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[Herpetology • 2018] Oreobates antrum • A New Cryptic Species of Oreobates (Anura: Craugastoridae) from the Seasonally Dry Tropical Forest of central Brazil

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Oreobates antrum 
Vaz-Silva, Maciel, Andrade & Amaro, 2018


Abstract
A new species of Oreobates Jiménez de la Espada, 1872 is described from the seasonally dry tropical forest associated to rocky outcrops of the northeastern Goiás State, Central Brazil. Oreobates antrum sp. nov. is diagnosable by the combination of morphological characters (e.g. small size, dorsal and ventral skin texture smooth to finely shagreened, and broadly enlarged truncate discs on Fingers III and IV), call attributes (composed of a single note and no harmonics with dominant frequency ranged 2070 Hz to 3273 Hz), and supported by molecular evidence (phylogenetic position and genetic divergence) with high degree of differentiation among other Oreobates species (divergences of 4.0–20.6% for 12S, 7.0–14% for 16S, 0.7–4.0% for RAG-1, and 1.1–8.0% for TYR). The new species was recovered as the sister of Oreobates remotus.

Keywords: Amphibia, Brachycephaloidea; Cerrado biome; Integrative taxonomy; Terrarana


reddish-brown Oreobates antrum sp. n. from the type locality at São Domingos, State of Goiás. 

FIGURE 3. Color patterns in live specimens of Oreobates antrum sp. n. from the type locality at São Domingos, State of Goiás.
Absence of dorsolateral bar (C), dorsolateral longitudinal stripes from post-ocular to sacral regions (D), diagonal labial bars slightly faded (E), light brown blotches between the eyes and nostrils (F).
Photos by D.L. Santos, S.P. Andrade and E.P. Victor-Junior.

Oreobates antrum sp. nov.

Etymology. The specific name antrum is a Latin adjective meaning “hollow, cave or cavity”. This name refers to the habitats where this species is found, caves of the calcareous rocky outcrops of the Cerrado associated to dry forests.


Wilian Vaz-Silva, Natan Medeiros Maciel, Sheila Pereira de Andrade and Renata Cecília Amaro. 2018. A New Cryptic Species of Oreobates (Anura: Craugastoridae) from the Seasonally Dry Tropical Forest of central Brazil. Zootaxa. 4441(1); 89–108. DOI:  10.11646/zootaxa.4441.1.5


[PaleoOrnithology • 2018] A North American Stem Turaco, and the Complex Biogeographic History of Modern Birds

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Field & Hsiang, 2018.

bird images by International Touraco Society

Abstract
Background: 
Earth’s lower latitudes boast the majority of extant avian species-level and higher-order diversity, with many deeply diverging clades restricted to vestiges of Gondwana. However, palaeontological analyses reveal that many avian crown clades with restricted extant distributions had stem group relatives in very different parts of the world.

Results:
Our phylogenetic analyses support the enigmatic fossil bird Foro panarium Olson 1992 from the early Eocene (Wasatchian) of Wyoming as a stem turaco (Neornithes: Pan-Musophagidae), a clade that is presently endemic to sub-Saharan Africa. Our analyses offer the first well-supported evidence for a stem musophagid (and therefore a useful fossil calibration for avian molecular divergence analyses), and reveal surprising new information on the early morphology and biogeography of this clade. Total-clade Musophagidae is identified as a potential participant in dispersal via the recently proposed ‘North American Gateway’ during the Palaeogene, and new biogeographic analyses illustrate the importance of the fossil record in revealing the complex historical biogeography of crown birds across geological timescales.

Conclusions: 
In the Palaeogene, total-clade Musophagidae was distributed well outside the range of crown Musophagidae in the present day. This observation is consistent with similar biogeographic observations for numerous other modern bird clades, illustrating shortcomings of historical biogeographic analyses that do not incorporate information from the avian fossil record.

Keywords: Biogeography, Palaeontology, Turaco, Musophagidae, Phylogeny, Fossils, Gondwana, Dispersal, Otidimorphae, Macroevolution


Fig. 1 Skeletal morphology of total clade musophagids.
(a) Complete skeleton of Foro panarium holotype USNM 336261. Scale bar equals 10 cm.
(b) 3-dimensional CT rendering of the pectoral region of Ross’s Turaco (Musophaga rossae) GCO 1142 (Georgia College Ornithology, Georgia College and State University, Milledgeville, GA). LF – left ramus of furcula, RC – right coracoid, RF – right ramus of furcula, S – sternum. 153:1 denotes unfused midline of furcula, which optimizes as an unambiguous synapomorphy of a Foro + Musophagidae clade. (c) Pectoral region of F. panarium. LH – left humerus, RS – right scapula. (d) Cranial region of USNM 336261. 50:1 processus costales of axis absent. 152:1 bill short and stout with broad processus maxillaris of the os nasale. (e) Distal end of right leg of USNM 336261. 109:0 – trochlea metatarsi IV without large trochlea accessoria. 106:0 tendon of musculus flexor hallucis longus not enclosed in bony canal

  


    


Daniel J. Field and Allison Y. Hsiang. 2018. A North American Stem Turaco, and the Complex Biogeographic History of Modern Birds. BMC Evolutionary Biology. 18:102.  DOI: 10.1186/s12862-018-1212-3
Feathered fruit-eater frozen in fossil form - tinyurl.com/ybmtujr9 @BMC_Series

    

[Botany • 2012] Rhododendron rawatii (Ericaceae) • A New Species from the Western Himalaya, India

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Rhododendron rawatii  I. D. Rai& B. S. Adhikari

in Rai & Adhikari, 2012.

 ABSTRACT
A new species of RhododendronR. rawatii is illustrated and described from the Western Himalaya. The species is sporadically found in the subalpine-timberline zone of Uttarakhand state. Fascicled white cottony hairs on the abaxial surface in between lateral veins of leaves, bright pink and shine-less corolla and comparatively large calyx with hairy margins distinguish the new species from its nearest ally R. fulgens. The populations of the species were found in two geographically distinct localities in the Rudraprayag and Pithoragarh districts of Uttarakhand state. The distinguishing morphological characters, affinities with other species and various ecological aspects of the new species are discussed here.





Rhododendron rawatii I. D. Rai & B. S. Adhikari sp. nov. 

Etymology:— The epithet rawatii acknowledges Prof. Gopal Singh Rawat, one of the leading phytotaxonomists and ecologists of India.


 Ishwari Datt Rai and Bhupendra S. Adhikari. 2012. Rhododendron rawatii (Ericaceae), A New Species from the Western Himalaya, India. PHYTOTAXA. 71(1):10-16   DOI:  10.11646/phytotaxa.71.1.3

[Crustacea • 2018] Xiphocaridinella otapi • Cryptic Diversity of Stygobiotic Shrimp Genus Xiphocaridinella Sadowsky, 1930 (Decapoda: Atyidae): The First Case of Species Co-occurrence in the Same Cave System in the Western Caucasus

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Xiphocaridinella otapi Marin, 2018


Abstract
DNA barcoding of stygobiotic shrimps of the genus Xiphocaridinella Sadowsky, 1930 (Crustacea: Decapoda: Atyidae) collected in underground streams flowing inside two neighboring large karst caves (Otap and Abrskil сaves) revealed the presence of two distinct genetic lineages representing the first case of species co-occurrence in the Western Caucasus. The paper presents the complete morphological re-description of stygobiotic atyid shrimp Xiphocaridinella ablaskiri (Birštein, 1939) and the description of a new species using genetic and morphological analysis. Other known cases of co-occurrence of several stygobiotic shrimp species in the same cave system as well as new genetic data (COI mtDNA) on Western Caucasian species of the genus Xiphocaridinella are discussed in the paper.

Keywords: Crustacea, Decapoda, Atyidae, Xiphocaridinella, stygobiotic, stygobiont, shrimps, new species, species co-occurrence, Western Caucasus




Ivan Marin. 2018. Cryptic Diversity of Stygobiotic Shrimp Genus Xiphocaridinella Sadowsky, 1930 (Crustacea: Decapoda: Atyidae): The First Case of Species Co-occurrence in the Same Cave System in the Western Caucasus. Zootaxa. 4441(2); 201–224.  DOI:  10.11646/zootaxa.4441.2.1
Ivan Marin. 2017. Troglocaris (Xiphocaridinellakumistavi sp. nov., A New Species of Stygobiotic Atyid Shrimp (Crustacea: Decapoda: Atyidae) from Kumistavi Cave, Imereti, Western Georgia, Caucasus. Zootaxa. 4311 (4), 576–588. DOI: 10.11646/zootaxa.4311.4.9

[Paleontology • 2018] Ceratosaur Palaeobiology: New Insights on Evolution and Ecology of the Southern Rulers

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 The hypothetical phylogenetic relationships of ceratosaurs based on current topologies. 
The main source is from Wang et al. (2016).

Hypothetical reconstruction of two abelisaurids showing the soft tissues on the head inferred from osteological morphology of the skull. On the top, Carnotaurus; on the bottom, PycnonemosaurusArt by Maurilio Oliveira. 

in Delcourt, 2018. 

Abstract
Ceratosaur theropods ruled the Southern Hemisphere until the end of the Late Cretaceous. However, their origin was earlier, during the Early Jurassic, a fact which allowed the group to reach great morphological diversity. The body plans of the two main branches (Noasauridae and new name Etrigansauria: Ceratosauridae + Abelisauridae) are quite different; nevertheless, they are sister taxa. Abelisaurids have lost the ability to grasp in the most derived taxa, but the reduced forelimb might have had some display function. The ontogenetic changes are well known in Limusaurus which lost all their teeth and probably changed the dietary preference at maturity. The results presented here suggest that abelisaurids had different soft tissues on the skull. These tissues might have been associated with evolution of a strong cervicocephalic complex and should have allowed derived taxa (e.g. Majungasaurus and Carnotaurus) to have low-displacement headbutting matches. The ability to live in different semi-arid environment plus high morphological disparity allowed the ceratosaurs to become an evolutionary success.


Figure 1 The hypothetical phylogenetic relationships of ceratosaurs based on current topologies. The main source is from Wang et al. (2016). The phylogenetic position of Chenanisaurus is from Longrich et al.(2016) and the Ligabueino, Austrocheirus, Majungasaurinae and Brachyrostra are from Filippi et al.(2011).

 Figure 4 Skin structures inferred for abelisaurids. Dorsal surface of the skull of (A) Rugops (MNN IGU1), (C) Carnotaurus (MACN-CH 894) and dorsal surface of the fused nasal of (B) Abelisaurus (MPCA 11908). Scales bar: 5 cm. 


Figure 6 Hypothetical reconstruction of two abelisaurids showing the soft tissues on the head inferred from osteological morphology of the skull. On the top, Carnotaurus; on the bottom, Pycnonemosaurus.
Art by Maurilio Oliveira.

Rafael Delcourt. 2018. Ceratosaur Palaeobiology: New Insights on Evolution and Ecology of the Southern Rulers. Scientific Reports. 8, 9730.  DOI:   10.1038/s41598-018-28154-x 

[Herpetology • 2018] Sky, Sea, and Forest Islands: Diversification in the African Leaf‐folding Frog Afrixalus paradorsalis (Anura: Hyperoliidae) of the Lower Guineo‐Congolian Rain Forest

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Afrixalus paradorsalis  Perret, 1960

in Charles, Bell, Blackburn, et al., 2018. 
photo: Daniel M. Portik

Abstract
Aim: 
To investigate how putative barriers, forest refugia, and ecological gradients across the lower Guineo‐Congolian rain forest shape genetic and phenotypic divergence in the leaf‐folding frog Afrixalus paradorsalis, and examine the role of adjacent land bridge and sky‐islands in diversification.

Location: The Lower Guineo‐Congolian Forest, the Cameroonian Volcanic Line (CVL), and Bioko Island, Central Africa.

Taxon: Afrixalus paradorsalis (Family: Hyperoliidae), an African leaf‐folding frog.

Methods: 
We used molecular and phenotypic data to investigate diversity and divergence among the A. paradorsalis species complex distributed across lowland rain forests, a land bridge island, and mountains in Central Africa. We examined the coincidence of population boundaries, landscape features, divergence times, and spatial patterns of connectivity and diversity, and subsequently performed demographic modelling using genome‐wide SNP variation to distinguish among divergence mechanisms in mainland (riverine barriers, forest refugia, ecological gradients) and land bridge island populations (vicariance, overwater dispersal).

Results: 
We detected four genetically distinct allopatric populations corresponding to Bioko Island, the CVL, and two lowland rain forest populations split by the Sanaga River. Although lowland populations are phenotypically indistinguishable, pronounced body size evolution occurs at high elevation, and the timing of the formation of the high elevation population coincides with mountain uplift in the CVL. Spatial analyses and demographic modelling revealed population divergence across mainland Lower Guinea is best explained by forest refugia rather than riverine barriers or ecological gradients, and that the Bioko Island population divergence is best explained by vicariance (marine incursion) rather than overseas dispersal.

Main conclusions: 
We provide growing support for the important role of forest refugia in driving intraspecific divergences in the Guineo‐Congolian rain forest. In A. paradorsalis, sky‐islands in the CVL have resulted in greater genetic and phenotypic divergences than marine incursions of the land bridge Bioko Island, highlighting important differences in patterns of island‐driven diversification in Lower Guinea.

Keywords: Africa amphibian, historical demography, land bridge island, Lower Guinea, phylogeography


Figure 1: Sampling localities of Afrixalus paradorsalis paradorsalis (circles) and A. p. manengubensis (triangles) in the Lower Guinean forests of continental Central Africa and Bioko Island. Sampling localities are coloured according to the mitochondrial (mtDNA) haplotype groups and distinct genetic lineages identified in analyses of the ddRADseq (nuDNA) dataset (Figure 2). Symbols with white borders reflect localities with only mtDNA sequence data and symbols with no border reflect localities with only morphological data. The right panel depicts the locations of key mountains along the Cameroon Volcanic Line


Kristin L. Charles, Rayna C. Bell, David C. Blackburn, Marius Burger, Matthew K. Fujita, Václav Gvoždík, Gregory F.M. Jongsma, Marcel Talla Kouete, Adam D. Leaché and Daniel M. Portik. 2018. Sky, Sea, and Forest Islands: Diversification in the African Leaf‐folding Frog Afrixalus paradorsalis (Anura: Hyperoliidae) of the Lower Guineo‐Congolian Rain Forest. Journal of Biogeography. DOI: 10.1111/jbi.13365

[Diplopoda • 2018] The Genus Eviulisoma Silvestri, 1910 (Polydesmida, Paradoxosomatidae), in the Udzungwa Mountains, Tanzania, and related species from other Eastern Arc Mountains. With notes on Eoseviulisoma Brolemann, 1920, and Suohelisoma Hoffman, 1963 [A Mountain of Millipedes VII]

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Eviulisoma zebra Enghoff, 2018
one of the strikingly marked species from the Udzungwa Mts. 

Photograph by Martin Nielsen.

Abstract

 Twenty-two new species of the genus Eviulisoma Silvestri, 1910, from the Eastern Arc Mountains, Tanzania, are described: Eviulisoma acaciae sp. nov., E. aequilobatum sp. nov., E. akkariae sp. nov., E. angulatum sp. nov., E. articulatum sp. nov., E. biquintum sp. nov., E. breviscutum sp. nov., E. cetafi sp. nov., E. chitense sp. nov., E. commelina sp. nov., E. coxale sp. nov., E. ejti sp. nov., E. grumslingslak sp. nov., E. kalimbasiense sp. nov., E. navuncus sp. nov., E. nessiteras sp. nov., E. ottokrausi sp. nov., E. paradisiacum sp. nov., E. sternale sp. nov. andE. zebra sp. nov. from the Udzungwa Mts,E. culter sp. nov. from the Rubeho Mts andE.kangense sp. nov. from the Kanga Mts. Eviulisoma kwabuniense Kraus, 1958, and E. dabagaense Kraus, 1958, both from the Udzungwa Mts, are redesribed based on new material. Notes are provided on E. iuloideum (Verhoeff, 1941) based on type material. Eoseviulisoma Brolemann, 1920, is synonymized under Eviulisoma, based on newly collected material of E. julinum (Attems, 1909), type species of Eoseviulisoma. New material of Suohelisoma ulugurense Hoffman, 1964, type species of Suohelisoma Hoffman, 1964, has revealed that the gonopod structure is more similar to that of Eviulisoma than originally thought, but Suohelisoma is retained as a valid genus. Four species groups are recognized among Eviulisoma species from the Udzungwa Mts, but the need for a revision of the entire genus is emphasized. Two types of epizootic fungi are recorded from Eviulisoma spp., and an enigmatic amorphous mass, which may be a kind of plugging substance, is recorded from the gonopod tips and excavated sixth sternum of several species. 

Keywords: Taxonomy, new species, epizootic fungi, copulatory plug. 


Fig. 1. Eviulisoma zebra sp. nov., one of the strikingly marked species from the Udzungwa Mts.
Photograph by Martin Nielsen.


Henrik Enghoff. 2018. A Mountain of Millipedes VII: The Genus Eviulisoma Silvestri, 1910, in the Udzungwa Mountains, Tanzania, and related species from other Eastern Arc Mountains. With notes on Eoseviulisoma Brolemann, 1920, and Suohelisoma Hoffman, 1963 (Diplopoda, Polydesmida, Paradoxosomatidae)European Journal of Taxonomy. 445: 1–90. DOI: 10.5852/ejt.2018.445

[Herpetology • 2018] Cnemaspis tanahjampea • A New Bent-toed Gecko (Cyrtodactylus: Squamata: Gekkonidae) from the Island of Tanahjampea, South Sulawesi, Indonesia

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Cyrtodactylus tanahjampea
Riyanto, Hamidy & McGuire, 2018


Abstract
The recent description of Cyrtodactylus tahuna from Sangihe Island and descriptions of other new species from remote islands in the Indo-Australian Archipelago indicate the important role of oceanic dispersal and isolation in the evolution and diversification of the genus Cyrtodactylus. We provide another example involving Tanahjampea Island, a remote island 155 km south of the Southwestern Peninsula of Sulawesi, Indonesia. Here, we describe a new species on the basis of 11 specimens collected from that island. This new species is an intermediate sized Cyrtodactylus with a snout–vent length of up to 76.1 mm in adult males and 72.8 mm in females. It is easily distinguished from all recognized species occurring on Sulawesi as well as in the Moluccas and Lesser Sunda Islands by the following unique combination of characters: (1) brachium and antebrachium tuberculated, (2) ventrolateral folds with tubercles, (3) 20–23 irregularly aligned rows of keeled tubercles, (4) 31–34 paravertebral tubercles, (5) 29–34 ventral scales between ventrolateral folds, (6) no precloacal depression, (7) enlarged precloacofemoral scales in continuous series, (8) males with 20–24 precloacofemoral pores in wide Ʌ-shape, (9) enlarged post precloacal scales present, (10) 19–21 fourth toe subdigital lamellae, (11) enlarged transversely median subcaudals absent, (12) tail not prehensile, (13) tubercles extend along 71% of original tail length, and (14) the original tails reaching 147% of snout–vent length. We also provide an identification key to the bent toed gecko species that occur in the Wallacea region.

Keywords: Reptilia, oceanic dispersal, isolation, evolution, diversification




Awal Riyanto, Amir Hamidy and Jimmy A. McGuire. 2018. A New Bent-toed Gecko (Cyrtodactylus: Squamata: Gekkonidae) from the Island of Tanahjampea, South Sulawesi, Indonesia. Zootaxa. 4442(1); 122–136. DOI:  10.11646/zootaxa.4442.1.6


[Botany • 2018] Nine New Species of Hymenasplenium (Aspleniaceae) from Asia

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Hymenasplenium phamhoanghoi 

in Xu, Zhang, Lu, et al., 2018. 

Abstract
Nine new species of Hymenasplenium (Aspleniaceae) from Asia are here described based on both morphology and our recent molecular phylogenetics of the genus. Of the nine new species, H.chingii, H. denticulatum, H. sinense, H. speluncicola, and H. wangpeishanii are from southern China, whereas H. distans, H. ngheanense, H. phamhoanghoiand H. quangnamense are from Vietnam. These new species are morphologically similar to but distinguishable from those of the H. unilaterale s.l. group (H. apogamum, H. hondoense, and H. murakami-hatanakae). All except one new species were included in a recent phylogenetic analysis and were well supported as distinct lineages based on molecular data. All new species are illustrated and the information on their distributions, habitats, and major distinguishing characters is provided.

Keywords: Guangxi, Guizhou, limestone caves, Vietnam, Yunnan




Ke-Wang Xu, Liang Zhang, Ngan Thi Lu, Xin-Mao Zhou, Hai He, Thien Tam Luong, Ralf Knapp, Wen-Bo Liao and Li-Bing Zhang. 2018. Nine New Species of Hymenasplenium (Aspleniaceae) from Asia. Phytotaxa. 358(1); 1–25. DOI:  10.11646/phytotaxa.358.1.1

[Paleontology • 2018] Endocerids: Suspension Feeding Nautiloids?

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 endocerids with their filtering apparatus

in Mironenko, 2018. 
Reconstruction by Andrey Atuchin

ABSTRACT
For a long time all extinct cephalopods of the subclass Nautiloidea were considered as ecological analogues of the Recent Nautilus. Recently this view has been rejected: it is now known that among the nautiloids there were not only demersal predators but also epipelagic animals whose life-style and reproduction differed from those of the Nautilus. However, the habits of some nautiloid orders is still poorly understood. One of the most enigmatic cephalopods is the Early Paleozoic nautiloid order Endocerida. Endocerids differ from other nautiloids: they reached gigantic sizes (up to 9 meters), had a wide siphuncle tube and were widespread and numerous during the Ordovician. Since they were an important component of many Ordovician ecosystems, without the understanding of their habits and feeding strategies a correct reconstruction of these ecosystems is impossible. Until now, endocerids have been considered as dominant apex predators, however, this assumption is based on an analogy with the Nautilus mode of life, while the features of the structure of endocerid shells do not confirm this idea and furthermore contradict it. In this article, a new hypothesis is proposed and debated: according to it, the endocerids were planktotrophic cephalopods and the largest of them were giant suspension feeders.

KEYWORDS: Ordovician, Nautiloidea, Endocerida, suspension-feeding, plankton


Figure 2. Hypothetical reconstruction of endocerids with their filtering apparatus. A thin and expansible membrane stretched between their arms is based on the membrane in modern cirrate octopuses and Vampiroteutis.

Drawn by Andrey Atuchin, based on the sketch of the author.

Aleksandr A. Mironenko. 2018. Endocerids: Suspension Feeding Nautiloids? Historical Biology: An International Journal of Paleobiology.   DOI: 10.1080/08912963.2018.1491565

Missed It? | Full list of the 85 paleontological papers published this week go.shr.lc/2lKrKKr via @Paleowire


[Paleontology • 2018] Reanalysis of the Phylogenetic Status of Nipponosaurus sachalinensis (Ornithopoda: Dinosauria) from the Late Cretaceous of Southern Sakhalin

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Nipponosaurus sachalinensis Nagao, 1936

in Takasaki, Chiba, Kobayashi, et al., 2018
ニッポノサウルス || DOI: 10.1080/08912963.2017.1317766 


Abstract
Nipponosaurus sachalinensis is the only definitive lambeosaurine hadrosaurid from Sakhalin Island of Russia. Previous studies suggested it was a member of Lambeosaurini (derived lambeosaurines). However, its phylogenetic status within Lambeosaurini remains controversial. In addition, some studies argued the juvenile ontogenetic stage of the holotype and regarded Nipponosaurus as an invalid taxon. In order to solve these problems, its definite growth stage is determined through histological studies. Absence of a line of arrested growth, presence of osteons with large vascular spaces, and presence of primary bone remnants even in the highly modified regions of the femur confirm that the holotype was a juvenile. More than a hundred of the 350 characters used to determine the phylogenetic position of Nipponosaurus are ontogenetically variable characters based on the different ontogenetic stages of Hypacrosaurus stebingeri. Our phylogenetic analysis reveals that Nipponosaurus is a basal lambeosaurine hadrosaurid, much further down in the tree than previously suggested, and shows a polytomy with Blasisaurus and Arenyisaurus. This study also indicates that Nipponosaurus is a valid taxon because it possesses unique characters within the Lambeosaurinae (presence of massive surangular anterodorsal process, presence of lateral shelf of the dentary, and a relatively short ulna), which are independent of ontogeny.

Keywords: Dinosaur, Ornithopoda, Hadrosauridae, Nipponosaurus, ontogeny, histology



Cross section of a thighbone of Nipponosaurus (A) with an enlarged photo of the rectangular area (B). The latter shows the changing directions of the vascular canals.  



ニッポノサウルスの孤独 - GET AWAY TRIKE !
 
blogs.yahoo.co.jp/rboz_05/35175912.html   
Conclusions:
 Histological observations provide the first direct evidence that Nipponosaurus is an immature specimen. By comparing different ontogenetic stages of H. stebingeri and reviewing previous studies, up to 102 characters previously used in phylogenetic analyses are considered ontogenetically controlled within Hadrosauridae. Our phylogenetic analysis positions Nipponosaurus within a monophyletic clade of Arenysaurus and Blasisaurus, which has a sister clade relationship with the clade comprised of Parasaurolophini and Lambeosaurini. This newly recovered phylogenetic position supports a strong affinity of Asian and European lambeosaurids. The resulting relationships of this genus suggest that this taxon is valid, and represents one of the few hadrosaur specimens in Far East Asia.

Ryuji Takasaki, Kentaro Chiba, Yoshitsugu Kobayashi, Philip J. Currie and Anthony R. Fiorillo. 2018. Reanalysis of the Phylogenetic Status of Nipponosaurus sachalinensis (Ornithopoda: Dinosauria) from the Late Cretaceous of Southern Sakhalin. Historical Biology: An International Journal of Paleobiology.  5; 694-711.   DOI: 10.1080/08912963.2017.1317766

 ニッポノサウルスの孤独 - GET AWAY TRIKE ! - Yahoo!ブログ  blogs.yahoo.co.jp/rboz_05/35175912.html
#ブログ #その他自然科学 #鳥脚類
【動画】NスペPlus 7200万年前の巨大恐竜“むかわ竜”がよみがえる! - 世界でも珍しい全身骨格化石を手がかりに、“むかわ竜”の姿をよみがえらせました。 #むかわ竜 #恐竜 #化石  nhk.or.jp/special/plus/videos/20170522/index.html

Unraveling the mysteries of Nipponosaurus phys.org/news/2017-06-unraveling-mysteries-nipponosaurus.html via @physorg_com
Duck-Billed Dinosaur Is Japan’s Largest Complete Fossil asianscientist.com/2017/06/in-the-lab/largest-dinosaur-skeleton-nipponosaurus

    

[Botany • 2018] Argyreia gyrobracteata • Species Delimitation of Some Argyreia (Convolvulaceae) Using Phenetic Analyses: Insights from Leaf Anatomical Data Reveal A New Species from northeastern Thailand

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Argyreia gyrobracteata Traiperm & Chitchak

in Chitchak, Traiperm, Staples, et al., 2018. 
   DOI:  10.1139/cjb-2017-0108 

ABSTRACT
Argyreia Lour. is one of the most taxonomically complex genera of the morning glory family (Convolvulaceae). The number of named species is now 135, and new species are regularly being described. There are several species complexes that are morphologically similar and difficult to tell apart. Therefore, the aim of this study is to explore the species identification criteria for Argyreia, especially new sources for taxonomically informative characters. Ten accessions representing three morphologically similar Argyreia operational taxonomic units (OTUs) were collected and their anatomical characters were investigated using the leaf peeling technique and paraffin sectioning method. Anatomical character states were analyzed using two phenetic analysis methods: clustering analysis (CA) and principal component analysis (PCA). Three distinct clusters were clearly separated in both PCA and CA at the internal similarity coefficient of 0.48 with a high R-value of 0.89757. Nineteen effectively distinguishable character states were derived from the high loadings of the first two components. In conclusion, two of the separated groups were matched with known species, and the third separated group is here delineated as a new species. Therefore, a new species, Argyreia gyrobracteata Traiperm & Chitchak, is described and illustrated together with ecological data and a preliminary conservation assessment.

Keywords: cluster analysis, cryptic species, morphometrics, principal component analysis, species delimitation

Fig. 7. Argyreia gyrobracteata Traiperm & Chitchak sp. nov.:
 (A) flower in front view; (B) flower in side view; (C) interaction with an insect visitor, oriental carpenter bee (Xylocopa nasalis); (D) plant habit
(all photos taken by P. Rattanakrajang from live plants vouchered as P. Rattanakrajang et al. 104).

Argyreia gyrobracteata Traiperm & Chitchak, sp. nov. 

TYPE: Thailand. Ubon Ratchathani, Sirindhorn district, ..., in the edge of dipterocarp forest, August 2016, P. Rattanakrajang, N. Chitchak & P. Traiperm 110 (holotype BKF!; isotypes K!, QBG!)

DIAGNOSIS: The new species is similar to A. mekongensis in having a white campanulate corolla, but differs from that species by the linear-oblong to narrowly lanceolate bract shape (versus lanceolate or oblong-lanceolate), the curly or twisted bract orientation (versus falcate), the larger sepals, and the multicellular, uniseriate, villous trichomes restricted to a small, dense, triangular patch on the adaxial side of the filaments, above the insertion point of the filaments on the corolla tube (versus dispersed in a band 3–5 mm wide surrounding the free filament, above the insertion point on the corolla tube).
....

DISTRIBUTION: Known so far from discrete populations in two different districts within Ubon Ratchathani province, Thailand. One population is close to the border of Thailand–Laos and possibly A. gyrobracteata occurs across the border in Laos.

ETYMOLOGY: The specific epithet refers to the curly/twisted bracts of this species, which have not been observed in any other known species of Argyreia

 Natthaphong Chitchak, Paweena Traiperm, G. Staples, Pantamith Rattanakrajang and Pirada Sumanona. 2018. Species Delimitation of Some Argyreia (Convolvulaceae) Using Phenetic Analyses: Insights from Leaf Anatomical Data Reveal A New Species. Botany. 96(4); 217-233.  DOI:  10.1139/cjb-2017-0108 

[Botany • 2018] Odontochilus putaoensis (Orchidaceae) • A New Species from Myanmar

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Odontochilus putaoensis X.H. Jin, L.A. Ye & A.T. Mu

in Ye, Mu & Jin, 2018.  


Abstract
Odontochilus putaoensis, a new species of Orchidaceae, is described and illustrated from Putao Township, Kachin State, Myanmar. Odontochilus putaoensis is close to O. duplex, but can be easily distinguished from the latter by having a light yellow lip, a bisaccate hypochile with a small, erect, blade-like and emarginate callus within each sac, a mesochile with a pair of dentate-pectinate flanges and a bilobed epichile with a pair of widely diverging lobes that are erect and concave. An identification key to the Southeast Asian species of Odontochilus and colour photographs of O. putaoensis are provided. A preliminary conservation assessment according to the IUCN Red List Categories and Criteria is given for the new species.

Keywords: Cranichideae, Kachin State, key, new species, southeast Asia, terrestrial orchid

Figure 1. Odontochilus putaoensis X.H.Jin, L.A.Ye & A.T.Mu.
 A Habit of Odontochilus putaoensis B Front view of flower, showing lip epichile with a pair of erect and concave lobes C Hypochile of Odontochilus putaoensis, indicating small, erect, blade-like, emarginate callus within each sac D Dissected flower, showing pedicel and ovary, column, sepals, petals, lip and a pair of clavate pollinia E Dorsal view of flower, showing dorsal sepal forming a hood with petals. Photographed by X.H. Jin.

Odontochilus putaoensis X.H. Jin, L.A. Ye & A.T. Mu, sp. nov.

Diagnosis: Odontochilus putaoensis is similar to O. duplex, but can be easily distinguished from the latter by having a light yellow lip composed of a bisaccate hypochile with a small, erect, blade-like and emarginate callus within each sac, a mesochile with a pair of dentate-pectinate flanges and bilobed epichile with a pair of widely diverging lobes that are erect and concave.

Type: MYANMAR. Kachin State: Putao Township, Hponkanrazi Wildlife Sanctuary, subtropical, evergreen, broad-leaved, montane forest, 2000 m a.s.l., 20 October 2014, Xiaohua Jin et al, PT-ET 959 (Holotype, PE!).

....

Etymology: The new species is named after Putao, the northernmost town of Myanmar, near which it was discovered in a vast area of undisturbed mountain forest.

Distribution and habitat: Odontochilus putaoensis grows in shaded and damp humus in humid, broad-leaved, evergreen forest, at an elevation of about 1500-2000 m. At present, O. putaoensis is only known from the type locality.




Ye Lwin Aung, Aye Thin Mu and Xiaohua Jin. 2018. Odontochilus putaoensis (Cranichideae, Orchidaceae), A New Species from Myanmar. PhytoKeys. 103: 19-26.   DOI: 10.3897/phytokeys.103.25913

  

[Herpetology • 2018] Megophrys lancip • A Megophrys Kuhl and Van Hasselt (Amphibia: Megophryidae) from southwestern Sumatra, Indonesia

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Megophrys lancip 
 Munir, Hamidy, Farajallah & Smith, 2018 


Abstract
Megophrys lancip sp. nov., from the Bukit Barisan mountain range of southwestern Sumatra, Indonesia, is described on the basis of molecular and morphological evidence. The new species is distinguished from its congeners in Sumatra, Java, Borneo, and the Philippines by having a medium-sized body, snout with an extremely pointed rostral appendage, a medium-sized triangular eyelid appendage, a dorsolateral fold extending from just behind the eye to the groin, vomerine teeth, vocal slits, nuptial pads on the dorsomedial surface of the first and second fingers in males, and in lacking a Y, X, or H-shaped fold on the dorsum. Morphologically, the new species is most similar to M. montana, but it has a longer rostral appendage, shorter eyelid appendages, and less developed toe webbing. We also evaluate the taxonomic status of M. parallela and comment on the occurrence of M. aceras in Sumatra.

Keywords: Amphibia, Megophrys lancip, new species, Sundaland


Misbahul Munir, Amir Hamidy, Achmad Farajallah and Eric N. Smith. 2018.  A New Megophrys Kuhl and Van Hasselt (Amphibia: Megophryidae) from southwestern Sumatra, Indonesia. Zootaxa. 4442(3); 389–412. DOI: 10.11646/zootaxa.4442.3.3

[Botany • 2018] Begonia medogensis • A New Species of Begoniaceae from Western China and Northern Myanmar

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Begonia medogensis JianW.Li, Y.H.Tan & X.H.Jin

in Li, Tan, Wang, et al., 2018.

Abstract
Begonia medogensis JianW.Li, Y.H.Tan & X.H.Jin, a new species of Begoniaceae, is described and illustrated by colour photographs. Begonia medogensis is distributed in western China and northern Myanmar. It has erect stems, is tuberless, has many triangular to lanceolate leaves, base slightly asymmetric, margins remotely and irregularly denticulate; staminate flowers have 4 perianth segments, with outer 2 segments broadly ovate, inner 2 spathulate; pistillate flowers have 5 perianth segments, unequal, outer 4 broadly ovate, inner 1 spathulate. The new species is assigned to section Platycentrum and can easily be distinguished from the other species in the section.

Keywords: Begonia, Begonia medogensis, sect. Platycentrum, new species, China, Myanmar


Figure 1. Begonia medogensis JianW.Li, Y.H.Tan & X.H.Jin.
 A Habitat B–E Flowers F Pedicel and ovary (showing large wing) G Male flowers (face view) H Ovary (showing loculus) I Flowers J Dissection of female flower K Dissection of male flower L Leaves M Anther with filament (under dissection mirror, bar = 1 mm) N Female flower (face view).
(photographed by Jian-Wu Li).

Begonia medogensis JianW.Li, Y.H.Tan & X.H.Jin, sp. nov.

Diagnosis: Begonia medogensis is morphologically similar to B. goniotis, B. griffithiana, B. nepalensis and B. sandalifolia, but can be easily distinguished from them by having leaves ovate-lanceolate, 6.0–8.0 × 1.5–2.5 mm, base slightly asymmetric, margins remotely and irregularly denticulate; triangular to lanceolate stipules; staminate flowers with outer 2 segments broadly ovate, inner 2 spathulate; pistillate flowers with perianth segments unequal, outer 4 larger, broadly ovate, inner 1 smallest, spathulate; cylindroid ovary, larger wing oblong, apex truncate.

Type: CHINA. Tibet, Medog County, Beibeng town, semi-evergreen forest in a subtropical area, 29°15'09"N, 95°13'31"E. 1381 m a.s.l., 16 November 2017, flowering, Xiaohua Jin, Jianwu Li, Xilong Wang & Chengwang Wang 19331 (holotype: HITBC!, isotype: HITBC!, PE!, K!)


Distribution and habitat: This new species grows in subtropical areas in Beibeng town, Medog County, Tibet, China, at an elevation of 700–1400 m and in Putao district, Kachin state, Myanmar, at an elevation of 600–1200 m.

Etymology: The species is named after the holotype locality, Medog County, in Tibet, China.


 Jian-Wu Li, Yun-Hong Tan, Xi-Long Wang, Cheng-Wang Wang and Xiao-Hua Jin. 2018. Begonia medogensis, A New Species of Begoniaceae from Western China and Northern Myanmar. PhytoKeys.  103: 13-18.  DOI: 10.3897/phytokeys.103.25392



[Ornithology • 2018] Pelecanoides whenuahouensis • Analyses of Phenotypic Differentiations Among South Georgian Diving Petrel (Pelecanoides georgicus) Populations Reveal An Undescribed and Highly Endangered Species from New Zealand

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Pelecanoides whenuahouensis 
Fischer, Debski, Miskelly, Bost, Fromant, Tennyson, Tessler, Cole, Hiscock, Taylor & Wittmer, 2018

Whenua Hou Diving Petrel  ||   DOI:  10.1371/journal.pone.0197766 

Abstract
Unresolved taxonomy of threatened species is problematic for conservation as the field relies on species being distinct taxonomic units. Differences in breeding habitat and results from a preliminary molecular analysis indicated that the New Zealand population of the South Georgian Diving Petrel (Pelecanoides georgicus) was a distinct, yet undescribed, species. We measured 11 biometric characters and scored eight plumage characters in 143 live birds and 64 study skins originating from most populations of P. georgicus, to assess their taxonomic relationships. We analysed differences with principal component analyses (PCA), factorial ANOVAs, and Kruskal-Wallis rank sum tests. Results show that individuals from New Zealand differ significantly from P. georgicus from all other populations as following: 1) longer wings, 2) longer outer tail feathers, 3) deeper bills, 4) longer heads, 5) longer tarsi, 6) limited collar extent, 7) greater extent of contrasting scapulars, 8) larger contrasting markings on the secondaries, 9) paler ear coverts, 10) paler collars, and 11) paler flanks. Furthermore, we used a species delimitation test with quantitative phenotypic criteria; results reveal that the New Zealand population of P. georgicus indeed merits species status. We hereby name this new species Pelecanoides whenuahouensis sp. nov. Due to severe reductions in its range and the very low number of remaining birds (~150 individuals limited to a single breeding colony on Codfish Island/Whenua Hou) the species warrants listing as ‘Critically Endangered’. 

S1 Fig. Lateral view of the holotype of Pelecanoides whenuahouensis  (NMNZ OR.21058) (Johannes H. Fischer).

The new species of diving petrel, named Whenua Hou Pelecanoides whenuahouensis, is already marked as critically endangered. File size: 13.5 MB Attribution: Jake Osborne

Pelecanoides whenuahouensis sp. nov.  

Etymology: P. whenuahouensis is named after the name of Codfish Island in the Māori language/Te Reo Māori: Whenua Hou (pronounced 'fɛnua 'hou, meaning ‘new land’). This island hosts the only extant colony of this species. This name was selected by the Ngāi Tahu, the Māori people who still hold a genealogical, cultural, and spiritual connection to both the island and this species, which they consider a taonga (treasure).

Common name: We propose the English common name ‘Whenua Hou Diving Petrel’.

Generic placement: P. whenuahouensis clearly belongs in Pelecanoides (family: Pelecanoididae, order: Procellariiformes) based on a combination of black and white plumage, short, paddle-like wings, short tail, small and compact build, and bill morphology (short, broad based bill with hooked tip, a paraseptal process in nostrils, and gular pouch).

Diagnosis: P. whenuahouensis differs from P. garnottii, through bill morphology/coloration (a shorter, slimmer bill, with much smaller nostrils, the presence of lavender blue on the lower mandible, and a less well-defined paraseptal process (but both species have the paraseptal process placed at approximately 50%) and a smaller overall size (resulting in shorter wings, tarsi, and a much lower bodyweight). P. whenuahouensis, however, does appear to have a longer tail than P. garnottii. Furthermore, P. whenuahouensis exhibits 1) a much larger extent of contrasting ear coverts, 2) continuous and pure white scapulars, 3) a limited (light grey) collar, 4) much paler (light grey) flanks and axillaries, and 5) white underwings including primaries. In addition, P. whenuahouensis can also be readily distinguished from P. garnottii based on vocalisations.
......



Distribution: All known study skins of P. whenuahouensis originate from either Dundas Island, Enderby Island (both Auckland Islands, New Zealand), or Codfish Island, New Zealand. P. whenuahouensis remains extant only on Codfish Island, where it breeds in a minute (0.018 km2) strip of coastal, sandy foredunes in Sealers Bay. The historic distribution of P. whenuahouensis in New Zealand likely encompassed the Otago Peninsula on the South Island, Mason’s Bay on Stewart Island, Enderby and Dundas Islands on the Auckland Islands and the Chatham Islands.

The offshore distribution of P. whenuahouensis remains unknown. Prey species found in two specimens indicate that P. whenuahouensis forages on the edge of the continental shelf during the breeding season. The only documented P. georgicus record for Australia (Bellambi Beach, New South Wales) likely pertained to P. whenuahouensis, based on the reported biometrics (most notably a tail length of 41 mm), indicating at least considerable vagrancy potential, and perhaps a larger offshore distribution than previously assumed, as recently demonstrated in P. u. urinatrix.


Fig 6. Study skins of Pelecanoides georgicus from different populations (Johannes H. Fischer). (A) Dorsal view. (B) Ventral view. (C) Lateral view. SAO = NMNZ OR.18421; origin: South Georgia, U.K., South Atlantic Ocean. SIO = NMNZ OR.24768; origin: Heard Island, Australia, South Indian Ocean. NZ = NMNZ OR.21631; origin: Dundas Island, Auckland Islands, New Zealand. Note differences in bill depth (NZ having the highest/deepest), collar extent (SIO having the largest), extent of contrasting scapulars (NZ having the largest), and contrasting white markings on secondaries (NZ having the largest) among others.

Conclusion: 
Here, we provide evidence of the distinctiveness of the Whenua Hou Diving Petrel (Pelecanoides whenuahouensis sp. nov.; previously part of the South Georgian Diving Petrel P. georgicus complex), which is a ‘Critically Endangered’ species. The conservation status of this species has remained “hidden” to global conservation interests due to its inclusion in a polytypic “species”. New Zealand, however, maintains a national threat classification system and therefore, the dire situation of P. whenuahouensis has been acknowledged within New Zealand. Consequently, we advocate the continuing use of national threat classification systems, as in cases like this, it has complemented the global threat classification system, by protecting taxa for which the taxonomy is still unclear. In addition, we urge taxonomists to focus new research on polytypic species that are likely to include threatened taxa, for conservation efforts depend on species being a clear and single ecological unit.


Johannes H. Fischer, Igor Debski, Colin M. Miskelly, Charles A. Bost, Aymeric Fromant, Alan J. D. Tennyson, Jake Tessler, Rosalind Cole, Johanna H. Hiscock, Graeme A. Taylor and Heiko U. Wittmer. 2018. Analyses of Phenotypic Differentiations Among South Georgian Diving Petrel (Pelecanoides georgicus) Populations Reveal An Undescribed and Highly Endangered Species from New Zealand. PLoS ONE. 13(6): e0197766.  DOI:  10.1371/journal.pone.0197766

New diving petrel critically endangered  scimex.org/newsfeed/new-diving-petrel-critically-endangered

[Entomology • 2018] Lepidotrigona satun • A New Species of Lepidotrigona (Hymenoptera: Apidae) from Thailand with the Description of Males of L. flavibasis and L. doipaensis and Comments on Asymmetrical Genitalia in Bees

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Lepidotrigona satun Attasopa & Bänziger, 2018

in Attasopa, Bänziger, Disayathanoowat & Packer, 2018.

Abstract
We describe Lepidotrigona satun Attasopa and Bänziger new species from southern Thailand based upon associated males and females (workers). The new species is a member of the L. ventralis species group, which is otherwise represented in Thailand only by L. flavibasis and L. doipaensis. We also describe the males of the latter two species, associated with nests from close to their type localities in northern Thailand. Lepidotrigona doipaensis Schwarz and L. flavibasis (Cockerell) had previously often been misidentified as L. ventralis (Smith), a species confirmed only from Borneo. Based upon differences in male morphology, especially of the metasomal sterna, we conclude that the male described from Vietnam by Sakagami (1975) as belonging to L. flavibasis represents an undescribed species. Our findings support previous taxonomic studies that highlight the importance of including males in the differentiation of closely related species of meliponines and their association with workers. The three species whose males we describe have asymmetric penis valves with the asymmetry differentially developed among the three. We compare this genitalic asymmetry with that known from a different apid genus, Tarsalia.

Keywords: Hymenoptera, Asymmetry, Lepidotrigona satun n. sp., L. ventralis, stingless bees, taxonomy, Trigona


FIGURE 4. Lepidotrigona satun n. sp., dorsal habitus. (A) male holotype and (B) worker paratype.

Lepidotrigona satun Attasopa and Bänziger n. sp. 

Etymology. The specific epithet refers to the province in Thailand where the species was collected; it is a noun in apposition.

 Diagnosis. Lepidotrigona satun is a member of the“ventralis” species group based primarily on size: body and forewing length each less than 5 mm. It is the only species in the group known from the lower peninsula of Thailand. Males can be differentiated from those of the other two species of the “ventralis” group confirmed as occurring in Thailand (L. flavibasis and L. doipaensis) based upon external morphology as follows: margin of mesoscutum of L. satun with plumose, scale-like, yellow hairs (Fig. 4: A) (no such hairs in the other two species). S4 of L. satun is angularly emarginate apicomedially (Fig. 2: A1) (convex medially and bisinuate laterally in L. flavibasis, slightly concave in L. doipaensis). The apicosubmedial lobes of S5 in L. satun are apically rounded each with 4–7 thick, long setae (Fig. 2: A2) (the lobes are pointed in the other two species and bear only 1–2 setae which are very short in L. flavibasis (Fig. 2: B2) or with one very long and, if present, a second much shorter in L. doipaensis (Fig. 2: C2)). S5 gradulus does not touch the antecosta in L. satun (Fig. 2: A2) whereas it does touch it in the other two species, briefly in L. flavibasis (Fig. 2: B2) and extensively in L. doipaensis (Fig. 2: C2).
....

FIGURE 5. Lepidotrigona satun n. sp., lateral habitus. (A) male holotype and (B) worker paratype. 

 FIGURE 6. Lepidotrigona satun n. sp., head, frontal view. (A) male holotype and (B) worker paratype.

....


Final Comments on the Lepidotrigona ventralis species group. 
Our data clearly demonstrate that what has been considered by some to be a single (Ascher & Pickering 2017), albeit perhaps variable (Sakagami 1975), species termed L. ventralis, is a complex of species (as recognized by Rasmussen 2008) whose members are readily differentiable using pubescence coloration characteristics, morphological measurements and, where males are available, details of male metasomal sterna and genitalia. The male external metasomal sterna and the genital capsules of L. satun n. sp. provide excellent characters for species delimitation, and also permit the differentiation of other species in the L. ventralis group: L. flavibasis and L. doipaensis and the undescribed species thought to belong to the former by Sakagami (1975). We encourage others to make the, often considerable, effort required to find males of Meliponini from nests, as our data suggest they may often have more diagnostic species level characters than do the workers, as has been noted by others (Schwarz 1939; Sakagami 1975, 1978; Sakagami & Inoue 1978; Camargo & Moure 1994; Camargo et al. 2000; Gonzalez & Griswold 2011, 2012; Dollin et al. 2015; Halcroft et al. 2016; Engel et al. 2017b). However, we would argue against nest destruction in order to find them: all the males we describe here were collected as they left the nest entrance associated with conspecific nestmate workers. Lepidotrigona ventralis differs from the new species not only by morphology of the holotype as indicated in the original description by Smith (1857), Schwarz’s (1939) identification key (as L.ventralis s.s.), and the holotype examined by Rasmussen (2016, pers. comm. with H.B.), but also our examined museum specimens from the type locality and nearby areas, in which all the hairs on the dorsal surface of the metatibia are white. 

There are biogeographic differences between the new species and the others in the L. ventralis species group in Thailand. The new species’ nests were discovered from a low altitude area, 100 m a.s.l. in Satun province, which is around 480 km away from the Isthmus of Kra to the South. Kra is a biogeographically important region; it is an ecotone between the evergreen forests south of it and the forests with a marked dry season north of it (van Steenis 1950; Woodruff 2003). In contrast, L. doipaensis and L. flavibasis, for which type material and our own specimens agree, come from higher altitudes, of at least 500–1100 and 925–1700 m a.s.l. respectively in northern Thailand, some 1,300 km north of Satun. Moreover, L. ventralis itself is known only from the island of Borneo which is at least 1,200 km across the South China Sea from the type locality of the new species. Although L. ventralis s.s. has been recorded from several other countries, including Thailand (as listed in Rasmussen 2008), Schwarz (1939) never verified this species from anywhere except the type locality. All supposed L. ventralis s.s. H.B. has seen from Thailand were misidentified.


Korrawat Attasopa, Hans Bänziger, Terd Disayathanoowat and Laurence Packer. 2018. A New Species of Lepidotrigona (Hymenoptera: Apidae) from Thailand with the Description of Males of L. flavibasis and L. doipaensis and Comments on Asymmetrical Genitalia in Bees. Zootaxa. 4442(1); 63–82. DOI:  10.11646/zootaxa.4442.1.3

[Botany • 2018] Manihot takape (Euphorbiaceae) • A New Tuberous Subshrub from the Paraguayan Chaco

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Manihot takape  De Egea & Peña-Chocarro 
in De Egea Elsam, Carmen Peña-Chocarro, Mereles & Céspedes, 2018 

Abstract
Manihot takape De Egea & Peña-Chocarro, sp. nov. is described and illustrated as a new species from the Paraguayan Chaco. It was collected while carrying out fieldwork related to the study of the most important Wild Crop Relatives of the country’s flora. Morphological characteristics that differentiate this species from closely related taxa, as well as its habitat, geographical distribution and conservation status are provided.

Keywords: Paraguay, dry Chaco, Manihotae, endemism

Figure 1. Manihot takape.
A Habit (Krapovickas & Cristóbal 44224) B Pistillate flower with calyx open (Krapovickas & Cristóbal 44224) C Staminate flower (Aquino & Quarti 470) D Staminate flower with calyx split and open (Aquino & Quarti 470) E Dried capsule (J. De Egea et al. 1793) F Seed, ventral side (J. De Egea et al. 1793). Drawn by Laura Simón.

Manihot takape De Egea & Peña-Chocarro, sp. nov.
  
Diagnosis: Subshrubs 0.5−0.8(−1) m tall, all parts glabrous; stems branched from base, suberect to decumbent; petiole attachment basal to occasionally narrowly peltate (less than 0.2 cm from lamina base), lamina unlobed or shallowly to deeply 3(−5)−lobed, several intermediate states found in the same plant; inflorescence a cluster of 2−6 subspicate racemes 14−33 cm long; flowers creamy-white, occasionally reddish, glabrous; pistillate flowers geminate, long pedicellate, sepals distinct, disc plicate; staminate flowers numerous, subsessile, sepals connate 1/4 their length, disc lobulate; capsules light green, unwinged, smooth when fresh, rough when dried.
....

Figure 3. Manihot takape  (J. De Egea et al. 1793).
 A Habit B Uprooted plant C Roots in cross-section D–E Leaves - note the variability in leaf forms F Immature fruit.

Distribution and ecology: This species has been collected in dry areas of the Paraguayan Chaco, more specifically within the Departments of Boquerón and Presidente Hayes (Fig. 4). These areas are characterised by sandy and loose soils (regosols) resulting from silted palaeo-riverbeds of the Pilcomayo river delta. The species is frequent in open wooded savannahs, locally called espartillares, dominated by the grass Elionurus muticus (Spreng.) Kuntze (espartillo) and scattered with tree species such as Schinopsis cornuta Loes. (Anacardiaceae), Astronium fraxinifolium Schott (Anacardiaceae), Jacaranda mimosifolia D.Don (Bignoniaceae) and Tabebuia aurea Benth. & Hook.f. ex S.Moore (Bignoniaceae). Based on the data available so far, the restricted distribution of Manihot takape could represent an endemism of the dry Chaco. However, more surveys and collections will be needed to confirm the extension of the species distribution range.

Etymology: The specific epithet stems from the vernacular name takape (Guarani language). This word is used for a particular habitat characterised by a wooded savannah or open woodland (Bertoni 1940). The word is also applied to small woody plants (i.e. subshrubs). This is based on the word takã (twig or branch) and the suffix ‘pe’ (short or dwarf). Both meanings fit the newly described species of Manihot.


 Juana De Egea Elsam, María del Carmen Peña-Chocarro, Fátima Mereles and Gloria Céspedes. 2018. Manihot takape sp. nov. (Euphorbiaceae), A New Tuberous Subshrub from the Paraguayan Chaco. PhytoKeys. 103: 1-12. DOI:  10.3897/phytokeys.103.26307


[Entomology • 2018] Rhumosa n. gen. • A New Genus and Five New Species of Anostostomatidae (Orthoptera: Ensifera) from the Lesser Antilles

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Rhumosa macoucheriei
Hugel & Desutter-Grandcolas, 2018


Abstract
Most high volcanic islands of Lesser Antilles harbor one single genus of Anostostomatidae: Rhumosa n. genRhumosa bolognei n. gen. n. sp. in Guadeloupe, Rhumosa macoucheriei n. gen. n. sp. in Dominica, Rhumosa depazei n. gen. n. sp. in Martinique, Rhumosa admiralrodneyei n. gen. n. sp. in Saint Lucia, Rhumosa captainblighei n. gen. n. sp., in Saint Vincent. These species are restricted to well preserved rainforests; species from northern islands apparently occurring at higher elevation than species of southern islands. The distribution and generic position of Rhumosa n. gen. species is discussed, as well as the generic position of Lutosa cubaensis (Haan, 1843).

Keywords: Orthoptera, endemism, Caribbean, Windward islands, Leeward islands, latitudinal gradients


Rhumosa macoucheriei n. gen. n. sp.  
Genus Rhumosa n. gen.

Type species. Rhumosa bolognei n. gen., n. sp, here designated.

Distribution. Central America, Caribbean, Lesser Antilles.


Derivatio nominis. This genus is named after the French word for rum, all species of the genus displaying the color of dark rum, and coming from a major rum-producing region. All species described in the present article are named after a rum produced near their respective type locality. We wish to emphasise that this is intended in the spirit of honouring local expertise in rum production, and the flavour of local rums, not the people after whom these rums are named (some of whom, paradoxically, may have been unsavoury characters).


Sylvain Hugel and Laure Desutter-Grandcolas. 2018. A New Genus and Five New Species of Anostostomatidae from the Lesser Antilles (Orthoptera: Ensifera). Zootaxa. 4425(3); 511–526. DOI:  10.11646/zootaxa.4425.3.5

[Herpetology • 2018] Speciation in the Mountains and Dispersal by Rivers: Molecular Phylogeny of Eulamprus Water Skinks and the Biogeography of Eastern Australia

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Top left is a topographic map of the Australian continent (red = high, green = low, major drainage lines = white). 
Bottom left map shows finer‐scale drainage lines (Global Map Australia 1M 2001, Geoscience Australia) overlain on to a digital elevation model image (Shuttle Radar Topography Mission) where light grey equates to areas of high elevation, and dark grey equates to areas of low elevation. 

Right panel shows the distribution of the five Eulamprus species; E. quoyii (A, purple), E. kosciuskoi and E. leuraensis (B, yellow and red, respectively), E. heatwolei (C, green) and E. tympanum (D, pink). 
(Photos: Stephen Zozaya & Stewart Macdonald).

in Pepperm, Sumner, Brennan, et al., 2018.
  DOI: 10.1111/jbi.13385  


Abstract
Aim: 
To develop a robust phylogeny for the iconic Australian water skinks (Eulamprus) and to explore the influence of landscape evolution of eastern Australia on phylogeographic patterns.

Location: Eastern and south‐eastern Australia.

Methods: 
We used Sanger methods to sequence a mitochondrial DNA (mtDNA) locus for 386 individuals across the five Eulamprus species to elucidate phylogeographic structure. We also sequenced a second mtDNA locus and four nuclear DNA (nDNA) loci for a subset of individuals to help inform our sampling strategy for next‐generation sequencing. Finally, we generated an anchored hybrid enrichment (AHE) approach to sequence 378 loci for 25 individuals representing the major lineages identified in our Sanger dataset. These data were used to resolve the phylogenetic relationships among the species using coalescent‐based species tree inference in *BEAST and ASTRAL.

Results: 
The relationships between Eulamprus species were resolved with a high level of confidence using our AHE dataset. In addition, our extensive mtDNA sampling revealed substantial phylogeographic structure in all species, with the exception of the geographically highly restricted E. leuraensis. Ratios of patristic distances (mtDNA/nDNA) indicate on average a 30‐fold greater distance as estimated using the mtDNA locus ND4.

Main conclusions: 
The major divergences between lineages strongly support previously identified biogeographic barriers in eastern Australia based on studies of other taxa. These breaks appear to correlate with regions where the Great Escarpment is absent or obscure, suggesting topographic lowlands and the accompanying dry woodlands are a major barrier to dispersal for water skinks. While some river corridors, such as the Hunter Valley, were likely historically dry enough to inhibit the movement of Eulamprus populations, our data indicate that others, such as the Murray and Darling Rivers, are able to facilitate extensive gene flow through the vast arid and semi‐arid lowlands of New South Wales and South Australia. Comparing the patristic distances between the mitochondrial and AHE datasets highlights the continued value in analysing both types of data.

Keywords: anchored hybrid enrichment, Eastern Australia, gene flow, great dividing range, Murray–Darling Basin, Newer Volcanics Province


Figure 1: Phylogenomic analyses provide consistent support of interspecific relationships among Eulamprus water skinks, regardless of reconstruction method. Lizard images to the left depict the relative size and appearance of each species. The first and third trees in this figure were constructed using anchored phylogenomics data (nuclear exons—nDNA), resulting in identical topologies between the full (378) and filtered (281) datasets. On these two trees (nDNA starBEAST and nDNA ASTRAL), nodes labelled with a white circle denote fully supported relationships (posterior probability = 1, bootstrap = 100), with all other nodes labelled according to estimated support. Note terminal branch lengths in ASTRAL analysis are fixed, and not to scale. The middle phylogeny has been reconstructed using the mitochondrial locus ND4 (mtDNA), with nodes labelled by a red circle constrained to match the nuclear species tree topology. Intraspecific relationships of the mtDNA tree remained unconstrained, and are used to illustrate the sampling depth and relative diversity of each species. Labels on the far right of this figure match the nDNA ASTRAL tree, run on phased haplotype data, where each taxon is represented by two terminal tips representing the phased alleles. Sampling data for each individual can be found in Table S1. Colours designated for each species correspond to sampling maps in Figure 2, and intraspecific mtDNA phylogenies in supplemental materials (Figures S1–S4)

Figure 2: Top left is a topographic map of the Australian continent (red = high, green = low, major drainage lines = white). Bottom left map shows finer‐scale drainage lines (Global Map Australia 1M 2001, Geoscience Australia) overlain on to a digital elevation model image (Shuttle Radar Topography Mission) where light grey equates to areas of high elevation, and dark grey equates to areas of low elevation. Thick dark grey lines indicate biogeographic barriers mentioned in the text. Stippled blue lines indicate the major rivers; Darling River (DR), Lachlan River (LR), Murrumbidgee River (MBR) and Murray River (MR). Coloured symbols represent sampling localities for two clades that use rivers to facilitate long‐distance gene flow. Purple triangles indicate one of the E. quoyii clades, while green circles representing our sample localities for one of the E. heatwolei clades. State boundaries are shown by thin grey lines. QLD = Queensland, SA = South Australia, NSW = New South Wales, ACT = Australian Capital Territory, VIC = Victoria.

Right panel shows the distribution of the five Eulamprus species; E. quoyii (A, purple), E. kosciuskoi and E. leuraensis (B, yellow and red, respectively), E. heatwolei (C, green) and E. tympanum (D, pink). Different coloured shapes on each map refer to major clades within each species, whereas small black + symbols refer to museum locality records. Relevant biogeographic barriers from the larger map to the left have been overlain 
(Photo credit: Stephen Zozaya & Stewart Macdonald).


Mitzy Pepperm, Joanna Sumner, Ian G. Brennan, Kate Hodges, Alan R. Lemmon, Emily Moriarty Lemmon, Garry Peterson, Daniel L. Rabosky, Lin Schwarzkopf, Ian A. W. Scott, Glenn Shea and J. Scott Keogh. 2018. Speciation in the Mountains and Dispersal by Rivers: Molecular Phylogeny of Eulamprus Water Skinks and the Biogeography of Eastern Australia. Journal of Biogeography. DOI: 10.1111/jbi.13385

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