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Wednesday, June 10th, 2020

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    12:24a
    [Botany • 2020] Winitia thailandana • Generic Status of Winitia (Annonaceae, Miliuseae) Reaffirmed by Molecular Phylogenetic Analysis, Including A New Species and A New Combination from Thailand

    แสดทักษิณา Winitia thailandana Chaowasku & Aongyong

    in Chaowasku, Aongyong, Damthongdee, et al., 2020.
    DOI: 10.5852/ejt.2020.659
     facebook.com/MartySiamocananga

    Abstract
    The generic status of Winitia Chaowasku (Annonaceae Juss., Miliuseae Hook.f. & Thomson) is reaffirmed by an extensive phylogenetic reconstruction using seven plastome regions (matK, ndhF, rbcL, ycf1 exons; trnL intron; psbA-trnH, trnL-trnF intergenic spacers) and including, among others, seven accessions of Winitia plus two accessions of its sister group, Stelechocarpus Hook.f. & Thomson. The results disclosed a maximally supported clade of Winitia, as well as of Stelechocarpus. The sister relationship of the two genera is still rather poorly supported and the branch uniting them is very short, whereas the branches leading to Winitia and to Stelechocarpus are relatively long, corresponding to their considerable morphological differences. Additionally, in Miliuseae there is a particular indel of eight continuous base pairs in the trnL-trnF intergenic spacer potentially diagnostic for generic discrimination, i.e., members in the same genus possess the same indel structure (absence or presence of a gap), and this indel differentiates Winitia from StelechocarpusWinitia cauliflora (Scheff.) Chaowasku appears polyphyletic and Winitia longipes (Craib) Chaowasku & Aongyong comb. nov. based on Stelechocarpus longipes Craib is consequently proposed. Furthermore, our phylogenetic data support a new species, Winitia thailandana Chaowasku & Aongyong sp. nov. from southern Thailand, which is described and illustrated. A key to genera in the sageraeoid clade (Sageraea-Winitia-Stelechocarpus) and a key to the four species of Winitia are provided.

    Keywords: identification key; Malmeoideae; phylogenetics; systematics; taxonomy

    Taxonomy
    Order Magnoliales Juss. ex Bercht. & J.Presl
    Family Annonaceae Juss., nom. cons.
    Tribe Miliuseae Hook.f. & Thomson

    Genus Winitia Chaowasku

    Winitia longipes (Craib) Chaowasku & Aongyong comb. nov.

    Stelechocarpus longipes Craib, The Journal of the Natural History Society of Siam 6: 43 (Craib 1923). 
    Type: THAILAND · Khao Rum [Nakhon Si Thammarat Prov.]; fl; Native Collector s.n. (Herb. Eryl Smith 643); holotype: K[K000382080]; isotype: BK.

    (A-B) Flowers of Winitia thailandana Chaowasku & Aongyong sp. nov.  Flower.

    (lower) Flowers of Winitia cauliflora (Scheff.) Chaowasku and 
    Winitia longipes (Craib) Chaowasku & Aongyong comb. nov.  


    Fig. 4. Flowers and floral organs of Winitia thailandana Chaowasku & Aongyong sp. nov.
    A–B. Flower. C. Flower with petals removed. D. Stamen, abaxial (above) and adaxial (below) sides. E. Back side of flower, showing sepals (abaxial side). 
    A, B from Gardner & Sidisunthorn ST0817 (L), photographs by S. Gardner; C–E from Aongyong 9 (CMUB).

    Winitia thailandana Chaowasku & Aongyong sp. nov. 

    Diagnosis:Morphologically similar to Winitia expansa, differs by having a non-glaucous appearance on the petal adaxial surface (glaucous in W. expansa) and shallow pits on the adaxial surface of the inner petals (no pitted structures in W. expansa). Moreover, its inflorescences are mostly clustered on large roots and at the unswollen base of trunks, whereas the inflorescences of W. expansa are mostly clustered at the swollen base of trunks. 

    Etymology: Named after Thailand, a country where this species is endemic. 

         


    Tanawat Chaowasku, Kithisak Aongyong, Anissara Damthongdee, Hathaichanok Jongsook and David M. Johnson. 2020. Generic Status of Winitia (Annonaceae, Miliuseae) Reaffirmed by Molecular Phylogenetic Analysis, Including A New Species and A New Combination from Thailand. European Journal of Taxonomy. 659; 1–23. DOI: 10.5852/ejt.2020.659

          

    แสดทักษิณา Winitia thailandana Chaowasku & Aongyong พืชชนิดใหม่ของโลก พบที่เขาหินปูนจังหวัดสุราษฎร์ธานีเท่านั้น ดอกมีความคล้ายชมพูภิรมย์ Winitia expansa Chaowasku ซึ่งพบที่จังหวัดพัทลุง นอกจากนี้ยังพบว่างำเงาะจากประเทศไทย แตกต่างจากตัวอย่างต้นแบบของชื่อ Winitia cauliflora จึงได้ชื่อใหม่ว่า Winitia longipes (Craib) Chaowasku & Aongyong ซึ่งย้ายมาจากสกุล Stelechocarpus

    1:33a
    [Crustacea • 2020] On the Taxonomy of the Endemic Inle Lake Crab, Inlethelphusa acanthica (Kemp, 1918) (Brachyura: Potamidae) of Myanmar

    Inlethelphusa acanthica (Kemp, 1918)

    in Ng, Mar & Yeo, 2020. 
     RAFFLES BULLETIN OF ZOOLOGY. 68

    Abstract
     The potamid freshwater crab, Inlethelphusa acanthica (Kemp, 1918), is endemic to Inle Lake, in Shan state, Myanmar, and was hitherto known only from the types and several small specimens collected in the 1930s. The species, the type of Inlethelphusa Yeo & Ng, 2007, is redescribed from a good series of fresh specimens. The taxonomy of the species is discussed and variations in the armature of the carapace anterolateral margin, male pleon, chela, as well as the male first gonopod structure are documented. Significantly, the male first gonopod of smaller specimens has the terminal segment straight and more cylindrical, with the tip truncate or weakly bifurcated, in contrast to that of larger males, which is more elongate, with the distal part gently curved upwards and the tip sharp. 

    Key words: Decapoda, freshwater crab, redescription, variation, diagnostic characters, wetland conservation


    Fig. 8. Inlethelphusa acanthica (Kemp, 1918), female (40.4 × 28.5 mm) (ZRC 2019.1794). Colour in life. Photograph: P.Y.C. Ng.


    TAXONOMY
    Family Potamidae Ortmann, 1896
    Subfamily Potamiscinae Bott, 1970 sensu Yeo & Ng, 2004

    Inlethelphusa Yeo & Ng, 2007
    Type species. Potamon (Potamon) acanthicum Kemp, 1918, 
    by monotypy.

    Diagnosis. Carapace broader than long, relatively low; dorsal surface gently convex; epigastric cristae low, distinct, not sharp, anterior to postorbital cristae, distinctly separated from postorbital cristae by groove; postorbital cristae low, blunt, not confluent with epibranchial teeth; external orbital angle well developed, separate from rest of anterolateral margin by deep cleft; epibranchial tooth well developed, spiniform; anterolateral margins prominently serrated, with anterior serrations larger; antennular fossae subrectangular, broad; epistome posterior margin with low but distinct median tooth; endostomial ridge absent. Third maxilliped with long exopod, with long flagellum. Ambulatory legs short; merus without subdistal spine on dorsal margin. Suture between male thoracic sternites 2 and 3 distinct; thoracic sternite 8 completely separated by a longitudinal medial line; sternopleonal cavity almost reaching imaginary line joining anterior edges of cheliped bases; male pleon triangular. G1 subterminal segment with distal third bent outward, appears neck-like, being distinctly tapered or constricted; G1 terminal segment slender, elongate, tubular to tapering, tip truncate or sharp, upcurved, dorsal flap absent. G2 longer than G1, distal segment distinctly less than half length of basal segment.

    Inlethelphusa acanthica (Kemp, 1918) (Figs. 1–8) 

    Potamon (Potamon) acanthicum Kemp, 1918: 85, fig. 2, pl. 24 figs. 3, 4. 
    Lobothelphusa acanthia – Bott, 1970: 150; Yeo & Ng, 1999: 640. 
    Inlethelphusa acanthica – Yeo & Ng, 2007: 283, fig. 6; Ng et al., 2008: 163.

    Ecological notes. Kemp (1918: 89) notes that this “is apparently the only crab that makes its way into the central region of the Inle Lake, on the bottom of which it is occasionally found. It is more abundant among the roots of the floating islands at the edge of the lake, and also frequents small hill-streams.” The series of recent specimens (ZRC 2018.1370) were from the centre of the lake and were collected in the nets of fishermen. Two other specimens (ZRC 2018.0736) were from small streams flowing into Inle Lake. Nothing else is known about its ecology. This potamid species occupies a lacustrine niche in northern Indochina that, in other parts of Southeast Asia, is normally filled by crabs of the family Gecarcinucidae Rathbun, 1904. The chelae of I. acanthica are gaped in large males and females (Fig. 3D, E), similar to those of the analagous lentic gecarcinucids found in swamps and lakes in Thailand and Cambodia, and are not specifically adapted for feeding on molluscs (see Ng & Naiyanetr, 1993; Ng, 1995). In ancient lakes in Sulawesi, molluscivorous species have large molariform teeth at the base of the gaping fingers (see Chia & Ng, 2006; Schubart & Ng, 2008), while there is no evidence of incipient development or evolution of any such molariform teeth in I. acanthica.



     Peter K. L. Ng, Win Mar and Darren C. J. Yeo. 2020. On the Taxonomy of the Endemic Inle Lake Crab, Inlethelphusa acanthica (Kemp, 1918) (Crustacea: Brachyura: Potamidae) of Myanmar. RAFFLES BULLETIN OF ZOOLOGY. 68; 453–463.  

           

    1:34a
    [Paleontology • 2020] Dietary Palaeoecology of An Early Cretaceous Armoured Dinosaur (Ornithischia; Nodosauridae) Based on Floral Analysis of Stomach Contents

    Borealopelta markmitchelli Brown, et al., 2017

    in Brown, Greenwood, Kalyniuk, et al., 2020. 
     Illustration by Julius Csotonyi.

     Abstract
    The exceptionally well-preserved holotype of the armoured dinosaur Borealopelta markmitchelli (Ornithischia; Nodosauridae) from the Early Cretaceous (Clearwater Formation) of northern Alberta preserves a distinct mass within the abdominal cavity. Fourteen independent criteria (including: co-allochthony, anatomical position, gastroliths) support the interpretation of this mass as ingested stomach contents—a cololite. Palynomorphs in the cololite are a subset of the more diverse external sample. Analysis of the cololite documents well-preserved plant material dominated by leaf tissue (88%), including intact sporangia, leaf cross-sections and cuticle, but also including stems, wood and charcoal. The leaf fraction is dominated (85%) by leptosporangiate ferns (subclass Polypodiidae), with low cycad–cycadophyte (3%) and trace conifer foliage. These data represent the most well-supported and detailed direct evidence of diet in an herbivorous dinosaur. Details of the dietary palaeoecology of this nodosaur are revealed, including: selective feeding on ferns; preferential ingestion of leptosporangiate ferns to the exclusion of Osmundaceae and eusporangiate ferns such as Marattiaceae; and incidental consumption of cycad–cycadophyte and conifer leaves. The presence of significant (6%) charcoal may represent the dietary use of recently burned conifer forest undergoing fern succession, early evidence of a fire succession ecology, as is associated with many modern large herbivores.

    Keywords: cololite, Ankylosauria, diet, Canada, Clearwater Formation, Cretaceous


    Figure 1. Location of abdominal mass, including stomach contents (cololite), within the well-preserved nodosaur Borealopelta markmitchelli (TMP 2011.033.0001).
    Photograph (a) and scientific line drawing (b) of the specimen in dorsal view. Schematic drawing (c) of specimen showing position and extent of abdominal mass, as well as extrapolated body outline. Inset (d) of i, showing close up photograph of dorsal view of posterior margin of abdominal mass. Inset (e) of ii, showing detailed map of extent of abdominal mass. (f) Schematic drawing of Kunbarrasaurus ieversi (GM F18101) scaled to (c), showing relative size and positon of cololite. Solid orange, observed cololite; hatched orange, inferred cololite. A, anterior; L, lateral. Scale bars in (a,b,c,f) are 1 m, and in (d,e) are 10 cm.

    Figure 4. Palaeobotanical elements observed on the cololite histological slides.
    (a) Clubmoss (Lycopodiopsida) sporangium type C with Echinatisporis sp. (Lycopodiaceae or Selaginellaceae), (b–d) isolated leptosporangiate fern sporangia with spores in situ, (b) sporangium type F with Cicatricosisporites sp. (Schizaeaceae), (c) sporangium type E with Deltoidospora sp. (fam. indet.) or Biretrisporites sp. (Matoniaceae-Cyatheaceae-Dicksoniaceae), (d) sporangium type A (spore indet.), (e) charcoal/blackened plant fragment, (f) square stem cross-section, (g) cuticle without stomata displaying sinuous lateral cell walls (Type 1), (h) leaf cross section, (i) cuticle with stomata and sinuous lateral cell walls (Type 2), (j) cuticle with stomata Type B, (k) thickened cells/ sclerenchyma, (l) cuticle with stomata (Type A), (m) twig cross-section showing annual rings. (c,d,j,k) scale bars = 40 µm; (a,b,e,g,h,i,l) scale bars = 100 µm; (m,f) scale bars = 400 µm.

    Figure 6. Composition of the cololite determined from microscopy of thin sections.
    (a) Breakdown of slide area (slide 2 only) occupied by gastroliths, matrix, plant fragments and void space as only slide 2 was scored for the non-plant composition. Breakdown of the plant fragment composition only (across all slides) into tissue types (b) and leaf specific tissue types. Breakdown of plant fragments (across all slides) into broad taxonomic groups (c).

    Figure 3. Gates Formation (Grand Cache Member) plant fossils from central Alberta.
    (a) Pterophyllum sp. (TMP 1990.027.0021), (b) Sphenopteris sp. (TMP 1981.055.0103), (c) Gleichenites sp. (USask 925-7273), (d) Ginkgoites sp. (TMP 1990.027.0020), (e) Taeniopteris sp. (TMP 1981.055.0006), (f) Cladophlebis sp. (top left) and Elatides sp. (arrow) (TMP 1981.055.0012), (g) Elatides curvifolia (TMP 2015.006.0469), (h) Sagenopteris sp. (TMP 1981.055.0033), (i) Equisetites sp. (USask 750-7557), (j) conifer cone (TMP 1981.055.0044) and (k) Coniopteris sp. (TMP 1981.055.0058). Scale bars = 1 cm.

    Life reconstruction of the Cretaceous Period armoured dinosaur Borealopelta markmitchelli, which lived 110 million years ago in what is now Alberta, eating ferns.
     Royal Tyrrell Museum of Palaeontology. Illustration by Julius Csotonyi.


    Caleb M. Brown, David R. Greenwood, Jessica E. Kalyniuk, Dennis R. Braman, Donald M. Henderson, Cathy L. Greenwood and James F. Basinger. 2020. Dietary Palaeoecology of An Early Cretaceous Armoured Dinosaur (Ornithischia; Nodosauridae) Based on Floral Analysis of Stomach Contents.  Royal Society Open Science.   DOI: 10.1098/rsos.200305 

    A Nodosaur’s Last Meal
     The world’s best-preserved armoured dinosaur, the nodosaur Borealopelta markmitchelli, continues to answer important questions about its biology and behaviour.

    2:00a
    [Mammalogy • 2020] Uncovering the Species Diversity of Subterranean Rodents at the End of the World: Three New Species of Patagonian Tuco-tucos (Rodentia, Hystricomorpha, Ctenomys)

    Holotype of Ctenomys bidaui n. sp. (CFA-MA 11867). 
    Skins of the holotypes of Ctenomys bidaui n. sp. (A, B), Ctenomys contrerasi n. sp. (C, D), and Ctenomys thalesi n. sp. (E, F)
     Teta & D’Elía​, 2020

    Abstract
    Ctenomys Blainville 1826 is one of the most diverse genera of South American caviomorph rodents. Currently, six species of this genus are reported from Patagonia, south of 42°S. In this contribution, we assessed the taxonomic status of several populations from eastern and central Chubut province, northern Patagonia. Based on phylogenetic analyses of DNA sequences, morphology assessment (qualitative and quantitative), and previously published karyological data, we describe three new species of this genus, one formed by two subspecies, endemic to northern Patagonia. In addition, we include C. coyhaiquensis Kelt and Gallardo 1994 into the synonymy of C. sericeus J.A. Allen 1903. Finally, we discussed the need for additional integrative approaches, including field collection of specimens, to better understand the diversity of this highly speciose rodent genus.


    Figure 4: Skins of the holotypes of Ctenomys bidaui n. sp.Ctenomys contrerasi n. sp., and Ctenomys thalesi n. sp.
    Dorsal (A, C, E) and ventral (B, D, F) views of the skins of the holotypes of Ctenomys bidaui n. sp. (A, B; CFA-MA 11867), C. contrerasi n. sp. (C, D; CFA-MA 11853), and C. thalesi n. sp. (E, F; CFA-MA 11849).

    Figure 5: Holotype of Ctenomys bidaui n. sp. (CFA-MA 11867).
    Dorsal (A), ventral (B) and lateral (C) views of the skull and labial view of the mandible (D) and selected cranial traits (E–J) of the holotype of Ctenomys bidaui n. sp. (CFA-MA 11867). E: nasals (nl) and premaxillae (pm); F: interparietal (ip); G; lateral view of the zygomatic arch; H: incisive (fi) and interpremaxillary (fh) foramina; I: tympanic bullae (tb) in posterolateral view; J: condyloid process (clp) of the mandible in dorsal view.
    Other abbreviations: fr, frontals; mr, masseteric ridge; pp, paraoccipital process; ppj, postorbital process of jugal; va, ventrolateral apophysis of the postcondyloid process. Scale = 5 mm.

    Ctenomys bidaui n. sp.
     Bidau’s tuco-tuco
    Tuco-Tuco de Bidau

    Morphological diagnosis—A medium-sized tuco-tuco of the C. magellanicus species group with moderately differentiated dorsal and ventral colorations; dorsum Light Brownish Olive to Brownish Olive; venter Pale Olive Buff with Gray colored basal hairs. Skull strongly built; interorbital processes of frontals slightly developed; zygomatic arches robust; premaxillo-frontal suture at the level of the naso-frontal suture; interparietal broad and short; incisive foramina moderately short and broad, recessed in a common fossa of straight outer borders and incompletely separated by a bony septum; interpremaxillary foramen large; auditory bullae inflated and ovate.

    Distribution—Known only from three localities near coastal areas of Península de Valdés, Chubut, Argentina (Fig. 1). Possibly, also correspond to this species the late Holocene fossil remains referred by Udrizar Sauthier & D’Agostino (2017) from this same general area.

    Etymology—We named this species in honor of the late Claudio J. Bidau (1953-2018), an Argentinian biologist with an extensive and varied scientific production, of which an important fraction is aimed to elucidate the complex evolutionary history of the genus Ctenomys. Claudio was a much-appreciated member of the South American community of mammalogists where he is well remembered. The species name is a patronym in the genitive singular.


    Ctenomys contrerasi n. sp.
    Contreras’tuco-tuco
    Tuco-Tuco de Contreras

    Morphological diagnosis—A small to medium sized tuco-tuco of the C. magellanicus species group with dorsal and ventral colorations moderately differentiated; dorsum Brownish Olive to Olive or Tawny Olive; venter Pale Olive Buff with Gray colored basal hairs. Skull moderately robust, interorbital region with posteriorly divergent outer margins; premaxillo-frontal suture placed slightly to well behind from the naso-frontal suture; zygomatic arch thin to moderately robust, with slightly developed postorbital and mandibular processes of jugal and a conspicuous zygomatic depression; interparietal completely fused; incisive foramina moderately long and narrow, recessed in a common fossa of straight to slightly convex outer borders and completely separated by a thin bony septum; interpremaxillary foramen small to large; paraoccipital process fan-shaped; auditory bullae inflated, and pyrifom.

    Distribution—This species has an apparently disjunct distribution, being recorded at four localities close to the Atlantic coast, between the Chubut river in the south and the Ameghino Isthmus to the north, and other two populations in west-central Chubut, south of the Chubut river (Fig. 1). Both distributional areas are about 335 km apart.

    Etymology—This species of Ctenomys is named in honor of Julio R. Contreras (1933-2017), an Argentinean mammalogist and ornithologist who dedicated more than 45 years of his life to the study of the taxonomy, systematics, and biogeography of the genus Ctenomys (see Teta & Ríos, 2019). Contreras described more than a dozen of new species of tuco-tucos, both from Argentina and Paraguay. Together with C. Bidau (Contreras & Bidau, 1999), he authored one of the first attempts to summarize the complex evolutionary history of this genus, proposing a general hypothesis about its diversification. The species name is a patronym in the genitive singular.

    Ctenomys contrerasi contrerasi n. subsp.

    Ctenomys contrerasi navonae n. subsp.

    Etymology—This subspecies of Ctenomys is named in honor of our colleague and friend Graciela T. Navone, an Argentinean parasitologist with a large career studying small mammal endoparasites. Graciela is also a prominent and active member of the Sociedad Argentina para el Estudio de los Mamíferos (SAREM). The species name is a patronym in the genitive singular.


    Ctenomys thalesi n. sp.
     Thales’s tuco-tuco
    Tuco-Tuco de Thales

    Morphological diagnosis— A small-sized tuco-tuco of the C. magellanicus species group with dorsal and ventral coloration moderately differentiated; dorsum Light Brownish Olive; venter Pale Olive Buff with gray colored basal hairs. Skull moderately robust, interorbital region with posteriorly divergent outer margins; premaxillo-frontal suture placed slightly behind the naso-frontal suture; zygomatic arch thin, with slightly developed postorbital and mandibular processes of jugal and a conspicuous zygomatic depression; interparietal completely fused; incisive foramina moderately short and narrow, recessed in a common fossa of nearly convex outer borders and completely separated by a thin bony septum; interpremaxillary foramen small to absent; paraoccipital process hook-shaped; auditory bullae inflated, and pyrifom.

    Distribution— Known only from two localities on northeastern Chubut province, close to the Atlantic coast, south of Chubut river (Fig. 1).

    Etymology— We name this species in honor of Thales Renato Ochotorena de Freitas, a Brazilian geneticist who leads a productive research program mostly centered on Brazilian species of Ctenomys, covering among others, aspects of taxonomy, cytogenetics, speciation, phylogeography, and conservation genetics. The species name is a patronym in the genitive singular.


    Ctenomys sericeus Allen, 1903
    Silky tuco-tuco
    Tuco-Tuco sedoso

    Morphological diagnosis—pelage short, soft, and glossy (Fig. 5S, on Data S2); general color above Olive Brown to Sepia strongly varied with Black, the hairs being Dark Gray for the basal three fourths, then banded narrowly with pale Yellowish Brown, and tipped with Black; top of nose and top of head like median dorsal region, which is darker than the sides, sometimes forming a dark median dorsal band extending from the nose to the base of the tail; flanks lighter than dorsum and venter Isabella; ears very small, blackish; upper surface of feet grayish to yellowish; tail Tawny Olive, with a median dusky stripe along the apical half of the upper surface. Skull moderately robust (Fig. 6S, on Data S2), interorbital region with posteriorly divergent outer margins; premaxillo-frontal suture placed behind from the naso-frontal suture; zygomatic arches robust, with conspicuously and moderately developed postorbital and mandibular processes of jugal, respectively, and a well-marked zygomatic depression; interparietal absent to very small; incisive foramina moderately short and broad, recessed in a common fossa of convex outer borders and completely separated by a thin bony septum; interpremaxillary foramen large to inconspicuous; paraoccipital hook-shaped; auditory bullae inflated, and pyrifom.


    Distribution— C. sericeus occurs in open shrubby to herbaceous steppes from southwestern Chubut (Argentina) in the north to the northern margin of the Santa Cruz river (Santa Cruz, Argentina) in the south, and adjacent open areas of Aysen, Chile (Fig. 1).


    Conclusions: 
    The integrative analyses of morphological, molecular, and karyotipic data of Patagonian specimens of Ctenomys allowed as to describe three new species endemics to the open areas of northern Patagonia. The three new species belong to the C. magellanicus species group. In addition, we consider the geographically restricted C. coyhaiquensis (Kelt & Gallardo, 1994) as a junior synonym of the widespread C. sericeus (Allen, 1903). Our results also shown that as currently understood, C. haigi is likely a composite of two lineages of species level; tentatively, we refer to then as C. haigi s.s. and C. cf. C. lentulus. Our findings, together with the fact that large Patagonian areas still remain unstudied, suggest that the diversity of Patagonian species of Ctenomys is only partially understood. Therefore, to fill in this gap of knowledge, it is needed to carry out additional integrative taxonomic studies, based on the field collection of additional specimens.


    Pablo Teta and Guillermo D’Elía​. 2020. Uncovering the Species Diversity of Subterranean Rodents at the End of the World: Three New Species of Patagonian Tuco-tucos (Rodentia, Hystricomorpha, Ctenomys).   PeerJ. 8:e9259. DOI: 10.7717/peerj.9259

    2:02a
    [Botany • 2020] Tillandsia dichromantha (Tillandsioideae; Bromeliaceae) • A New Species from the State of Oaxaca, Mexico

    Tillandsia dichromantha Hern.-Cárdenas, López-Ferr. & Espejo.


    in Hernández-Cárdenas, Espejo-Serna, López-Ferrari & Lara-Godínez, 2020. 

    Abstract
    Tillandsia dichromantha, a new species from the state of Oaxaca, Mexico, is described and illustrated. The proposed taxon is compared with T. achyrostachys and T. ilseana, species with which it has some similarities. Images and a distribution map are included.

    Keywords: Endemic, Monocots, Poales

    FIGURE 1. Tillandsia dichromantha Hern.-Cárdenas, López-Ferr. & Espejo.
    A. Habitat in San Juan Mixtepec, Oaxaca. B. Habitat in Santos Reyes Tepejillo, Oaxaca. C. Plant at the type locality. D. Detail of the spike. E. Flower. F. Floral bract. G. Sepals. H. Petals. I. Stamens. J. Pistil.
    (Photographs A–C by R. Hernández-Cárdenas; D–J by A. Espejo-Serna).



    Tillandsia dichromantha Hern.-Cárdenas, López-Ferr. & Espejo, sp. nov. 

    The new species is similar to Tillandsia ilseana and T. achyrostachys but differs in the height of the flowering plants (45–55 vs. ± 100, and 24–45 cm), the number of spikes (6–9 vs. (4)9–15, and one), the ecarinate and conspicuosly nerved floral bracts (vs. carinatesmooth, and ecarinate-conspicuosly nerved), the floral bracts width (1.3–1.6 vs. 0.7–0.8, and 1.6–2.3 cm), the sepals size (2.3–2.5 × 0.5–0.6 vs. ±2.8 × 0.8–0.9, and 2.7–2.9 × 0.6–0.7 cm), the petal color (violet + green-chartreuse vs. very pale violet [T. ilseana], and chartreuse green [T. achyrostachys]), and in the style length (6–6.5 vs. 5.5–6, and 4.5–5 cm).

    FIGURE 3. A–B. Tillandsia dichromantha Hern.-Cárdenas, López-Ferr. & Espejo. A. Holotype. B. Paratype.
    C. Herbarium specimen of T. achyrostachys E. Morren ex Baker, coll. A. Mendoza R. 1397 (UAMIZ).
    D. Isotype of T. ilseana W. Till, Halbritt. & Zecher, coll. E.& I. Zecher 8/80 (UAMIZ).

    FIGURE 2. Distribution map of Tillandsia dichromantha Hern.-Cárdenas, López-Ferr. & Espejo.

    Distribution and habitat:— Tillandsia dichromantha is only known from Oaxaca (Figure 2): the Sierra Madre del Sur in the municipalities of San Juan Mixtepec; and Santos Reyes Tepejillo, in the district of Juxtlahuaca, where it grows epiphytically on Quercus spp. and Acacia sp. in dry oak (Quercus) forests, Pinus forests, and tropical deciduous forests with species of Arecaceae, Ipomoea species, Bursera species, and Juniperus species (Figures 1A–B). Tillandsia dichromantha grows among other Tillandsia species like T. achyrostachys, T. dugesii Baker (1887: 278), T. recurvata L. (1762: 410), and T. usneoides L. (1762: 411). Plants of T. dichromantha inhabit localities between 1,730 and 1,960 m elevation and blooms from December to January. It should be mentioned that we found only three individuals during all the visits to the zone along a year, so probably the plants are scarce. 

    Etymology:— The specific epithet refers to the bicolorous petals, violet and chartreuse green, that distinguish this new species. 


    Rodrigo Alejandro Hernández-Cárdenas, Adolfo Espejo-Serna, Ana Rosa López-Ferrari and Sofía Ana Lucrecia Lara-Godínez. 2020. Tillandsia dichromantha (Tillandsioideae; Bromeliaceae), A New Species from the State of Oaxaca, Mexico. Phytotaxa. 447(2); 81–87. DOI: 10.11646/phytotaxa.447.2.1

           

    2:03a
    [Herpetology • 2020] Platypelis laetus • Frogs of the Genus Platypelis from the Sorata Massif in northern Madagascar: Description of A New Species and Reports of Range Extensions

    Platypelis laetus 
    Rakotoarison, Scherz, Köhler, Ratsoavina, Hawlitschek, Megson, Vences & Glaw, 2020

    DOI: 10.3897/zse.96.47088 

    Abstract
    We describe a new species of arboreal microhylid frog, genus Platypelis, from northeastern Madagascar and report the expansion of distribution ranges of two other species. Platypelis laetus sp. nov. is small to medium-sized (24.3–25.6 mm snout-vent length) compared to other Platypelis, exhibits a greenish colored throat and was found in bamboo forest of the Sorata Massif. Its advertisement call consists of a single short tonal note repeated at regular intervals in long call series. Based on DNA sequences of a fragment of the mitochondrial 16S rRNA gene, the new species was placed in a clade with Platypelis olgae from the Tsaratanana Massif, and with two other, unconfirmed candidate species from the Sorata Massif and from Andravory, herein named Platypelis sp. Ca12 and Ca13. Molecular divergences among these lineages were substantial, amounting to 7.6‒8.1% uncorrected 16S p-distance to the closest nominal species, P. olgae, from which the new species is also distinguished by a lack of allele sharing in the nuclear RAG-1 gene. We also provide new records of Platypelis alticola and P. tsaratananaensis from the Sorata Massif, supported by molecular analysis. This confirms a wider distribution of these two species that previously were considered to be endemic to the Tsaratanana Massif. However, their populations in Sorata were characterized by a certain degree of genetic differentiation from Tsaratanana populations suggesting they require more detailed taxonomic assessment.

    Key Words: Amphibia, Anura, Cophylinae, distribution, Microhylidae, molecular genetics, Platypelis laetus sp. nov., Platypelis alticola, Platypelis tsaratananaensis, Sorata, systematics



    Figure 3. Photographs in life of Platypelis laetus sp. nov. from the Sorata massif:
    a–c ZSM 5652/2012 (FGZC 3761), holotype; d, e ZSM 5651/2012 (FGZC 3588), paratype; f, g ZSM 5653/2012 (FGZC 3762), paratype; h Eggs and embryos found in the same bamboo hole with the specimens ZSM 5652/2012 and ZSM 5653/2012.

    Platypelis laetus sp. nov.

    Diagnosis: Assigned to the genus Platypelis in the microhylid subfamily Cophylinae based on enlarged terminal discs on fingers and toes, absence of nuptial pads, and molecular phylogenetic relationships. The species can be identified among other cophylines by the combination of the following character states: (1) medium-sized species (adult male SVL 24.3–25.6 mm); (2) manus with second finger slightly shorter than fourth and pes with third toe much shorter to very slightly shorter than fifth; (3) males with prepollical tubercle but lacking a finger-like prepollex as typical for Anodonthyla; (4) throat greenish in life; (5) chest and anterior belly translucent gray, with distinct white spotting that is absent on the posterior belly; (5) absence of red color on limbs and ventral side.

    Distribution: The species is known only from the Sorata Massif, northern Madagascar, at elevations of 1339‒1541 m above sea level (Fig. 2).

    Natural history: Platypelis laetus sp. nov. occurs in rainforest on the Sorata Massif, but most of the specimens were collected in the bamboo forest of the massif. The holotype was calling from a bamboo hole at about 5 m above the ground. The bamboo node was occupied by another specimen, was water-filled, and contained 35 whitish eggs and embryos, probably of this species, in at least two different developmental stages (Fig. 3h). Another male was found on a palm tree at around 4 m above the ground. Calling occurred around dusk.

    Etymology: The specific epithet is a masculine Latin adjective meaning “happy”. The new species is so named in reflection of the joy and happiness of the first author to get to work on the cophyline microhylid frogs of Madagascar.

           


     Andolalao Rakotoarison, Mark D. Scherz, Jörn Köhler, Fanomezana M. Ratsoavina, Oliver Hawlitschek, Steven Megson, Miguel Vences and Frank Glaw. 2020. Frogs of the Genus Platypelis from the Sorata Massif in northern Madagascar: Description of A New Species and Reports of Range Extensions.  Zoosystematics and Evolution. 96(1): 263-274. DOI: 10.3897/zse.96.47088


    2:04a
    [Botany • 2020] Michaelmoelleria vietnamensis (Gesneriaceae) • A New Lithophilous Dwelling Genus and Species with Zigzag Corolla Tube from southern Vietnam

    Michaelmoelleria vietnamensis  F. Wen, Z.B. Xin & T.V. Do

    in Wen, Xin, Fu, Li, Su, et al., 2020. 
    DOI:  10.3897/phytokeys.146.49731
    Photos by Fang Wen

    Abstract
    Michaelmoelleria, a new genus from southern Vietnam is described with a single species, M. vietnamensis. The new genus is morphologically most similar to Deinostigma and Tribounia but it differs from the latter two by having four fertile stamens. Nuclear ribosomal internal transcribed spacer (ITS) region and plastid trnL-F intron spacer (trnL-F) DNA sequence data from the new genus and eighty-seven species representing 42 genera within tribe Didymocarpeae are used to resolve its generic placement. The molecular evidence reveals that it is most closely related to Cathayanthe rather than Deinostigma and Tribounia. The chromosome number is counted as 2n = 36 that further clarified its distinction comparing to the related genera within tribe Didymocarpeae. A global conservation assessment is also performed and classifies Michaelmoelleria vietnamensis as Critically Endangered (CR).

    Keywords: Cathayanthe, cliff-dwelling, Deinostigma, Didymocarpoideae, flora of Vietnam, IUCN, phylogeny, Tribounia


    Figure 1. Photos of the new genus, Michaelmoelleria, the population in natural habitat.Michaelmoelleria vietnamensis F.Wen, Z.B.Xin & T.V.Do
    A habitat along the La stream B habit C plants in flower D frontal view of flower in natural habitat E lateral view of flower in natural habitat.
    Photos by Fang Wen, arranged by Wen-Hua Xu.


    Figure 4. Photos of new genus, Michaelmoelleria F. Wen, Y.G. Wei & T.V. Do.
    Michaelmoelleria vietnamensis F. Wen, Z.B. Xin & T.V. Do
    A flowering potted plant in GCCC’s greenhouse B frontal view of the corolla and the corolla tube C different angles of a lateral view of corolla and corolla tube (I) D different angles of lateral view of the corolla and the corolla tube (II) E cyme F bracts (above: adaxial surface; below: abaxial surface) G calyx lobes H lateral view of flower and bud I calyx lobes (the left three: adaxial calyx lobes surfaces; the right two: abaxial calyx lobes surfaces) J opened corolla showing stamens and staminode K our fertile anthers L pistil and calyx M stigma.
    Photos by Fang Wen, arranged by Wen-Hua Xu.

    Michaelmoelleria F. Wen, Y.G. Wei & T.V. Do, gen. nov.

     Diagnosis: Michaelmoelleria resembles monotype genus Cathayanthe, but differs from the latter by leaf blade glabrous (vs. sericeous to pubescent in Cathayanthe, same as order followings); calyx actinomorphic (vs. zygomorphic); fertile stamens 4 (vs. 2), stigma 2, both developed ligulate (vs. 1, subcapitate, divided on 1 side); capsule long linear (vs. fleshly, narrowly ellipsoid). The new genus is also morphologically similar to Deinostigma and Tribounia, but is easily distinguished from both by having corolla tube narrowly curving to zigzag infundibuliform-tubular, and bent at about 90° angle in the middle of corolla tube (vs. infundibuliform in Deinostigma; of a narrow lower tube which widens into an infundibuliform & upper tube which has a prominent boss on the dorsal surface in Tribounia, same as order followings), fertile stamens number 4 (vs. 2; 2) and stigma 2-lobed, lobes often gathering together (vs. upper lip usually vestigial and only lower lip developing, broad, flat and weakly 2-lobed; capitate).

    Type and only known species: Michaelmoelleria vietnamensis F. Wen, Z.B. Xin & T.V. Do, sp. nov.

    Etymology: Michaelmoelleria was named in honor of Prof./Dr. Michael Möller from the Royal Botanic Garden Edinburgh. He is a well-known botanist studying Old World Gesneriaceae, especially in Africa (Madagascar) and Asia (China), and mentor of the senior author from the 1990s to the present. “Michaelmoeller-” (means “Michael Möller”) stands for his full name. “moeller” is the English modification of the German family name, “Möller”. Initially, we planned to use “Moelleria” as the genus name. However, this name was used in different places three times. They are Moelleria Cleve (Bacillariophyta, incertae sedis) [non Moelleria Scop. (Spermatophyta, Flacourtiaceae) (≡ Iroucana Aubl.)]; [nec Moelleria Bres. (Fungi, Clavicipitaceae) (≡ Moelleriella Bres.)] [nec Moelleria (Freng.) Freng. (Bacillariophyta, Naviculaceae)] (Blanco and Wetzel 2016). Thus, to prevent confusion with those mentioned above, three existing and existed “Moelleria”, we consider that using the variant of Dr. Michael Möller’s full name, “Michaelmoeller”, to name this new genus to be most appropriate.

    Distribution and habitat: Endemic to southern Vietnam, under broadleaved forests in a montane granite area at 140–200 m altitude.



    Michaelmoelleria vietnamensis F. Wen, Z.B. Xin & T.V. Do, sp. nov.

    Etymology: The genus is named for the famous botanist, Dr. / Prof. Michael Möller, from the Royal Botanic Garden Edinburgh, and the species is named for Vietnam, which holds the first discovered and only known location for the species.


    Figure 6. Photos of Deinostigma W.T.Wang & Z.Y.Li (A–E) and Tribounia D.J.Middleton (F–I),
    the morphologically similar genera and species of Michaelmoelleria F.Wen, Y.G.Wei & T.V.Do (M. vietnamensis F.Wen, Z.B.Xin & T.V.Do)

    A Deinostigma eberhardtii (Pellegr.) D.J.Middleton & H.J.Atkins B D. tamiana (B.L.Burtt) D.J.Middleton & H.J.Atkins C D. cycnostyla (B.L.Burtt) D.J.Middleton & H.J.Atkins D D. cicatricosa (W.T.Wang) D.J.Middleton & Mich.Möller E D. cyrtocarpa (D.Fang & L.Zeng) Mich.Möller & H.J.Atkins
    F–G Tribounia venosa (Barnett) D.J.Middleton H–I T. grandiflora D.J.Middleton.
    A–E photos by Fang Wen F–I photos by David Middleton, arranged by Wen-Hua Xu.

           

     Fang Wen, Zi-Bing Xin, Long-Fei Fu, Shu Li, Lan-Ying Su, Stephen Maciejewski, Zhang-Jie Huang, Truong Van Do and Yi-Gang Wei. 2020. Michaelmoelleria (Gesneriaceae), A New Lithophilous Dwelling Genus and Species with Zigzag Corolla Tube from southern Vietnam. PhytoKeys. 146: 89-107. DOI:  10.3897/phytokeys.146.49731

        

    9:52a
    [PaleoMammalogy • 2020] Juchuysillu arenalesensis • A New Typothere Notoungulate (Mammalia: Interatheriidae) from the Miocene Nazareno Formation of Southern Bolivia

    Juchuysillu arenalesensis
    Croft & Anaya, 2020

     Illustration: Velizar Simeonovski 

    Abstract
    We describe a new interatheriid notoungulate, Juchuysillu arenalesensis gen. et sp. nov., based on six partial upper and lower dentitions from the early to middle Miocene Nazareno Formation of southern Bolivia. A specimen is also referred to J. arenalesensis from the early middle Miocene (Langhian) locality of Cerdas, Bolivia (ca. 100 km to the northwest). The new species is distinguished by its very small size (ca. 15% smaller than Protypotherium minutum) and the unique combination of shallow ectoloph sulci on P3-4, length of M1 > M2 > M3, trapezoidal upper molars, and absence of a buccal talonid sulcus on m3. A second, larger interatheriid species is present at Nazareno but is not represented by remains sufficiently complete for a more precise identification. A phylogenetic analysis indicates that J. arenalesensis represents a unique lineage within Interatheriinae that diverged after Protypotherium sinclairi but before Miocochilius anomopodus, Caenophilus tripartitus, Miocochilius federicoi, and several species of Protypotherium, including Protypotherium australeJuchuysillu arenalesensis is one of two small (< ca. 3 kg) typotheres at Nazareno; its body mass is estimated at 1.1 kg. An updated faunal list for the Nazareno Formation includes 19 species of mammals pertaining to seven orders and 15 families; fragmentary turtle (Testudinidae?) and bird (Phorusrhacidae) remains are also present. The precise age of Nazareno Formation vertebrates is unknown, but the presence of at least three notoungulate species shared with Cerdas suggests a similar (∼16–15 Ma) age for the fossil-bearing levels.


      




    Darin A. Croft and Federico Anaya. 2020. A New Typothere Notoungulate (Mammalia: Interatheriidae), from the Miocene Nazareno Formation of Southern Bolivia. Ameghiniana. 57(2); 189-208. DOI: 10.5710/AMGH.11.01.2020.3271  

           

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