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[Herpetology • 2016] A Reassessment of Melanophidium Günther, 1864 (Serpentes: Uropeltidae) from the Western Ghats of peninsular India, with the Description of A New Species; Melanophidium khairei

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Melanophidium khairei 
 Gower, Giri, Captain & Wilkinson, 2016 


Abstract

A new species of the uropeltid snake genus, Melanophidium Günther, 1864 is described based on a series of eight specimens. Melanophidium khairei sp. nov. is the fourth species described in the genus, and the first for 144 years. Superficially M. khairei sp. nov. resembles M. punctatum Beddome, 1871 in being piebald and punctate (and it was previously misidentified as M. punctatum), but in many scalation characters it more closely resembles M. wynaudense (Beddome, 1863). The new species occurs in southern Maharashtra, Goa, and northern Karnataka, in the Western Ghats region of peninsula India. It is the most northerly member of its genus. Lectotypes and paralectotypes are designated for M. wynaudense, M. bilineatum Beddome, 1870, and M. punctatum. A new key to the species of Melanophidium is presented. Aspects of the morphology, taxonomy and distribution of the three previously described species of Melanophidium are reviewed and revised.

Keywords: Reptilia, Alethinophidia, shieldtail, snake, systematics, taxonomy






 David J. Gower, Varad Giri, Ashok Captain and Mark Wilkinson. 2016. A Reassessment of Melanophidium Günther, 1864 (Squamata: Serpentes: Uropeltidae) from the Western Ghats of peninsular India, with the Description of A New Species. ZOOTAXA. 4085(4); 481-503. http://www.mapress.com/j/zt/article/view/zootaxa.4085.4.2

Snake that remained hidden for 145 years found - @NatureInd
 http://www.natureasia.com/en/nindia/article/10.1038/nindia.2016.33


[Herpetology • 2016] Raorchestes honnametti • Integrative Taxonomic Approach for Describing a New Cryptic Species of Bush Frog (Raorchestes: Anura: Rhacophoridae) from the Western Ghats, India

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Raorchestes honnametti 
Gururaja, Priti, Roshmi & Aravind, 2016

Abstract

A new cryptic species of bush frogRaorchestes honnametti sp. nov. is described from the south-eastern part of the Western Ghats, India. This newly described species belongs to the Charius clade and is morphologically similar to other clade members—R. charius and R. griet. Therefore, an integrative taxonomic approach based on molecular and bioacoustic analysis along with morphology was used to delimit the new species. Raorchestes honnametti sp. nov., is currently known only from Biligiri Rangaswamy Temple Tiger Reserve, a part of Biligiri Rangaswamy horst mountain range (a mountain formed due movement of two faults) formed during the Late Quaternary period (1.8–2.58 Ma). Discovery of cryptic species from a highly speciose and well-studied genus Raorchestes hints at the possible existence of several more cryptic species in this genus. We discuss the possible reasons for crypsis and emphasize the need for continued systematic surveys of amphibians across the Western Ghats.


Raorchestes honnametti sp. nov. Gururaja, Priti, Roshmi and Aravind
urn:lsid:zoobank.org:act:071B913C-BB18-4E6A-97C6-6BA2621F8D6E

Suggested common name: Honnametti Bush Frog.

Holotype: BNHS 5941, an adult male collected by authors from Strobilanthus shrubs at 0.48m above ground at Honnametti, on 13th October 2012 at 20:20 h from Biligiri Rangaswamy hills (11.8987° N, 77.1741° E, 1659 m amsl).

Paratypes: BNHS 5942, BNHS 5943, BNHS 5945 and BNHS 5946, male individuals collected by authors in Honnametti, collection date and place same as holotype. BNHS 5944, a male collected by authors on 14th October 2012 at 19:45 h Dodda Sampige (11.9473° N and 77.1836° E, 1142 m amsl).

Fig 4. Holotype (BNHS 5941) of Raorchestes honnametti sp. nov.
a-— Live specimen; — ventral view; — dorsal view; — ventral view of hind limb; — ventral view of forelimb; — lateral profile of head; — Schematic view of webbing in hind limb.

Diagnosis:Raorchestes honnametti belongs to the genus Raorchestes as they are relatively small sized frogs (15–45 mm), active in night, vomerine teeth absent, transparent/translucent vocal sac while calling and direct development without free swimming tadpoles. It is a small sized adult (male: 21.7–24.8 mm, n = 6); snout longer than the horizontal diameter of eye; groin uniform light brown with 3–4 yellow blotches; both anterior and posterior part of thigh uniform light brown with small round to oval shaped yellow blotches and relatively short hind limbs ShL/SVL ratio <0.5. It belongs to the Charius clade and morphologically similar to R. charius and R. griet.

Etymology: Named after the locality of holotype – Honnametti. Honnametti is treated as an invariable noun in apposition to the generic name.

Fig 1. Biligiri Rangaswamy Temple Tiger Reserve and sampling sites of Raorchestes honnametti sp. nov. (blue circles).

Natural history: Raorchestes honnametti sp. nov. is known only from Biligiri Rangaswamy hills and is one of the very common frogs in that landscape. It is found in shola forests, evergreen forests, semi-evergreen forests and around human habitations. Individuals were found calling in an open area within Ageratina adenophora (Asteraceae) and Strobilanthus bushes. Some individuals were also found on tree saplings in the understory. Individuals call at a perched height between 0.48–1.00 m from ground. Call starts at around 6 pm and goes till early morning. During monsoon (June to September), individuals call almost throughout the day except on days with heavy rains or dry days. Other anuran species like Pseudophilautus sp., Hylarana sp., Fejervarya sp., Duttaphrynus melanostictus, Microhyla sholigari, M. ornata, M. rubra and Euphlyctis cyanophlyctis co-occur with R. honnametti in Biligiri Rangaswamy hills.




Conservation:
There are no immediate threats from human activities to this newly described species as Biligiri Rangaswamy hills is a tiger reserve and enjoys high level of protection. However, in the last one decade, a significant area of the Reserve has been taken over by highly invasive species like Lantana camara (Verbenaceae) and Ageratina adenophora (Asteraceae). On subsequent visits, we have seen several calling males of R. honnametti on Lantana and Ageratina bushes, indicating that this species might have adapted to the presence of these invasive species. However, a systematic research needs to be undertaken to assess the impact of invasive species on R. honnametti.


H. Priti , Rekha Sarma Roshmi, Badrinath Ramya, H. S. Sudhira, G. Ravikanth, Neelavara Anantharam Aravind, Kotambylu Vasudeva Gururaja. 2016. Integrative Taxonomic Approach for Describing a New Cryptic Species of Bush Frog (Raorchestes: Anura: Rhacophoridae) from the Western Ghats, India. PLoS ONE. DOI: 10.1371/journal.pone.0149382

[Botany • 2016] Disporum sinovietnamicum sp. nov. (Colchicaceae) from southwestern Guangxi, China

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Disporum sinovietnamicum R. C. Hu & Y. Feng Huang sp. nov. is described and from southwestern Guangxi, China. It is morphologically closest to D. jinfoshanense X. Z. Li, D. M. Zhang & D. Y. Hong, but differs by having stems that are 35–90 cm tall, narrowly lanceolate and thinly leathery leaves, and ovate and glabrous tepals.


Ren-Chuan Hu, Wei-Bin Xu and Yun-Feng Huang. 2016. Disporum sinovietnamicum sp. nov. (Colchicaceae) from southwestern Guangxi, China.
 Nordic Journal of Botany.  DOI:  10.1111/njb.00989 

[Ornithology • 2016] Nondestructive Raman Spectroscopy confirms Carotenoid-pigmented Plumage in the Pink-headed Duck Rhodonessa caryophyllacea

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FIGURE 1. Dorsal view of a Pink-headed Duck (Rhodonessa caryophyllacea, USNM 608914), close view of the pink crown feathers, and a Raman spectrum collected from the pink feathers. The Raman spectrum was collected at 100 mW for 60 s through a 10× microscope objective. Each of the 3 carotenoid-identifying peaks in the spectrum has been labeled with the vibrational mode it represents.

ABSTRACT
A small group of pigment classes is responsible for the wide range of plumage colors in modern birds. Yellow, pink, and other “warm” feather colors of many species are attributed to carotenoid pigments, a plumage trait that has an uneven distribution across modern bird species. Carotenoid plumage pigments are especially rare among fowl (superorder Galloanseres), and until recently, the Pink-eared Duck (Malacorhynchus membranaceus) from Australia provided the only evidence that any species of waterfowl (order Anseriformes) exhibits carotenoid-pigmented plumage. We analyzed a Pink-headed Duck (Rhodonessa caryophyllacea) study skin using Raman spectroscopy, without plucking or otherwise damaging the specimen. Raman spectra confirmed that the pink feathers of Rhodonessa are pigmented with carotenoids. Spectra from Rhodonessa were similar to those from Malacorhynchus, which suggests that the same carotenoid is the primary plumage pigment in both species. Moreover, spectra from Rhodonessa were similar to spectra from other taxa pigmented with ketocarotenoids. Malacorhynchus and Rhodonessa are distant relatives within Anseriformes, so these findings indicate multiple evolutionary origins of plumage carotenoids within the waterfowl or (less likely) many losses of plumage carotenoids from duck species. Our results show that pigment chemistry can be studied in precious ornithological specimens without damaging the specimens, and provide new evidence that the (apparently extinct) Rhodonessa possessed what is evolutionarily an extremely rare trait among waterfowl.

Keywords: Anseriformes, coloration, feather, pigmentation, Raman spectroscopy, Rhodonessa


Female and male Pink-headed Duck Rhodonessa caryophyllacea
illustrated by Henrik Grönvold  wikipedia.org


Daniel B. Thomas and Helen F. James. 2016. Nondestructive Raman Spectroscopy confirms Carotenoid-pigmented Plumage in the Pink-headed Duck [La espectrometría Raman no destructiva confirma la pigmentación con carotenoides del plumaje de Rhodonessa caryophyllacea].  The Auk. 133(2) 147-154. DOI: 10.1642/AUK-15-152.1

Extinct pink-headed duck derived its unique color from carotenoids  http://phy.so/373134159 via @physorg_com
Carotenoid pigments make extinct duck a rare bird indeed http://smithsonianscience.si.edu/2016/03/red-headed-duck/

RESUMEN
Un pequeño grupo de clases de pigmentos es responsable del amplio rango de colores del plumaje en las aves modernas. Amarillo, rosa y otros colores “cálidos” de las plumas de muchas especies son atribuidos a los pigmentos carotenoides, un rasgo del plumaje que tiene una distribución desigual entre las especies de aves modernas. Los pigmentos carotenoides del plumaje son especialmente raros entre las aves de caza (superorden Galloanseres) y hasta hace poco, la especie Malacorhynchus membranaceus de Australia representaba la única evidencia de una especie de ave acuática (orden Anseriformes) con plumaje pigmentado con carotenoides. Analizamos una piel de estudio de Rhodonessa caryophyllacea usando espectrometría Raman sin perforar o dañar el espécimen. El espectro Raman confirmó que las plumas rosas de Rhodonessa están pigmentadas con carotenoides. Los espectros de Rhodonessa fueron similares a aquellos de Malacorhynchus, sugiriendo que el mismo carotenoide es el principal pigmento del plumaje en cada especie. Más aun, los espectros de Rhodonessa fueron similares a los espectros de otros taxa pigmentados con ceto-carotenoides. Malacorhynchus y Rhodonessa son parientes distantes adentro de los Anseriformes, indicando orígenes evolutivos múltiples de los carotenoides del plumaje adentro de las aves acuáticas, o (menos probable) muchas pérdidas de los carotenoides del plumaje en las especies de patos. Nuestros análisis muestran que la química de los pigmentos puede ser estudiada en especímenes ornitológicos valiosos sin dañarlos, y brinda nueva evidencia de que la especie (aparentemente extinta) Rhodonessa poseía lo que es un rasgo evolutivo extremadamente raro entre las aves acuáticas.

Palabras clave: Anseriformes, coloración, espectrometría Raman, pigmentación, plumas, Rhodonessa

[Crustacea • 2011] Samarplax principe • A New Genus and Species of Anchialine Hymenosomatidae (Decapoda, Brachyura) from Samar, Philippines

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Samarplax principe 
Husana, Tan & Kase, 2011

ABSTRACT

A new genus and species of brachyuran crab, Samarplax principe (family Hymenosomatidae) is described from an anchialine cave in Samar Island, Philippines. This cavernicolous species lacks rostrum and has degenerated eyes, possesses two small spines at the lateral margin of the carapace, has a proportionally shorter projected merus of the third maxilliped, an almost flat epistome and brush-like setae instead of teeth along the cutting edges of the chelae. The complete loss of visual organs and pigmentation, the long but slender ambulatory legs and large egg size suggest a completely hypogeal lifestyle for this species. This is the first species of Hymenosomatidae recorded from an anchialine cave in the Philippines exhibiting true troglomorphic adaptations. 


 Daniel Edison M. Husana. Swee Hee Tan and Tomoki Kase. 2011. A New Genus and Species of Anchialine Hymenosomatidae (Crustacea, Decapoda, Brachyura) from Samar, Philippines. Zootaxa. 3109: 49–59 

[Herpetology • 2014] Phylogeography of the Asian Softshell Turtle Amyda cartilaginea (Boddaert, 1770): Evidence for A Species Complex

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Fig. 3. Live Asian softshell turtles from the Great Sunda Islands.
Note in (A), (D) and (E) the saddle-shaped dark mark on the carapace.
(A) Amyda species (candidate species A?), juvenile, Loagan Bunut National Park, Sarawak, Malaysia (Borneo). Photo: Indraneil Das.
(B) Amyda cartilaginea cartilaginea (terminal clade 2), West Java, Indonesia (trade specimen). Yellow-spotted form of van Dijk (1992). Photo: Mark Auliya.
(C) Amyda species (not studied genetically). Rantauprapat, Sumatera Utara, Indonesia (northern Sumatra). Yellowspotted form of van Dijk (1992). Photo: Maren Gaulke.
(D) Amyda cartilaginea maculosa subsp. nov. (terminal clade 3), Balai Ringin, near Serian, Sarawak, Malaysia (Borneo). Photo: Indraneil Das.
(E) Amyda cartilaginea maculosa subsp. nov. (terminal clade 3), juvenile, Tanjung Lasa, Kapuas Hulu, West Kalimantan, Indonesia (Borneo). Note the different facial pattern compared to (A). Photo: Mark Auliya.

Fig. 4. Live Asian softshell turtles from Mainland Southeast Asia.
(A) Amyda ornata ornata (terminal clade 6), southern Vietnam or Cambodia. Arrow-headed form of van Dijk (1992). Note the smooth rear carapace. Photo: Timothy McCormack.
(B, C) Amyda ornata phayrei (terminal clade 5), Thailand. Note the different head colouration compared to A. o. ornata and the pronounced shell tubercles. Photos: Peter Praschag.
 (D, E) Amyda ornata subspecies (terminal clade 4), Chittagong Hills, Bangladesh. Note the pale shell colouration, the indistinct head pattern and the pronounced shell tubercles. Photos: Peter Praschag.

Abstract
Using up to 2456 bp mtDNA and up to 2716 bp nDNA of fresh samples and short sequences of three mitochondrial genes of historical museum material, we examine the phylogeography of Amyda cartilaginea. This data set provides evidence for the existence of deeply divergent genetic lineages which we interpret as three distinct species, two of which are polytypic. On the Great Sunda Islands, the distribution ranges of the two subspecies of Amyda cartilaginea (Boddaert, 1770) sensu stricto and of an undescribed species match palaeodrainage systems. Amyda cartilaginea cartilaginea occurs in the East Sunda palaeodrainage, with records in eastern Borneo and Java. Also a record from Sulawesi, most probably not representing a native population, refers to A. c. cartilaginea. In the North Sunda palaeodrainage (Sumatra, western Borneo) livesAmyda cartilaginea maculosa subsp. nov., which is described herein. One sample from the Baram river (Sarawak, Malaysia) is genetically highly distinct and represents a new species. We refrain from naming this taxon until more material becomes available for morphological characterization. For the continental populations, we resurrect the species Amyda ornata (Gray, 1861). We identify Asian softshell turtles from the Mekong drainage with the nominotypical subspecies, while the genetically distinct populations from Thailand and Myanmar are assigned to Amyda ornata phayrei (Theobald, 1868). Samples from Bangladesh are also genetically distinct and represent an undescribed subspecies and the first country record for Amyda.
Key words: Amyda cartilaginea cartilaginea; Amyda cartilaginea maculosa subsp. nov.; Amydaornata ornata; Amyda ornata phayrei; Great Sunda Islands; Southeast Asia, Subspecies; Taxonomy; Testudines; Trionychidae.


Fig. 3. Live Asian softshell turtles from the Great Sunda Islands.
Note in (A), (D) and (E) the saddle-shaped dark mark on the carapace.
 (A) Amyda species (candidate species A?), juvenile, Loagan Bunut National Park, Sarawak, Malaysia (Borneo). Photo: Indraneil Das.
(B) Amyda cartilaginea cartilaginea (terminal clade 2), West Java, Indonesia (trade specimen). Yellow-spotted form of van Dijk (1992). Photo: Mark Auliya.
 (C) Amyda species (not studied genetically). Rantauprapat, Sumatera Utara, Indonesia (northern Sumatra). Yellowspotted form of van Dijk (1992). Photo: Maren Gaulke.
 (D)Amyda cartilaginea maculosa subsp. nov. (terminal clade 3), Balai Ringin, near Serian, Sarawak, Malaysia (Borneo). Photo: Indraneil Das.
(E) Amyda cartilaginea maculosa subsp. nov. (terminal clade 3), juvenile, Tanjung Lasa, Kapuas Hulu, West Kalimantan, Indonesia (Borneo). Note the different facial pattern compared to (A). Photo: Mark Auliya.

Fig. 4. Live Asian softshell turtles from Mainland Southeast Asia.
(A) Amyda ornata ornata (terminal clade 6), southern Vietnam or Cambodia. Arrow-headed form of van Dijk (1992). Note the smooth rear carapace. Photo: Timothy McCormack.
(B, C)
ตะพาบน้ำ | Amyda ornata phayrei (terminal clade 5), Thailand. Note the different head colouration compared to A. o. ornata and the pronounced shell tubercles. Photos: Peter Praschag.
(D, E) Amydaornata subspecies (terminal clade 4), Chittagong Hills, Bangladesh. Note the pale shell colouration, the indistinct head pattern and the pronounced shell tubercles. Photos: Peter Praschag.

Uwe Fritz, Richard Gemel, Christian Kehlmaier, Melita Vamberger and Peter Praschag. 2014. Phylogeography of the Asian Softshell Turtle Amyda cartilaginea (Boddaert, 1770): Evidence for A Species Complex. Vertebrate Zoology. 64(2): 229–243. 


[Herpetology • 2015] Insights from Integrative Systematics Reveal Cryptic Diversity in Pristimantis Frogs (Anura: Craugastoridae) from the Upper Amazon Basin

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Fig 1. Phylogeny and distribution of the Pristimantis acuminatus group in the Amazon Basin.
 (A) Optimal maximum likelihood tree (log likelihood = -6762.95) inferred from a partitioned analysis of 1997 aligned sites of the 12S, 16S and COI (by codon position) mtDNA genes, showing the phylogenetic relationships among 33 specimens identified as P. acuminatussensu lato and P. tantanti from the Amazon basin. Clade A = Pristimantis limoncochensis sp. nov., clade B =P. omeviridis sp. nov., clade C = P. acuminatus sensu stricto, clade D = P. enigmaticus sp. nov., and clade E = P. tantanti. Stars denote clades with Bayesian posterior probability values1; numbers below clades represent non-parametric bootstrap support values.
(B) Areas of distribution for species in the complex. Dotted circles = Localities of collection from specimens used for the phylogenetic analyses; Polygons = occurrence areas drawn as minimum convex polygons for each clade based on specimens reviewed in collections (S2 Table). Colors of clades in the phylogenetic tree correspond to colors of polygons and dotted circles on the map.

Abstract

Pluralistic approaches to taxonomy facilitate a more complete appraisal of biodiversity, especially the diversification of cryptic species. Although species delimitation has traditionally been based primarily on morphological differences, the integration of new methods allows diverse lines of evidence to solve the problem. Robber frogs (Pristimantis) are exemplary, as many of the species show high morphological variation within populations, but few traits that are diagnostic of species. We used a combination of DNA sequences from three mitochondrial genes, morphometric data, and comparisons of ecological niche models (ENMs) to infer a phylogenetic hypothesis for the Pristimantis acuminatus complex. Molecular phylogenetic analyses revealed a close relationship between three new species — Pristimantis enigmaticus sp. nov.,P. limoncochensis sp. nov. andP. omeviridis sp. nov. — originally confused with Pristimantis acuminatus. In combination with morphometric data and geographic distributions, several morphological characters such as degree of tympanum exposure, skin texture, ulnar/tarsal tubercles and sexual secondary characters (vocal slits and nuptial pads in males) were found to be useful for diagnosing species in the complex. Multivariate discriminant analyses provided a successful classification rate for 83–100% of specimens. Discriminant analysis of localities in environmental niche space showed a successful classification rate of 75–98%. Identity tests of ENMs rejected hypotheses of niche equivalency, although not strongly because the high values on niche overlap. Pristimantis acuminatus and P.enigmaticus sp. nov. are distributed along the lowlands of central–southern Ecuador and northern Peru, in contrast with P. limoncochensis sp. nov. and P. omeviridis sp. nov., which are found in northern Ecuador and southern Colombia, up to 1200 m in the upper Amazon Basin. The methods used herein provide an integrated framework for inventorying the greatly underestimated biodiversity in Amazonia.

Fig 9. Living specimens of the Pristimantis acuminatus complex and their relatives in the Amazon Basin.
(A) Pristimantis acuminatus, QCAZ 53263, (B) Pristimantis tantanti, CORBIDI 12987, (C-D) night and daylight color variation in Pristimantis limoncochensis sp. nov., QCAZ 52987, (E) amplectant pair of Pristimantis omeviridis sp. nov., holotype female QCAZ 55392 and paratype male QCAZ 55391, (F) Pristimantis padiali, specimen not collected, (G-H) night and daylight color variation in Pristimantis enigmaticus sp. nov., specimen not collected.

 Photographs of (B) by V. Durán, (E) by Santiago Ron, (F) by Omar Rojas; all other photographs by H. M. Ortega-Andrade.  DOI: 10.1371/journal.pone.0143392


H. Mauricio Ortega-Andrade, Octavio R. Rojas-Soto, Jorge H. Valencia, Alejandro Espinosa de los Monteros, Juan J. Morrone, Santiago R. Ron and David C. Cannatella. 2015. Insights from Integrative Systematics Reveal Cryptic Diversity in Pristimantis Frogs (Anura: Craugastoridae) from the Upper Amazon Basin. PLoS ONE. 10(11): e0143392. DOI: 10.1371/journal.pone.0143392

[Herpetology • 2016] Systematic Revision of the Marbled Velvet Geckos (Oedura marmorata species complex, Diplodactylidae) from the Australian Arid and Semi-Arid Zones

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FIGURE 5. Species in the Oedura marmorata complex in life:
 
AOedura cincta, Eastern ESU, Winton Region, Queensland; BO. cincta, Eastern ESU, Danggalli Conservation Park, South Australia; COcincta, central ESU, Simpson’s Gap, Northern Territory; DO. cincta, central ESU, hatchling, Simpson’s Gap, Northern Territory; E. Oedura bella sp. nov., Doomadgee area, Queensland; FO. bella sp. nov. holotype, 10 km south of Mt Isa, Queensland; GOedura fimbria sp. nov., Little Sandy Desert, Western Australia; HO. fimbria sp. nov., Pannawonnica, Western Australia. 
Photographs: A, C–E. S. Macdonald; B. M. Hutchinson; F. P.M. Oliver; G. B. Maryan; H. R. Ellis.   DOI: 10.11646/zootaxa.4088.2.1

Abstract

Lizards restricted to rocky habitats often comprise numerous deeply divergent lineages, reflecting the disjunct nature of their preferred habitat and the capacity of rocky habitats to function as evolutionary refugia. Here we review the systematics and diversity of the predominantly saxicoline Australian marbled velvet geckos (genus Oedura) in the Australian arid and semi-arid zones using newly-gathered morphological data and previously published genetic data. Earlier work showed that four largely allopatric and genetically divergent lineages are present: Western (Pilbara and Gascoyne regions), Gulf (west and south of the Gulf of Carpentaria), Central (central ranges) and Eastern (Cooper and Darling Basins). None of these four populations are conspecific with true O. marmorata, a seperate species complex that is restricted to the Top End region of the Northern Territory. Top End forms share a short, bulbous tail whereas the other four lineages treated here possess a long, tapering tail. Morphological differences among the arid and semi-arid lineages include smaller body size, tapering lamellae and a shorter tail for the Gulf population, and a partially divided rostral scale in the Western population compared to the Central and Eastern populations. Accordingly, we resurrect O. cinctade Vis from synonymy for the Central and Eastern lineages, and regard this species as being comprised of two evolutionary significant units. We also describe the Gulf and Western lineages as new species: Oedura bella sp. nov. and Ofimbria sp. nov., respectively. We note that a predominantly arboreal lineage (the Eastern lineage of Ocincta) is more widely distributed than the other lineages and is phylogenetically nested within a saxicoline clade, but tends to have a deeper head and shorter limbs, consistent with morphological variation observed in other lizard radiations including both saxicoline and arboreal taxa.

Keywords: Reptilia, arboreal, central ranges, Cooper Basin, gecko, de Vis, Gulf Country, new species, Oedura cinctaOedura bella sp. nov., Oedura fimbria sp. nov., Pilbara, saxicoline, taxonomy






Oedura cincta de Vis, 1888
Inland marbled velvet gecko

Lectotype. QM J226, Charleville, Queensland, Australia (collected by Kendall Broadbent in 1885). Paralectotypes. AMS R5602, AMS R5603, as for lectotype.
Synonomy. Oedura derelicta Wells & Wellington, 1985,
holotype—NTM R11413, Jessie Gap, Alice Springs, Northern Territory.



Oedura bella sp. nov. Gulf marbled velvet gecko

Distribution and habitat. Restricted to the ranges around the south and western edges of the Gulf of Carpentaria; from the Selwyn Range around Mt Isa in the southeast, north to Riversleigh and Musselbrook regions in the Queensland-Northern Territory border, as far west as the McArthur River and Borroloola regions of Northern Territory, with a further apparently isolated insular population on Groote Eylandt to the north (see comments), and another isolated record from the northern edge of the Barkly Tablelands (Fig. 2). Field observations suggest this species is primarily saxicoline, using both horizontal screes and vertical faces (including road cuttings), however, it has also been recorded under bark around the base of trees (but in rocky country) (G. Bourke, pers. comm.). 

Etymology. From the Latin masculine adjective bellum (used in its feminine form), meaning amongst other things pretty, handsome, charming, fine, lovely, neat, pleasant, agreeable, active, gallant or good. In reference to the very attractive contrasting yellow and dark colour pattern of this species. 


Oedura fimbria sp. nov.Western marbled velvet gecko

Distribution and habitat. Occurs in the Pilbara, Gascoyne and Murchison regions of mid-western Western Australia (Fig. 2). In the north (Pilbara), this species extends to the southern edge of the Great Sandy Desert, east to Karlamilyi National Park, and west to the Burrup Peninsula. In the south it occurs in the Gascoyne, western Murchison and Yalgoo regions, east as far as the Barlee Range, south to Mt Magnet and Gullwa, and east to the Little Sandy Desert. From collector’s notes associated with voucher specimens, this species was recorded as occurring on relatively massive ranges, rocky outcrops and breakaways, caves and gorges 114 times, whereas there are only 4 occurrences on trees and one under tin. We have only observed this species on rocky outcrops with large boulders (Pilbara) or on cliff faces (Kennedy Range).

 Etymology. Fimbria is Latin for fringe in reference to the lateral fringes of expanded lamellae along the sides of the digits. Used as a noun in apposition. 


Oliver, Paul M. & Paul Doughty. 2016. Systematic Revision of the Marbled Velvet Geckos (Oedura marmorata species complex, Diplodactylidae) from the Australian Arid and Semi-Arid Zones. Zootaxa. 4088(2): 151–176.  DOI: 10.11646/zootaxa.4088.2.1



[Herpetology • 2016] Systematics and Phylogeny of Sitana (Reptilia: Agamidae) of Peninsular India, with the Description of One New Genus, Sarada, and Five New Species

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Fig. 14. Images of Sarada spp. in life with photos of their habitat:
A. Adult male Sarada deccanensiscomb. nov. B. Habitat at Jalna, the type locality of S. deccanensis.
C. Adult male Sarada superba sp. nov. in breeding display. D. Habitat at Chalkewadi, the type locality of S. superba sp. nov.
E. Adult male Sarada darwini sp. nov. in breeding display. F. Habitat at Bidnal, the type locality of S. darwini sp. nov.
ABSTRACT

We revise the taxonomy of the agamid genus Sitana Cuvier, 1829, a widely distributed terrestrial lizard from the Indian subcontinent based on detailed comparative analyses of external morphology, osteology and molecular data. We sampled 81 locations spread over 160,000 sq.km. in Peninsular India including type localities, which represented two known and five previously undescribed species. Based on general similarity in body shape and dewlap all species were hitherto identified as members of the genus Sitana. However, Sitana deccanensis and two other morphotypes, which are endemic to north Karnataka and Maharashtra in Peninsular India, are very distinct from the rest of the known members of the genus Sitana based on their external morphology and osteology. Moreover, members of this distinct morphological group were monophyletic in the molecular tree, and this clade (clade 1) was sister to two well-supported clades (2 and 3) constituting the rest of the Sitana. The interclade genetic divergence in mtDNA between clade 1 and clades 2 and 3 was 21-23%, whereas clade 2 and clade 3 exhibited 14-16% genetic divergence. Thus, we designate a new genus name “Saradagen. nov. for species represented in Clade 1, which also includes the recently resurrected Sitana deccanensis. We describe two new species in Sarada gen. nov. and three new species in Sitana. Similarity in the dewlap of Sitana and Sarada gen. nov. is attributed to similar function (sexual signaling) and similarity in body shape is attributed to a similar terrestrial life style and/or common ancestry.

Key words: cryptic, dewlap, genetics, morphology, osteology, taxonomy 


Family Agamidae Gray, 1827
Genus Sitana Cuvier, 1829

Fig. 9. Sitana spp. (Cuvier, 1829) in life and their habitat:
Sitana ponticeriana. A. Adult male from type locality, B. Habitat type in the type locality, Puducherry.
 Sitana visiri sp. nov. C. Adult male, D. Habitat type in the type locality, Tuticorin.
Sitana laticeps sp. nov. E. Adult male in breeding display, F. Habitat type in the type locality, Bopdev Ghat.
Sitana spinaecephalus sp. nov. G. Adult male H. Habitat type in the type locality, Halol.


Sitana Cuvier, 1829. Le Regne Animal Distribué, d’apres son Organisation, pur servir de base à l’Histoire naturelle des Animaux et d’introduction à l’Anatomie Comparé. 43. Type species: Sitana ponticeriana.
Semiophorus Wagler, 1830. Natürliches System der Amphibien: mit vorangehender Classification der Säugethiere und Vögel: ein Beitrag zur vergleichenden Zoologie. 152. Type species: Sitana ponticeriana (named as pondicerianus)
Litana Kelaart, 1854. Catalogue of reptiles collected in Ceylon. The Annals and magazine of natural history (2) 13: 138. Litana ponticereana.
Content.Sitana ponticeriana Cuvier, 1829;Sitana fusca Schleich and Kästle, 1998;Sitanasivalensis Schleich, Kästle and Shah, 1998;Sitana schleichi Anders and Kästle, 2002;Sitana bahiri Amarsinghe, Ineich, and Karunarathna, 2015;Sitana devakai Amar­singhe, Ineich, and Karunarathna, 2015.

English name. Fan-throated lizards (Das, 1997).

Etymology. Cuvier (1829) in his description did not mention anything about the generic name. Jerdon (1853) mentioned that Sitana is the name that it was known by at Puducherry, with the genus name a Latin termination of the word “Shaitan” or Devil. Jerdon also notes that the name was sometimes applied to it by the Musulmans of South India. More recently Schleich and Kästle (2002), without any reference, suggested that the generic name is derived from the Tamil language sit wona, small lizard. Sit wona does not translate to small lizard in Tamil: it is either siriyawona or chinnawona. There is no mention about the etymology of the genus by past herpetologists (Günther, 1864, Boulenger, 1890, Smith, 1935). Since Jerdon’s information was published during the same century, we suggest his version of the genus etymology is more likely to be accurate.

Diagnosis. Small to medium-sized lizards, male SVL 36.6-56.6 mm, females 36.4-52.1 mm; head-scales unequal, strongly keeled; supraciliary edge sharp; fourth toe extending well beyond third, fifth toe absent; exposed tympanum, no preanal or femoral pores, no prominent dorsal crest; presence of enlarged scales on the lateral side of the trunk and a single enlarged keeled scale on the thigh region. Scales on the dorsum within the dark brown line marking are relatively larger than the adjoining smaller scales on the lateral side of the body. Dewlap size varies from small to large depending on the species. Sitana can be differentiated from their closest living genus Otocryptis by the absence of fifth toe and an exposed tympanum.

Distribution and habit. Widely distributed in the Indian Subcontinent from Jammu and Kashmir in the north, the Sind region of Pakistan in the west, West Bengal in the east, and Sri Lanka in the south. (Stoliczka, 1872; Murray, 1886; Sahi and Duda, 1981).Sitana are primarily terrestrial, but also climb onto low bushes, herbs and small rocks (Fig. 9). Breeding starts approximately a month and a half before the monsoon (Rao and Rajabai, 1972; Subramanean and Reddy, 2010; Pal et al., 2010; Trivedi et al., 2011).

 • Sitana ponticeriana (Cuvier, 1829)
 • Sitana visiri Deepak sp. nov.
 • Sitana spinaecephalus Deepak, Vyas and Giri sp. nov.
 • Sitana laticeps Deepak and Giri sp. nov.

---------------------------------




Sarada Deepak, Karanth and Giri, gen. nov.
Suggested English name. Large fan-throated lizards.

Type species. Sitana deccanensis Jerdon, 1870.
Content.Saradadeccanensis (Jerdon, 1870) comb. nov., Sarada darwini sp. nov., Sarada superba sp. nov.
Etymology. The generic epithet is derived from the word ‘Sarada,’ which is the Marathi word for agamid lizards in Maharashtra and some parts of Karnataka, where this genus is endemic.

Diagnosis. Sarada gen. nov. can be easily diagnosed from all other agamid lizards from the Indian subcontinent except Sitana in having five fingers and four toes. Sarada gen. nov. is closely related to two genera from Indian subcontinent, Otocryptis Wagler 1830 and Sitana Cuvier (1829). Sarada gen. nov. can be easily differentiated from Otocryptis by the absence of fifth toe and exposed tympanum. Sarada gen. nov. can be diagnosed from Sitana by following unique combination of characters: breeding males with iridescent blue, orange and black colour with yellow stripes, the orange colour in some individuals extending all the way to the vent; absence of enlarged scale on the thigh; scales on flanks homogeneous, absence of enlarged scales on the lateral side of the body, absence of enlarged, strongly keeled scales around the tympanum; additionally Sarada gen. nov. can be distinguished from the Sitana sivalensis complex by the following set of characters: large body size (range 52.9-74.4 mm SVL males; range 43.6-64.3 mm SVL females); very large dewlap with enlarged overlapping scales extending all the way to middle of the abdomen (mean 51% up to 73% of TRL). Osteologically, Sarada gen. nov. can be distinguished from Sitana ponticeriana and Sitana spinaecephalus clades by the additional phalange on the fourth finger and in having one less trunk vertebra (Fig. 7 and Table 6). Dorsum pale brown to dark brown with four black brown-edged rhomboidal markings, the one on the nuchal region is darker than the remainder, and the back is bordered on each side with a thin cream coloured band. One prominent buff coloured line begins below the eye extending to the forearam, and another is comparatively broad and extends from behind the eye to the neck; a prominent dark brown interorbital patch is present but does not reach the eyes. Limbs and tail with dark brown or black bands of variable widths.

Distribution. Restricted distribution in Maharshtra and north Karnataka, the northern most records are from Nashik in Maharashtra, and the southernmost are in Bellary and Bidnal in north Karnataka. The easternmost records are from Chanda (Chandrapur) (Blanford, 1870; Amarasinghe et al., 2015). Based on the available records, it appears that they are not found in the lowlands and coastal plateaus on the western part of the distribution of the genus.

 • Sarada deccanensis (Jerdon, 1870) comb. nov.
 • Sarada darwini Deepak, Karanth, Dutta and Giri sp. nov.
 • Sarada superba Deepak, Zambre, Bhosale and Giri sp. nov.


V. Deepak, Varad B. Giri, Mohammad Asif, Sushil Kumar Dutta, Raju Vyas, Amod M. Zambre, Harshal Bhosale and K. Praveen Karanth. 2016. Systematics and Phylogeny of Sitana (Reptilia: Agamidae) of Peninsular India, with the Description of One New Genus and Five New Species. CONTRIBUTIONS TO ZOOLOGY [Bijdragen tot de Dierkunde]85(1)


[PaleoEntomology • 2016] Alienoptera – A New Insect Order in the Roach - Mantodean Twilight Zone

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Alienopterus brachyelytrus 
Bai, Beutel, Klass, Wipfler et Zhang, 2016

Highlights
• A new insect order, Alienoptera ord. Nov., is described from Burmese amber.
• It displays a bizarre combination of characters occurring in different insect orders.
• †Alienopterus was an evolutionary dead end in the roach-mantis transition zone.

Abstract
A new insect species (Alienopterus brachyelytrus Bai, Beutel, Klass, Wipfler et Zhang gen. et sp. nov.) of a new order and family is described, based on a single male embedded in Cretaceous Burmese amber (ca. 99 Ma). Unusual characters are shortened forewings combined with fully developed, operational hindwings, similar as in Dermaptera, and specialized attachment pads otherwise only found in mantophasmatodeans (heelwalkers). A cladistic analysis suggests a placement as sister to Mantodea, supported by a profemoral brush and other characters. The male genitalia show the same pattern in both groups. Specialized features are the unusual flight apparatus, attachment structures adapted for locomotion on leaves, and a dense profemoral setation suitable for catching small prey. †Alienopterus was apparently able to fly and likely a predator of small arthropods in bushes or trees. An impressive radiation of Mantodea started in similar habitats at least 35 Ma later in the early Cenozoic. In contrast, †Alienopterus was an evolutionary dead end in the roach-mantis transition zone.

Keywords: mantis; fossil; amber; Cretaceous; Polyneoptera; Dictyoptera; Mantodea; Alienopterus; raptorial leg


  Systematic palaeontology

Order Alienoptera Bai, Beutel, Klass, Wipfler et Zhang ord. Nov.

Family Alienopteridae Bai, Beutel, Klass, Wipfler et Zhangfam. Nov.

Alienopterus Bai, Beutel, Klass, Wipfler et Zhang gen. Nov.

Type species:Alienopterus brachyelytrus Bai, Beutel, Klass, Wipfler et Zhang sp. nov.

 Material: Currently only one nearly complete specimen is known (No. BU-001,057). This adult male is designated as the holotype of the new species. The (type) specimen is currently on long-term loan in the Institute of Zoology, Chinese Academy of Sciences (IZAS) (specimen available for study by contacting MB or WWZ). From 2026 it will be deposited in the currently established Three Gorges Entomological Museum, Chongqing, China.

  Etymology: The genus name “Alienopterus” refers to the unusual (Latin “alienus”) combination of characters including the wings (New Latin “-pterus” = − winged, from Greek “pterón” = wing) of the new species. The species epithet refers to the short (Greek “brachys”) and apparently hardened forewings (“elytron”, as generally used for the hardened forewings of beetles).

Ming Bai, Rolf Georg Beutel, Klaus-Dieter Klass, Weiwei Zhang, Xingke Yang, Benjamin Wipfler 2016. †Alienoptera – A New Insect Order in the Roach - Mantodean Twilight Zone. Gondwana Research. DOI: 10.1016/j.gr.2016.02.002 


[Ichthyology • 2016] Pegasus tetrabelos • Integrated Taxonomy Reveals Hidden Diversity in Northern Australian Fishes: A New Species of Seamoth (Genus Pegasus)

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Short-spined Seamoth | Pegasus tetrabelos  
 Osterhage, Pogonoski, Appleyard & White, 2016

Abstract

Fishes are one of the most intensively studied marine taxonomic groups yet cryptic species are still being discovered. An integrated taxonomic approach is used herein to delineate and describe a new cryptic seamoth (genus Pegasus) from what was previously a wide-ranging species. Preliminary mitochondrial DNA barcoding indicated possible speciation in Pegasus volitans specimens collected in surveys of the Torres Strait and Great Barrier Reef off Queensland in Australia. Morphological and meristic investigations found key differences in a number of characters between P. volitans and the new species, Pegasus tetrabelos. Further mt DNA barcoding of both the COI and the slower mutating 16S genes of additional specimens provided strong support for two separate species. Pegasus tetrabelos and P. volitans are sympatric in northern Australia and were frequently caught together in trawls at the same depths.

Diagnosis and Description

Pegasus tetrabelos Osterhage, Pogonoski, Appleyard and White sp. nov.
  urn:lsid:zoobank.org:act:359804F0-30D0-4ECC-B355-D60D45556018.


Fig 2. Holotype of Pegasus tetrabelos (CSIRO H 6553–03, 110 mm PCL). (A) dorsal; (B) lateral; and (C) ventral views.

Diagnosis: Tail rings 12, anteriormost 9 mobile, articulating laterally, remaining 3 fused together, attenuated and dorsoventrally flattened; terminodorsal-lateral (tdl) and terminoventral-lateral (tvl) plates each with an anteriorly and posteriorly directed spine; terminal-lateral plates (tl) absent; interpectoral plate (ip) present; single ventral preopercular notch present; rostrum spatulate; carapace with three small posteriorly directed tubercles along each dorsal ridge, one at the centre of each dorsal plate; scales not present on orbit; pectoral fin composed of 9–10 (usually 10) soft rays, 5th ray stouter than other rays; abdominal centra 7, caudal centra 14, total centra 21; tail with 4 dark saddles, no dark saddle on tail ring XI.


Distribution: Pegasus tetrabelos is known from the east coast of Queensland and Torres Strait between latitudes 9°15’ S and 22°01’ S, and in the Northern Territory from the Beagle Gulf to off Darwin (Fig 8). Specimens collected during the Torres Strait and Great Barrier Reef trawl surveys formed three distinct clusters (Fig 9). The first cluster was located in the Torres Strait between latitudes 9°15’ S and 10°51’ S; the second cluster in Princess Charlotte Bay (~14°15’ S); and the third from Bowling Green Bay (19°26’ S) south to Broad Sound (22°01’ S). Despite intensive trawling, no specimens of the new species (or P. volitans) were caught between these clusters in the trawl survey. This likely reflects specific habitat preferences. There are currently no records of this species from the Gulf of Carpentaria or Western Australia.

Specimens of P. tetrabelos were collected at depths of 8–45 m, mostly in depths less than 30 m. Although the trawling surveys of the Great Barrier Reef and Torres Strait were conducted to depths of 100 m, P. tetrabelos was not collected in depths greater than 40 m.

Etymology: The species name tetrabelos is a combination of the Greek ‘tetra’ meaning four and ‘belos’ meaning dart or arrow in allusion to the four backward pointing spines on the terminal tail ring (two on each side). The name is treated as a noun in apposition.

Vernacular names: Short-spined Seamoth.


Conservation and management implications: 

This study has delineated and described a new cryptic species, Pegasus tetrabelos, from what was previously a commonly-recognised, wide-ranging species. This has been strongly supported by multiple taxonomic tools through an integrated taxonomy approach, and will provide a basis for scientific studies, and informed management and conservation efforts into the future.

A consequence of having a single wide-ranging species split into two, with one species having a much more restricted range, is that there is a need to reassess management or impacts relevant to each species. Pegasus species are caught as bycatch in northern Australian commercial prawn trawl fisheries, where they are discarded. The abundance of ‘P. volitans’ was reported to have declined in the southeast Gulf of Carpentaria after 20 years of prawn trawl fishing, with demersal fish surveys recording a reduction in catches of 32%. In the East Coast Trawl Fishery and Torres Strait Prawn Fishery, ‘P. volitans’ were found to be caught in ~24 and 41% of prawn trawls, respectively. Although it is not possible to determine the relative contribution of P. volitans and P. tetrabelos from this data, it is likely both species are encountered in these two fisheries.

Although pegasids are not utilised in large quantities in Australian waters, there is evidence of far greater exploitation of pegasids in some Asian countries. In a single Philippine province, it is estimated 43,000–62,000 seamoths/year (predominantly P. volitans) are caught live for the aquarium trade, with an additional 130,000–620,000 P. volitans/year caught incidentally by fishers and sold to traditional Chinese medicine markets. Sales of P. volitans for traditional medicine in China are estimated to be in the millions each year, provided by suppliers throughout Southeast Asia. This highlights the need for further taxonomic work on this group outside of Australia. If the wide-ranging P. volitans is found to be a complex of species with more restricted ranges, such localised heavy exploitation could be a more significant threat than currently recognised.


Deborah Osterhage, John J. Pogonoski, Sharon A. Appleyard and William T. White. 2016. Integrated Taxonomy Reveals Hidden Diversity in Northern Australian Fishes: A New Species of Seamoth (Genus Pegasus). PLoS ONE. 11(3): e0149415.   DOI: 10.1371/journal.pone.0149415

[Crustacea • 2016] “Symmetrical” Hermit Crabs of the Family Pylochelidae (Decapoda: Anomura) collected by the “BIOPAPUA” and “PAPUA NIUGINI” expeditions in the Papua New Guinea, with Descriptions of Two New Species

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Trizocheles sakaii  Forest, 1987 

Abstract

Collections made during the recent expeditions to Papua New Guinea (“BIOPAPUA”, 2010; “PAPUA NIUGINI”, 2012) yielded a total of 12 species from the “symmetrical” hermit crab family Pylochelidae, including two new to science: Bathycheles incisus (Forest, 1987), B. integer (Forest, 1987), Cheiroplatea laticauda Boas, 1926, C. pumicicola Forest, 1987, Cheiroplatea rotundioculus n. sp., Pylocheles mortensenii Boas, 1926, and Xylocheles macrops (Forest, 1987) (Pylochelinae); Parapylocheles scorpio (Alcock, 1894), Trizocheles manningi Forest, 1987, T. moosai Forest, 1987, T. sakaii Forest, 1987, and Trizocheles spinidigitus n. sp. (Trizochelinae). Affinities of the two new species are discussed. Parapylocheles scorpio, Trizocheles manningi and T. sakaii are recorded from the South Pacific for the first time. Revised identification keys to species of Cheiroplatea and Trizocheles are provided. 

Keywords: Crustacea, Bathycheles, Cheiroplatea, Parapylocheles, Parapylochelidae, Pylocheles, Trizocheles, Xylocheles


Tomoyuki Komai and Tin-Yam Chan. 2016. “Symmetrical” Hermit Crabs of the Family Pylochelidae (Crustacea: Decapoda: Anomura) collected by the “BIOPAPUA” and “PAPUA NIUGINI” expeditions in the Papua New Guinea, with Descriptions of Two New Species.
Zootaxa. 4088(3)  http://mapress.com/j/zt/article/view/zootaxa.4088.3.1

[Botany • 2016] New Orchid Species of Stigmatodactylus (Orchidoideae; Diurideae) from central Palawan, Philippines; Stigmatodactylus dalagangpalawanicum & S. aquamarinus

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Stigmatodactylus aquamarinus  A.S.Rob. & E.Gironella, 2016
FIGURE 4. Stigmatodactylus aquamarinus growing in situ in the Mount Victoria massif.


Abstract
Two new species of Stigmatodactylus from Palawan Island in the Philippines are described and illustrated. The taxa, which represent the first records for the genus Stigmatodactylus in the Philippines, are restricted to the ultramafic peaks of central Palawan. Cryptostylis carinata, originally described from New Guinea, is also documented, representing a first record for this species in Palawan.

Keywords: Acianthinae, Diurideae, Malesia, Orchidoideae, Philippine flora



Stigmatodactylus dalagangpalawanicum A.S.Rob., 2016
FIGURE 2.Stigmatodactylus dalagangpalawanicum growing in situ in the Mount Victoria massif.

Stigmatodactylus dalagangpalawanicum A.S.Rob., 2016

Conservation status: This species is known from three small populations across a 2 km transect in closed canopy upper montane forest. The total population across all three sites comprises ca. 18 mature individuals. Direct observations satisfy the IUCN Red List Criteria B2ac(iv);D (IUCN, 2001) as CR (Critically Endangered). The occurrence of this taxon in the surrounding forest above 1400 metres can be inferred, potentially satisfying the criteria for an EN assessment, but the ephemeral nature of Stigmatodactylus populations and their apparent sensitivity to environmental disturbance nonetheless puts them at high risk.

Distribution and Ecology: Growing terrestrially in humus layer overlying ultramafic rock in upper montane, closed canopy forest below summit scrub zone. The known populations of Stigmatodactylus dalagangpalawanicum comprise fewer than 20 documented individuals growing within a narrow elevational range of 1400–1700 m. Plants grow singly or in sparsely scattered groups beneath stunted summit trees, 2.0–3.5 m tall. June temperatures achieve 25 ºC in the shade during the day, 12–14 ºC at night, with frequent clouds and periodic rains (pers. obs.). Associated genera
include Leptospermum (Myrtaceae), Vaccinium (Ericaceae), Rhododendron (Ericaceae) and Quercus (Fagaceae).

Phenology: Inflorescences bearing flowers observed in June, July, October, November and December, suggesting a tendency to flower following the rainy spring months into the start of the dry season, which is most pronounced from January through to April. Exploratory root excavation in October showed no apparent tubers, although they have been noted at other times of year, suggesting that these are newly produced at the end of each growing season; the noted absence of tubers in other perennating Stigmatodactylus taxa (Kores 1991, Schlechter 1911) may thus be a function of timing, although this cannot be stated with certainty in the absence of multiple observations.

Etymology: The specific epithet, dalagangpalawanicum, is the Tagalog (Filipino) words dalaga ng Palawan (Maiden of Palawan), a reference to the pretty and diminutive form of the plants and a name now adopted by the local Tagbanua tribe for the plant since our research began. This designation is made in particular honour to the second author, Elizabeth Gironella, in the year following her official retirement after decades of work as curator of the herbarium at Palawan State University

Stigmatodactylus aquamarinus A.S.Rob. & E.Gironella, 2016
FIGURE 4. Stigmatodactylus aquamarinus growing in situ in the Mount Victoria massif.

Stigmatodactylus aquamarinus A.S.Rob. & E.Gironella, 2016

Conservation status: This species is known from three small populations of just 1–2 individuals each. Direct observations satisfy the IUCN Red List Criteria B2ac(iv);D (IUCN, 2001) as CR (Critically Endangered). Despite numerous visits with successful sightings of its sister taxon, Stigmatodactylus dalagangpalawanicum, S. aquamarinus has not yet been observed at the same location more than once.

Distribution and Ecology: Growing terrestrially in moss pads overlying matted tree roots or steeply inclined ultramafic rock, generally occurring singly beneath closed canopy forest of upper montane trees 4–6 m tall or climbing bamboo; or in ultramafic rubble in open summit scrub, sheltered by large boulders. The known populations of Stigmatodactylus aquamarinus occur between 1430–1680 m.

Phenology: Plants and inflorescences bearing flowers observed in October, November and December, during the latter part of the wet season. Vegetative parts have been notably absent at other times of year, and the recurrence of plants at the same site in consecutive years has yet to be documented. This may suggest ephemeral colonisation of suitable sites, but data are too scant to be conclusive.

Etymology: The specific epithet, aquamarinus, is derived from the Latin aqua (water) and marinus (of the sea) = aquamarine, a reference to the unusual bluish to turquoise colour of the petals and sepals.


Alastair S. Robinson, Elizabeth P. Gironella and Jehson M. Cervancia. 2016. New Orchid Species of Stigmatodactylus (Orchidoideae; Diurideae) and A New Record of Cryptostylis carinata from central Palawan, Philippines. Phytotaxa. 252(2): 99–113. DOI:   10.11646/phytotaxa.252.2.2

Buod (Pilipino)
Inilarawan at iginuhit sa artikulong ito ang dalawang bagong species ng Stigmatodactylus mula sa isla ng Palawan sa Pilipinas. Ito ang pinakaunang tala ng genus Stigmatodactylus sa Pilipinas at matatagpuan lamang sa ultramafic na bundok sa gitnang Palawan. Ang ultramafic na bundok ay may mataas na mga sangkap na Magnesium at Iron. Inihayag rin sa sulating ito ang unang tala sa Palawan ng 1 species na Cryptostylis carinata, na unang naitalâ sa bansang New Guinea.

[Herpetology • 2015] Pristimantis macrummendozai • A New Species of the Genus Pristimantis (Anura: Craugastoridae) from the Merchán-Iguaque páramos Region (Boyacá, Colombia)

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Pristimantis macrummendozai 
Acosta-Galvis, 2015 

 ABSTRACT
During an exploratory field trip, made to identify possible study areas in one of the isolated paramos north of the Arcabuco region (Boyacá, Colombia), a species of terrestrial frog assignable to the unistrigatus species group of the genus Pristimantis was discovered. It is similar in morphology to the species group with reduced discs formed by Pristimantis mnionaetesP. nervicus and Pnicefori of the Cordillera Oriental of Colombia. These species allow the recognition of 10 species of this genus associated with high mountain environments in the Eastern Cordillera of Colombia. Data on their morphology, distribution and natural history and associated anurans reported from this geographical area are presented.

Key words. Pristimantis. Paramo. Boyaca. Andean. New species. 


 Andrés Rymel Acosta-Galvis. 2015. Una nueva especie del género Pristimantis (Anura: Craugastoridae) del complejo de páramos Merchán-Iguaque (Boyacá, Colombia) [A New Species of the Genus Pristimantis (Anura: Craugastoridae) from the Merchán-Iguaque páramos Region (Boyacá, Colombia)].  BIOTA. 16(2): 107-127. 


Resumen 
Durante el desarrollo de una salida exploratoria, con el fin de identificar áreas de estudio en una de las unidades de páramos aisladas al norte de la región de Arcabuco (Boyacá, Colombia), se realiza el hallazgo de una nueva especie del género Pristimantis asignable al grupo unistrigatus. Esta especie es similar en su morfología al grupo de especies con discos reducidos, conformado por Pristimantis mnionaetes, P. nervicus y P. nicefori propias de los páramos de la cordillera Oriental de Colombia. Estas especies permiten en conjunto el reconocimiento de diez especies de este género asociadas a los ambientes de alta montaña en la cordillera Oriental de Colombia. Se presentan datos relacionados con su morfología, distribución e historia natural y se reporta la anurofauna asociada a esta área geográfica. 

Palabras clave. Pristimantis. Páramo. Boyacá. Andes. Nueva especie 


  
New species of high-altitude Andean frog discovered in Colombia http://thecitypaperbogota.com/news/new-species-of-high-altitude-andean-frog-discovered-in-colombia/12146 via @thecitypaperbogota
Descubren nueva especie de rana en Colombia http://tinyurl.com/zkw3qph via @elespectador

[Herpetology • 2016] Microhyla laterite • A New Species of Microhyla Tschudi, 1838 (Anura: Microhylidae) from a Laterite Rock Formation in South West India

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Laterite Narrow-mouthed Frog | Microhyla laterite 
Seshadri, Singal, Priti, Ravikanth, Vidisha, Saurabh, Pratik & Gururaja, 2016


Abstract

In recent times, several new species of amphibians have been described from India. Many of these discoveries are from biodiversity hotspots or from within protected areas. We undertook amphibian surveys in human dominated landscapes outside of protected areas in south western region of India between years 2013–2015. We encountered a new species of Microhyla which is described here as Microhyla laterite sp. nov. It was delimited using molecular, morphometric and bioacoustics comparisons. Microhyla laterite sp. nov. appears to be restricted to areas of the West coast of India dominated by laterite rock formations. The laterite rock formations date as far back as the Cretaceous-Tertiary boundary and are considered to be wastelands in-spite of their intriguing geological history. We identify knowledge gaps in our understanding of the genus Microhyla from the Indian subcontinent and suggest ways to bridge them.


Fig 4. Plate depicting a laterite pool habitat of Microhyla laterite sp. nov. and adult male in life (a) laterite pool habitat at type locality. (b) Dorso-lateral view of adult male.

Microhyla laterite sp. nov.
urn:lsid:zoobank.org:act:321B8493-CD5C-4774-B664-6D6A36EAB0B2

Suggested common name: Laterite narrow-mouthed frog

Holotype: BNHS 5964, an adult male collected from laterite rocks in Kodanga, Herga village, Manipal, Udupi District by KSS and RS at 19:30–20:00 h on 26th June 2015.

Paratypes: Two males (BNHS 5965, 5966) and one female (BNHS 5967) were collected in same locality, date and time as holotype by KSS and RS.

Diagnosis: The new species is assigned to the genus Microhyla owing to the following set of characters sensu Parker (25), Dutta and Ray (26) and Matsui, Hamidy [27]: Small sized adults with circular pupil; dorsal skin smooth, with markings from back of eye to vent; supratympanic fold present; paratoid glands absent; fingers without webbing, free with or without dilations; tongue oval, entire and free at the base; snout less than twice the diameter of eye; tympanum hidden by skin; palmar tubercles distinct; distinct oval shaped inner metatarsal tubercle and rounded outer metatarsal tubercle; rudimentary webbing in foot.

Microhyla laterite sp. nov. can be distinguished from all other congeners in the Indian subcontinent by the following suite of characters: (i) A very small sized adult frog (Male: 15.3–16.6 mm, n = 3 and Female: 18.4 mm, n = 1); (ii) snout obtuse in dorsal and ventral view with indistinct canthus rostralis, snout protrudes beyond mouth in ventral view (iii) tongue obovate, margin irregular, without lingual papilla (iv) tympanum hidden; (v) head wider than long; (vi) skin smooth on dorsum and venter; (vii) short, dark horizontal band on dorsum on the same plane as forelimbs. (viii) Throat with dense purplish-black pigmentation, reducing in intensity towards belly; (ix) reduced webbing in feet; (x) discs with circum-marginal groves on fingers and toes.


An adult male Microhyla laterite.
Photo: R. Singal 

An adult female Microhyla laterite.
Photo: K. S. Seshadri 

Variations: Sexes dimorphic, female larger than male (SVL: male, 15.3–16.6 mm, female: 18.4 mm); Sub-gular skin fold absent and when gravid, un-pigmented eggs visible near flanks, belly and groin.

Etymology: This species is named after the laterite rock formations in the type locality and other parts of its geographic range (Fig 4A). The specific name is an invariable noun in the nominative singular in apposition to generic name.


Ecology and Natural History Observations
Microhyla laterite sp. nov. was observed in and around the type locality during the south west monsoon seasons between April–August from 2013–2015. The species was found to be restricted to laterite habitats near rural and peri-urban areas. This species inhabits ephemeral ponds and other marshy areas in laterite habitats. They also occur in wet paddy fields where they were observed to vocalize from the embankment. Vocalization begins about 18:00 h and peaks between 19:15–21:30 h. The vocalization is very similar to that of ground crickets. Males can be located on leaf litter and other debris in dense grass clusters and often change their position while vocalizing. Upon disturbance, a few males were observed to stop calling and retreat backwards into small cavities in laterite rock formations where they lay low and hide for a few minutes.

The tadpoles of M. laterite sp. nov. are small, blackish overall and seen in shoals of over 100 individuals. We have observed Euphlyctis mudigere Joshy, Alam, Kurabayashi, Sumida, and Kuramoto, 2009, to feed on these tadpoles. Other species observed in the type locality are M. ornata; Fejervarya sahyadris (Dubois, Ohler, and Biju, 2001); F. caperata Kuramoto, Joshy, Kurabayashi, and Sumida, 2008; Hoplobatrachus tigerinus (Daudin, 1802); Polypedates maculatus (Gray, 1830) and Euphlyctis cyanophlyctis (Schneider, 1799).

Geographic Range and IUCN Status: 
Microhyla laterite sp. nov. was found from very few locations in and around Manipal, Udupi District (between 13.2868°–13.3757° N and 74.7795°–74.8731° E, 50 m amsl) and Konaje, Mangaluru District (12.8183° N, 74.9319° E, 80m amsl) M.lateritii, Karnataka State (Fig 1). The geographic extent of occurrence was 146.13 km2. As per IUCN Red List criteria [24], this species qualifies to be listed as endangered (EN) under B1ab(iii),(iv).


K. S. Seshadri, Ramit Singal, H. Priti, G. Ravikanth, M. K. Vidisha, S. Saurabh, M. Pratik and Kotambylu Vasudeva Gururaja. 2016. Microhyla laterite sp. nov., A New Species of MicrohylaTschudi, 1838 (Amphibia: Anura: Microhylidae) from a Laterite Rock Formation in South West India. PLoS ONE.  DOI:  10.1371/journal.pone.0149727

Singapore, India researchers discover new frog species in India’s wastelands http://bit.ly/1TOjghS



[Paleontology • 2016] Extinction of Fish-shaped Marine Reptiles associated with reduced Evolutionary Rates and Global Environmental Volatility

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Two ichthyosaurs Pervushovisaurus bannovkensi wander through a middle Cenomanian low latitude ecosystem that will prevail for most of the Late Cretaceous: high sea level and sea temperatures, rudist reefs (Ichthyosarcolites, Hippurites), newly radiating neoselacian sharks and acanthomorph fishes Aipichthyoides.
Artwork by Andrey Atuchin 

Despite their profound adaptations to the aquatic realm and their apparent success throughout the Triassic and the Jurassic, ichthyosaurs became extinct roughly 30 million years before the end-Cretaceous mass extinction. Current hypotheses for this early demise involve relatively minor biotic events, but are at odds with recent understanding of the ichthyosaur fossil record. Here, we show that ichthyosaurs maintained high but diminishing richness and disparity throughout the Early Cretaceous. The last ichthyosaurs are characterized by reduced rates of origination and phenotypic evolution and their elevated extinction rates correlate with increased environmental volatility. In addition, we find that ichthyosaurs suffered from a profound Early Cenomanian extinction that reduced their ecological diversity, likely contributing to their final extinction at the end of the Cenomanian. Our results support a growing body of evidence revealing that global environmental change resulted in a major, temporally staggered turnover event that profoundly reorganized marine ecosystems during the Cenomanian.





Figure 1: Phylogeny and ecological diversity of parvipelvian ichthyosaurs.
(a) Time scaled strict consensus tree arising from equal weight maximum parsimony analysis. Numbers denote >1 Bremer decay indices. Grey bars denote range extensions by specimens identified at the generic level. Colour coding of taxa refers to the results of b. (b) Cluster dendrogram based on the ecological data set, with gut-content data and the general features of each guild. (c) Teeth representative of each guild across the Late Albian–Cenomanian interval, illustrating the ecological extinction at the beginning of the Cenomanian. ‘Platypterygius campylodon’ and ‘Platypterygius’ sp. from the US are early Cenomanian in age, Pervushovisaurus bannovkensis is Middle Cenomanian in age and ‘Platypterygius’ sp. from Germany is Late Cenomanian in age. *denotes taxa from the Stoilensky/Kursk fauna. Scale bar, 50 mm.


Valentin Fischer, Nathalie Bardet, Roger B. J. Benson, Maxim S. Arkhangelsky and Matt Friedman. 2016. Extinction of Fish-shaped Marine Reptiles associated with reduced Evolutionary Rates and Global Environmental Volatility. Nature Communications. 7, Article number: 10825 DOI: 10.1038/ncomms10825

Slower evolution and climate change drove ichthyosaurs to extinction http://phy.so/376640171 via @physorg_com


[Herpetology • 2014] Brachytarsophrys popei • A New Species of the Genus Brachytarsophrys Tian and Hu, 1983 (Anura: Megophryidae) from Southern China Based on Molecular and Morphological Data

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 Brachytarsophrys popei
Zhao, Yang, Chen, Chen & Wang. 2014 

ABSTRACT

A new species, Brachytarsophrys popei sp. nov., is described based on a series of specimens collected from Mount Jinggang, Jiangxi Province, Taoyuandong Nature Reserve, Hunan Province and Nanling Nature Reserve, Guangdong Province, China. The new species can be easily distinguished from other known congeners by morphology, morphometrics and molecular data of the mitochondrial 16S rRNA gene. It is characterized by its relatively small size with 86.2 mm in snout-vent length in adult female and 70.7 mm–83.5 mm in males; vomerine teeth bearing on two markedly elevated ridges, which projecting behind far beyond the posterior level of the choanae, widely separated by a distance nearly 1.5 times length of one; margin of tongue deeply notched behind; toes about one-third to two-thirds webbed in males, at most one-third webbed in female; the webs extending as a wide fringes along either side of toes; upper eyelid with tubercles, one of which is enlarged and becoming a remarkably prominent, bluntly conical light- yellow horn; black tiny nuptial spines on the dorsal surface of the first finger and second finger base, single vocal sac in males; gravid females bear pure yellowish oocytes; tadpoles with a transverse white stripe on ventral surface and two longitudinal white stripes along the sides of body. The new species represents the fifth known Brachytarsophrys species.

  Figure 3 General aspect of Brachytarsophrys popei sp. nov.
A: Dorsolateral view of the adult male holotype SYS a001867 in life. B: Dorsolateral view of the adult female paratype SYS a001875 in life. C: Ventral view of the holotype SYS a001867 in life. D: Ventral view of the paratype SYS a001875 in life.

Etymology: The  specific  name  “popei”  is  in  honour  of  the noted American herpetologist Clifford H. Pope (1899–1974), in recognition of his efforts on biodiversity surveys and  research  of  amphibians  and  reptiles  in  Southeast  China.  We  propose  the  standard  name  “Pope’s  Short-legged Toad”, chinese name “Po Shi Duan Tui Chan”.

Distribution: Currently, B.  popei sp.  nov.  is  distributed  in the middle section of Luoxiao Mountains and Nanling Mountains  in  southern  China,  including  three  type  localities:  the  Mount  Jinggang,  Jiangxi  Province,  the  adjacent  Taoyuangdong  NR,  Hunan  Province,  and  the  Nanling  NR,  Guangdong  Province,  China.  In  addition,  the  Yizhang  County,  Hunan  Province  bordered  with  the  Nanling Nature Reserve, thus, population as B. carinense from Yizhang County of Hunan should be the B. popei sp. nov.


Jian Zhao, Jian-Huan Yang, Guo-Ling Chen, Chun-Quan Chen and Ying-Yong Wang. 2014. Description of A New Species of the Genus Brachytarsophrys Tian and Hu, 1983 (Amphibia: Anura: Megophryidae) from Southern China Based on Molecular and Morphological Data. ASIAN HERPETOLOGICAL RESEARCH. 5(3):150-156  DOI:  10.3724/SP.J.1245.2014.00150

[Herpetology • 2016] Abronia cuetzpali • A New Species of Abronia (Squamata: Anguidae) from the Sierra Madre del Sur of Oaxaca, Mexico

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Abronia cuetzpali  
Campbell, Solano-Zavaleta, Flores-Villela, Caviedes-Solis & Frost. 2016  DOI:  10.1670/14-162


Abstract
A newly discovered species of arboreal alligator lizard of the genus Abronia is described from the Sierra Madre del Sur of Oaxaca, Mexico. It appears to be most closely related to A. mixteca and A. oaxacae, but differs from these species (and others in the subgenus Abronia) in a number of features, including the combination of having two primary temporals contacting the postocular series, the anterior superciliary contacting the cantholoreal, six to eight nuchals in a transverse row across the nape, minimally seven to eight scales between large nuchals and ventral scales on neck, and 32–35 transverse rows of dorsal scales. This new species is the only species of Abronia known from the central and western portions of the Sierra de Miahuatlán in the southern part of the Sierra Madre del Sur, although A. oaxacae occurs to the east in this range. Many of the arboreal and secretive species of Abronia have avoided discovery until relatively recently, with about a third of known species described in the last 3 decades.



Abronia cuetzpali sp. nov. 
Sierra de Miahuatlán Abronia — Dragoncito de Sierra de Miahuatlán

Etymology. — The specific name is a noun in apposition taken from the Nahuatl word for lizard,  “cuetzpali,” although there are various alternative spellings.

Habitat and Distribution. — On the basis of the three known specimens of A. cuetzpali, its distribution extends in the Sierra Madre del Sur of Oaxaca from near Santa Catarina Juquila to San Miguel Suchixtepec, a distance of about 70 km. The known elevational distribution is from 1,711 to 2,150 m. Suitable elevations above 1,500 m and temperate forest are continuous between these localities. There is no reason to believe that A. cuetzpali does not range farther to the west and east, where suitable habitat also exists. The area inhabited by A. cuetzpali is covered by pine–oak forest (sensu Leopold, 1959) that may have a prominent hardwood component including oaks and a heavy broadleaf understory in some places (Fig. 7).




Jonathan A. Campbell, Israel Solano-Zavaleta, Oscar Flores-Villela, Itzue W. Caviedes-Solis and Darrel R. Frost. 2016. A New Species of Abronia (Squamata: Anguidae) from the Sierra Madre del Sur of Oaxaca, Mexico.  Journal of Herpetology.   50(1): 149-156.  DOI:  10.1670/14-162

Resumen
Se describe una nueva especie de lagartija lagarto arbórea del género Abronia de la Sierra Madre del Sur de Oaxaca, México. Parece estar más relacionada a A. mixteca y A. oaxacae, pero difiere de estas especies y de otras del subgénero Abronia en varios caracteres, incluyendo la combinación de tener dos temporales primarias contactando la serie postocular, la superciliar anterior en contacto con la cantoloreal, 6–8 nucales en hilera transversal sobre la nuca, un mínimo de 7–8 escamas entre las nucales grandes y las escamas ventrales del cuello, y 32–35 hileras transversales de escamas dorsales. Esta nueva especie es la única del género Abronia conocida de las porciones central y occidental de la Sierra de Miahuatlán en la región sur de la Sierra Madre del Sur, aunque A. oaxacae ocurre al oriente de esta serranía. Muchas de las especies de Abronia con hábitos secretos y arbóreos han evadido ser descubiertas hasta hace poco, aproximadamente una tercera parte de las especies han sido descritas en las últimas tres décadas.

[Botany • 2016] Lilium procumbens and its Allies in the Flora of Vietnam

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Lilium procumbens  Aver. & N.Tanaka, 2016

ABSTRACT
 Lilium procumbens – a new species discovered at a limestone ridge in northern Vietnam is unique in having a slender procumbent stem. This paper presents a detailed taxonomic account of the species including a description, illustrations, information on the type, ecology, phenology and distribution, affinity with other congeners, and expected conservation status. A key to all the known Lilium species from Vietnam and an annotated list of them are also provided.

KEY WORDS: Lilium, nature protection, new species, plant diversity, plant taxonomy, Vietnam.


Lilium procumbens Aver. & N.Tanaka, sp. nov.

Etymology: The specific epithet refers to the procumbent habit of the plant.

Distribution: Endemic to VIETNAM, Cao Bang province (Nguyen Binh district, Ca Thanh municipality).


 Lilium species from Vietnam
The name of cultivated species is marked with an asterisk* 

1.Lilium procumbens Aver. & N.Tanaka, sp. nov. 
2. Lilium eupetes J.M.H. Shaw, 2008, Plantsman n.s., 7: 39.
3.Lilium poilanei Gagnep., 1934, Fl. Indo-Chine 6: 810, fig. 80, 1 
4. Lilium brownii F.E. Brown ex Miellez, 1841, Cat. Expos. Soc. Hort. Lille

5. Lilium concolor Salisb.*, 1806, Parad. Lond. t. 47
6.Lilium longiflorum Thunb.*, 1794, Trans. Linn. Soc. London 2: 333
7.Lilium lancifolium Thunb.*, 1794, Trans. Linn. Soc. London 2: 333


 Leonid V. Averyanov, Noriyuki Tanaka and Khang Sinh Nguyen. 2016. New Species - Lilium procumbens and its Allies in the Flora of Vietnam.
 Taiwania.61(1): 1‒7. DOI:  10.6165/tai.2016.61.1

[Ichthyology • 2016] Amaralia oviraptor • A New Species of Amaralia Fowler (Siluriformes: Aspredinidae) from the Paraná-Paraguay River Basin

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Amaralia oviraptor
 Friel& Carvalho, 2016

Abstract

A new species of the banjo catfish genus Amaralia is described from the Paraná-Paraguay River Basin in central-western Brazil, Paraguay and northern Argentina. Amaralia oviraptor is distinguished from its single and allopatric congener, Amaralia hypsiura, by the greater number of dorsal-fin rays (3 vs. 2); by the absence of lateral contact between middle and posterior nuchal plates (vs. middle and posterior nuchal plates contacting each other laterally); and by a longer cleithral process (17.4–19.5 % of SL, mean 18.2 % vs. 14.0–17.2 % of SL, mean=15.5 %). Comments on the peculiar oophagic diet of Amaralia and an extended diagnosis of the genus are provided.

Keywords: Pisces, Neotropical, biodiversity, banjo catfish, osteology, oophagy


FIGURE 1. Amaralia oviraptor, MZUSP 4423, holotype, 68 mm SL
Brazil, Mato Grosso, Santo Antônio do Leverger municipality, rio Cuiabá.


Distribution. Amaralia oviraptor is widely distributed in the Paraná-Paraguay River system, found throughout the Paraguay River Basin in Brazil, Paraguay and northern Argentina and also in the Paraná drainage in Argentina and Brazil (Fig. 8). The new species seems to be absent in some portions of this system such as the Uruguay River Basin and the main tributaries of the upper Paraná.
Etymology. The epithet oviraptor is a combination of the Latin ovum (ovi), meaning egg; and raptor, a robber or plunderer, commonly used term for a predator, here referring to the peculiar dietary preferences observed in this species. Treated as a noun in apposition.
Ecological notes. An interesting aspect of Amaralia is its apparent dietary specialization on both the eggs and developing embryos of other catfishes (Friel, 1994; Roberts, 2015). Direct evidence of such oophagy is based on examination of the stomach contents from 23 preserved Amaralia specimens (17 A. hypsiura and six A. oviraptor ). Seven of these specimens (six female and one male) contained masses of ova or developing embryos in their stomach. The source of the eggs and embryos is most likely those of loricariid catfishes, and in least in one instance, the caudal fin-ray counts of the embryos fall within the range for loricariid catfishes. One male contained a single scoloplacid catfish specimen in its stomach, and the remaining 15 specimens (seven female and eight male) had empty stomachs. These observations differ significantly from the documented diets of other aspredinids, where stomach contents typically contained some organic detritus along with various aquatic and terrestrial insect prey.





John P. Friel and Tiago P. Carvalho. 2016. A New Species of Amaralia Fowler (Siluriformes: Aspredinidae) from the Paraná-Paraguay River Basin. Zootaxa. 4088(4) 

Resumo: 
Uma nova espécie de Amaralia é descrita da bacia do Paraná-Paraguai no Centro-Oeste do Brasil, Paraguai e Norte da Argentina. Amaralia oviraptor difere-se do seu único congênere de distribuição alopátrica, Amaralia hypsiura, pelo maior número de raios da nadadeira dorsal (3 vs. 2); pela ausência de um contato lateral entre a placa nucal mediana e a placa nucal posterior (vs. placa mediana e posterior contatando uma a outra lateralmente); e por um processo cleitral mais longo (17.4–19.5 % do CP, média = 18.2 % vs. 14.0–17.2 % do CP, média = 15.5 %). Comentários sobre o gênero são feitos acerca de sua dieta oofágica e uma diagnose entre os aspredinídeos é fornecida. 
Palavras-chave: Neotropical, biodiversidade, bagre banjo, osteologia, oofagia.

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