Thursday, November 21, 2019

[Paleontology • 2019] New Skulls and Skeletons of the Cretaceous Legged Snake Najash, and the Evolution of the Modern Snake Body Plan


Najash rionegrina Apesteguía & Zaher, 2006

in Garberoglio, Apesteguía, Simões, et al., 2019. 
Illustration: Raúl O. Gómez.

Abstract
Snakes represent one of the most dramatic examples of the evolutionary versatility of the vertebrate body plan, including body elongation, limb loss, and skull kinesis. However, understanding the earliest steps toward the acquisition of these remarkable adaptations is hampered by the very limited fossil record of early snakes. Here, we shed light on the acquisition of the snake body plan using micro–computed tomography scans of the first three-dimensionally preserved skulls of the legged snake Najash and a new phylogenetic hypothesis. These findings elucidate the initial sequence of bone loss that gave origin to the modern snake skull. Morphological and molecular analyses including the new cranial data provide robust support for an extensive basal radiation of early snakes with hindlimbs and pelves, demonstrating that this intermediate morphology was not merely a transient phase between limbed and limbless body plans.


Fig. 1 Najash specimens from LBPA. (A) MPCA 500, skull with atlas-axis in right lateral view. (B) MPCA 591, partial skull with articulated vertebrae in right lateral view. (C) MPCA 581, partial skull with atlas in left lateral view. (D) MPCA 564, articulated specimen with partial skull and postcranium in ventral view. (E) MPCA 419, dentary and associated vertebrae and ribs. (F) MPCA 480, partial skull with atlas in dorsal view. (G) MPCA 536, partial skull in ventral view. (H) MPCA 386, partial skull in ventral view. bo, basioccipital; ti, tibia.

 Fig. 2 CT scan reconstructions of the articulated skull of Najash (MPCA 500). (A) Right lateral view. (B) Left lateral view. (C) Dorsal view. (D) Ventral view.
 II, optic foramen; V, trigeminal foramen; aiaf, anterior inferior alveolar foramen; amf, anterior mylohyoid foramen; at, atlas-axis; ang, angular; bo, basioccipital; cb, compound bone; co, coronoid; cri, crista interfenestralis; crt, crista tuberalis; d, dentary; ept, ectopterygoid; fr, frontal; iof, infraorbital foramen; j, jugal; mf, mental foramina; mx, maxilla; n, nasal; ot, otoccipital; pa, parietal; pbs, parabasisphenoid; pal, palatine; pmx, premaxilla; pof, postfrontal; prf, prefrontal; pro, prootic; pt, pterygoid; q, quadrate; smx, septomaxilla; so, supraoccipital; sp, splenial; st, supratemporal; stf, stapedial footplate; vo, vomer.

the legged snake Najash.
Illustration: Raúl O. Gómez, 
Universidad de Buenos Aires, Buenos Aires, Argentina


Fernando F. Garberoglio, Sebastián Apesteguía, Tiago R. Simões, Alessandro Palci, Raúl O. Gómez, Randall L. Nydam, Hans C. E. Larsson, Michael S. Y. Lee and Michael W. Caldwell. 2019. New Skulls and Skeletons of the Cretaceous Legged Snake Najash, and the Evolution of the Modern Snake Body Plan. Science Advances. 5(11); eaax5833. DOI:  10.1126/sciadv.aax5833

New fossils shed light on how snakes got their bite and lost their legs
phys.org/news/2019-11-fossils-snakes-lost-legs.html via @physorg_com


[Botany • 2019] Ombrophytum chilensis (Balanophoraceae) • A New Species of Ombrophytum from Chile, with Notes on Subterranean Organs and Vegetative Reproduction in The Family


Ombrophytum chilensis Kuijt & Delprete

in Kuijt & Delprete, 2019

Abstract
The Chilean desert specimens of Ombrophytum (Balanophoraceae) reported in the literature as O. subterraneum (Asplund) Hansen differ structurally in several respects from that species, which was described from moist tropical forest in Bolivia. Therefore the Chilean specimens are treated as a narrowly endemic, separate species, Ombrophytum chilensis Kuijt & Delprete, on the basis of the type specimen and published photographs. Discussions on morphology, distribution and conservation status are provided for this species. Critical comments on the underground organs and reproduction in Neotropical Balanophoraceae are also presented.

Keywords: Corynaea, Helosis, Langsdorffia, Thonningia, parasitic plants, underground structures, Eudicots

FIGURE 2. Ombrophytum chilensis, details from holotype specimen (Martin 468 (SI [Sheet A]).
 A, Specimen from upper envelope (see Fig. 1), view from external side; B, Same specimen, view from dissected side. Courtesy M. Belgrano. 

FIGURE 3. Inflorescences of Ombrophytum chilensis, from Murata (1997).
Photograph by J.D. Mauseth (near Chiu Chiu, Chile).

Ombrophytum chilensis Kuijt & Delprete, sp. nov. 

Diagnosis:— Ombrophytum chilensis differs from the other species of the genus in the translucent scales on the young peduncle (Fig. 3), while the other species apparently have naked peduncles, except for O. subterraneum having some scattered scales. Equally distinctive are the large, mostly tridentate fertile bracts (i.e., subtending inflorescence branches) that intergrade with the scales below (i.e., on the peduncle), while in other species of the genus they have a truncate-obconical stalk and a hemi-ellipsoid head in O. guayanensis Delprete (2014: 264, figs. 1D, F)), or they are clavate in O. violaceum B. Hansen (1977: 231; Hansen 1980: 58), or with a filiform stalk and distally obtriangular in O. microlepis B. Hansen (1980: 60, figs. 24F, G), or with a flat stalk and a “subulate to bifurcate or irregularly incised dent protruding upward from its lower part” (Hansen 1980: 64) in O. subterraneum.
...

 Distribution and Ecology:— At this time it appears that the above cited Antofagasta site represents the only Chilean one, not just for the genus, but for Balanophoraceae generally. Ecologically, the present species is unusual in existing in one of the most arid regions worldwide, while other species of the genus are mostly found in moist tropical forests, with the possible exception of the Galapagos population that has previously been assigned to O. subterraneum.

 Vernacular name:— Siicha (H.C. Martin 486).

Job Kuijt and Piero G. Delprete. 2019. A New Species of Ombrophytum (Balanophoraceae) from Chile, with Notes on Subterranean Organs and Vegetative Reproduction in The Family. Phytotaxa. 420(4); 264–272. DOI: 10.11646/phytotaxa.420.4.2

[Ichthyology • 2019] Netuma patriciae • A New Sea Catfish (Siluriformes: Ariidae) from the Philippines


Netuma patriciae  
Takahashi, Kimura & Motomrua, 2019


Abstract
A new sea catfish (Ariidae), Netuma patriciae, is described based on the holotype and nine paratypes, 127.3–303.4 mm in standard length, collected from Panay and Luzon islands, Philippines. The new species most resembles N. thalassina (Rüppell 1837), in sharing counts of anal-fin rays (17–19 in N. patriciae, 15–17 in N. thalassina) and a distinct dorsomedian head groove (longitudinal length of the groove, 33.7–40.1% of head length, 22.3–31.0%). However, the new species can be easily distinguished from the latter in having fused vomerine tooth patches, and more numerous free vertebrae (43–44 vs. 41–42 in N. thalassina). Although N. bilineata (Valenciennes in Cuvier and Valenciennes 1840a) has also fused vomerine tooth patches, the new species is distinguished by having fewer free vertebrae (43–44 vs. 47–51 in N. bilineata) and longer dorsomedian head groove (33.7–40.1% of head length vs. 0–9.7%). The new species can also be easily distinguished from both N. thalassina and N. bilineata by having a filamentous dorsal-fin ray (longest dorsal-fin ray 26.9–35.9% of standard length vs 20.3–23.3% in N. thalassina, 20.9–25.3% in N. bilineata, standard length > 127 mm) and a U-shaped junction of dorsomedian head ridge (vs. V-shaped in both species).

Keywords: Teleostei, Fork-tailed catfish, Netuma thalassina, Netuma bilineata, Taxonomy 


Netuma patriciae sp. nov. KAUM–I. 98403, holotype, 200.1 mm SL, Iloilo, Panay Island, Philippines, fresh condition;

Netuma patriciae sp. nov.
(New English name: Whipfin Sea Catfish)

Etymology. The specific name patriciae is in honor of Patricia J. Kailola, the University of the South Pacific and Pacific Dialogue Ltd, in recognition of her research on the catfish family Ariidae.

Distribution. Known only from Panay Island and Manila Bay, Philippines. Type locality Iloilo, Panay Island, Philippines.


Yumeka Takahashi, Seishi Kimura and Hiroyuki Motomrua. 2019. A New Sea Catfish, Netuma patriciae (Siluriformes: Ariidae), from the Philippines. Ichthyological Research.  DOI: 10.1007/s10228-019-00719-4 


[Entomology • 2019] Diversity and Distribution of Pleioplectron Cave Wētā (Orthoptera: Rhaphidophoridae: Macropathinae), with the Synonymy of Weta and the Description of Seven New Species


A. Pleioplectron auratum sp. nov., adult ♂, Whites Beach, Rarangi. 
B. P. gubernator  sp. nov., two adult ♂♂, Three Pointer, Gouland Downs, Heaphy Track. 

C. P. caudatum sp. nov., adult ♂, Blowfly Hut, Moeraki River, South Westland. 

D. P. flavicorne sp. nov., sub-adult ♀, Blowfly Hut, Moeraki River, South Westland.
 E–F. P. crystallae sp. nov. E. Adult ♂, Cave Brook, Gouland Downs, Kahurangi NP. F. Adult ♀ feeding on Racomitrium Brid. moss, Salisbury Lodge, Mt Arthur, Kahurangi NP.

Hegg, Morgan-Richards & Trewick, 2019

Abstract
The genus Pleioplectron was first described by Hutton (1896) and included six New Zealand species. This genus has since had three species moved, one each to the genera Pachyrhamma Brunner von Wattenwyl, 1888, Miotopus Hutton, 1898 and Novoplectron Richards, 1958. Here we clarify the status and appearance of Pleioplectron simplex Hutton, 1896 (incl. P. pectinatum Hutton, 1896 syn. nov.) and P. hudsoni Hutton, 1896, as well as P. thomsoni (Chopard, 1923) comb. nov., which is transferred from the genus Weta Chopard, 1923. The genus Weta is newly synonymised with Pleioplectron. We also describe seven new species of Pleioplectron from South Island, New Zealand: P. auratum sp. nov., P. caudatum sp. nov, P. crystallae sp. nov., P. flavicorne sp. nov., P. gubernator sp. nov., P. rodmorrisi sp. nov and P. triquetrum sp. nov. We base these descriptions on morphology using fresh specimens of both male and female adults, and provide support for each with DNA sequence variation (mtDNA, partial COI).

Keywords: Cave wētā; Pleioplectron; Rhaphidophoridae; systematics; New Zealand


Fig. 14. Live Pleioplectron Hutton, 1896 in their natural environments.
A–B. P. simplex Hutton, 1896, Hinewai Reserve, Banks Peninsula. A. Adult ♀ feeding on a small native snail Flammulina zebra (Le Guillou, 1842). B. Adult ♂. The different colouration is due to individual variation, not sexual dimorphism.
C–D. P. thomsoni (Chopard, 1923) comb. nov. C. Adult ♂ in natural cave, Trotters Gorge, Otago. D. Adult ♀ in mining tunnel in Bannockburn, Central Otago, where a population of nearly white colour exists.
E. P. hudsoni Hutton, 1896, adult ♀, Otaki Forks, Tararua Forest. F. P. triquetrum sp. nov., ♂, Hinau Track, Kaikōura.

Fig. 15. Live Pleioplectron Hutton, 1896 in their natural environments.
A. P. auratum sp. nov., adult ♂, Whites Beach, Rarangi. B. P. gubernator sp. nov., two adult ♂♂, Three Pointer, Gouland Downs, Heaphy Track.
C. P. caudatum sp. nov., adult ♂, Blowfly Hut, Moeraki River, South Westland. D. P. flavicorne sp. nov., sub-adult ♀, Blowfly Hut, Moeraki River, South Westland.
E–F. P. crystallae sp. nov. E. Adult ♂, Cave Brook, Gouland Downs, Kahurangi NP. F. Adult ♀ feeding on Racomitrium Brid. moss, Salisbury Lodge, Mt Arthur, Kahurangi NP.

Fig. 18. Known distribution of cave wētā in the genus Pleioplectron Hutton, 1896.
A. North Island, New Zealand, showing the distribution of P. hudsoni. B–J. South Island, New Zealand, showing the distribution of the remaining nine species.


Danilo Hegg, Mary Morgan-Richards and Steven A. Trewick. 2019. Diversity and Distribution of Pleioplectron Hutton Cave Wētā (Orthoptera: Rhaphidophoridae: Macropathinae), with the Synonymy of Weta Chopard and the Description of Seven New Species. European Journal of Taxonomy.  577;1–46.  DOI: 10.5852/ejt.2019.577

[Entomology • 2019] Thitarodes shambalaensis • A New Species of Ghost Moth (Lepidoptera, Hepialidae) from Yanzigou Glacier, Mt. Gongga, Sichuan, China: A New Host of the Caterpillar Fungus Ophiocordyceps sinensis supported by Genome-wide SNP Data


Thitarodes shambalaensis 
Wang, Zhuang, Wang & Pierce, 2019


Abstract
A new species of ghost moth, Thitarodes shambalaensis sp. nov., is described from Yanzigou glacier, Mt. Gongga, Sichuan, China. The species is a host of the economically important caterpillar fungus Ophiocordyceps sinensis. Establishment of this new species is supported by morphology and genetic differentiation measured in a CO1 phylogeny and in genome-wide SNP coverage. A summary tree from 538 sequences of different genetic markers from Thitarodes (including sequences extracted from caterpillar fungus sclerotium samples) support the genus Thitarodes as a monophyletic group, and indicate that Thitarodes is the host genus for O. sinensis. Sampling efforts so far have centered on half of the known phylogenetic diversity of Thitarodes, with some species-level clusters (separated by < 2.5% genetic distance) containing 17 described species. Fifteen clusters are known from either a single “orphan taxon” or a single sequence from a caterpillar fungus sclerotium sample. We provide suggestions for building a more robust phylogeny of the genus Thitarodes and highlight some of the conservation threats that species from this genus face due to unprecedented habitat exploitation.

Keywords: RAD-Seq, phylogeny, new species, caterpillar fungus, Kangding, Mt. Gongga, Sichuan, China


Figure 1. Thitarodes shambalaensis sp. nov. 
A holotype, male, dorsal view B paratype, female, dorsal view C holotype, male, ventral view D paratype, female, dorsal view E resting position in habitat (photograph credit Hua Zhang). Scale bar: 1 cm.

Figure 2. A Natural habitat of Thitarodes shambalaensis sp. nov. at Yanzigou glacier entrance point, Mt. Gongga, Sichuan, China (photograph credit Meng Li, May 2018) B disturbed habitat of Thitarodes shambalaensis sp. nov. due to excavation of T. shambalaensis pupae, at Haizidang, Yanzigou glacier (photograph credit Wenbin Ju, May 2019). 

Figure 3. Thitarodes shambalaensis sp. nov. A forewing (up) and hindwing (bottom) venation from dorsal view B antenna, front view C labial palp, caudal view, covered under setae. Scale bar: 1 mm.

Thitarodes shambalaensis sp. nov.

Etymology: From the Sanskrit word शम्भल (Shambala). In Hindu and Tibetan Buddhist tradition, the term refers to a mythical kingdom hidden in the snow mountains. The name refers to the magnificence of the species’ alpine habitat under Mt. Gongga.



 Zhengyang Wang, Hailing Zhuang, Min Wang and Naomi E. Pierce. 2019. Thitarodes shambalaensis sp. nov. (Lepidoptera, Hepialidae): A New Host of the Caterpillar Fungus Ophiocordyceps sinensis supported by Genome-wide SNP Data. ZooKeys. 885: 89-113. DOI: 10.3897/zookeys.885.34638

[Arachnida • 2019] Salticidae (Araneae) of New Caledonia: Genus Corambis Simon, 1901


Corambis pantherae
Patoleta & Żabka, 2019


Abstract
The genus Corambis Simon, 1901 includes five species; three of them, C. jacknicholsoni sp. nov., C. logunovi sp. nov. and C. pantherae sp. nov., are described here as new. The female of the C. foeldvarii Szűts, 2002 is described for the first time and a new generic diagnosis is proposed. The distribution and relationships of Corambis are discussed in terms of the geological and bioclimatic history of New Caledonia.

Keywords: jumping spiders; New Caledonia; endemism; taxonomy


Corambis jacknicholsoni sp. nov. 

 Diagnosis Differs from other species of the genus by its hook-like embolus (Fig. 4E–F) and the lateral location of ag2 in females (Fig. 5G). 

Etymology This beautiful spider is named for Mr. Jack Nicholson, the great American actor, three times Oscar winner.


Corambis logunovi sp. nov. 

Diagnosis Differs from other species of the genus by its darker coloration, legs with no fringe, longer chelicerae, and much wider and heavier embolus (Fig. 6E–F). Copulatory openings oriented antero-laterally, accessory glands situated posteriorly on spermathecae (Fig. 7G).

Etymology This species is named for Dr. Dmitri Logunov, a distinctive Russian arachnologist (now at the University of Manchester), a friend of ours.



Fig. 8. Corambis pantherae sp. nov., holotype, ♀ (QMB S35653).
A–C. Dorsal and frontal views. D. Chelicerae, maxillae and labium. E, G. Internal genitalia. F. Epigyne.

Corambis pantherae sp. nov. 

Diagnosis Differs from other species of the genus by its relatively wider cephalothorax and spotted abdominal pattern. Copulatory openings oriented laterally, ag2 situated postero-laterally (Fig. 8). 

Etymology This species is named for its abdominal pattern.


Barbara Patoleta and Marek Żabka. 2019. Salticidae (Arachnida: Araneae) of New Caledonia: Genus Corambis Simon, 1901. European Journal of Taxonomy. 578: 1–18. DOI: 10.5852/ejt.2019.578


Wednesday, November 20, 2019

[Herpetology • 2019] Trachischium apteii • A New Species of Fossorial Natricid Snakes of the Genus Trachischium Günther, 1858 (Serpentes: Natricidae) from the Himalayas of northeastern India


Trachischium apteii  
Bhosale, Gowande & Mirza, 2019


Abstract
A new species of natricid snakes, Trachischium apteii sp. nov. is described from the northeastern Indian State of Arunachal Pradesh. The new species differs from its congeners in the following suite of characters: dorsal scales in 15:15:15 rows, SVL 293–299 mm, higher ventral count 143–150, very faint dorsal longitudinal lines, absence of yellow patch on the neck and the belly being pale yellow. Preliminary discussion on the phylogenetic position of the members of the genus Trachischium is presented. This discovery of a new snake species advocates the need for dedicated surveys to document biodiversity across Arunachal Pradesh and the neighbouring States of northeastern India.

Keywords: Biodiversity hotspot, Molecular phylogeny, Natricidae, Taxonomy, Species complex


Fig. 2. Trachischium apteii sp. nov. holotype female BNHS 3550 in life. 

Trachischium apteii sp. nov.

Diagnosis: Large-sized member of the genus, reaching SVL of 293–299 mm. Tail comprising of 11–13% of total length. Dorsal scales smooth and glossy, arranged in 15 rows throughout the body. Six supralabials, third and fourth in contact with orbit. Temporals 1 + 1, anterior temporal long. Ventrals 143–150, subcaudals 25–28. Dorsum colouration dark brown to black with faint dorsal longitudinal lines, lacking yellow patch on the neck and the belly being yellowish.
...

Etymology: The specific epithet is a patronym, honouring Dr. Deepak Apte, Director of the Bombay Natural History Society, marine biologist and conservationist for his contribution to conservation, and for his continued support to HB and to the Arunachal Expedition, which led to the discovery of the new species.

Natural history notes: The holotype, paratype, and another uncollected individual were found under logs during a daytime search. The individuals were likely seeking refuge under the logs during the day. Locals informed the scientific team that the snakes have also been found while digging during non-monsoon seasons.


 Harshal S. Bhosale, Gaurang G. Gowande and Zeeshan A. Mirza. 2019. A New Species of Fossorial Natricid Snakes of the Genus Trachischium Günther, 1858 (Serpentes: Natricidae) from the Himalayas of northeastern India. Comptes Rendus Biologies. In Press. DOI: 10.1016/j.crvi.2019.10.003
  #herpetology #TheArunachalExpedition #newspecies #ArunachalPradesh #northeast #northeastIndia #talleyvalley #talle #singinawaconservationfoundation #nhm #singinawajunglelodge #convservation #biodiversity #research #biology #BBC #natgeo #discovery #animals #snakes #reptiles #media

[Botany • 2019] Ombrophytum villamariensis (Balanophoraceae) • A New Species of Ombrophytum, A Genus not previously recorded for Colombia


Ombrophytum villamariensis S. Guzmán-Guzmán

in Guzmán-Guzmán, 2019.

Abstract
A new species of Balanophoraceae, Ombrophytum villamariensis Guzmán-Guzmán, is described for Colombia, where the genus has not previously been recorded. At least the first part of the development of the inflorescence is underground. Inflorescences have simple lateral branches, bearing male flowers in the upper part of the inflorescence and female flowers in the lower part. The apical parts (peltas) of the inflorescence branches are morphologically different in the two areas. The first stages of the plants are ball-shaped, within which inflorescences are formed endogenously. When the latter finally emerge, they lift the ball’s surface layer which usually splits, leaving an irregular volva at the base of the inflorescence.


Keywords: Eudicots, Balanophoraceae, Caldas, Cordiaceae, Cordillera Central Andina, endogenous inflorescences, Lophophytoideae, parasitic plant, Oxycorynina

FIGURE 1. Ombrophytum villamariensis in situ.
 A. Inflorescence emerging from the ground; the calyptra is on the left. B. Mature tuber with two lateral tubers in development. C. Bract apex between female branches (red arrow). D. Old male inflorescences where the female part has remained underground.
 Scale bar: A, C, D = 20 mm; B = 4 mm. 
Photos by A. Montaña (A and C) & H. F. Arias (B and D).


Ombrophytum villamariensis S. Guzmán-Guzmán, sp. nov.

Diagnosis: Ombrophytum villamariensis is similar to O. microlepis of low Amazonian areas of Peru and Brazil. However, differ in a much shorter peduncle (30 mm or absent vs 60 mm), longer male and female inflorescence branches (9–10 mm vs. 3–7 mm and 4–6 mm vs. 4 mm, respectively) and two entirely different types of peltas.

Etymology: The epithet refers to the municipality where the new species was discovered, a municipality that stands out for the beauty of its landscapes, its beauty immortalized in its hymn: “…De Colombia, Villa de las flores, y de Caldas bella rosa en botón…”

FIGURE 2. Types of rupture of the volva of Ombrophytum villamariensis and ecological interactions.
A. Inflorescence emerging from the tubercle producing a trilobular volva. B. “Calyptra” with irregular ruptures partially covering the inflorescence. C. Beetle of the subtribe Oxycorynina observed between the female and male inflorescence branches (red arrow). D. Bite marks of possible rodent (see enlarged section); tuber and host roots to the left.
Scale bar: A = 6 mm; B, D (and section) = 20 mm; C = 4 mm. 
Photos by A. Montaña (D) & J. C. Tovar (A, C and B).



Habitat and distribution: This species is found in Andean forests of the Central Cordillera of Colombia between 2400–2500 m, in the municipality of Villamaria, department of Caldas, Colombia. In addition to the two hosts mentioned above, other genera found at the site were Brunellia Ruiz & Pavón (1794: 71) (Brunelliaceae), Chamaedorea Willdenow (1806: 638) (Arecaceae), Saurauia Willdenow (1801: 407) (Actinidiaceae), Oreopanax Decaisne & Planchon (1854: 107) (Araliaceae), Cyathea Smith (1793: 416) (Cyatheaceae), Juglans Linnaeus (1753: 997) (Juglandaceae) and Croton Linnaeus (1753: 1004) (Euphorbiaceae).


Santiago Guzmán-Guzmán. 2019. A New Species of Ombrophytum (Balanophoraceae), A Genus not previously recorded for Colombia. Phytotaxa. 424(1); 61–66. DOI:  10.11646/phytotaxa.424.1.6

Tuesday, November 19, 2019

[Herpetology • 2019] Leptobrachella namdongensis • A New Species of Leptobrachella Smith 1925 (Anura: Megophryidae) from Thanh Hoa Province, Vietnam


Leptobrachella namdongensis 
Chung, Nguyen, Luu, Nguyen & Jiang, 2019

RAFFLES BULLETIN OF ZOOLOGY. 67

Abstract
 Based on the results of molecular and morphological systematics analyses, a new species, Leptobrachella namdongensis, is recognised from Nam Dong Conservation Area in Thanh Hoa Province, Vietnam. Genetic divergences in the16S rRNA gene between the new form and other species in the genus range from 4.7 to 21.0% and average at approximately 24%. The new species is most similar to L. petrops and L. puhoatensis, but can be distinguished from them and other congeners by a combination of the following morphological characters: size medium (30.9 mm in the adult male and 32.1–35.3 mm in adult females); head wider than long; tympanum distinct; throat immaculate white, chest and belly with dark specking on outer margins; toes with basal webbing; supratympanic fold edged by a distinct black line; inter-orbital region with distinct black blotches; iris bicoloured, upper half copper, fading to golden in its lower half; head without dorsolateral markings. 

Key words: Nam Dong Conservation Area, phylogenetics, Vietnam, taxonomy


Fig. 3. Dorsolateral view (A) and ventral view (B) of the holotype (VNUF A.2017.37, male) of Leptobrachella namdongensis, new species in life. 
Photos by Vinh Q. Luu.

Fig. 6. Paratypes of Leptobrachella namdongensis, new species in life.
 A, female VNUF A.2017.95 (SVL 32.1mm); B, female VNMN2019.04 (SLV 33.0mm); C, female IEBR 4512 (SVL 32.2mm).
 Photos by Vinh Q. Luu.

Leptobrachella namdongensis, new species

Diagnosis. Leptobrachella namdongensis, new species is distinguished from its congeners by a combination of the following morphological characters: size medium (30.9 mm in the adult male and 32.1–35.3 mm in adult females); head wider than long; tympanum distinct; throat immaculate white, chest and belly with dark specking on outer margins; toes with basal webbing and without lateral fringe; supratympanic fold edged by a distinct black line; inter-orbital region with distinct black blotches; iris bicoloured, upper half copper, fading to golden in its lower half; head without dorsolateral markings.

Etymology. Specific epithet is in reference to the type locality of the Nam Dong Conservation Area. We recommend “Nam Dong litter frog” as the common English name and “Cóc mày nam động” as the Vietnamese name.

Distribution and ecological notes. Leptobrachella namdongensis, new species is currently known from Nam Dong Conservation Area and Pu Hu Nature Reserve (NR), Thanh Hoa Province, Vietnam. All specimens of the new species were found on rocks in small streams or near cascade streams in evergreen forest at elevations between 500 and 740 m a.s.l. (Fig. 7). Leptobrachella namdongensis, new species occurs sympatrically with Leptobrachella ventripunctata.

Fig. 7. Habitat of Leptobrachella namdongensis, new species in Nam Dong Conservation Area, Thanh Hoa Province, Vietnam.



Hoang Van Chung, Nguyen Thien Tao, Luu Quang Vinh, Nguyen Quang Truong and Jiang Jianping. 2019. A New Species of Leptobrachella Smith 1925 (Anura: Megophryidae) from Thanh Hoa Province, Vietnam. RAFFLES BULLETIN OF ZOOLOGY. 67;  536–556.  

     


Sunday, November 17, 2019

[Herpetology • 2019] Hyalinobatrachium adespinosai • A New Glassfrog (Centrolenidae: Hyalinobatrachium) from the Topo River Basin, Amazonian Slopes of the Andes of Ecuador


Hyalinobatrachium adespinosai
Guayasamin, Vieira, Glor & Hutter, 2019


Abstract
A new species of glassfrog (Centrolenidae) is described from the San Jacinto River, an affuent of the Topo River, on the Amazonian slopes of the Ecuadorian Andes. The new species, Hyalinobatrachium adespinosai sp. nov., can be differentiated from all other centrolenids by the combination of its coloration (transparent peritoneum and pericardium) and vocalization (call duration = 0.38–0.44 s, with 9–13 pulses per call; dominant frequency = 4,645–5,001 Hz). However, H. adespinosai sp. nov. is morphologically cryptic with H. anachoretus, H. esmeralda, and H. pellucidum, from which it differs by call traits (in H. anachoretus: call duration = 0.32–0.37 s, with 5 or 6 pulses per call, dominant frequency = 4,670–4,800 Hz; in H. esmeralda: call duration = 0.218–0.257 s, tonal call, dominant frequency = 4,739–5,580 Hz; in H. pellucidum: call duration = 0.112– 0.140 s, tonal, dominant frequency = 5,000–5,710 Hz). Biogeographically, the new species is separated from H. anachoretus by a considerable distance and, also, the Marañon valley. Finally, following IUCN conservation criteria, the status of the new species is considered as Data Defcient. 

Keywords: Amphibia, Anura, Ecuador, Pastaza basin, phylogeny, Tungurahua Province 


Fig. 2. Hyalinobatrachium adespinosai sp. nov. in life, holotype.

    

 Hyalinobatrachium adespinosai new species
Suggested English name: Adela’s Glassfrog
 Suggested Spanish name: Rana de Cristal de Adela 

Holotype. ZSFQ 1648 (JMG 583, Fig. 2), adult male from riverine vegetation along the San Jacinto River (1.3447°S, 78.1814°W; 1,795 m asl), Tungurahua Province, Ecuador, collected by CRH, REG, and KC on 4 August 2017. Paratypes. ZSFQ 1650–52, 1647, adult males with same data as holotype. 


Generic placement. The new species is placed in the genus Hyalinobatrachium (Ruiz-Carranza and Lynch, 1991, as modifed by Guayasamin et al. 2009) on the basis of morphological and molecular data. The main diagnostic phenotypic traits of Hyalinobatrachium are: (1) ventral parietal peritoneum completely transparent; (2) digestive tract and bulbous liver covered by iridophores; (3) humeral spines absent; (4) white bones in life; (5) males call from the underside of leaves; (6) females place the eggs on the underside of leaves; and (7) males provide extended parental care. All the aforementioned characteristics are shared by the new species. Additionally, analyses of the mitochondrial 16S gene place the new species as a close relative of other Hyalinobatrachium species (Fig. 1); thus, generic placement in Hyalinobatrachium is unambiguous.

 Diagnosis. Within the genus Hyalinobatrachium, the new species is diagnosable mainly by having a transparent pericardium. However, the new species is morphologically cryptic with three closely related taxa (H. anachoretus, H. pellucidum, H. esmeralda). Based on comparisons with specimens examined (see Appendix 1), all these species display a similar size and color pattern (pale green dorsum with yellow dots and a transparent venter and pericardium; red heart visible ventrally). However, calls between species diverge noticeably; the major difference is the structure of the call, with two species (H. adespinosai sp. nov. and H. anachoretus) having pulsed calls and the others having tonal vocalizations (Fig. 3; Table 1). The call of H. adespinosai sp. nov. is further differentiated from that of H. anachoretus by being longer, having more pulses per note, and being produced at a higher rate (Table 1). Toe webbing (Toe IV) is less extensive in the new species (21/3 IV 2+) than in H. anachoretus (1+ IV 1+; Twomey et al. 2014). Additionally, the new species and H. anachoretus are separated by considerable distance (airline distance = 473 km), including one of the most important biogeographic barriers in South America, the Marañon valley (see Duellman 1999; Winger and Bater 2015 and references therein). Uncorrected p genetic distances for the mitochondrial gene 16S between H. adespinosai sp. nov. and its closest relatives are summarized in Table 2.

Fig. 5. Distribution of Hyalinobatrachium adespinosai sp. nov. in Ecuador.

Fig. 4. Natural history and in-situ photographs of the new species. (A) Adult male of Hyalinobatrachium adespinosai near his egg clutch; other males were observed on the same leaf as the egg clutch. (B) Close-up of the egg clutch. (C) Spider predation on an unattended egg clutch.

Ecology. All individuals of the new species were found on the underside of leaves of riverine vegetation along the San Jacinto River. The section of river was fast-fowing and had visible rapids. Although the population is locally abundant (as heard from numerous advertisement calls), individuals are very diffcult to observe because they are usually found at the canopy level (4–16 m above ground level). The type series consists of males exclusively; they were calling in the months of July and August. One male (ZSFQ 1648) was apparently guarding an egg clutch containing 22 embryos; both the adult male and the egg clutch were on the same leaf most of the time, but the male also moved to nearby leaves (Fig. 4). 

Distribution. Hyalinobatrachium adespinosai sp. nov. is only known from the type locality: San Jacinto River (...; 1,795 m asl), Tungurahua Province, Ecuador (Fig. 5). 

Evolutionary relationships. The phylogenetic analyses recover Hyalinobatrachium adespinosai sp. nov. haplotypes as sister to haplotypes sampled from H. anachoretus and nested within other members of a monophyletic clade comprised of all other sampled species of Hyalinobatrachium (Fig. 1). The most closely related species to H. adespinosai sp. nov. share several morphological traits, including a red heart exposed ventrally (H. adespinosai + H. anachoretus + H. pellucidum + H. yaku). 


Etymology. The specifc epithet adespinosai honors Adela Espinosa, an Ecuadorian conservationist and board member of the Jocotoco Foundation (http:// www.jocotoco.org). Adela’s work has focused on the conservation of species and ecosystems. The new glassfrog described here is found only within the limits of a natural reserve owned by Adela and her husband, Antonio Páez. We are delighted to recognize Adela’s devotion to nature with this marvelous species.


Juan M. Guayasamin, José Vieira, Richard E. Glor and Carl R. Hutter. 2019. A New Glassfrog (Centrolenidae: Hyalinobatrachium) from the Topo River Basin, Amazonian Slopes of the Andes of Ecuador. Amphibian & Reptile Conservation. 13(2) [General Section]: 133–144 (e194). amphibian-reptile-conservation.org/



Resumen.— Describimos una nueva especie de rana de cristal (Centrolenidae) del río San Jacinto, afuente del río Topo, en la vertiente amazónica de los Andes del Ecuador. La especie nueva, Hyalinobatrachium adespinosai sp. nov., se diferencia de todos los centrolénidos por la combinación de su coloración ventral (peritoneo y pericardio transparentes) y las características de su canto (duración del canto = 0.382–0.430 s, con 9–13 pulsos por canto; frecuencia dominante = 4,645–5,001 Hz). Sin embargo, es morfológicamente críptica con H. anachoretus, H. esmeralda y H. pellucidum, especies de las cuales difere por su canto (en H. anachoretus: duración del canto = 0.32–0.37 s, con 5 or 6 pulsos por canto, frecuencia dominante = 4,670–4,800 Hz; en H. esmeralda: duración del canto = 0.218–0.257 s, tonal, frecuencia dominante = 4,739–5,580 Hz; en H. pellucidum: duración del canto = 0.112–0.140 s, tonal, frecuencia dominante = 5,000–5,710 Hz). Finalmente, siguiendo los criterios de la UICN, sugerimos que Hyalinobatrachium adespinosai sp. nov. sea ubicada en la categoría de Datos Insufcientes. 
Palabras clave. Amphibia, Anura, Cuenca del Pastaza, Ecuador, flogenia, Tungurahua Province