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[Ornithology • 2017] Myzomela irianawidodoae • A Colourful New Species of Myzomela Honeyeater from Rote Island in eastern Indonesia ---ScRaBBlE

Myzomela irianawidodoae Prawiradilaga, Baveja, Suparno, Ashari, Ng, Gwee, Verbelen & Rheindt, 2017  photo:   Philippe Verbelen  e-journ...

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Showing posts with label 2016. Show all posts
Showing posts with label 2016. Show all posts

Wednesday, March 20, 2019

[Ichthyology • 2016] A Taxonomic Revision of the Neotropical Electric Fish Genus Brachyhypopomus (Gymnotiformes: Hypopomidae), with Descriptions of 15 New Species ---ScRaBBlE


Fig. 1: Live individuals of 12 sympatric species of Brachyhypopomus and one species of Microsternarchus from the vicinity of Tefé, Amazonas, Brazil (Amazonas dr.). 

aBrachyhypopomus batesibBrachyhypopomus beebeicBrachyhypopomus belindaedBrachyhypopomus bennettieBrachyhypopomus brevirostris.

 f. Brachyhypopomus flavipomusg. Brachyhypopomus hamiltonih. Brachyhypopomus hendersoniiBrachyhypopomus pinnicaudatus.

 jBrachyhypopomus reganikBrachyhypopomus sullivanilBrachyhypopomus walterimMicrosternarchus bilineatus

Crampton, De Santana, Waddell, & Lovejoy, 2016

ABSTRACT

The bluntnose knifefish genus Brachyhypopomus Mago-Leccia, 1994, is diagnosed from other Rhamphichthyoidea (Rhamphichthyidae + Hypopomidae) by the presence of a disk-like ossification in the anterior portion of the palatoquadrate, and by the following external characters: short snout, 18.7-32.6% of head length (vs. 33.3-68.6% in Hypopomus, Gymnorhamphichthys, Iracema, and Rhamphichthys), absence of a paired accessory electric organ in the mental or humeral region (vs. presence in Hypopygus and Steatogenys), presence of 3-4 pectoral proximal radials (vs. 5 in Akawaio), presence of the antorbital + infraorbital, and the preopercular cephalic lateral line canal bones (vs. absence in Racenisia). Brachyhypopomus cannot be diagnosed unambiguously from Microsternarchus or from Procerusternarchus on the basis of external characters alone. Brachyhypopomus comprises 28 species. Here we describe 15 new species, and provide redescriptions of all 13 previously described species, based on meristic, morphometric, and other morphological characters. We include notes on ecology and natural history for each species, and provide regional dichotomous keys and distribution maps, based on the examination of 12,279 specimens from 2,787 museum lots. A lectotype is designated for Brachyhypopomus pinnicaudatus (Hopkins, Comfort, Bastian & Bass, 1990). Brachyhypopomus species are abundant in shallow lentic and slow-flowing freshwater habitats from southern Costa Rica and northern Venezuela to Uruguay and northern Argentina. Species diversity is highest in Greater Amazonia, where 20 species occur: Brachyhypopomus alberti, new speciesBrachyhypopomus arrayae, new species, and Brachyhypopomus cunia, new species, in the upper rio Madeira drainage; Brachyhypopomus batesi, new species, in the central Amazon and rio Negro; B. beebei, B. brevirostrisBrachyhypopomus regani, new speciesBrachyhypopomus sullivani, new species, and B. walteri, widespread through the Amazon and Orinoco basins and the Guianas; Brachyhypopomus belindae, new species, in the central Amazon basin; Brachyhypopomus benjamini, new species, and Brachyhypopomus verdii, new species, in the upper Amazon basin; B. bennetti, in the upper, central, and lower Amazon, lower Tocantins, and upper Madeira basins; B. bullocki in the Orinoco, Negro and Essequibo drainages; B. diazi in the Orinoco Llanos; Brachyhypopomus flavipomus, new species, and Brachyhypopomus hamiltoni, new species, in the central and upper Amazon basin; Brachyhypopomus hendersoni, new species, in the central Amazon, lower Negro and Essequibo basins; B. pinnicaudatus in the central and lower Amazon, lower, upper Madeira, lower Tocantins and Mearim basins, and coastal French Guiana; and Brachyhypopomus provenzanoi, new species, in the upper Orinoco and upper Negro basins. Five species are known from the Paraná-Paraguay-Uruguay basin and adjacent southern Atlantic drainages: B. bombilla in the lower Paraná, upper, central, and lower Paraguay, Uruguay and Patos-Mirim drainages; B. brevirostris in the upper Paraguay basin; B. draco in the lower Paraná, lower Paraguay, Uruguay, Patos-Mirim, and Tramandaí basins; B. gauderio in the lower Paraná, upper, central, and lower Paraguay, Uruguay, Patos-Mirim and Tramandaí basins; and B. walteri in the lower Paraná and upper Paraguay basins. Two species occur in small Atlantic drainages of southern Brazil: B. janeiroensis in the São João, Paraíba and small intervening drainages; and B. jureiae in the Ribeira de Iguape and Una do Prelado. One species occurs in the middle and upper São Francisco basin: Brachyhypopomus menezesi, new species. Three species occur in trans-Andean drainages: B. diazi in Caribbean drainages of northern Venezuela; B. occidentalis in Atlantic and Pacific drainages of southern Costa Rica and Panama to Darién, and the Maracaibo, Magdalena, Sinú and Atrato drainages; and Brachyhypopomus palenque, new species, in Pacific drainages of Ecuador.

Keywords: Biogeography; Bluntnose knifefish; Electroreception; Identification key; Rhamphichthyoidea


Fig. 1: Live individuals of 12 sympatric species of Brachyhypopomus and one species of Microsternarchus from the vicinity of Tefé, Amazonas, Brazil (Amazonas dr.).
a. Brachyhypopomus batesi MCP 45312 (WC01.191293b), immature, 102 mm TL. b. Brachyhypopomus beebei head - uncat., immature, 75 mm TL; body - MCP 45450 (WC04.090600), female, 178 mm TL. c. Brachyhypopomus belindae MCP 45430, paratype, immature, 104 mm TL (photographed out of water, close up of head not available). d. Brachyhypopomus bennetti MCP 45451, male, 196 mm TL. e. Brachyhypopomus brevirostris uncat., immature, 224 mm TL. f. Brachyhypopomus flavipomus MCP 45453 (WC09.090600), female, 98 mm TL. g. Brachyhypopomus hamiltoni MCP 45482 (WC05.080301), holotype, female, 97 mm TL. h. Brachyhypopomus hendersoni MCP 45489, female, 164 mm TL. i. Brachyhypopomus pinnicaudatus MCP 45455, female, 135 mm TL. j. Brachyhypopomus regani, MCP 45285 (WC02.100301), male, 119 mm TL. k. Brachyhypopomus sullivani MCP 45464 (WC04.210201), immature, 79 mm TL. l. Brachyhypopomus walteri MCP 45458 (WC 03.090600), male, 161 mm TL. m. Microsternarchus bilineatus uncat., 85 mm TL. 

Brachyhypopomus alberti
, Brachyhypopomus arrayae, Brachyhypopomus batesi,   
Brachyhypopomus belindae, Brachyhypopomus benjamini, Brachyhypopomus cunia,   
Brachyhypopomus flavipomus, Brachyhypopomus hamiltoni, Brachyhypopomus hendersoni,   
Brachyhypopomus menezesi, Brachyhypopomus palenque, Brachyhypopomus provenzanoi 
Brachyhypopomus regani, Brachyhypopomus sullivani, Brachyhypopomus verdii 
 Crampton, De Santana, Waddell, & Lovejoy, 2016

William G. R. Crampton, Carlos D. de Santana, Joseph C. Waddell and Nathan R. Lovejoy. 2016.  A Taxonomic Revision of the Neotropical Electric Fish Genus Brachyhypopomus (Ostariophysi: Gymnotiformes: Hypopomidae), with Descriptions of 15 New Species.
Neotropical Ichthyology.  14(4); DOI: 10.1590/1982-0224-20150146 


RESUMO: Peixes elétricos do gênero Brachyhypopomus Mago-Leccia, 1994, são diagnosticados dos outros Rhamphichthyoidea (Rhamphichthyidae + Hypopomidae) pela presença de uma ossificação discóide na porção anterior do palatoquadrado, e pelos seguintes caracteres externos: focinho curto, 18,7-32,6% do comprimento da cabeça (vs. 33,3-68,6% em Hypopomus, Gymnorhamphichthys, Iracema e Rhamphichthys), ausência de um órgão elétrico acessório pareado na região mental ou humeral (vs. presença em Hypopygus e Steatogenys), presença de 3-4 proximais peitorais radiais (vs. 5 em Akawaio), presença do antiorbital + infraorbital, e dos canais ossificados da linha lateral da região cefálica do pré-opérculo (vs. ausência em Racenisia). Brachyhypopomus não pode ser diagnosticado de maneira não-ambígua de Microsternarchus ou Procerusternarchus, com base em caracteres de morfologia externa. Brachyhypopomus compreende 28 espécies válidas. Aqui nós descrevemos 15 espécies novas, e fornecemos a redescrição de 13 espécies previamente descritas, baseado em caracteres merísticos, morfométricos e outros caracteres morfológicos. Nós incluímos notas sobre à ecologia e história natural para cada uma das espécies, e fornecemos chaves dicotômicas regionais e mapas de distribuição baseado no exame de 12.279 espécimes de 2.787 lotes de museus. Um lectótipo é designado para Brachyhypopomus pinnicaudatus (Hopkins, Comfort, Bastian & Bass, 1990). Espécies de Brachyhypopomus são abundantes em habitats de águas rasas lênticas e com correntes fracas, ocorrendo do sul da Costa Rica e norte da Venezuela ao Uruguai e norte da Argentina. A diversidade de espécies é maior na Grande Amazônia, onde 20 espécies ocorrem: B. alberti, espécie nova, B. arrayae, espécie nova e B. cunia, espécie nova, na drenagem do alto rio Madeira; B. batesi, espécie nova, na Amazônia central e rio Negro; B. beebei, B. brevirostris, B. regani, espécie nova, B. sullivani, espécie nova e B. walteri, amplamente distribuídas nas bacias Amazônicas e do Orinoco, e nas Guianas; B. belindae, espécie nova, bacia Amazônica central; B. benjamini, espécie nova e B. verdii, espécie nova, na bacia do alto Amazonas; B. bennetti, no alto, médio e porções baixas da bacia Amazônica, baixo Tocantins e alto rio Madeira; B. bullocki nas drenagens do Orinoco, Negro e Essequibo; B. diazi nos Llanos do Orinoco; B. flavipomus, espécie nova e B. hamiltoni, espécie nova, no médio e alto Amazonas; B. hendersoni, espécie nova, na Amazônia central, baixo Negro e Essequibo; B. pinnicaudatus no médio e baixo Amazonas, baixo e alto Madeira, baixo Tocantins, bacia do Mearim e rios costeiros da Guiana Francesa; e B. provenzanoi, espécie nova, nas bacias do alto Orinoco e alto Negro. Cinco espécies são conhecidas das bacias Paraná-Paraguai-Uruguai e bacias adjacentes das drenagens do sul do Brasil: B. bombilla no alto, médio e baixo Paraguai, baixo Paraná, Uruguai e drenagens Patos-Mirim; B. brevirostris da bacia do alto Paraguai; B. draco das bacias do baixo Paraguai, baixo Paraná, Uruguai, Patos-Mirim e Tramandaí; B. gauderio das bacias do alto, médio e baixo Paraguai, baixo Paraná, Uruguai, Patos-Mirim e Tramandaí; e B. walteri das bacias do alto Paraguai e baixo Paraná. Duas espécies ocorrem nas drenagens costeiras do sudeste do Brasil: B. janeiroensis no São João, Paraíba e em drenagens menores nas adjacências; e B. jureiae no Ribeira de Iguape e Una do Prelado. Uma espécie ocorre no médio e alto rio São Francisco: B. menezesi, espécie nova. Três espécies ocorrem nas drenagens trans-Andinas: B. diazi nas drenagens do Caribe no norte da Venezuela; B. occidentalis nas drenagens do Atlantico e Pacífico do sul da Costa Rica e Panamá até Darién, e nas drenagens do Maracaibo, Magdalena, Sinú e Atrato; e B. palenque, espécie nova, nas drenagens do Pacífico no Equador.

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روابط التحميل والمشاهدة، الروابط المباشرة للتحميل
او
شاهد هذا الفيديو القصير لطريقة التحميل البسيطة


كيف تحصل على مدونة جاهزة بآلاف المواضيع والمشاركات من هنا
شاهد قناة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على اليوتيوب لمزيد من الشرح من هنا
رابط مدونة منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات في أي وقت حــــتى لو تم حذفها من هنا
شاهد صفحة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على الفيس بوك لمزيد من الشرح من هنا
تعرف على ترتيب مواضيع منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات (حتى لا تختلط عليك الامور) من هنا

ملاحظة هامة: كل عمليات تنزيل، رفع، وتعديل المواضيع الجاهزة تتم بطريقة آلية، ونعتذر عن اي موضوع مخالف او مخل بالحياء مرفوع بالمدونات الجاهزة بآلاف المواضيع والمشاركات، ولكم ان تقوموا بحذف هذه المواضيع والمشاركات والطريقة بسيطة وسهلة. ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــسلامـ.

[Entomology • 2016] Revision of the Oriental subfamily Heteropteryginae Kirby, 1896 (Phasmatodea: Areolatae: Heteropterygidae), with A Re-arrangement of the family Heteropterygidae and the Descriptions of Five New Species of Haaniella Kirby, 1904 ---ScRaBBlE


Heteropteryx dilatata  (Parkinson, 1798)


Abstract  

The areolate Oriental family Heteropterygidae Kirby, 1893 is critically reviewed and the results of the present study contradict the arrangement suggested by Zompro (2004), but in most aspects agree with a molecular study presented by Whiting et al (2003) and a phylogenetic study presented by Bradler (2009). The family is critically discussed and new hypotheses are presented for the phylogeny and intra-familiar relationships, placing the subfamily Dataminae Rehn & Rehn, 1939 as the basalmost clade of Heteropterygidae. The subfamilies Obriminae Brunner v. Wattenwyl, 1893 and Heteropteryginae Kirby, 1893 together represent the sister-group of Dataminae. Arguments and a tree are presented to support this hypothesis. New diagnoses and lists of genera are provided for all three subfamilies contained in Heteropterygidae, along with keys to distinguish between them.

        The subfamily Obriminae is critically reviewed and the distinction between the three tribes Obrimini Brunner v. Wattenwyl, 1893, Eubulidini Zompro, 2004 and Miroceramiini Zompro, 2004 introduced by Zompro (2004) is shown to be poorly supported. While Obrimini sensu Zompro, 2004 is generally accepted (but now also contains genera that were placed in Eubulidini or Miroceramiini by Zompro (2004)), the tribes Eubulidini and Miroceramiini are not supported. A new arrangement is introduced, which is based on morphological characters neglected or overlooked by Zompro (2004) but were partly discussed by Bradler (2009). The genus Mearnsiana Rehn & Rehn, 1939 is removed from Miroceramiini and transferred to Obrimini. The genera Eubulides Stål, 1877Heterocopus Redtenbacher, 1906Theramenes Stål, 1875 and Stenobrimus Redtenbacher, 1906 are removed from Eubulidini and also transferred to Obrimini. Consequently, Eubulidini is synonymised with Obrimini (n. syn.). Miroceramiini is a monotypical tribe and only includes the Wallacean genus Miroceramia Günther, 1934. The new tribe Tisamenini n. trib. is established for the three basal genera Tisamenus Stål, 1875Ilocano Rehn & Rehn, 1939 and Hoploclonia Stål, 1875 all of which were placed in Eubulidini by Zompro (2004). The latter genus differs from the other two genera by the morphology of the female genitalia, which is unique amongst the entire family. Three generic groups are recognized within Obrimini, the Obrimus-group, Stenobrimus-group and Theramenes-group. Keys are presented to distinguish between the three tribes now contained in the Obriminae, i.e. Obrimini, Tisamenini n. trib. and Miroceramiini. The genus Hennobrimus Conle, 2006 is synonymised with Mearnsiana Rehn & Rehn, 1939, based on the fact that the type-species of both genera are conspecific (n. syn.). Hennobrimus hennemanni Conle, 2006, the type-species of Hennobrimus, and Trachyaretaon manobo Lit & Eusebio, 2005 are synonymised with Mearnsiana bullosa Rehn & Rehn, 1939, the type-species of Mearnsiana (n. syn.). Theramenes dromedarius Stål, 1877 from the Philippines is removed from synonymy with the Wallacean Theramenes olivaceus (Westwood, 1859) and re-established as a valid species (rev. stat.).

        The subfamily Heteropteryginae Kirby, 1896 is revised at the species-level and a new diagnosis is presented. Keys to the two genera and all 16 known species are provided along with new descriptions, differential diagnoses, lists of examined material, detailed information on the known distributions, measurements and illustrations of the insects and eggs. The intra-subfamiliar and intra-generic relationships are discussed and a cladogram is presented. Heteropteryginae contains two genera: Heteropteryx Gray, 1835 (Type-species: Phasma dilatatum Parkinson, 1798) and Haaniella Kirby, 1896 (Type-species: Phasma (Heteropteryx) muelleri de Haan, 1842). The distribution of this subfamily is restricted to Sundaland with the exception of a single species that is found in Vietnam. All other species are distributed in Borneo, Sumatra, the Mentawai Islands, Singapore, Peninsular Malaysia and Thailand. Heteropteryginae contains the largest and most striking members of the entire family Heteropteryginae, some of which are amongst the heaviest insects known. The subfamily is characterized by apomorphies such as the presence of wings, having a tympanal area (= stridulatory organ) in the basal portion of the alae, straight profemora, strongly shortened tarsi, lack of rough sensory-areas on the prosternum and typically X-shaped micropylar plate of the eggs. The sister-group of Heteropteryginae is represented by the Obriminae, with which it shares a beak-like secondary ovipositor in the females and presence of a medio-apical spine on the area apicalis. Both features are synapomorphies of Heteropteryginae + Obriminae.

        The genus Haaniella Kirby, 1904 contains 16 known species, five of which are newly described herein. The genus Miniopteryx Zompro, 2004 (Type-species: Haaniella parva Günther, 1944) is synonymised with Haaniella on the basis that the distinguishing feature mentioned in the original description is a character that is frequently found throughout the genus (n. syn.). The type-species H. parva Günther, 1944 is automatically retransferred to Haaniella (rev. stat.). Haaniella aculeata n. sp. from western Sumatra is described from the male. Haaniella macroptera n. sp. from Singapore and the Johor state in southern Peninsular Malaysia is described from both sexes and the eggs. Haaniella gintingi n. sp. from Central Sumatra is described from both sexes and the eggs and Haaniella kerincia n. sp. from Western Sumatra is described from the insects only, the eggs being still unknown. One new species, Haaniella gorochovi n. sp., is the only representative of the genus and subfamily Heteropteryginae known from Vietnam and both sexes as well as the eggs are described. Haaniella erringtoniae (Redtenbacher, 1906) is endemic in Peninsular Malaysia, here removed from synonymy with H. muelleri (de Haan, 1842) and re-established as a valid species (rev. stat.). The Sumatran Haaniella glaber (Redtenbacher, 1906) is removed from synonymy with H. muelleri (Haan, 1842) and re-established as a valid species (rev. stat.). Leocrates glaber Redtenbacher, 1906 and Haaniella muelleri simplex Günther, 1944 are removed from synonymy with H. muelleri (Haan, 1842) (rev. stat.) and synonymised with H. glaber. Haaniella mecheli (Redtenbacher, 1906) and H. rosenbergii (Kaup, 1871) are removed from synonymy with H. muelleri (Haan, 1842) and re-established as valid species (rev. stat.). Haaniella erringtoniae novaeguineae Günther, 1934 and Haaniella muelleri var. b. (Haan, 1842) are synonymized with H. rosenbergii (Kaup, 1871) (n. syn.). The type-species Haaniella muelleri (Haan, 1842) is shown to be a fairly rare species that is restricted to Sumatra. All subsequent records of H. muelleri from outside Sumatra and references to captive breeding of stock originating from Peninsular Malaysia in Europe relate to H. erringtoniae (Redtenbacher, 1906). The previously unknown males and eggs of H. rosenbergii (Kaup, 1871) as well as the previously unknown females and eggs of H. parva Günther, 1944 are described and illustrated for the first time. Based on morphological characters of the insects and eggs three distinct species-groups are recognized within Haaniella. The muelleri species-group contains nine species that are distributed throughout Sumatra, the Mentawei Islands, Singapore and Peninsular Malaysia. These are characterized by the smooth ventral surface of the meso- and metafemora and lemon-shaped eggs which entirely lack the setae seen in the two other species-groups. The grayii species-group comprises four species, two of which are endemic in Borneo, one endemic in Sumatra and the fourth species being the only known representative of the subfamily in Vietnam. These species are characteristic for the prominent pair of spines on the abdominal tergites II–IV of males and long apically multidentate epiproct of females. The echinata species-group contains three exceptionally Bornean species, which are characterized by the long and apically pointed subgenital plate of females, which clearly projects beyond the epiproct, as well as the sub-basal lateral tooth of the anal segment of males. The muelleri species-group is sister to the remainder two species-groups.

        Heteropteryx Gray, 1853 is a monotypical genus and only contains the type-species H. dilatata (Parkinson, 1798), which is found throughout Peninsular Malaysia, Thailand, Sumatra and Northeastern Borneo. This genus differs from Haaniella by the strongly conically elevated head, which posteriorly projects over the anterior margin of the pronotum, females being bright green or yellow in colour with plain and translucent pink alae and having distinct spines on the abdominal tergites, and males having a strongly shortened mesothorax and dull pink alae. 

Lectotypes are designated for Haaniella parva Günther, 1944, Heteropteryx echinata Redtenbacher, 1906, Heteropteryx saussurei Redtenbacher, 1906 and Heteropteryx scabra Redtenbacher, 1906 to guarantee stability of these names.

        Information on the habitats, host-plants, biology, life cycle, parasitism and captive breeding of the species of Heteropteryginae is presented and a list summarising all taxonomic changes presented herein.

Keywords: Phasmatodea, Heteropterygidae, Heteropteryginae, Obriminae, Dataminae, HeteropteryxHaaniella, taxonomic revision, classification, new tribe, new species, new subspecies, new synonyms, lectotypes, keys, differentiations, descriptions, illustrations, eggs




Frank H. Hennemann, Oskar V. Conle, Paul D. Brock and Francis Seow-Choen. 2016. Revision of the Oriental subfamily Heteropteryginae Kirby, 1896, with A Re-arrangement of the family Heteropterygidae and the Descriptions of Five New Species of Haaniella Kirby, 1904. (Phasmatodea: Areolatae: Heteropterygidae).  Zootaxa. 4159(1); 1–219. DOI: 10.11646/zootaxa.4159.1.1

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روابط التحميل والمشاهدة، الروابط المباشرة للتحميل
او
شاهد هذا الفيديو القصير لطريقة التحميل البسيطة


كيف تحصل على مدونة جاهزة بآلاف المواضيع والمشاركات من هنا
شاهد قناة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على اليوتيوب لمزيد من الشرح من هنا
رابط مدونة منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات في أي وقت حــــتى لو تم حذفها من هنا
شاهد صفحة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على الفيس بوك لمزيد من الشرح من هنا
تعرف على ترتيب مواضيع منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات (حتى لا تختلط عليك الامور) من هنا

ملاحظة هامة: كل عمليات تنزيل، رفع، وتعديل المواضيع الجاهزة تتم بطريقة آلية، ونعتذر عن اي موضوع مخالف او مخل بالحياء مرفوع بالمدونات الجاهزة بآلاف المواضيع والمشاركات، ولكم ان تقوموا بحذف هذه المواضيع والمشاركات والطريقة بسيطة وسهلة. ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــسلامـ.

[Mammalogy • 2016] Euroscaptor orlovi & E. kuznetsovi • Secrets of the Underground Vietnam: An Underestimated Species Diversity of Asian Moles (Lipotyphla: Talpidae: Euroscaptor) ---ScRaBBlE


Euroscaptor orlovi
Zemlemerova, Bannikova, Lebedev, Rozhnov & Abramov, 2016


ABSTRACT
 A study of the Southeast Asian moles of the genus Euroscaptor based on a combined approach, viz. DNA sequence data combined with a multivariate analysis of cranial characters, has revealed a high cryptic diversity of the group. An analysis of mitochondrial cytochrome b gene and five nuclear genes has revealed two deeply divergent clades: the western one (E. klossi + E. malayana + E. longirostris from Sichuan + Euroscaptor spp. from northern Vietnam and Yunnan, China), and the eastern one (E. parvidens s.l. + E. subanura). The pattern of genetic variation in the genus Euroscaptor discovered in the present study provides support for the existence of several cryptic lineages that could be treated as distinct species based on their genetic and morphological distinctness and geographical distribution. The moles from southern China and northern Vietnam form three distinct groups. The specimens from Sichuan (including the one collected from the type locality of E. longirostris) were clearly distinct from the northwestern Vietnam and Yunnan samples that were previously attributed to this species. We argue that the real distribution of E. longirostris is restricted to Sichuan, northward of Yangtze River, whereas the populations occurring southward of this isolation barrier evidently represent a new species Euroscaptor orlovi sp. nov. (northwestern Vietnam and Yunnan, southern China). Moreover, Red River that divides the western and eastern parts of northern Vietnam beyond doubt separates the population of E. orlovi from the moles occurring in northeastern Vietnam (Vinh Phuc and Cao Bang provinces); the latter are described here as Euroscaptor kuznetsovi sp. nov. Yet, genetic data are in favour of a close affinity of E. subanura with E. parvidens. A combined analysis of both genetic and morphological data has revealed a strong geographic segregation of E. parvidens samples. The populations from Dalat Plateau (southern Vietnam), including the moles from Loc Bao, Bi Dup and Chu Yang Sin, form a well-supported clade and can be considered true E. parvidens. The specimens from central Vietnam (Kon Tum and Quang Nam provinces) are significantly different from them, yet their monophyly has been supported by the mtDNA only. The moles from central Vietnam have been described here as a new subspecies Euroscaptor parvidens ngoclinhensis ssp. nov. All the studied samples of E. subanura have shown a low genetic and morphological variability despite their wide geographic range. 

Key words: cryptic species, Euroscaptor, multilocus phylogeny, multivariate analyses, taxonomy




SYSTEMATICS 
Genus Euroscaptor Miller, 1940
 Type species: Talpa klossi Thomas, 1929. 

Distribution: widely distributed in South Asia, occurring in China, Nepal, Laos, Vietnam, Myanmar, Thailand, and Peninsular Malaysia. 

Composition: Euroscaptor klossi (Thomas, 1929), Euroscaptor longirostris (Milne-Edwards, 1870), Euroscaptor malayana (Chasen, 1940), Euroscaptor parvidens (Miller, 1940), Euroscaptor subanura Kawada et al., 2012, Euroscaptor orlovi sp. nov., and Euroscaptor kuznetsovi sp. nov. (see descriptions below). Probably, also includes Euroscaptor grandis Miller, 1940 and Euroscaptor micrura (Hodgson, 1841). The taxonomic status of “Talpacryptura Blyth, 1843 from Darjeeling, India remains obscure. 


Euroscaptor orlovi sp. nov.

Diagnosis. Large-sized mole, comparable to E. longirostris. Pelage blackish brown. Tail long and club-shaped. Rostral part of skull elongated and narrow. Posterolingual border of P4 deeply concave. Anterior parts of auditory bullae flatted and straddling. A new species distinguished by the mitochondrial gene cytochrome b and five nuclear genes (BRCA1, BRCA2, ApoB, RAG1 and A2ab) (see Figs 2–4).

Etymology. The new species is named in honour of Dr. Nikolai L. Orlov (Zoological Institute, Russian Academy of Sciences, Saint Petersburg, Russia) in recognition of his remarkable contributions to the study of animals of Vietnam. 

Distribution. Found in northern Vietnam (Lao Cai Province, Sa Pa District) and southern China (Yunnan Province). It may have a wider distribution in the highlands of northern Laos and in northwestern Vietnam, probably westward of Red River.


Euroscaptor kuznetsovi sp. nov.

Diagnosis. Large-sized mole, comparable to E. longirostris and E. orlovi sp. nov. Pelage blackish brown. Tail long and club-shaped. Rostral part of skull elongated and relatively wide. Posterolingual border of P4 deeply concave. Anterior parts of auditory bullae flatted and straddling. A new species distinguished by the mitochondrial gene cytochrome b and five nuclear genes (BRCA1, BRCA2, ApoB, RAG1 and A2ab) (see Figs 2–4).

Etymology. The new species is named in honour of Dr. German V. Kuznetsov (A.N. Severtsov Institute of Ecology and Evolution, Russian Academy of Sciences, Moscow) in recognition of his many contributions to the study of mammals of Vietnam. 

Distribution. Distributed in north-eastern Vietnam. It is recorded from Vinh Phuc Province (Tam Dao) and Cao Bang Province (Nguyen Binh District). Found at the elevations of 750–950 m a.s.l. Probably, the record from Guangxi, south-eastern China (Hoffman and Lunde 2008) belongs to this species as well. 


Euroscaptor parvidens ngoclinhensis subsp. nov.

Diagnosis. Small-sized mole, comparable only to E. subanura, and smaller on average in its external and cranial measurements than the nominotypical E. parvidens. The fourth upper premolar with a well developed parastyle. A new species distinguished by the mitochondrial gene cytochrome b (see Fig. 2).

Etymology. The subspecies is named after the Ngoc Linh Mountain in Kon Tum Province of Vietnam, from where it was collected for the first time. 

Distribution. Known from the Central Highlands of Vietnam (Kon Tum and Quang Nam provinces). Probably, the moles from Gia Lai Province (Abramov et al. 2013a) belong to this subspecies. 



E.D. Zemlemerova, A.A. Bannikova, V.S. Lebedev, V.V. Rozhnov and A.V. Abramov. 2016. Secrets of the Underground Vietnam: An Underestimated Species Diversity of Asian Moles (Lipotyphla: Talpidae: Euroscaptor[ТАЙНЫ ПОДЗЕМНОГО ВЬЕТНАМА: НЕДООЦЕНЕННОЕ ВИДОВОЕ РАЗНООБРАЗИЕ АЗИАТСКИХ КРОТОВ (LIPOTYPHLA: TALPIDAE: EUROSCAPTOR)]. Proceedings of the Zoological Institute RAS. 320(2); 193–220.   istina.msu.ru/publications/article/22015267 

Stranger Species shar.es/1M90OQ

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روابط التحميل والمشاهدة، الروابط المباشرة للتحميل
او
شاهد هذا الفيديو القصير لطريقة التحميل البسيطة


كيف تحصل على مدونة جاهزة بآلاف المواضيع والمشاركات من هنا
شاهد قناة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على اليوتيوب لمزيد من الشرح من هنا
رابط مدونة منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات في أي وقت حــــتى لو تم حذفها من هنا
شاهد صفحة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على الفيس بوك لمزيد من الشرح من هنا
تعرف على ترتيب مواضيع منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات (حتى لا تختلط عليك الامور) من هنا

ملاحظة هامة: كل عمليات تنزيل، رفع، وتعديل المواضيع الجاهزة تتم بطريقة آلية، ونعتذر عن اي موضوع مخالف او مخل بالحياء مرفوع بالمدونات الجاهزة بآلاف المواضيع والمشاركات، ولكم ان تقوموا بحذف هذه المواضيع والمشاركات والطريقة بسيطة وسهلة. ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــسلامـ.

[Botany • 2016] Floral Specialization for Different Pollinators and Divergent Use of the Same Pollinator Among Co-occurring Impatiens Species (Balsaminaceae) from Southeast Asia ---ScRaBBlE


Researchers have presented their results on specialization in pollination techniques in flowers of the genus Impatiens. For two months in 2014, they have studied 7 co-occurring species of the genus Impatiens in the Chiang Dao Wildlife Sanctuary in Chiang Mai, Thailand.

 Ruchisansakun, Tangtorwongsakul, Cozien, et al. 2016.

Floral variation among closely related species is thought to often reflect differences in pollination systems. Flowers of the large genus Impatiens are characterized by extensive variation in colour, shape and size and in anther and stigma positioning, but studies of their pollination ecology are scarce and most lack a comparative context. Consequently, the function of floral diversity in Impatiens remains enigmatic. This study documents floral variation and pollination of seven co-occurring Impatiens spp. in the Southeast Asian diversity hotspot. To assess whether floral trait variation reflects specialization for different pollination systems, we tested whether species depend on pollinators for reproduction, identified animals that visit flowers, determined whether these visitors play a role in pollination and quantified and compared key floral traits, including floral dimensions and nectar characteristics. Experimental exclusion of insects decreased fruit and seed set significantly for all species except I. muscicola, which also received almost no visits from animals. Most species received visits from several animals, including bees, birds, butterflies and hawkmoths, only a subset of which were effective pollinators. Impatiens psittacina, I. kerriae, I. racemosa and I. daraneenae were pollinated by bees, primarily Bombus haemorrhoidalis. Impatiens chiangdaoensis and I. santisukii had bimodal pollination systems which combined bee and lepidopteran pollination. Floral traits differed significantly among species with different pollination systems. Autogamous flowers were small and spurless, and did not produce nectar; bee-pollinated flowers had short spurs and large floral chambers with a wide entrance; and bimodally bee- and lepidopteran-pollinated species had long spurs and a small floral chamber with a narrow entrance. Nectar-producing species with different pollination systems did not differ in nectar volume and sugar concentration. Despite the high frequency of bee pollination in co-occurring species, individuals with a morphology suggestive of hybrid origin were rare. Variation in floral architecture, including various forms of corolla asymmetry, facilitates distinct, species-specific pollen-placement on visiting bees. Our results show that floral morphological diversity among Impatiens spp. is associated with both differences in functional pollinator groups and divergent use of the same pollinator. Non-homologous mechanisms of floral asymmetry are consistent with repeated independent evolution, suggesting that competitive interactions among species with the same pollination system have been an important driver of floral variation among Impatiens spp.

Keywords: autogamy; bee pollination; butterfly pollination; floral asymmetry; nectar robbing; nectar spur; pollen placement; sympatry; tropics



Figure 3. Impatiens flowers, showing variation in colour and shape and floral visitors:
 I. muscicola (A); 
I. santisukii pollinated by Polytremis lubricans lubricans (B) and Bombus haemorrhoidalis (C);
I. racemosa pollinated by B. haemorrhoidalis (D);
I. chiangdaoensis pollinated by Notocrypta curvifascia (E) and visited by a nectar-robbing B. haemorrhoidalis (F);
 I. psittacina pollinated by B. haemorrhoidalis (G);
  
I. kerriae pollinated by B. haemorrhoidalis (H) and visited by Apis cerana (I), Macroglossum belis (J), and Aethopyga gouldiae (K).
  I. daraneenae pollinated by an unknown bee species (Apidae) (L).



Black arrow in (A) indicates the typical position of the shed anthers onto the lower lateral united petals, facilitating autonomous self-pollination. All other arrows indicate pollen placement sites on visiting bee species (C, D, G, H, L). Scale bar in (A) represents 1 mm, all other scale bars represent 10 mm.


Saroj Ruchisansakun, Pornpimon Tangtorwongsakul, Ruth J. Cozien, Erik F. Smets FMLS and Timotheüs van der Niet. 2016. Floral Specialization for Different Pollinators and Divergent Use of the Same Pollinator Among Co-occurring Impatiens Species (Balsaminaceae) from Southeast Asia. Botanical Journal of the Linnean Society. 181(4); 651–666.  DOI: 10.1111/boj.12427


In a study in the Botanical Journal of the Linnean Society, researchers (including 4  from Naturalis) have presented their results on specialization in pollination techniques in flowers of the genus Impatiens. For two months in 2014, they have studied 7 co-occurring species of the genus Impatiens (see video) in the Chiang Dao Wildlife Sanctuary in Chiang Mai, Thailand.

Impatiens develops diff. floral shapes to specialize in pollination techniques + avoid competition! Blog+video https://science.naturalis.nl/en/about-us/news/onderzoek/flowers-impatiens-genus-and-their-specialization-pollination-techniques/?platform=hootsuite


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روابط التحميل والمشاهدة، الروابط المباشرة للتحميل
او
شاهد هذا الفيديو القصير لطريقة التحميل البسيطة


كيف تحصل على مدونة جاهزة بآلاف المواضيع والمشاركات من هنا
شاهد قناة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على اليوتيوب لمزيد من الشرح من هنا
رابط مدونة منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات في أي وقت حــــتى لو تم حذفها من هنا
شاهد صفحة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على الفيس بوك لمزيد من الشرح من هنا
تعرف على ترتيب مواضيع منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات (حتى لا تختلط عليك الامور) من هنا

ملاحظة هامة: كل عمليات تنزيل، رفع، وتعديل المواضيع الجاهزة تتم بطريقة آلية، ونعتذر عن اي موضوع مخالف او مخل بالحياء مرفوع بالمدونات الجاهزة بآلاف المواضيع والمشاركات، ولكم ان تقوموا بحذف هذه المواضيع والمشاركات والطريقة بسيطة وسهلة. ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــسلامـ.

[Botany • 2016] Zingiber sirindhorniae | ไอยริศ • A Remarkable New Species in Zingiber section Dymczewiczia (Zingiberaceae) from Thailand ---ScRaBBlE


ไอยริศ |   Zingiber sirindhorniae Triboun & Keerat.


ABSTRACT
 Zingiber sirindhorniae Triboun and Keerat., a new species from Thailand, is described and illustrated. It belongs to Zingiber section Dymczewiczia (Horan.) Benth. because of its terminal inflorescence which is rather rare in Zingiber.

KEY WORDS: new species, ZingiberDymczewiczia, Zingiberaceae, Thailand



Zingiber sirindhorniae Triboun and Keerat., sp. nov.

Diagnosis: Zingiber sirindhorniae belongs to Zingiber section Dymczewiczia (Horan.) Benth. due to the terminal infl orescence on the leafy shoot. It is most similar to Zingiber plicatum Škorničk. and Q.B. Nguyễ n in having terminal inflorescence and the limestone habitat, but they differ by the former having a short and small terminal inflorescence on a leafy stem and by the dark maroonish flowers.

Figure 2. Zingiber sirindhorniae Triboun and Keerat.:
A. habitat, B. habit, C. rhizomes, and D. inflorescence with opened flowers.

Photographed by Pramote Triboun. 

Distribution. Endemic to Thailand. So far known only from Loei Province. 

 Ecology. In humus among rocks in partially shaded dry evergreen forest on limestone hills, alt. 350-450 m. 

 Phenology. Flowering in June to August and fruiting in July to October. 

 Etymology. The specific epithet honours Her Royal Highness Princess Sirindhorn of Thailand who has taken a keen interest in the conservation of plants. Vernacular. Aiyarit (ไอยริศ), name given by Her Royal Highness Princess Sirindhorn.
  

Notes. Four Thai species of Zingiber produce a terminal inflorescence; the inflorescence is always terminal in Z. pellitum Gagnep. and Z. gramineum Blume, while Z. barbatum Wall. and Z. junceum Gagnep. occasionally produce a terminal inflorescence. These four species are taller (to 1 m tall or taller) and are terrestrial, while Z. sirindhorniae is rather slender and small (40-70 cm tall), and grows in humus in crevices on limestone cliffs. In habit Zingiber sirindhorniae is more like Z. plicatum Škorničk. and Q.B. Nguyễn. The inflorescence of the new species is rather fragile and delicate.



  

Pramote Triboun and Kaweesak Keeratikiet. 2016. Zingiber sirindhorniae, A Remarkable New Species in Zingiber section Dymczewiczia (Zingiberaceae) from Thailand.  The Thailand Natural History Museum Journal. 10(1); 1-6.  www.THNHMJournal.com



 ตราไปรษณียากร ชุด ปีใหม่ 2559 (ชุดที่ 1) ‘พืชตระกูลขิง’ 
Thailand • New Year 2016 Postage Stamps (1st Series) ‘Gingers (Zingiberaceae)’

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روابط التحميل والمشاهدة، الروابط المباشرة للتحميل
او
شاهد هذا الفيديو القصير لطريقة التحميل البسيطة


كيف تحصل على مدونة جاهزة بآلاف المواضيع والمشاركات من هنا
شاهد قناة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على اليوتيوب لمزيد من الشرح من هنا
رابط مدونة منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات في أي وقت حــــتى لو تم حذفها من هنا
شاهد صفحة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على الفيس بوك لمزيد من الشرح من هنا
تعرف على ترتيب مواضيع منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات (حتى لا تختلط عليك الامور) من هنا

ملاحظة هامة: كل عمليات تنزيل، رفع، وتعديل المواضيع الجاهزة تتم بطريقة آلية، ونعتذر عن اي موضوع مخالف او مخل بالحياء مرفوع بالمدونات الجاهزة بآلاف المواضيع والمشاركات، ولكم ان تقوموا بحذف هذه المواضيع والمشاركات والطريقة بسيطة وسهلة. ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــسلامـ.

[PaleoOrnithology • 2017] Piscivorenantiornis inusitatus • The First Known Piscivorous Enantiornithine Bird from the Early Cretaceous of China ---ScRaBBlE


Piscivorenantiornis inusitatus 
Wang & Zhou, 2017  


ABSTRACT
A fish-eating enantiornithine bird with a gastric pellet composed of fish bones has recently been reported from the Lower Cretaceous Jiufotang Formation of Liaoning Province, northeastern China. Along with other discoveries, this specimen reveals that distinct features of modern avian digestive system were well established in those early birds. On the basis of a detailed anatomical study presented here, we show that this fish-eating enantiornithine bird represents a new taxon, Piscivorenantiornis inusitatus, gen. et sp. nov. The well-preserved elements of the skull, neck, sternum, and pelvis further enrich our understanding of the morphological diversity in early enantiornithines. Most notably, the cranial articular facet of the caudal cervical vertebra is dorsoventrally concave and mediolaterally convex, a feature otherwise unknown among other birds and with unclear functional significance.



  Life reconstruction of the fish-eating enantiornithine bird, eating – and vomiting – habits.
Illustration: SHI Aijuan 

SYSTEMATIC PALEONTOLOGY
AVES Linnaeus, 1758
ORNITHOTHORACES Chiappe, 1995
ENANTIORNITHINES Walker, 1981

PISCIVORENANTIORNIS, gen. nov.

Type Species:— Piscivorenantiornis inusitatus, sp. nov.

Etymology:— The generic name is derived from Latin ‘pisci’ and ‘vor,’ intended to convey ‘a fish-eating enantiornithine bird.’


PISCIVORENANTIORNIS INUSITATUS, sp. nov.
Etymology:— The specific name is from Latin ‘inusitatus,’ referring to the unusual cranial articular facet of the caudal cervical vertebra. 

FIGURE 1. Photograph of the holotype of Piscivorenantiornis inusitatus, gen. et sp. nov., IVPP V22582.
Scale bar equals 10 mm. 

Figure 3. A Sketch Reconstruction of the Fish-Eating Enantiornithine Bird Represented by IVPP V22582 



Min Wang and Zhonghe Zhou. 2017. A Morphological Study of the First Known Piscivorous Enantiornithine Bird from the Early Cretaceous of China.  Journal of Vertebrate Paleontology. DOI:  10.1080/02724634.2017.1278702

Min Wang, Zhonghe Zhou and Corwin Sullivan. 2016. A Fish-Eating Enantiornithine Bird from the Early Cretaceous of China Provides Evidence of Modern Avian Digestive Features. Current Biology. 26; 1170–1176.  DOI: 10.1016/j.cub.2016.02.055


Fish-eating enantiornithine bird provides evidence of modern avian digestive features http://phy.so/381743208 via @physorg_com

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روابط التحميل والمشاهدة، الروابط المباشرة للتحميل
او
شاهد هذا الفيديو القصير لطريقة التحميل البسيطة


كيف تحصل على مدونة جاهزة بآلاف المواضيع والمشاركات من هنا
شاهد قناة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على اليوتيوب لمزيد من الشرح من هنا
رابط مدونة منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات في أي وقت حــــتى لو تم حذفها من هنا
شاهد صفحة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على الفيس بوك لمزيد من الشرح من هنا
تعرف على ترتيب مواضيع منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات (حتى لا تختلط عليك الامور) من هنا

ملاحظة هامة: كل عمليات تنزيل، رفع، وتعديل المواضيع الجاهزة تتم بطريقة آلية، ونعتذر عن اي موضوع مخالف او مخل بالحياء مرفوع بالمدونات الجاهزة بآلاف المواضيع والمشاركات، ولكم ان تقوموا بحذف هذه المواضيع والمشاركات والطريقة بسيطة وسهلة. ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــسلامـ.

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