptobrachella niveimontis sp. nov. is the fifth known species of the genus inhabiting elevations above 2 000 m, and to the best of our knowledge it also occurs at the highest elevation as compared to other Chinese species of Leptobrachella. During our field surveys, calling males were recorded mostly inside the rocky crevices, and some were found hiding under leaf litter. Ubiquitous orthopteran-like calls could be heard along the stream from April to May, and very few calls were detected during July. The gravid female collected in April carried pure white eggs.

      


Figure  7.  Holotype of Leptobrachella flaviglandulosa sp. nov. (KIZ032626) in life
A: Dorsolateral view; B: Ventral view; C: Dorsal view; D: Lateral view; E: Hand in ventral view; F: Foot in ventral view; G: Iris coloration; H: Dorsal view of thighs; L: Posteroventral view of thigh.

Leptobrachella flaviglandulosa sp. nov. Chen, Wang & Che

Diagnosis: Leptobrachella flaviglandulosa sp. nov. can be distinguished from its congeners by the following combination of morphological characters: (1) body size small (SVL 22.99–26.97 mm in 13 adult males, 29.30 mm in single adult female); (2) tympanum distinct, partially covered by black marking; (3) black supratympanic line present; (4) skin on dorsum shagreened with fine yellowish-brown tubercles; (5) venter whitish with small black speckling on throat, chest and belly margins; (6) supra-axillary gland, femoral, pectoral and ventrolateral glands yellowish; (7) ventrolateral glands forming a discontinuous line; (8) finger webbing and fringes absent; (9) toe webbing poorly developed and lateral fringes narrow; (10) longitudinal ridges distinct under toes and interrupted at the articulations; (11) distinct black blotches scattered on dorsum and flanks; (12) “\ /”-shaped yellow markings on dorsum in scapular region; (13) pectoral glands larger than femoral glands; (14) iris distinctly bicolored, typically golden-orange in upper half, fading to whitish grey in lower half.


Etymology: The species epithet, “flaviglandulosa”, is a Latin adjective in feminine gender, derived from Latin “flavus” for “yellow color” and “glandula” for “gland”, in reference to characteristic life coloration of femoral, pectoral and ventrolateral glands in the new species.
 For the common name, we recommend “Yellow-gland Leaf Litter Toad” (English) and “Huang Xian Zhang Tu Chan” (黄腺掌突蟾) (Chinese).

Figure  9.  Breeding habitat and general aspect in field of Leptobrachella spp. in Xiaoqiaogou Nature Reserve
A1: Breeding stream in Fadou Station, which harbors three co-occurring species: Leptobrachella bourreti, L. flaviglandulosa sp. nov., and L. nyx. A2: Stream in Nanchang Station, which harbors two co-occurring sympatric species: Leptobrachella flaviglandulosa sp. nov. and L. nyx. A3: Stream in Xiaoqiaogou Station, which harbors two sympatric species: L. bourreti and Leptobrachella feii sp. nov.
B1: Leptobrachella bourreti in the field. B2: Leptobrachella flaviglandulosa sp. nov. in the field. B3: Leptobrachella feii sp. nov in the field.

Distribution and habits: Leptobrachella flaviglandulosa sp. nov. is currently known only from Xiaoqiaogou Nature Reserve, Xichou County, Wenshan City, Yunnan Province, China. The species was found in the environs of the Fadou, Shangchang and Nanchang stations of the nature reserve. The new species was recorded along small seeps or clear-water rocky mountain streams in well-preserved montane evergreen broadleaf forest at elevations between 1000 and 1400 m a.s.l. (Figure 9). The new species was recorded in sympatry with L. bourreti and L. nyx. During our field surveys, calling males were found mostly while sitting on vegetation, and some were calling from rocky crevices. An insect-like calls could be heard along the stream from March to June; gravid female was collected in March bearing pure-white eggs.


Figure  10.  Holotype of Leptobrachella feii sp. nov. (KIZ032625) in life
A: Dorsolateral view; B: Ventral view; C: Dorsal view; D: Lateral view; E: Hand in ventral view; F: Foot in ventral view; G: Iris coloration; H: Dorsal view of thighs; L: Posteroventral view of thigh.

Leptobrachella feii sp. nov. Chen, Yuan & Che

Diagnosis: Leptobrachella feii sp. nov. can be distinguished from its congeners by a combination of the following morphological characters: (1) body size small (SVL 21.51–22.75 mm in 5 adult males, 25.67 mm in a single adult female); (2) tympanum distinct, partially covered by black marking; (3) distinct black supratympanic line; (4) skin on dorsum shagreened with small tubercles and unequal dermal ridges; (5) distinct black blotches scattered on the creamy white chest and belly; (6) small black spots densely covering the throat; (7) ventrolateral glands present, forming a distinct continuous white line; (8) finger webbing and fringing absent; (9) toe webbing rudimentary with narrow lateral fringes; (10) longitudinal ridges under toes distinct and uninterrupted at the articulations; (11) small white pectoral glands; (12) black patches scattered on lateral sides of the body; (13) relatively long head (HDL/SVL=0.38–0.43 in males); and (14) iris distinctly bicolored, typically golden orange in upper half, fading to silver white in lower half.

Etymology: The specific epithet “feii” is a patronymic noun in the genitive singular; derived from the name of Prof. Liang Fei of the Chengdu Institute of Biology, CAS, China, in recognition of his long-term and significant contribution to the advancement of amphibian research in China, particularly his research on the family Megophryidae. 
For the common name, we recommend “Fei's Leaf Litter Toad” (English) and “Fei Shi Zhang Tu Chan” (费氏掌突蟾) (Chinese).

Distribution and habits: Leptobrachella feii sp. nov. is currently known to occur at two disjunct localities: Xiaoqiaogou Nature Reserve, Xichou County, Wenshan City, Yunnan Province, China, and Daweishan Nature Reserve, Pingbian County, Yunnan Province, China (Figure 1); these two sites are separated by a flying distance about 150 km. The new species was found along small seeps in well-preserved montane evergreen broadleaf forest at elevations between 1 577 m and 1 850 m a.s.l. (Figure 9). The new species is sympatric with L. bourreti. During our field surveys, males were usually recorded while calling sitting on vegetation (usually on the members of the family Acanthaceae species; see Figure 9). Advertisement calls of the new species, resembling calling of orthopterans, could be heard along the streams from March to June; gravid female collected in April was swollen with pure white eggs.


Jin-Min Chen, Kai Xu, Nikolay A. Poyarkov, Kai Wang, Zhi-Yong Yuan, Mian Hou, Chatmongkon Suwannapoom, Jian Wang and Jing Che. 2020. How Little is Known about “the Little Brown Frogs”: Description of Three New Species of the Genus Leptobrachella (Anura: Megophryidae) from Yunnan Province, China. Zoological Research. DOI: 10.24272/j.issn.2095-8137.2020.036

[Herpetology • 2020] Amolops tuanjieensis • A New Species of the Genus Amolops (Anura: Ranidae) from Yunnan, China


Amolops tuanjieensis Gan, Yu & Wu, 2020

Tuanjie Cascade Frog | 团结湍蛙 || 

 A new species of the genus AmolopsAmolops tuanjieensis sp. nov., is described from Yunnan, China. The new species can be distinguished by the following characters: dorsolateral folds present; dorsal and ventral surfaces smooth; top of head and dorsum brown-red with irregular gray and dark spots; flank green; side of head black, from tip of snout, diffusing posteriorly to axilla, continuing as black streak below edge of dorsolateral fold; SVL 39.5–40.4 mm in males, 56.8–60.7 mm in females; tympanum distinct; supratympanic fold indistinct; vomerine teeth in two oblique rows between choanae, closer to each other than choanae; vocal sacs present; nuptial pads present; outer metatarsal tubercle absent, supernumerary tubercles absent; all fingertips expanded into discs; limbs dorsally brown with dark brown bars and irregular dark brown blotches.

 Collection site of Amolops tuanjieensis sp. nov. from Yunnan, China (A) and
Bayesian phylogram of Amolops species inferred from a combination of 16S rRNA, CO1, and ND2 (B).
Numbers above branches are Bayesian posterior probabilities (only values above 50% are shown).





Dorsal (C) and ventral (D) views of holotype of Amolops tuanjieensis sp. nov. (GXNU YU110005) in preservative. Ventral view of hand (E) and foot (F) of holotype in preservative. 



Dorsal (G) and lateral (H) views of paratype of Amolops tuanjieensis (GXNU YU110034) in life and
dorsal (I) and ventral (J) views of paratype (GXNU YU110034) in preservative.

Amolops tuanjieensis sp. nov.

Diagnosis: Amolops tuanjieensis sp. nov. differs from other members in the genus Amolops by the following characters: (1) SVL 39.5–40.4 mm in males and 56.8–60.7 mm in females; (2) dorsolateral folds present; (3) side of head dark with light-colored upper lip stripe extending to axilla; (4) skin on dorsal and ventral surfaces smooth; (5) tympanum distinct, less than half of eye diameter; (6) supratympanic fold indistinct; (7) vomerine teeth in two oblique rows between choanae, closer to each other than to choanae; (8) top of head and dorsum brown-red with irregular black and gray spots; (9) loreal regions dark black; (10) lateral green; (11) pineal body present; (12) nuptial pad velvety; (13) two external subgular vocal sacs in males; (14) all fingertips expanded; (15) two palmar tubercles present; (16) inner metatarsal tubercle oval, outer metatarsal tubercle absent; (17) supernumerary tubercles absent.


Etymology: The specific epithet is named for the type locality, Tuanjie Township, Gengma Dai and Wa Autonomous County, Yunnan Province, China.
We suggest the English common name as “Tuanjie Cascade Frog” 
and the Chinese common name as “团结湍蛙”.

Distribution and ecology: The new species is known only from the type locality (Supplementary Figure S1). The holotype and paratypes were found on leaves and small branches, less than 1 m above the ground along a stream. No tadpoles or vocal recordings were collected for the new species.

Comments: 
In China, species of Amolops have been assigned to different species groups based on morphological characters (Fei et al., 2009). However, consistent with Lyu et al. (2019a), our phylogenetic analysis revealed that the division of some species groups needs further investigation. Firstly, A. chayuensis, which was placed in the A. monticola group by Sun et al. (2013) based on the presence of dorsolateral folds, did not group together with the clade consisting of the new species and other members of the same group, indicating that the A. monticola group is not monophyletic and that assignment of species groups based on dorsolateral folds only is problematic. Comprehensive morphological and molecular comparisons using A. monticola data are necessary to clarify the division of the A. monticola group.

In addition to the problems at the species group level in Amolops, species diversity within this genus also needs further investigation. Amolops marmoratus, which has been confused with A. afghanus and A. indoburmanensis (Dever et al., 2012; Lyu et al., 2019a), is mainly distributed in southern Tibet, as well as Myanmar, Bangladesh, Nepal, and eastern Himalaya in India (Frost, 2019), with distribution in Thailand according to Chan-ard (2003). This species is certainly known from Myanmar, but the statuses of other populations remain problematic (Frost, 2019). In this study, we found that the genetic distance between A. marmoratus from Thailand and A. marmoratus from Myanmar reached 4.48% for the 16S sequences, indicating that A. marmoratus from Thailand possibly represents a cryptic species.


Yu-Lu Gan, Guo-Hua Yu and Zheng-Jun Wu. 2020. A New Species of the Genus Amolops (Anura: Ranidae) from Yunnan, China. Zoological Research. 41(2); 188-193. DOI: 10.24272/j.issn.2095-8137.2020.018

Friday, April 24, 2020

[Herpetology • 2020] Oreolalax longmenmontis • A New Species of the Toothed Toad Oreolalax (Anura, Megophryidae) from Sichuan Province, China


Oreolalax longmenmontis
Hou, Shi, Hu, Deng, Jiang, Xie & Wang, 2020 

Longmen Mountains Toothed Toad  ||  DOI: 10.3897/zookeys.929.49748

Abstract
The toad genus Oreolalax is widely distributed in southwest China and northern Vietnam. A new species of the genus is described from Sichuan Province, China. Phylogenetic analyses based on the mitochondrial 12S rRNA and 16S rRNA gene sequences supported the new species as an independent clade clustered into the clade also containing O. nanjiangensis and O. chuanbeiensis. The new species can be distinguished from its congeners by a combination of the following characters: body size moderate (SVL 51.2–64.2 mm in males); head broad; tympanum hidden; interorbital region with dark triangular pattern; belly with marbling; male lacking spines on lip margin; spiny patches on chest small with thick sparse spines in male; nuptial spines thick and sparse; tibio-tarsal articulation reaching beyond nostril when leg stretched forward; toe webbing at base.

Keywords: Molecular phylogenetic analyses, morphology, southwest China, taxonomy

Figure 3. Photos of the holotype CIB20180522001 of Oreolalax longmenmontis sp. nov. in life
 A dorsal view B ventral view C lateral view D view of chest E view of oral cavity E dorsal view of fingers G view of femoris posterior H ventral view of foot I ventral view of hand. Key: 1 indicates tympanum hidden; 2 denotes a pair of spinal patches with large and sparse spines on chest; 3 denotes nuptial spines on the dorsal surface of fingers I and II; 4 denotes two small posterior femoral glands.

Figure 5. Colour variations in Oreolalax longmenmontis sp. nov. A, B dorsal and ventral view of the paratype CIB20180527002
C, D dorsal and ventral view of the paratype CIB20180526001.


Oreolalax longmenmontis sp. nov.

Diagnosis: 
Oreolalax longmenmontis sp. nov. is assigned to the genus Oreolalax by its molecular phylogenetic position and the following morphological characters: the maxillary teeth prominent; back rough scattered with large warts, covered with oval black spots; pupil vertical; tongue oval, notched posteriorly; femoral glands prominent; pectoral and axillary gland present in males in breeding season; inner two fingers with black nuptial spines in males in breeding season.

Oreolalax longmenmontis could be distinguished from its congeners by a combination of the following characters: body size moderate (SVL 51.2–64.2 mm in males); head broad; tympanum hidden; interorbital region with dark triangular pattern; belly with marbling; male lacking spines on lip margin; spiny patches on chest small with thick and sparse spines in male; nuptial spines thick and sparse; tibio-tarsal articulation reaching beyond nostril when leg stretched forward; toe webbing at base.


Figure 7. Habitats of Oreolalax longmenmontis sp. nov. in the type locality, Sichuan White River National Nature Reserve in Pengzhou City, Sichuan Province, China
A landscape of montane forests B a montane stream with a small pond occupied by toad (insert: the holotype CIB20180522001 in life).

Distribution and ecology: Oreolalax longmenmontis sp. nov., is currently known only from the type locality, the White River National Nature Reserve, Pengzhou City, Sichuan Prov., China at elevations of 1300–1450 m. The new species inhabits subtropical evergreen broad-leaved forests and is frequently found near the ponds in the montane streams (Fig. 7). The breeding season is currently uncertain. Three sympatric amphibian species, i.e., Amolops chunganensis (Pope, 1929), Odorrana margaratae (Liu, 1950), and Quasipaa boulengeri (Günther, 1889), were found in the same habitat.

Etymology: The specific epithet longmenmontis refer to the type locality of the species, the central part of the Longmen Mountains, Pengzhou City of Sichuan Prov., China. 
We propose the common name “Longmen Mountains Toothed Toad” (English) and “long men shan chi chan” (Chinese).


Yinmeng Hou, Shengchao Shi, Daming Hu, Yue Deng, Jianping Jiang, Feng Xie and Bin Wang. 2020. A New Species of the Toothed Toad Oreolalax (Anura, Megophryidae) from Sichuan Province, China. ZooKeys. 929: 93-115. DOI: 10.3897/zookeys.929.49748