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[Botany • 2018] Polygala veadeiroensis (Polygalaceae) • A New Species of Polygala endemic to Chapada dos Veadeiros, Goiás, Brazil

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Polygala veadeiroensis  J. F. B. Pastore

in Pastore, 2018. 

Summary
 A new species, Polygala veadeiroensis (Polygalaceae) subgenus Polygala section Timutua DC. series Timoutoideae, is described from Chapada dos Veadeiros, Goiás State, Brazil. The infrageneric placement and its conservation status are assessed and its habitat and phenology are included. The new species is compared with its morphologically allied species, P. carphoides and P. cuspidata. Illustrations, photos of floral parts under magnification, and a distribution map are also provided.

Key Words: endemic species, subgenus Polygala, taxonomy 

Fig. 1. Polygala veadeiroensis. A habit; B raceme; C bract; D bracteole; E two upper outer sepals; F lower outer sepal; G androecium and lateral petals; H gynoecium; J fruit with persistent calyx; K, L seed.
From Pastore & Suganuma 417 (the type). 
Drawn by Carla Texeira de Lima.

Polygala veadeiroensis J. F. B. Pastore sp. nov. 
Type: Brazil, Goiás, Chapada dos Veadeiros, Cavalcante, estrada [Rodovia GO-118], entre Cavalcante e Santa Teresina de Goiás, 14°03'27"S 47º30'16"W, 6 March 2003, Pastore & Suganuma 417 (holotype CTBS!; isotype CEN!).

recognition:The crested keel places Polygala veadeiroensis within Polygala subgenus Polygala, in addition the spiciform raceme, yellowish spots on floral parts, sepals with acuminate apex, winged stems, and verticillate leaves at proximal nodes are all associated with species belonging to Polygala section Timutua series Timoutoideae Chodat. Polygala veadeiroensis is morphologically most similar to P. carphoides Chodat, from which it is readily separable by its leaves 2.5 – 4 × 1.1 – 1.9 cm, racemes 2 – 3 × 0.8 cm, and linear bracts 2.3 – 2.5 mm long (vs leaves 0.4 – 0.9 × 0.1 – 0.3 cm, racemes 0.5 – 1.5 × 0.35 – 0.5 cm, and lanceolate bracts 0.7 – 1.5 mm long in P. carphoides). On the other hand P. veadeiroensis can be easily recognised by the short bracts when compared with P. cuspidata (2.3 – 2.5 cm vs 4.8 – 9 cm in P. cuspidata).

Fig. 2. Polygala veadeiroensis. A bract; B bracteoles; C flower; D two upper outer sepals; E lower outer sepal; F one of the two inner sepals (wings); G keel; H androecium and lateral petals; J gynoecium; K style; L fruit with persistent calyx; M capsule; N seed; P appendage.
All from Pastore & Suganuma 417. photos: J. Floriano B. Pastore.

Fig. 3 Polygala veadeiroensis and its habitat.
A and D habit; B raceme; C flower in a young raceme; E habitat.
All from Pastore & Mota 5308 (CTBS). photos: J. Floriano B. Pastore.

Distribution: Most of the analysed specimens of Polygala veadeiroensis (except Pastore & Suganuma 648 and Cardoso et al. 2531) are likely to be derived from the same stretch of c. 20 km along the GO-118 road between Alto Paraíso de Goiás and Teresina de Goiás, on the borders of the Chapada dos Veadeiros National Park (CVNP). However, other populations are likely to occur inside the CVNP (Map 1).

Habitat: Polygala veadeiroensis occurs in rocky field areas, called campo limpo rupestre, in sandy soil; altitudes between c. 1,200 – 1,500 m. Fig. 3E.

Conservation status: Although Polygala veadeiroensis is likely to have a wider occurrence inside the area of CVNP (beyond the area estimated here), using the available data to determine the conservation status suggests the criterion VU (2B: a, b3) of IUCN (2012). The known area of occupancy is estimated to be less than 2,000 km2 (c. 228 km2) and because the only known habitat is quite near the interstate roads GO-118 and GO-239, a continued decline of habitat quality and quantity is anticipated.

Etymology: Polygala veadeiroensis refers to the Chapada Veadeirosregion in the northeast of the Goiás State in Brazil.


J. F. B. Pastore. 2018. Polygala veadeiroensis (Polygalaceae), A New Species of Polygala endemic to Chapada dos Veadeiros, Goiás, Brazil. Kew Bulletin. 73:37.  DOI: 10.1007/s12225-018-9759-0



[Herpetology • 2018] Leptophryne javanica • Detection of Cryptic Taxa in the Genus Leptophryne (Fitzinger, 1843) (Amphibia; Bufonidae) and The Description of A New Species from Java, Indonesia

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 Leptophryne javanica 
Hamidy, Munir, Mumpuni, Rahmania & Kholik, 2018

Kodok Merah Ciremai || facebook.com/BTNCiremai

Abstract
We investigated phylogenetic relationships among populations of two species within the genus Leptophryne, L. cruentata and L. borbonica, using the mitochondrial 16S rRNA gene. As a result, we identified two distinct lineages within populations currently considered Leptophryne cruentata: 1) a lineage containing L. cruentata from the type locality, and 2) a lineage from Mt. Slamet and Mt. Ciremai. On the basis of genetic and morphological differences, we describe the Mt. Slamet and Mt. Ciremai populations as a new speciesLeptophryne javanica sp. nov. The new species is distinguished from L. cruentata and L. borbonica by the following combination of morphological characters: the presence of distinct yellow mottling on the dorsum; relatively small body size (SVL male 22.2–24.0 mm, female 29.6 mm); relatively short hindlimbs (HLL 37.0–40.9 mm); relatively short fourth toe (4ToeL 4.3–6.0 mm); basal webbing on the hands, but well developed on toes; very protruding snout and an indistinct tympanum. In our preliminary phylogenetic analysis, we also detected four distinct lineages within Leptophryne borbonica: 1) a lineage containing true L. borbonica from west Java, 2) a lineage from Lampung (Sumatra I), 3) a lineage from northern Borneo, and 4) a lineage from Bengkulu (Sumatra II). Further studies are needed to determine taxonomic status of these lineages.

Keywords: Amphibia, Leptophryne javanica, new species, Sundaland, taxonomy


Leptophryne javanica sp. nov.: female paratype (MZB 28564)
photographs by Farist Alhadi.

Leptophryne javanica new species
 Leptophryne cruentata (Tschudi, 1838): Mumpuni 2014

Etymology. The specific epithet is in reference to Java, the island where the type series was collected.

Range. Leptophryne javanica sp. nov. is currently known only from the northwestern slope of Mt. Slamet and Mt. Ciremai (Fig. 1). Since L. cruentata is endemic to mountains in the west of Java, Leptophryne javanica sp. nov. is likely endemic to mountains in the central part of the island ....



  



Leptophryne cruentata from Cibereum waterfall, Mt. Gede.: male (MZB Amph 22257)
 photographs by Farist Alhadi


 Amir Hamidy, Misbahul Munir, Mumpuni Mumpuni, Mila Rahmania and Azis Abdul Kholik. 2018. Detection of Cryptic Taxa in the Genus Leptophryne (Fitzinger, 1843) (Amphibia; Bufonidae) and The Description of A New Species from Java, Indonesia. Zootaxa. 4450(4); 427–444. DOI:  10.11646/zootaxa.4450.4.2


 Spesies Baru “Kodok Merah Ciremai” 
#kodokMerahCiremai #LeptophryneJavanica #ayoketamannasional #gunungciremai #wonderfulindonesia #pesonaindonesia

     

[Ichthyology • 2018] Rhinogobius immaculatus • A New Species of Freshwater Goby (Teleostei: Gobiidae) from the Qiantang River, China

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Rhinogobius immaculatus
Li, Li & Chen, 2018


Abstract
A new freshwater goby, Rhinogobius immaculatus sp. nov., is described here from the Qiantang River in China. It is distinguished from all congeners by the following combination of characters: second dorsal-fin rays I, 7–9; anal-fin rays I, 6–8; pectoral-fin rays 14–15; longitudinal scales 29–31; transverse scales 7–9; predorsal scales 2–5; vertebrae 27 (rarely 28); preopercular canal absent or with two pores; a red oblique stripe below eye in males; branchiostegal membrane mostly reddish-orange, with 3–6 irregular discrete or connected red blotches on posterior branchiostegal membrane and lower operculum in males; caudal-fin base with a median black spot; and no black blotch on anterior part of first dorsal fin in males.

Keywords: Gobiidae, Rhinogobius, New species, Qiantang River, China

 Figure 5: Coloration of head and first dorsal fin of male  Rhinogobius immaculatus sp. nov. Specimen collected from Xiuning County, Anhui Province, China. Specimen not preserved.


Figure 4 Male (A) and female (B) Rhinogobius immaculatus sp. nov. 
Specimens collected from Xiuning County, Anhui Province, China. Specimens not preserved.  

Rhinogobius immaculatus sp. nov.

Diagnosis: Most similar to Rhinogobius wuyanlingensis in number of vertebrae (27) and preopercular canal pores (2 or 0 vs. 2), but differing by fewer pectoral-fin rays (14–15 vs. 17–18), fewer anal-fin rays (I, 6–7 vs. I, 8), fewer transverse scales (7–9, modally 8 vs. 9–10), absence of a black blotch on anterior part of first dorsal fin in males (vs. present), and branchiostegal membrane mostly reddish-orange, with irregular blotches posteriorly in males (vs. with red stripes).
....

Distribution and ecology: Known only from streams of the Qiantang River basin in Zhejiang and Anhui Provinces, China (Figure 6). Most often found in shallow (10–50 cm deep) low-gradient streams, with sand and gravel mixed substrate.
Adult Rhinogobiusimmaculatus sp. nov. are small in size. The smallest female with mature oocytes was 22.4 mm SL. The largest specimen collected in the field was 26.3 mm SL. The largest captive specimen kept in an aquarium for 29 months was 32.8 mm SL.

Etymology: The specific name, immaculatus, is derived from Latin in (without) and maculatus (spotted), an adjective, alluding to the absence of a black blotch on the anterior part of the dorsal fin in adult males.


Fan Li, Shan Li and Jia-Kuan Chen. 2018. Rhinogobius immaculatus, A New Species of Freshwater Goby (Teleostei: Gobiidae) from the Qiantang River, China. Zoological Research. 39(6); 396-405. DOI: 10.24272/j.issn.2095-8137.2018.065


[Entomology • 2018] A New Status for Aclogryllus Gorochov, 2009 (Phalangopsidae; Phalangopsinae) with A New Species, Aclogryllus manauensis, from Brazilian Amazon

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Aclogryllus manauensis da Silva & Martins

in da Silva, Martins, Pereira & Henriques, 2018

Abstract 
In this work, we propose to raise the subgenus Aclogryllus to generic status based on characteristics of external morphology and male genitalia. A new Amazonian species of Aclogryllus is also described. Photographs of nomenotypic species and the new Amazonian species are provided along with the description of morphological characteristics, diagnosis and photographs of male genitalia and female copulatory papilla. 


Key words: Crickets, Paragryllus, Paragryllina, Reserva Ducke, Amazon Forest, Brazil


Order Orthoptera Oliver, 1789
Suborder Ensifera Chopard, 1921

Superfamily Grylloidea Laicharding, 1781
Family Gryllidae Laicharting, 1781
Subfamily Phalangopsinae Blanchard, 1845

Tribe Paragryllini Desutter, 1987
Subtribe Paragryllina Desutter, 1987

Aclogryllus Gorochov, 2009 n. stat.
Type species: Aclogryllus crybelos (Nischk & Otte, 2000) n. comb.

Aclogryllus crybelos (Nischk & Otte, 2000) n. comb.


FIGURE 3. Aclogryllus manauensis n. sp., male habitus, dorsal view.

Aclogryllus manauensisda Silva & Martins n. sp. 
Etymology. The specific name refers to type locality, the municipality of Manaus.


 Lúciene Gimaque da Silva, Luciano De Pinho Martins, Marcelo Ribeiro Pereira and Augusto Loureiro Henriques. 2018. A New Status for Aclogryllus Gorochov, 2009 (Phalangopsidae; Phalangopsinae; Paragryllini) with A New Species from Brazilian Amazon. Zootaxa. 4433(1); 101–110.  DOI:  10.11646/zootaxa.4433.1.5

Resumo:Neste trabalho é proposto elevar o subgênero Aclogryllus para o status de gênero baseado em características da morfologia externa e genitália do macho. Também foi descrita uma nova espécie amazônica para Aclogryllus. Fotografias da espécie nominotípica e da nova espécie são apresentadas juntamente com a descrição das características morfológicas, diagnoses e fotografias da genitália masculina e da papila copulatória da fêmea. 
Palavras-chave: Grilos, Paragryllus, Paragryllina, Reserva Ducke, Floresta Amazônica, Brasil 

[Botany • 2018] Lysionotus bijantiae (Gesneriaceae) • A New Species of Lysionotus from Northeastern India

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Lysionotus bijantiae D. Borah & A. Joe

in Borah & Joe, 2018. 

Abstract
Lysionotus bijantiae, a new species of Lysionotus is described from Potin, Lower Subansiri District, Arunachal Pradesh, northeastern India. Detailed description, distribution along with color photographs are provided. A comparison chart of related species and a key to the taxa found in northeastern India are also provided.

Keyword: Arunachal Pradesh, Gesneriaceae, India, Lysionotus bijantiae, New species


Fig. 1. Lysionotus bijantiae:
A: Habitat. B: Habit. C: Flowering stem. D: Flowers. E: Bract. F: Calyx. G: Cut corolla inner surface with stamens and staminodes. H: Cut corolla outer surface. I: Stamens and staminodes. J: Stigma, style and a portion of ovary. K: Immature infructescence with persistent calyx.

Lysionotus bijantiae D. Borah & A. Joe, sp. nov. 

Lysionotus bijantiae is morphologically similar to L. gamosepalus but can be easily distinguished by a combination of characters such as erect sub-shrub (vs decumbent sub-shrub), stems pubescent (vs glabrous), leaves pubescent (vs glabrous), peduncles and petioles pubescent (vs glabrous), bracts lanceolate, villous (vs broadly ovate to orbicular, green, glabrous), calyx hairy, (vs glabrous), corolla cream (vs purplish), filaments curved (vs coiled), without connective appendage (vs horn-like connective appendage), pistil cream, pubescent (vs green, glabrous).

Etymology: The species is named after Bijanti Borah, mother of first author for her constant support. 

Distribution and ecology: Lysionotus bijantiae is known only from the type locality. The plant was found growing in wet shady areas. According to the IUCN red list categories and criteria (IUCN, 2012), L. bijantiaeshould be assessed as Critically Endangered (CR) based on the present situation: restricted geographic range of less than 2 km2 with only one single location (CR:B2a) and an estimated number of mature individuals of about 100.


Dipankar Borah and Alfred Joe. 2018. A New Species of Lysionotus (Gesneriaceae) from Northeastern India.  Taiwania. 63(3); 232-234. DOI: 10.6165/tai.2018.63.232 

 

[Botany • 2018] A Revision of Centaurea sect. Cynaroides (Asteraceae, Cardueae)

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 Centaurea iranshahrii Wagenitz & Esfandiari 

in Negaresh & Rahiminejad, 2018

Abstract
The taxonomic status of the taxa known to belong to Centaurea sect. Cynaroides and its close relatives was revised on the basis of herbarium specimens from the authors’ expeditions and other collections. It is established that Boissier is the correct author for C. sect. Cynaroides, and C. regia is designated as a lectotype of this section. Thirty seven species are recognised in the section. Three new species (Centaurea kamalnejadii, C. mozaffarianii, and C. zarrei), four new subspecies (C. amadanensis subsp. ranjbarii, C. cataonica subsp. syriaca, C. gigantea subsp. rechingeri, and C. kurdica subsp. ciliata) and two varieties (C. regia var. longispinosa and C. regia var. purpurea) are described. Two subspecies are reduced to the variety rank, and two varieties are elevated to the subspecies rank. Centaurea sect. Paraphysis is reduced as a synonym of C. sect. Cynaroides. Centaurea onopordifolia is transferred from C. sect. Cynaroides to a new section, i.e. C. sect. Cardueae. Three lectotypes are designated, six lectotypes from previous lectotypifications are rejected and the author names for six species are corrected. The recognized taxa, the relevant synonyms, type details, examined specimen lists, full descriptions and a taxonomic key are provided for this section. Distribution maps are provided for each sections, species, subspecies and varieties. Images of the type specimens of all taxa and also photos of the species in its natural habitat and related fields are provided. Five chromosome counts (2n = 18) are reported for C. amadanensis subsp. amadanensis, C. amadanensis subsp. gymnoclada, C. nemecii, C. regia var. regia, and C. regia var. purpurea. Biogeographical distribution and ecology of taxa of C. sect. Cynaroides are presented and discussed. In addition, cytotaxonomy, homoploidy and evolution of C. sect. Cynaroides are illustrated and discussed. Finally, the pollination of C. sect. Cynaroides is illustrated, and also images of the pollinators of some species of the section are provided.

Keywords: Eudicots, chromosome numbers, Compositae, identification key, lectotypifications, new combinations, new section, nomenclature, taxonomy

 Centaurea iranshahrii Wagenitz & Esfandiari (Negaresh & Asadbegy 19809, HUI, from typus, locus classicus); close up of involucres


Kazem Negaresh and Mohammad Reza Rahiminejad. 2018. A Revision of Centaurea sect. Cynaroides (Asteraceae, Cardueae—Centaureinae). Phytotaxa.  363(1); 1–131. DOI: 10.11646/phytotaxa.363.1.1


[Herpetology • 2018] First Appearance Deceives Many: Disentangling the Hemidactylus triedrus species complex Using An Integrated Approach; Hemidactylus whitakeri & H. sahgali

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Hemidactylus triedrus Daudin, 1802

Hemidactylus whitakeri 
 Hemidactylus sahgali
Mirza​, Gowande, Patil, Ambekar & Patel, 2018

 Abstract
The gekkonid lizard genus Hemidactylus Oken is the second most species-rich genus of geckos with greatest diversity in the tropical regions of the world. Some species of the genus are commensal and widespread; however, there are several endemic lineages with restricted distribution. India is home to at least 35 species, with 20 endemic species and the number is steadily increasing with exploration of new habitats and integrated taxonomic approach including molecular data. We made investigations into the molecular and morphological variation throughout the distribution of Hemidactylus triedrus Daudin, 1802 based on fresh specimens, literature review, museum material and molecular data. Results from morphological, molecular and micro-CT based anatomical data are unequivocal and show that H. triedrus is a species complex represented by three species, H. triedrus sensu stricto and two undescribed taxa. H. subtriedrus Jerdon, 1854 syn. nov. was found to be morphologically similar to the type specimen of H. triedrus, and genetically embedded in a clade containing H. triedrus sensu strictoand is here treated as a junior synonym of H. triedrus, whereas H. lankae Deraniyagala is referred to as nomen dubium given that the types are presently not traceable and the original description is inadequate in diagnosing the taxon. The populations from western-central India and parts of Pakistan, and from southern Karnataka are distinct and diagnosable, and are herein described as two new species, respectively. Morphological and molecular data support the distinctiveness of the new species. The present work resolves a taxonomic turmoil that lasted over two centuries highlighting the need for studies that integrate morphological and molecular data.

....


Hemidactylus triedrus species group
Species included: H. triedrus, H. sahgali sp. nov., H. whitakeri sp. nov.

Definition: Members of the group grow to a medium size ranging from 45–74 mm in SVL with a rather robust habitus. Dorsum with distinct dark bands may be edged with white or lighter shade of brown. Scales on the dorsal aspect of trunk granular intermixed with large keeled sub-trihedral or trihedral tubercles arranged in 15–20 fairly regular rows. Supralabial eight to nine and infralabials seven to eight to angle of jaw. Lamellae on digit one of manus and pes range from seven to eight and on digit four of manus and pes range from 8–10. Males possess a series of 7–15 precloacal femoral pores interrupted medially by a diastema of one to three non-pored scales. A single or a pair of sub-conical to rounded post cloacal spur. Tail with usually eight keeled tubercles in a whorl on segment I, the number subsequently reduces with progression of tail segments.

Distribution: Widespread across dry zones of India and Sri Lanka and parts of Pakistan.

Figure 4: Coloration in life of Hemidactylus triedrus.
 (A) male NCBS AU703 from Nellore, (B) an uncollected female from Pondicherry, (C) uncollected juvenile from Pondicherry.

Hemidactylus triedrus Daudin, 1802
Gecko triedrus Daudin, 1802:155
Hemidactylus triedrus Lesson, 1834:311; Boulenger, 1885:133 (in part); Smith, 1935:88 (in part)
Hemidactylus subtriedrus Jerdon, 1854:467; Smith, 1935:89 syn. nov.
Hemidactylus triedrus lankae Somaweera & Somaweera, 2009:180
Hemidactylus lankae Bauer et al., 2010:350

Diagnosis: A medium sized fairly stout gecko, adults ranging 58–76 mm in SVL. Dorsum in a shade of light brown with paired, thin black edged white bands at regular intervals. Dorsal scalation on trunk, granular, intermixed with enlarged, keeled 19–20 trihedral tubercle rows arranged in fairly regular longitudinal series. Seven lamellae under digit I of pes and manus, eight to nine under digit four of manus and pes. An angular series of seven to nine precloacal femoral pores separated at mid-pelvic by a diastema of one to three non-pored scales.

Suggested common name: Southern termite hill gecko.

Natural history: A species generally associated with termite mounds. Several individuals of different age classes can be seen occupying a single mound. Individuals can be seen at the entrance of the openings of termite mounds just after dusk and will retreat in the mound with the slightest disturbance. Juveniles when disturbed will attain a posture with their bodies high and the tail is moved slowly in a curling and uncurling manner, likely to draw attention toward the tail. Several individuals were found in a single mound when the termite mound was dug, along with scorpions of the genus Heterometrus sp., and frogs of the genus Uperodon sp. Individuals also seek shelter under boulders, abandoned houses during the day emerging just after dusk. Mostly terrestrial in its habits but will climb trees too. Breeding likely takes places from February to May as hatchlings and eggs have been seen in the months of April–May in Pondicherry and Kanyakumari. Occupies areas that are dry like scrub, dominated with boulders and even in cities closer to the coast. Widely distributed from Visakhapatnam in north to Kanyakumari in south and recorded from elevation ranging from 17 to 1,913 m AMSL. Recorded from the following states/Union territories in India: Kerala, Tamil Nadu, Andhra Pradesh and Pondicherry (Fig. 6).


Figure 7: Coloration in life of Hemidactylus whitakeri sp. nov. (A) Holotype female NCBS AU712, (B) uncollected juvenile from Bangalore.

Hemidactylus whitakeri sp. nov.
Hemidactylus subtriedrus Bauer et al., 2010
Hemidactylus triedrus Bansal & Karanth, 2010

Diagnosis: A medium sized fairly stout gecko, adults ranging 45–60 mm in SVL. Dorsum in a shade of light brown with paired, thin black edged white bands at regular intervals. Dorsal scalation on trunk granular, intermixed with enlarged, keeled 16–17 sub-trihedral tubercle rows arranged in fairly regular longitudinal series on dorsum. Seven lamellae (rarely six) under digit I of pes and manus, eight to nine under digit four of manus and pes. An angular series of seven to eight precloacal femoral pores separated at a mid-pelvic by a diastema of three non-pored scales.

Etymology: The specific epithet is a patronym honoring Romulus Earl Whitaker for his valuable contribution toward the study and conservation of reptiles of India.

Suggested common name: Whitaker’s termite hill gecko.

Natural history: The types were found moving actively at a quarry site around 20:30 h. The holotype female contains two eggs in her body cavity suggesting that this species breeds during the months of November. Several hatchlings of the new species were encountered at Kengiri near Bangalore in the month of April. Similar in its habits to H. triedrus and can be seen on termite mounds. Its distribution is not well known and known from Bangalore in the state of Karnataka and the Nilgiri district in Tamil Nadu (Fig. 6).


Figure 9: Coloration in life of Hemidactylus sahgali sp. nov.
(A) Paratype female NCBS AU709, (B) an uncollected male from Gautala Wildlife Sanctuary, Maharashtra, (C) uncollected juvenile from Pune.

Hemidactylus sahgali sp. nov.
Hemidactylus triedrus Boulenger, 1885:133 (in part); Smith, 1935:88 (in part); 
Minton, 1966:85; Bauer et al., 2010

Diagnosis: A medium sized fairly stout gecko, adults ranging 56–78 mm in SVL. Dorsum in a shade of light brown with paired, broad black edged white bands at regular intervals. Dorsal scalation on trunk, granular, intermixed with enlarged, keeled 15–16 trihedral tubercle rows arranged in fairly regular longitudinal series. Seven to eight lamellae under digit I of pes and manus, 8–10 under digit four of manus and pes. An angular series of 11–15 precloacal femoral pores separated at a mid-pelvic by a diastema of one to three non-pored scales.

Etymology: The specific epithet is a patronym honoring Bittu Sahgal, Editor and founder of Sanctuary Asia magazine for his contribution toward conservation of wildlife.

Suggested common name: Sahgal’s termite hill gecko.

Natural history: A species associated with termite mounds as its related species H. triedrus. Found in dry open scrub areas with boulders. Seen actively moving about on the ground just after dusk. Hatchlings have been seen in the month of May. Distributed throughout the Deccan Traps, its distribution extends beyond the traps north-west into Pakistan. In India, it is recorded from the following states: Maharashtra, Gujarat, Madhya Pradesh, Rajasthan and Chhattisgarh records ranging in elevation from 11 to 1,191 m AMSL. All records of the species from Pakistan are from elevation ranging from 15 to 25 m AMSL.


Zeeshan A. Mirza​, Gaurang G. Gowande, Rishikesh Patil, Mayuresh Ambekar and Harshil Patel. 2018. First Appearance Deceives Many: Disentangling the Hemidactylus triedrus species complex Using An Integrated Approach.  PeerJ. 6:e5341  DOI: 10.7717/peerj.5341

    

[Ichthyology • 2018] Hippocampus japapigu • A New Species of Pygmy Seahorse (Teleostei, Syngnathidae) from Japan, with A Redescription of H. pontohi

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Hippocampus japapigu
Short, Smith, Motomura, Harasti & Hamilton, 2018

Japanese Pygmy Seahorse | 日本のピグミータツノオトシゴ Hachijo-tatsu 
 DOI:  10.3897/zookeys.779.24799 

Abstract
The pygmy seahorseHippocampus japapigu sp. n. is described based on three specimens, 13.9–16.3 mm SL, collected from a mixed soft coral and algae reef at 11 m depth at Hachijo-jima Island, Izu Islands, Japan. The new taxon shares morphological synapomorphies with the previously described central Indo-Pacific pygmy seahorses, H. colemani, H. pontohi, H. satomiae, and H. waleananus, including extremely small size, 12 trunk rings, strongly raised continuous cleithral ring, snout spine, large spine on the eighth lateral and fifth and 12 superior trunk ridges, respectively, and unusual wing-like-protrusions immediately posterior to the head. Hippocampus japapigu sp. n. can be distinguished from all congeners by the following combination of features in the anterodorsal area of the trunk: bilaterally paired wing-like protrusions formed by a single pair of large, truncate spines projecting dorsolaterad on the first superior trunk ridge, followed by a unique elevated dorsal ridge formed by triangular bony mounds dorsally on the second to fourth superior trunk ridges. In contrast, H. pontohi possesses a pair of large truncate spines projecting strongly laterad on both the first and second superior trunk ridges followed by flat surfaces dorsally on the third and fourth superior trunk rings. The new species can be further differentiated by genetic divergence from H. pontohi (an uncorrected p-distance of 10.1% in the mitochondrial COI gene) and a striking reticulated white and brown lattice pattern on the head, trunk, and tail. Hippocampus japapigu sp. n. represents the fifth species of pygmy seahorse recorded in Japan.

Keywords: Acanthomorpha, computed tomography, reef fish, new species, systematics, taxonomy,  computed tomography

Figure 1. Hippocampus japapigu, UW 157506, female holotype directly after collection, 16.33 mm SL, Hachijo-jima Island, Izu Islands, Japan (photograph Hiroyuki Motomura). 

Figure 2. Hippocampus japapigu, paratypes directly after collection (A) UW 157507, male, 15.59 mm SL (B) KAUM-I. 111770, female, 14.54 mm SL, Hachijo-jima Island, Izu Islands, Japan (photographs Hiroyuki Motomura).

Hippocampus japapigu sp. n.

Diagnosis. Hippocampus japapigu sp. n. differs from its congeners by the following combination of characters: tail rings 28; dorsal fin rays 14; pectoral fin rays nine; subdorsal rings four; bilaterally paired wing-like protrusions formed by a pair of large truncate spines projecting laterad on first superior trunk ridge; elevated dorsal ridge formed by unique triangular bony mounds dorsally on second, third, and fourth trunk rings with the posterior mound less pronounced; large and prominent spine projecting laterad on eighth lateral trunk ridge.

Figure 4. Hippocampus japapigu in situ, Hachijo-jima Island, Izu Islands, Japan at 15 m depth (photograph Richard Smith). 

Figure 5. Hippocampus japapigu in situ, Hachijo-jima Island, Izu Islands, Japan from 10 m depth (photograph Richard Smith).

Distribution and habitat: Hippocampus japapigu sp. n. is only known to occur in Japan, from scattered localities including Kashiwa-jima Island, Sukumo Bay; Kushimoto, Kii Peninsula; Osezaki, Izu Peninsula; the Izu Islands of Miyake and Hachijo; Sagami Bay; and Chichi-jima, Ogasawara Islands. The specimens described herein were found off the northwest coast of Hachijo-jima Island at a depth of 10–13 m, and have been anecdotally reported elsewhere at 5–22 m by local divers. Owing to its diminutive size and extraordinary crypsis, this species may have a wider distribution within Japan. The new taxon is not associated with a particular host, and has been observed in association with mixed soft coral, the coralline algae Halimeda sp., and hydroids on rocky reef walls and large boulders in both exposed and semi-sheltered locations. During 15 dives initially spent searching ad hoc for this species by the second author in July 2013, 13 individuals were observed in an approximately 100 m stretch of rocky reef. These ranged in depth from 10 to 20 m and water temperature fluctuated between 19–24°C over 6 days. When one individual was discovered, another was often found in close proximity and appeared to represent male-female pairs. Returning in June 2015 with a larger group of experienced dive guides, with 10 dives searching for the species, only a single individual was found, possibly suggesting fluctuations in the abundance of the species. Several pregnant males were observed in July 2013, but it is unknown whether reproduction occurs seasonally or year-round.

Etymology: The specific epithet is from the colloquial Japanese name of the new species, Japan Pig, Japapigu, or 日本のピグミータツノオトシゴ. 

Common name: New common English and Japanese names, Japanese Pygmy Seahorse and Hachijo-tatsu, respectively, are proposed here for Hippocampus japapigu.

  

  

Figure 7. Comparison of live specimens of AHippocampus japapigu photographed off Hachijo-jima Island, Japan (Richard Smith), and its most similar congener BHippocampus pontohi photographed off Tomia Island, southeast Sulawesi, Indonesia (Richard Smith). Note the differences in the anterodorsal area of the trunk in H. japapigu vs. H. pontohi: single vs. double pair of bilaterally paired wing-like protrusions behind the head, raised dorsal ridge vs. laterodorsal flat surface, and large and prominent vs. small eighth lateral trunk ridge spine. Abbreviations: SP-WP, single pair of bilaterally paired wing-like protrusions; DP-WP, double pair of bilaterally paired wing-like protrusions; DR, raised dorsal ridge; FS, flat dorsal surface; P-8LTR, prominent eighth lateral trunk ridge spine; S-8LTR, small eighth lateral trunk ridge spine.

 Graham Short, Richard Smith, Hiroyuki Motomura, David Harasti and Healy Hamilton. 2018. Hippocampus japapigu, A New Species of Pygmy Seahorse from Japan, with A Redescription of H. pontohi (Teleostei, Syngnathidae). ZooKeys. 779: 27-49.  DOI:  10.3897/zookeys.779.24799

[Herpetology • 2018] Lepidophyma inagoi • A New Species of Lepidophyma (Squamata: Xantusiidae) from the Pacific Lowlands of Guerrero, Mexico

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Lepidophyma inagoi

Palacios-Aguilar, Santos-Bibiano & Flores-Villela, 2018
  DOI:  10.1670/17-061 
facebook.com/HerpMX

ABSTRACT
We describe a new species of the genus Lepidophyma from the Pacific lowlands of Guerrero, southern Mexico. Previously referred to as L. smithii, the new taxon is distinguished by a series of morphological characteristics, principally higher numbers of gulars, paravertebrals, and lateral tubercle rows. This new species increases the number of described Lepidophyma to 20 species.

FIG. 1. Adult female specimen of Lepidophyma inagoi in life (MZFC 30706, holotype).
FIG. 2. Dorsal and lateral view of the holotype of Lepidophyma inagoi (MZFC 30706).  

Lepidophyma inagoi, sp. nov. 
 Lepidophyma smithii Mendoza-Hernández and Santos-Barrera, 2004; 
Canseco-Ma´rquez et al., 2008; Vázquez-García et al., 2010.

Etymology.—The name inagoi is a patronym honoring our friend and colleague, Iván Nava González, who passed away in late December 2014.


Ricardo Palacios-Aguilar, Rufino Santos-Bibiano and Oscar Flores-Villela. 2018.
A New Species of Lepidophyma (Squamata: Xantusiidae) from the Pacific Lowlands of Guerrero, Mexico. Journal of Herpetology52(3); 327–331.  DOI:  10.1670/17-061


RESUMEN: Se describe una nueva especie del género Lepidophyma de las tierras bajas del Pacı´fico de Guerrero, sur de Me´xico. Esta nueva especie fue referida en el pasado a L. smithii pero puede ser diferenciada de esta por una serie de caracterı´sticas morfolo´gicas, principalmente por tener un mayor nu´mero de escamas gulares, paravertebrales e hileras de tube´ rculos laterales. Esta especie eleva el nu´mero de Lepidophyma descritas a 20.

[Crustacea • 2018] Caridina variabilirostris • A New Species of Freshwater Shrimp (Decapoda: Atyidae) from Pohnpei (Micronesia)

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Caridina variabilirostris 
Mazancourt, Marquet & Keith, 2018


Abstract
Recently, the status of a new species of atyid shrimp from Pohnpei (Micronesia) was discussed in relation to C. brachydactyla De Man, 1908 and C. mertoni J. Roux, 1911. By combining morphological data with a phylogenetic analysis with closely related species, this species is here described as Caridina variabilirostris sp. nov. Notes on its ecological distribution are also provided. The new species is characterized by a highly variable rostrum and is present in rivers all over Pohnpei Island. The status of this new species is clarified and it is shown that neither C. brachydactyla De Man 1908 nor C. mertoni J. Roux, 1911 occur on Pohnpei Island. 

Keywords: 16S, molecular, integrative taxonomy, island, morphology. 

Class Malacostraca Latreille, 1802 
Order Decapoda Latreille, 1802 

Family Atyidae De Haan, 1849 
Genus Caridina H. Milne Edwards, 1837 

Fig. 3.Caridina variabilirostris sp. nov.,
 showing the variation in rostrum length related to the altitude (a– c), drawings made from different specimens. a, m–n. ♂, cl 3.5 mm (MNHN-IU-2018-244). a. Rostrum. m. First pleiopod. n. Second pleiopod. b. ♀, cl 5.6 mm, rostrum (MNHN-IU-2018-252). c, j, o. ♀, cl 4.0 mm (MNHN-IU-2018-253) c. Rostrum. j. Uropodial diaeresis. o. Eggs. d–i, k. ♀, cl 3.5 mm (MNHN-IU-2018-250). d. First pereopod. e. Second pereopod. f. Third pereopod. g. Dactylus of third pereopod. h. Fifth pereopod. i. Dactylus of fifth pereopod. k. Telson. l. ♀, cl 4.3 mm, pre-anal carina (MNHN-IU-2018-256). of third pereopod. h. Fifth pereopod. i. Dactylus of fifth pereopod. k. Telson. l. ♀, cl 4.3 mm, pre-anal carina (MNHN-IU-2018-256).

Fig. 5. Caridina variabilirostris sp. nov., live coloration (Photos: P. Keith)

Caridina variabilirostris sp. nov. 

Etymology: The new species is named variabilirostris for its variable rostrum length.

Habitat: This species is found among macrophytes in flowing fresh water of the rivers of Pohnpei all along the course, showing good adaptability to different temperatures and hydrological conditions. It is more abundant in higher elevations due to reduced predator pressure.

Distribution: This new species is currently known from Pohnpei Island only. 



Valentin de Mazancourt, Gerard Marquet and Philippe Keith. 2018. Caridina variabilirostris (Crustacea: Decapoda: Atyidae), A New Species of Freshwater Shrimp from Pohnpei (Micronesia). European Journal of Taxonomy.  453; 1–16. DOI: 10.5852/ejt.2018.453

   

[PaleoIchthyology • 2018] Static Dental Disparity and Morphological Turnover in Sharks across the End-Cretaceous Mass Extinction

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in Bazzi, Kear, Blom,et al., 2018.

Highlights: 
• Shark teeth reveal morphological turnover during the end-Cretaceous mass extinction
• Fossil shark dental disparity is decoupled from taxonomic richness
 • Cretaceous–Palaeogene shark disparity was nearly static unlike other marine predators
• Prey availability and trophic cascades may have initiated Cenozoic shark radiations

Summary
The Cretaceous–Palaeogene (K–Pg) mass extinction profoundly altered vertebrate ecosystems and prompted the radiation of many extant clades. Sharks (Selachimorpha) were one of the few larger-bodied marine predators that survived the K–Pg event and are represented by an almost-continuous dental fossil record. However, the precise dynamics of their transition through this interval remain uncertain. Here, we apply 2D geometric morphometrics to reconstruct global and regional dental morphospace variation among Lamniformes (Mackerel sharks) and Carcharhiniformes (Ground sharks). These clades are prevalent predators in today’s oceans, and were geographically widespread during the late Cretaceous–early Palaeogene. Our results reveal a decoupling of morphological disparity and taxonomic richness. Indeed, shark disparity was nearly static across the K–Pg extinction, in contrast to abrupt declines among other higher-trophic-level marine predators. Nevertheless, specific patterns indicate that an asymmetric extinction occurred among lamniforms possessing low-crowned/triangular teeth and that a subsequent proliferation of carcharhiniforms with similar tooth morphologies took place during the early Paleocene. This compositional shift in post-Mesozoic shark lineages hints at a profound and persistent K–Pg signature evident in the heterogeneity of modern shark communities. Moreover, such wholesale lineage turnover coincided with the loss of many cephalopod and pelagic amniote groups, as well as the explosive radiation of middle trophic-level teleost fishes. We hypothesize that a combination of prey availability and post-extinction trophic cascades favored extant shark antecedents and laid the foundation for their extensive diversification later in the Cenozoic.

Keywords: K–Pg Boundary, Geometric Morphometrics, Sharks, Lamniformes, Carcharhiniformes, Macroevolution, Mass extinction, Teeth, Disparity



Late Maastrichtian marine assemblage.
 Illustration: Julius Csotonyi 


 Mohamad Bazzi, Benjamin P. Kear, Henning Blom, Per E. Ahlberg and Nicolás E.Campione. 2018. Static Dental Disparity and Morphological Turnover in Sharks across the End-Cretaceous Mass Extinction. Current Biology. In Press.  DOI: 10.1016/j.cub.2018.05.093

[Entomology • 2018] Speciation associated with Geographic and Ecological Divergence in Two Amazonian Heliconius Butterflies

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Rosser, Freitas, Huertas, Joron, Mérot, et al., 2018. 

Abstract
The evolution of reproductive isolation via a switch in mimetic wing coloration has become the paradigm for speciation in aposematic Heliconius butterflies. Here, we provide a counterexample to this, by documenting two cryptic species within the taxon formerly considered Heliconius demeter Staudinger, 1897. Amplified fragment length polymorphisms identify two sympatric genotypic clusters in northern Peru, corresponding to subspecies Heliconius demeter ucayalensis H. Holzinger & R. Holzinger, 1975 and Heliconius demeter joroni ssp. nov. These subspecies are reciprocally monophyletic for the mitochondrial genes COI and COII and the nuclear gene Ef1α, and exhibit marked differences in larval morphology and host plant use. COI sequences from 13 of the 15 currently recognized subspecies show that mtDNA differences are reflected across the range of H. demeter, with a deep phylogenetic split between the southern and northern Amazonian races. As such, our data suggest vicariant speciation driven by disruptive selection for larval performance on different host plants. We raise Heliconius demeter eratosignis (Joicey & Talbot, 1925) to Heliconius eratosignis based on nomenclatural priority, a species also comprising H. eratosignis ucayalensis comb. nov. and three other southern Amazonian races. Heliconius demeter joroni spp. nov. remains within H. demeter s.s., along with northern Amazonian and Guianan subspecies.

Keywords: butterflies, cryptic species, genotypic clusters, host plant shift, integrative taxonomy, mimicry, vicariant speciation

Figure 1. Distribution of races of H. demeter and H. eratosignis. Photos of type specimens are all males, except for H. e.ucayalensis. The inset shows fine-scale sympatry between H. d. joroni ssp. nov. and H. e. ucayalensis in the Tarapoto area of Peru. Heliconius demeter beebei Turner, 1966 and H. d. terrasanta appear to conform to the type specimens only around the type localities (in Terrasanta, Pará, and in Guyana). Between these, most populations appear to be either polymorphic or exhibit intermediate phenotypes (mixed square and cross symbols in the map). Heliconius demeter ssp. nov. refers to three males in the FLMNH recognized by W. Neukirchen as distinct from other described subspecies. These individuals may prove to have affinities to H. demeter titan. Distribution of races of H. demeter andH. eratosignis. Photos of type specimens are all males, except for H. e. ucayalensis. The inset shows fine-scale sympatry between H. d. joroni ssp. nov. and H. e. ucayalensis in the Tarapoto area of Peru. Heliconius demeter beebei Turner, 1966 and H. d. terrasanta appear to conform to the type specimens only around the type localities (in Terrasanta, Pará, and in Guyana). Between these, most populations appear to be either polymorphic or exhibit intermediate phenotypes (mixed square and cross symbols in the map). Heliconius demeter ssp. nov. refers to three males in the FLMNH recognized by W. Neukirchen as distinct from other described subspecies. These individuals may prove to have affinities to H. demeter titan.

Figure 3. Holotype ♂ of Heliconius demeter joroniLamas and Rosser ssp. nov.
Upper photo: dorsal, lower photo: ventral. Scale bar = 10 mm. Holotype ♂ of Heliconius demeter joroni Lamas and Rosser ssp. nov. Upper photo: dorsal, lower photo: ventral.
Scale bar = 10 mm.




Heliconius demeter joroni Lamas & Rosser ssp. nov.  
Heliconius demeter [ssp. nov.] Lamas, MS: Lamas, 2004: 268. Lamas & Jiggins, 2017: 224.

Diagnosis: Heliconius demeter joroni ssp. nov. is similar to H. demeter demeter, but differs from Staudinger’s syntypes of H. demeter from Iquitos, Loreto, Peru (now in the MNB) in having a much narrower yellow postmedian band on the dorsal forewing. It is known only from the Cordillera Escalera, near Tarapoto, Peru (Fig. 1), where its co-mimics include Heliconius eratosignis ucayalensis, Heliconius elevatus pseudocupidineus Neustetter, 1931, Heliconius aoede cupidineus Stichel, 1906 and Eueides tales michaeli Zikán, 1937, among others. Males are easily distinguishable from all sympatric taxa through the fused rays on the hindwing dorsum and the yellow costal streak on the forewing underside. Females may be distinguished from co-mimics through the configuration of the rays (which radiate from the cell), small size, length of the antennae (longer than the forewing discal cell) and the presence of the forewing underside yellow costal streak. Both sexes usually exhibit a single row of white submarginal dots along the anal margin of the ventral hindwing, which can be used to help separate the females fromH. erato emma and E. tales michaeli. This character can be faint or even missing in H. demeter joroni ssp. nov. and occasionally present in H. erato emma. However, the latter is confined to the Amazonian lowlands adjacent to the Cordillera Escalera, and at present there is no evidence to suggest that they regularly co-occur, barring occasional migrants.


Etymology: The subspecies name (a masculine noun in the genitive case) recognizes the contribution of the French evolutionary biologist Dr Mathieu Joron to the knowledge of the mimetic butterfly fauna of San Martín, Peru. Dr Joron is presently a Senior Scientist at the Centre d’Ecologie Fonctionnelle et Evolutive in Montpellier. He began studying the butterflies of San Martín during his PhD and has continued to do so throughout his career, with a particular focus on Heliconius numata.

Geographic distribution: Subspecies of H. demeter and H. eratosignis are mapped in Fig. 1, with photos of a type specimen of each race. Races of H. demeter occupy the Guianas and much of the Amazon basin. H. eratosignis races occur in the west and south of the Amazon basin. In Tarapoto, the two species fly together at a number of sites in the Cordillera Escalera. Only H. eratosignis has been recorded from the adjacent Amazonian lowlands, despite considerable sampling in the area. Museum data and observations by Keith Brown (1979) suggest that the two overlap (at least broadly) in the extreme south of Pará and northern Mato Grosso, in Brazil. There may well also be a contact zone on the Juruá River, between Porto Walter and Eirunepé, as both H. demeter demeter and H. eratosignis tambopata are known to occur there. However, the exact position of contact in this very large area is unclear. In data published by Brown (1979) two additional contact zones are indicated, at Pucallpa, Peru and near Cobija on the Brazilian/Bolivian border. We were unable to locate the relevant specimens in museum collections; however, we consider these points unreliable and excluded them from the distribution map in Fig. 1. The first is probably a generalized locality, with the specimens potentially coming from a large area of northern Peru. The second is likely explained through the co-occurrence of both H. eratosignis ulysses and H. eratosignis tambopata, as the latter was not described at the time (Lamas, 1985).


Neil Rosser, André V. L. Freitas, Blanca Huertas, Mathieu Joron, Gerardo Lamas Claire Mérot, Fraser Simpson, Keith R. Willmott, James Mallet and Kanchon K. Dasmahapatra. 2018. Cryptic Speciation associated with Geographic and Ecological Divergence in Two Amazonian Heliconius Butterflies. Zoological Journal of the Linnean Society. zly046.  DOI: 10.1093/zoolinnean/zly046


[Fungi • 2018] Gerronema kuruvense & G. keralense • Two New Species of Gerronema (Agaricales, Basidiomycota) from Kerala State, India

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Gerronema kuruvense 

in Latha, Nanu, Sharafudheen & Manimohan, 2018.

Abstract
Gerronema kuruvense sp. nov. and G. keralense sp. nov. are described from Kerala State, India, in the light of both morphology and molecular phylogenetic analysis. Comprehensive descriptions, photographs of both the basidiomes and the micro-structures, and comparisons with morphologically similar and phylogenetically related species are provided. Both morphology and nrITS-rDNA sequence-based molecular phylogenetic analysis proved the novelty of the species and their placement in the genus Gerronema. Both the species were collected from highland riverine islets.

Keywords: Fungi, Agaricomycetes, Marasmiaceae, phylogeny, taxonomy




K. P. Deepna Latha, Salna Nanu, Shahina A. Sharafudheen and Patinjareveettil Manimohan. 2018. Two New Species of Gerronema (Agaricales, Basidiomycota) from Kerala State, India. Phytotaxa. 364(1); 81–91. DOI:  10.11646/phytotaxa.364.1.5

[Botany • 2018] Thunbergia impatienoides (Acanthaceae) • A New Species from Thailand

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Thunbergia impatienoides Suwanph. & S.Vajrodaya

in Suwanphakdee & Vajrodaya, 2018

Abstract 
A new species, Thunbergia impatienoides, was discovered from Thailand and is here described. Detailed descriptions including pollen and seed morphologies, distribution, ecology and illustration are provided.

Key words: new species, pollen, Thailand, Thunbergia 


        

Thunbergia impatienoides Suwanph. & S.Vajrodaya, sp. nov.  

Etymology: The specific epithet refers to the gross appearance of its flower which is quite similar to a common ornamental balsam, Impatiens walleriana Hook.f. (Balsaminaceae).

Fig. 1 Thunbergia impatienoides Suwanph. & S.Vajrodaya.
 a–b. Flower bud; c. flower; d. corolla tube with glandular hairs; e. stamens; f. glandular hairs on filament base; g. anther; h. calyx and ovary; i. style and stigma; j. stigma; k. fruit; l. fruit close-up (C. Suwanphakdee 523 (BK, BKF, K, KKU, L, QBG)). — Photos: C. Suwanphakdee.

Distribution: Endemic to Thailand (border of northern and western Thailand in Tak province and in western Thailand in Kanchanaburi and Ratchaburi provinces). 

Habitat & Ecology: In shaded area in dipterocarp and mixed deciduous forests.

    



Chalermpol Suwanphakdee and Srunya Vajrodaya. 2018. Thunbergia impatienoides (Acanthaceae), A New Species from Thailand. Blumea. 63; 20-25.  DOI: 10.3767/blumea.2018.63.01.03 


[Botany • 2018] Berberis morii • A New Species of Berberis Sect. Wallichianae from Taiwan

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Berberis morii  Harber & C.C. Yu

in Harber, Chung & Yu, 2018.
  森氏小檗   DOI: 10.6165/tai.2018.63.235 

ABSTRACT
 In a revision of Berberis Sect. Wallichianae in Taiwan and Luzon, the Philippines, two of the authors recognized 11 species from Taiwan, including three new species. This article recognizes a further new species, Berberis morii, and places it in the same clade with other species from Taiwan. Rather than reproduce all the observations that were made there, we simply note that Taiwan is an important center of endemism of B. Sect. Wallichianae. In comparing the floral structure and overall morphology of B. morii with similar taxa from Taiwan, China and India, a series morphological differences, both qualitatively and quantitatively, were noted. Phylogenetic analysis was also used to evaluate the endemicity of B. morii.

KEY WORDS: Berberis, Cloud forest, Flora of Taiwan, Hualien, New species, Mori Ushinosuke. 



Berberis morii Harber & C.C. Yu, sp. nov. 
森氏小檗  

Type: TAIWAN: Cultivated; Hualian, Guangfu Logging Trail, ..., 1576 m, 20 March 2016, J. F. Harber & C. C. Yu 2016-01 (Holotype: HAST 141801!) 

Fig. 1. Berberis morii Harber & C.C. Yu
A. Plant in nature. B. Adventitious roots. C. Densely pruinose abaxial surface. D. Flower from plant in cultivation; abaxial view showing sepals. E. Petal with nectaries and stamen. F. Distribution of B. morii.

Fig. 3. Berberis morii Harber & C.C. Yu. 
A. Flowering branch. B. Flower, abaxial view. C. Flower, adaxial view. D. First whorl sepal. E. Inner sepals. F. Petal with pair of ovoid nectaries at base. G. Dehisced stamen. H. Stamen before dehiscence. 
Illustrations by HanYau Huang.

Distribution & habitat: eastern Taiwan, Hualien Hsien; known from only two small colonies, one on the side of Guangfu Logging Trail at 1576 m, the second at the summit of Mt. Wanwuta (Fig. 1F).

Etymology: Berberis morii is named for the Japanese ethnographer, Mori Ushinosuke, who was the first to collect plants in the area where B. morii was found. 


Julian Harber, Kuo-Fang Chung and Chih-Chieh Yu. 2018. A New Species of Berberis Sect. Wallichianae from Taiwan, Berberis moriiTaiwania. 63(3); 235-240, 2018 DOI: 10.6165/tai.2018.63.235


[Cetacea • 2017] A Common Bottlenose Dolphin (Tursiops truncatus) Prey Handling Technique for Marine Catfish (Ariidae) in the northern Gulf of Mexico

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Fig 1. Severed catfish head (Bagre marinus) found near dolphins demonstrating foraging behavior near Palma Sola Bay, FL (SAR). 
Fig 3. Bottlenose dolphin interacts with a hardhead catfish (
Ariopsis felis) near Palma Sola Bay, FL (SAR). The dorsal and pectoral spines of the fish appear locked in their defensive positions.

in Ronje, Barry, Sinclair, et al., 2017. 

Abstract
Few accounts describe predator-prey interactions between common bottlenose dolphins (Tursiops truncatus Montagu 1821) and marine catfish (Ariopsis felis Linnaeus 1766, Bagre marinus Mitchill 1815). Over the course of 50,167 sightings of bottlenose dolphin groups in Mississippi Sound and along the Florida coast of the Gulf of Mexico, severed catfish heads were found floating and exhibiting movements at the surface in close proximity to 13 dolphin groups that demonstrated feeding behavior. These observations prompted a multi-disciplinary approach to study the predator-prey relationship between bottlenose dolphins and marine catfish. A review was conducted of bottlenose dolphin visual survey data and dorsal fin photographs from sightings where severed catfish heads were observed. Recovered severed catfish heads were preserved and studied, whole marine catfish were collected and examined, and stranding network pathology reports were reviewed for references to injuries related to fish spines. Photographic identification analysis confirms eight dolphins associated with severed catfish heads were present in three such sightings across an approximately 350 km expanse of coast between the Mississippi Sound and Saint Joseph Bay, FL. An examination of the severed catfish heads indicated interaction with dolphins, and fresh-caught whole hardhead catfish (A. felis) were examined to estimate the presumed total length of the catfish before decapitation. Thirty-eight instances of significant trauma or death in dolphins attributed to ingesting whole marine catfish were documented in stranding records collected from the southeastern United States of America. Bottlenose dolphins typically adhere to a ram-feeding strategy for prey capture followed by whole prey ingestion; however, marine catfish skull morphology may pose a consumption hazard due to rigid spines that can puncture and migrate through soft tissue, prompting a prey handling technique for certain dolphins, facilitating consumption of the posterior portion of the fish without the head.

Fig 1. Severed catfish head (Bagre marinus) found near dolphins demonstrating foraging behavior near Palma Sola Bay, FL (SAR).  

Fig 3. Bottlenose dolphin interacts with a hardhead catfish (Ariopsis felis) near Palma Sola Bay, FL (SAR). The dorsal and pectoral spines of the fish appear locked in their defensive positions.

Conclusion: 
Bottlenose dolphin feeding morphology has evolved towards a ram-feeding mode without significant oral processing of prey; however, these observations of SCH suggest dolphins in the nGoMx have developed a prey handling technique to reduce potential complications from the venomous and sharp spines of marine catfish. The present study indicates some dolphins are targeting marine catfish when other prey is likely available, despite the additional energy presumably expended to decapitate each fish. Marine catfish in spawning aggregations may offer bottlenose dolphins a prey source with a positive energy trade-off due to their egg production and propensity for sonic activity. Generally, bottlenose dolphin diet studies find a relatively low occurrence of marine catfish, however, those data may reflect a lack of ingested otoliths due to successful decapitations or a bias towards a diet less representative of dolphins with extended movement patterns extralimital to the study population. The dorsal fin matches in dolphin groups associated with this rarely observed prey handling technique across these survey areas may indicate a need for specific studies (e.g., focal follows, remote tissue biopsy) to determine the extent to which this prey handling technique is related to factors such as ecology, genetics, or social transmission.


Errol I. Ronje, Kevin P. Barry, Carrie Sinclair, Mark A. Grace, Nélio Barros, Jason Allen, Brian Balmer, Anna Panike, Christina Toms, Keith D. Mullin and Randall S. Wells. 2017. A Common Bottlenose Dolphin (Tursiops truncatus) Prey Handling Technique for Marine Catfish (Ariidae) in the northern Gulf of Mexico. PLoS ONE. 12(7); e0181179.  DOI: 10.1371/journal.pone.0181179

     

In the Gulf of Mexico, dolphins have learned a deadly new trick.

[Paleontology • 2018] Bayannurosaurus perfectus • A Large-sized Basal Ankylopollexian from East Asia, Shedding Light on early Biogeographic History of Iguanodontia

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Bayannurosaurus perfectus 
 Xu, Tan, Gao, Bao, Yin, Guo, Wang, Tan, Zhang & Xing, 2018


Abstract
A presumably mostly quadrupedal ankylopollexian iguanodontian, Bayannurosaurus perfectus gen. et sp. nov., is reported here, and is represented by an excellently well-preserved skeleton from the Lower Cretaceous Bayingebi Formation of Inner Mongolia, China. The diagnosis of the taxon includes several autapomorphies, notably a dorsally directed, strap-like posterodorsal process of the jugal and a horizontally oriented preacetabular process of the ilium. The nearly complete caudal series retains eight posterior-most caudals with procoelous, trapezoidal centra in dorsal view, and the last three caudals are fully fused. The discovery of B. perfectus opens a critical new window on the early evolution and intercontinental dispersal of Iguanodontia. The skeleton displays a transitional morphology between non-hadrosauriform ankylopollexians and Hadrosauriformes. A phylogenetic analysis indicates that Bayannurosaurus is positioned higher on the tree than Hypselospinus, but below Ouranosaurus just outside of Hadrosauriformes. The tree topology of Iguanodontia with temporal and spatial constraints reveals a possible biogeographic scenario supported by the statistical dispersal-vicariance analysis: around the J/K boundary, non-hadrosauriform ankylopollexians experienced multiple dispersal events from Europe to Asia, accompanying the coeval fall of the global sea level.

Keywords: Non-hadrosauriform ankylopollexian; Lower Cretaceous; Bayingebi Formation; Inner Mongolia; Intercontinental dispersal

Fig. 1. Locality and horizon of the holotype (IMMNH PV00001) of Bayannurosaurus perfectus gen. et sp. nov.. (a) Fossil site at the quarry indicated by a white arrow. (b) Chulumiao locality in southwestern Inner Mongolia (China), where the holotype of B. perfectus was collected. (c) Stratigraphic distribution of B. perfectus within the upper Bayingebi Formation. (d) Holotype of B. perfectus originally exposed at the quarry.

Systematic palaeontology
Ornithischia Seeley, 1887
Ornithopoda Marsh, 1881

Iguanodontia Dollo, 1888 sensu Sereno, 1998
Ankylopollexia Sereno, 1986 sensu Sereno, 1998

Bayannurosaurus perfectus gen. et sp. nov.

 Etymology: Bayannur’, the name of the general geographic area where the fossil was retrieved; ‘saurus’, based on the Greek word ‘sauros’ for lizard. ‘perfectus’, in reference to the perfect preservation of the skeleton designated as the holotypic specimen.

Holotype: IMMNH PV00001 (housed at the Inner Mongolia Museum of Natural History, Hohhot, Inner Mongolia), a nearly complete, semi-articulated skeleton, including the entire caudal series.

 Locality and horizon: Chulumiao, ∼7 km north of Chaogewenduer Town, Urad Rear Banner, Bayannur, Inner Mongolia (Fig. 1b); middle part of the upper half of the Bayingebi Formation (Fig. 1c); Early Cretaceous (early Aptian).

Xing Xu, Qingwei Tan, Yilong Gao, Zhiqiang Bao, Zhigang Yin, Bin Guo, Junyou Wang, Lin Tan, Yuguang Zhang and Hai Xing. 2018. A Large-sized Basal Ankylopollexian from East Asia, Shedding Light on early Biogeographic History of Iguanodontia. Science Bulletin.  63(9); 556-563. DOI:  10.1016/j.scib.2018.03.016


Iguanodontia is among the first-discovered dinosaurian groups in the world, and has become one of the best studied ornithischian clades, which refers to its taxonomic, phylogenetic and ontogenetic significance for dinosaurian evolution. Ankylopollexia represents a relatively derived iguanodontian clade that displays large body size and many highly modified features for more efficient herbivory and locomotion. Although relevant studies on European and North American material enhanced our knowledge of the early evolution of Ankylopollexia, the extreme scarcity of non-hadrosauriform ankylopollexians in Asia had long hindered attempts to comprehensively elucidate evolutionary history and related issues of the global iguanodontians. The research team led by Dr. Xing Xu names and describes a new non-hadrosauriform ankylopollexian Bayannurosaurus perfectus represented by an excellently wellpreserved skeleton, from the Lower Cretaceous Bayingebi Formation, western Inner Mongolia, China. The discovery of this new taxon is very helpful in understanding the origin and early evolution of Hadrosauriformes, optimizing the phylogenetic framework of non-hadrosaurid iguanodontians and clarifying the global biogeographic history of Iguanodontia around the Jurassic–Cretaceous boundary (see the article by Xing Xu et al. on page 556).


[Herpetology • 2018] Trigonodactylus persicus • A New Species of Short-fingered Geckos Stenodactylus (Squamata, Geckonidae) from South Iran with Taxonomic Notes on Validity of the Genus Trigonodactylus Hass, 1957

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Trigonodactylus persicus 
Nazarov, Melnikov, Radjabizadeh & Poyarkov, 2018  


Abstract
In the present study we provide evidence for the validity of the genus Trigonodactylus Hass, 1957, improve the diagnosis for this genus and describe a new species that belongs to it—Trigonodactylus persicus sp. nov., from the sand dunes in Khuzestan Province, southwestern Iran. The new species is closely related to Trigonodactylus [Stenodactylus] arabicus sensu Hass, and can be distinguished by the following morphological characteristics: small size, maximum SVL 34 mm; SVL/TailL—approximately 1:1; ventral scales roundish, weakly keeled, 54–61 longitudinal rows at midbody and 190–25 along midbody. No enlarged postmentals. Fingers and toes slightly flattened dorso-ventrally. Lateral edge of digits fringed by series of projecting triangular scales. No web between digits. No preanal and femoral pores. Dorsal color pattern formed by thin, dark, irregular vermicular patches and spots. Sometimes these dark dorsal patterns blend with each other and form transverse bands. There is a narrow, dark, longitudinal line between forelimbs and hindlimbs on lateral sides. Dark, well developed ʌ-shaped marking on snout, which continues behind orbit on tympanum region, approaches the upper ear opening and ends on the pectoral arch. Labial scales white, in some cases with grey-brown dots. Dorsal surfaces of limbs and digits with irregular dark bands. Dorsal surface of tail with 8–10 wide, dark brown bands with irregular margins, same size as alternating light bands. Ventral surface of body and limbs white, tail with dark spots that become more distinct posteriorly.

Keywords: systematics, taxonomy, Reptilia, Middle East, zoogeography, new species, COI, DNA-barcoding,


FIGURE 2. ML-tree of studied Stenodactylus and Trigonodactylus species based on the analyses of 602 bp COI mtDNA gene fragment. Node colour indicates support values: black for well-supported and sufficiently supported nodes, grey for moderately or poorly supported nodes. Node support values are shown above or below tree nodes for ML BS/MP BS/BI PP analyses respectively.

Holotype of Trigonodactylus persicus sp. nov. in situ

Trigonodactylus persicus sp. nov.

Etymology: The new species was named after the geographic region, where it was found, Persia.

FIGURE 5. Members of the genus Trigonodactylus in situ:
a—Trigonodactylus persicus sp. nov.; b—T. sharqiyahensis (Metallinou & Carranza, 2013); c—T. arabicus Hass, 1957.

FIGURE 4. Dorsal (upper row), lateral (median row) and mental (lower row) views of heads of all members of the genus Trigonodactylus:
 T. arabicus holotype CAS 84321 (a; f; k); T. arabicus ZMMU R-14666-1 (b; e; l);
 Trigonodactylus persicus sp. nov. ZMMUR-14669 (c; h; m);  T. sharqiyahensis ZMMU R-14667-1 (d; i; n); T. pulcher holotype BMNH 1946.8.23.38. (e; j; o).

   


Roman A. Nazarov, Daniel A. Melnikov, Mehdi Radjabizadeh and Nikolay A. Poyarkov. 2018.  A New Species of Short-fingered Geckos Stenodactylus (Squamata, Geckonidae) from South Iran with Taxonomic Notes on Validity of the Genus Trigonodactylus Hass, 1957Zootaxa. 4457(1); 93–113. DOI:  10.11646/zootaxa.4457.1.4
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[Herpetology • 2017] Taxonomy of Litoria graminea (Anura: Hylidae), with Descriptions of Two closely related New Species; Litoria nullicedens & L. pallidofemora

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Litoria nullicedens Kraus, 2018


Abstract
I clarify the correct provenance and taxonomic identity of the poorly known canopy-dwelling frog, Litoria graminea, from New Guinea. I base my redescription upon analysis of relevant historical material as well as upon more recently obtained specimens from several localities in Papua New Guinea. Determining the correct identity of L. graminea makes clear that one recently named species (L. dux Richards & Oliver) is a junior synonym of that taxon and that additional close relatives of that species remain undescribed, two of which I describe here. The first is known from a series of localities along the southern versant of the Central Dividing Range and the Owen Stanley Mountains. The second is known from a single site in the foothills of the Owen Stanley Mountains in Central Province, Papua New Guinea. Differences among the species are largely confined to pigmentation features and the shape of the male nuptial pads. Further, I show that several morphometric and color-pattern features earlier thought to distinguish among members of this complex are encompassed by natural variation within true L. graminea, making the characters taxonomically uninformative. The two newly described species share the unusual feature of having green oral mucosa, although their bones were white in life. This coloration is presumably due to sequestration of biliverdin, as seen in a few other tropical treefrogs, but the function of this sequestration remains unknown.

Keywords: Litoria nullicedens sp. nov., Litoria pallidofemora sp. nov., Papua New Guinea, sibling species, species complex, treefrog, Amphibia




Fred Kraus. 2018. Taxonomy of Litoria graminea (Anura: Hylidae), with Descriptions of Two closely related New Species. Zootaxa. 4457(2); 264–284. DOI:  10.11646/zootaxa.4457.2.3


[Invertebrate • 2018] Taxonomic Reassessment and Redescription of Scolopendra arthrorhabdoides Ribaut, 1913 (Scolopendromorpha, Scolopendridae), with A Discussion on Its related Species

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Scolopendra arthrorhabdoides Ribaut, 1913

in Chagas-Jr & Jiménez, 2018.

Abstract
Scolopendra arthrorhabdoides Ribaut, 1913 is redescribed based on fresh material. Its taxonomic status is evaluated and compared with Scolopendra armata Kraepelin, 1903 and Scolopendra alternans Leach, 1816. The geographical distribution of S. arthrorhabdoides is also revised. Scolopendra armata is reported from Colombia for the first time.

Keywords: Myriapoda, Centipede, Chilopoda, Scolopendra, taxonomy, Colombia, Venezuela


FIGURE 1.Scolopendra arthrorhabdoides Ribaut, 1913. Habitus.
ICN-M.Ch- 0414, Icononzo, Department of Tolima.

Amazonas Chagas-Jr and Sebastián Galvis Jiménez. 2018. Taxonomic Reassessment and Redescription of Scolopendraarthrorhabdoides Ribaut, 1913, with A Discussion on Its related Species (Scolopendromorpha, Scolopendridae). Zootaxa. 4425(1); 153–164. DOI:  10.11646/zootaxa.4425.1.9

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