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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 Nymphalidae. Show all posts
Showing posts with label Nymphalidae. Show all posts

Wednesday, March 20, 2019

[Entomology • 2017] Melitaea acentria • A New Species of Melitaea from Israel, with Notes on Taxonomy, Cytogenetics, Phylogeography and Interspecific Hybridization in the Melitaea persea complex (Lepidoptera, Nymphalidae) ---ScRaBBlE


Melitaea acentria Lukhtanov, 2017

Photos by V. Lukhtanov    DOI: 10.3897/CompCytogen.v11i2.12370 

Abstract
Specimens with intermediate morphology are often considered to be the result of ongoing interspecific hybridization; however, this conclusion is difficult to prove without analysis of chromosomal and/or molecular markers. In the butterfly genus Melitaea, such an intermediacy can be detected in male genitalia, and is more or less regularly observed in localities where two closely related, presumably parental species are found in sympatry. Here I analyze a high altitude Melitaea population from Mt. Hermon in north Israel and show that its male genitalia are clearly differentiated from those found in phenotypically similar M. persea and M. didyma, but in some aspects intermediate between them. This hybrid-like population is unique because, although M. didyma is present on Mt. Hermon, the true, low-altitude M. persea has never been reported from Israel. Cytogenetic analysis revealed no apomorphic chromosomal characters to distinguish the Mt. Hermon population from other known taxa of the M. persea and M. didyma species groups. At the same time, DNA barcode-based phylogeographic study showed that this population is ancient. It was estimated to originate 1–1.6 million years ago in the Levantine refugium from a common ancestor with M. persea. Generally, the data obtained are incompatible with interpretation of the studied population as a taxon conspecific with M. persea or M. didyma, or a swarm of recent hybrids between M. persea and M. didyma, although the possibility of ancient homoploid hybrid speciation cannot be ruled out. I also argue that the name Melitaea montium assigned to butterflies from north Lebanon cannot be applied to the studied taxon from Mt. Hermon. Here I describe this morphologically and ecologically distinct entity as a new species Melitaea acentria sp. n., and compare it with other taxa of the M. persea complex.

Keywords: Chromosomes, COI, DNA barcoding, genitalia, homoploid hybrid speciation, interspecific hybridization, Middle East, Melitaea casta, Melitaea eberti, Melitaea higginsi, Melitaea deserticola, Melitaea trivia, morphology, nomenclature, taxonomy

Figure 2. Melitaea acentria sp. n.
  
holotype, male, 17949_A06, Israel, Mt. Hermon; upperside holotype, male; underside male, 25453_E09, Israel, Mt. Hermon d paratype, female, 25453_E11, Israel, Mt. Hermon  
Photos by V. Lukhtanov    DOI: 10.3897/CompCytogen.v11i2.12370

Melitaea acentria Lukhtanov, sp. n.

 Holotype: (Fig. 2a, b), male, BOLD process ID BPAL2191-13, field # CCDB-17949_A06, GenBank accession number # KY777529; Israel, Mt. Hermon, 2050 m, 01 June 2013, A. Novikova leg., deposited in the Zoological Institute of the Russian Academy of Science (St. Petersburg).

Figure 3. Melitaea acentria in nature. Female. Israel, Mt. Hermon, 1800 m, 07 May 2016.
Photos by V. Lukhtanov
 
 DOI: 10.3897/CompCytogen.v11i2.12370 

Figure 13. Melitaea acentria and its habitat. Israel, Mt. Hermon, 2040 m, 22 June 2013.  

Distribution: Melitaea acentria is known to occur at high altitudes (1730–2060 m above the sea level) of Mt. Hermon (Fig. 11). Within these altitudes it is sympatric and syntopic with M. trivia syriaca, M. deserticola and M. cinxia. At the altitudes 1730–1780 m there is an essential overlapping of the M. acentria and M. didyma liliputana ranges where both species were found to fly together in early May 2016. Two other Melitaea species known from Mt. Hermon, M. collina and M. telona, were found to fly mostly at lower altitudes 1000–1600 m.

Etymology: The name acentria is a noun of the feminine gender. This name originates from the Greek prefix “a” that means “not” and from the Latin word “centrum” (centre) derived from the Greek “κέντρον” (kentron, a sharp point). Acentria is the Internet nickname of Asya Novikova who collected the samples initiated this research.This name indicates also the peripheral position of the new species within the distribution range of the M. persea species complex.

Figure 2. Melitaea acentria sp. n. and M. persea persea.
Macentria sp. n., holotype, male, sample 17949_A06, Israel, Mt. Hermon; upperside Macentria sp. n., holotype, male, sample 17949_A06, Israel, Mt. Hermon; underside Macentria sp. n., paratype, male, sample 25453_E09, Israel, Mt. Hermon Macentria sp. n., paratype, female, sample 25453_E11, Israel, Mt. Hermon
e M. persea persea, male, 17966_A10, Iran, Fars prov., Fasa area, 20 km W Estahban, 2200 m, 9-11 May 2007, B. Denno coll., MGCL accession # 2010-20 f M. persea persea, female, 17951_B01, Iran, Fars prov., 20 km N Darab, 2100-2300 m, 24.05.1999, leg. P. Hofmann, MGCL g M. persea persea, male, 17966_A11, Iran, Fars prov., Fasa area, 20 km W Estahban, 2200 m, 9–11.05.2007, MGCL accession # 2008-43 h M. persea persea, male, 17951_B02, Iran, Char Mahall-o-Bahtiyari, Umg. Shahr-e-Kord, 2000 m, 28 May 2002, leg. P. Hofmann, MGCL.

Scale bar corresponds to 10 mm in all figures. 
Photos by V. Lukhtanov    DOI: 10.3897/CompCytogen.v11i2.12370

Figure 10. Melitaea persea persea, presumptive hybrid between M. interrupta and M. persea, M. persea paphlagonia, M. higginsi, M. didyma liliputana and M. interrupta.
a Melitaea persea persea, female, 17951_B03, Iran, Esfahan, Kuh-e-Marsenan, near Zefre, 2000 m, 26 May 2002, leg. Hofmann, MGCL b presumptive hybrid female between M. interrupta and M. persea, 17966_F12, Armenia, Zhangezur Range, Megri district, Litchk, 1800 m, 23 July 1999, A. Dantchenko leg., MGCL c M. persea paphlagonia, male, 17951_F11, Iran, Khorasan, Kuh-e-Binalut, 15 km SW Zoshk, 2300–2500 m, 7 June 1999, leg. P. Hofmann, MGCL d M. persea paphlagonia, male, 17951_F11, Iran, Khorasan, Kuh-e-Binalut, 15 km SW Zoshk, 2300-2500 m, 7 June 1999, leg. P. Hofmann, MGCL e M. higginsi, male, 17966_A12, Afghanistan, Hindukush, Panchir Valley, 20 June 2004, M.J.Simon collection, MGCL f M. higginsi, female, 17950_H10, Afghanistan, Badakhshan, Mt. Yamak N of Anjuman Pass, 3500-4000 m, 1-25 July 2004 M.J.Simon collection, MGCL g M. didyma liliputana, male, 17968_E10, Israel, Mt. Hermon h M. interrupta, male, 17966_F11, Armenia Armenia, Zhangezur Range, Kadjaran, 2500 m, 21–22 July 1999, leg. A. Chuvilin, MGCL; the wing underside is with black scales along the veins.
Scale bar corresponds to 10 mm in all figures. Photos by V. Lukhtanov    DOI: 10.3897/CompCytogen.v11i2.12370

Conclusion
The Melitaea persea species complex consists of the following taxa:

• M. persea Kollar, 1849
M. persea persea Kollar, 1849 (East Turkey, Armenia, Azerbaijan, Daghestan in Russian Caucasus, western, central and nothern parts of Iran)
M. persea paphlagonia Fruhstorfer, 1917 (NE Iran, probably also S. Turkmenistan)

• M. eberti Koçak, 1980 (N. Iran)

• M. higginsi Sakai, 1978 (Afghanistan)

• M. acentria Lukhtanov sp. n. (Mt. Hermon in Israel, definitely also the neighboring territories of Syria and Lebanon)

The identity and taxonomic status of the M. persea-similar samples from north Lebanon, Jordan, Iraq, Pakistan, and Afghanistan remain still unclear. The populations from Lebanon characterized by the mitochondrial haplogroup P2 (Fig. 9) could actually represent (i) a distinct subspecies of M. persea, (ii) an undescribed subspecies of M. acentria, or even (iii) an undescribed species. Further morphological, molecular and chromosomal studies are required to select between these hypotheses.


 Vladimir A. Lukhtanov. 2017. A New Species of Melitaea from Israel, with Notes on Taxonomy, Cytogenetics, Phylogeography and Interspecific Hybridization in the Melitaea persea complex (Lepidoptera, Nymphalidae). Comparative Cytogenetics. 11(2); 325-357.  DOI: 10.3897/CompCytogen.v11i2.12370

New butterfly species discovered in Israel for the first time in 109 years http://blog.pensoft.net/2017/05/09/new-butterfly-species-discovered-in-israel-for-the-first-time-in-109-years/

 

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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 • 2017] Remarkable Sexual Dimorphism, Rarity and Cryptic Species: A Revision of the ‘aegrota species group’ of the Neotropical Butterfly Genus Caeruleuptychia Forster, 1964 (Lepidoptera, Nymphalidae, Satyrinae) with the Description of Three New Species ---ScRaBBlE


male Sunburst Cerulean-Satyr, Caeruleuptychia helios  (Weymer, 1911)


Abstract

The ‘aegrota species group’ of the Neotropical nymphalid genus Caeruleuptychia Forster, 1964, in addition to three other superficially similar, enigmatic species in the genus, are revised. A lectotype is designated for Euptychia aegrota Butler, 1867, E. aetherialis Butler, 1877 stat. rev.E. helios Weymer, 1911 and E. pilata Butler, 1867, and C. aetherialis is resurrected from its synonymy with C. aegrotaCaeruleuptychia helios caelestissima Brévignon, 2010, syn. nov., and Magneuptychia keltoumae Brévignon & Benmesbah, 2012, syn. nov. are both regarded as junior subjective synonyms of C. helios (Weymer, 1911), as a result of the discovery and first illustration of the female of this taxon. The female of C. aegrota is also described and illustrated for the first time, and three new speciesCaeruleuptychia trembathi Willmott, Nakahara, Hall & Neild, sp. nov.C. scripta Nakahara, Zacca & Huertas, sp. nov., and C. maryzenderae Lamas & Nakahara, sp. nov. are described and named. We analyze morphological and molecular data separately, in addition to combining morphological data with molecular data, to provide the first phylogenetic hypothesis for the taxa treated in this revision.

Keywords: eastern Andes; Amazonian forest; DNA barcode; synonym; taxonomy; Euptychiina; lectotype; Magneuptychia

   
The iridescent blue male sunburst cerulean-satyr, Caeruleuptychia helios, top, was not linked with its female counterpart until DNA bar codes showed they were the same species.
 photos by Shinichi Nakahara, Florida Museum of Natural History

This iridescent blue male sunburst cerulean-satyr, Caeruleuptychia helios, was found at Villa Carmen Biological Station in Peru. Researchers attracted the butterfly with fermented fish and human urine.
Photo: Andrew Neild 

Caeruleuptychia trembathi  Willmott, Nakahara, Hall & Neild, 2017

DNA barcoding also revealed a new species: Trembath’s cerulean-satyr, or Caeruleuptychia trembathi. The male, top, is also strikingly different than the female.
 photos of male by Keith Willmott; photos of female by Andrew Neild 
  

Shinichi Nakahara, Thamara Zacca, Blanca Huertas, Andrew F. E. Neild, Jason P. W. Hall, Gerardo Lamas, Lauren A. Holian, Marianne Espeland and Keith R. Willmott. 2017. Remarkable Sexual Dimorphism, Rarity and Cryptic Species: A Revision of the ‘aegrota species group’ of the Neotropical Butterfly Genus Caeruleuptychia Forster, 1964 with the Description of Three New Species (Lepidoptera, Nymphalidae, Satyrinae).  Insect Systematics & Evolution. DOI: 10.1163/1876312x-00002167

A case of mistaken identity: DNA links male, female butterfly thought to be distinct species.

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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 • 2017] Preliminary Molecular Phylogeny and Biogeography of the Monobasic Subfamily Calinaginae (Lepidoptera, Nymphalidae) ---ScRaBBlE


Figure 2. Bayesian phylogeny of Calinaga estimated in BEAST using concatenated data. Purple squares are calibration points (root: 75 ± 3; Satyrinae + Charaxinae 70 ± 3.5, Charaxes + Euxanthe 22 ± 1). Monophyly was enforced on nodes marked with orange squares. The inset map shows the biogeographic regions used in DIVA analysis: A) Southwestern China ecozone, B) Himalaya-Tibetan plateau region, C) Northern Sino-Himalaya, D) Southern Sino-Himalaya, E) Indochina. Colored dots correspond to haplogroups on the tree.

Abstract
Calinaga (Moore 1857) is a rare and enigmatic Asian butterfly genus whose phylogenetic placement within Nymphalidae has only recently been established. The evolutionary history of Calinaga species however remains unknown. Here we explore the phylogeography of Calinaga using 1310 bp of sequence data from two molecular (mtDNA barcode and ribosomal protein S5 nuclear gene) and two morphological traits (genitalia and wing pattern). Within the proposed phylogenetic framework, we estimate the ages of divergence within the genus and reconstruct their historical biogeography. We found strong support for monophyly of Calinaga and support for the most recent accepted species in the genus. Our results indicate that the common ancestor of Calinaga first split in the Eocene (~43 million years ago) in southern China, probably as a consequence of geological and environmental impacts of the collision of the Indian and Asian subcontinents. In the Oligocene/Miocene, the extrusion of Indochina from the continent caused further dramatic orogenetic changes that promoted isolation and speciation events within the genus while Pleistocene climatic changes also influenced the distribution and further speciation. A dispersal–vicariance analysis suggests that vicariance events have played a far more important role than dispersal in the distribution of extant species.

Key Words: Calinaga, Calinaginae, Nymphalidae, mtDNA, butterfly, Indochina, Oligocene



Figure 1. (A) Approximate geographic distributions (Shirôzu 1960, Lang 2012) and sampling localities (circles) for the species of Calinaga included in this study (with the exception of the sample CBUD-INDIN for which we do not have an exact locality). Species as initially identified are highlighted and shown in different colours. Note that many of these initially attributed names subsequently proved erroneous. The map was obtained using Quantum GIS 2.8.2 based on a map from Natural Earth (www.naturalearthdata.com).
(B) Median-Joining Network of mtDNA. Circle size proportional to haplotype frequency; number of nucleotide substitutions indicated along connections, except for single or double substitutions. In both figures the species are highlighted and shown in different colours as initially identified. 

Conclusion
The genus Calinaga probably originated in the South-East Tibet in Eocene following the immense geological and environmental impact caused by the collision between Indian and Asian subcontinents. The extrusion of Indochina from the continent during the Oligocene/Miocene further prompted dramatic orogenetic changes that promoted isolation and speciation events in the genus. More recently, in the Pleistocene, climatic changes further modified the distribution of species and probably facilitated vicariant speciation events.

Since we did not sample or sequence specimens from all of the available names under Calinaga, we cannot make any definitive statements about the number of valid species warranted to be recognized as such, although the existence of many superfluous names is evident. From the names of the genus and the species coined by early British lepidopterists including F. Moore, it is apparent that they drew inspiration from Hindu mythological characters. In Sanskrit, Nāga refers to mythical reptilian creatures found in Indian religions (Hinduism, Buddhism and Janism) who were often worshipped as deities. Among them, “Kaliya” (or Kalya, “Kalia-Naga”, Calinaga) was a particularly notorious and poisonous one living in Yamuna river in Vrindavan (Uttar Pradesh). After an encounter with Krishna, Kaliya surrendered and was sent to exile (Bhagavata Purana, 16:10). It seems that the modern taxonomy of Calinaga is in need of a Krishna to conquer these superfluous names and cleanse its taxonomy albeit after careful examination of the types and sequencing of additional material.


 Valentina Todisco, Vazrick Nazari and Paul D.N. Hebert. 2017. Preliminary Molecular Phylogeny and Biogeography of the Monobasic Subfamily Calinaginae (Lepidoptera, Nymphalidae). Zoosystematics and Evolution. 93(2); 255-264. DOI: 10.3897/zse.93.10744

Origins of an enigmatic genus of Asian butterflies carrying mythological names decoded http://blog.pensoft.net/2017/04/18/origins-of-an-enigmatic-genus-of-asian-butterflies-carrying-mythological-names-decoded/

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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 • 2017] Phylogeny and Diversification of the Cloud Forest Morpho sulkowskyi Group (Lepidoptera, Nymphalidae) in the Evolving Andes ---ScRaBBlE



Abstract

The monophyletic Morpho sulkowskyi butterfly group, endemic of Andean cloud forests, was studied to test the respective contributions of Mio-Pliocene intense uplift period and Pleistocene glacial cycles on Andean biodiversity. We sampled nine taxa covering the whole geographical range of the group. Two mitochondrial and two nuclear genes were analysed using a Bayesian method. We established a dated phylogeny of the group using a relaxed clock method and a wide-outgroup approach. To discriminate between two hypotheses, we used a biogeographical probabilistic method. Results suggest that the ancestor of the M. sulkowskyi group originated during the Middle–Late Miocene uplift of the Eastern Cordillera in northern Peru. Biogeographical inference suggests that the M. sulkowskyi and Morpho lympharis clades diverged in the northern Peruvian Andes. The subsequent divergences, from the Late Miocene to the Late Pliocene, should have resulted from a dispersal towards the Northern Andes (M. sulkowskyi clade), after the closure of the West Andean Portal separating the Central and Northern Andes, and a southwards dispersal along the Peruvian and Bolivian Eastern Cordilleras (M. lympharis clade). Only a few divergences occurred at the very end of the Pliocene or during the Pleistocene, a period when the more recent uplifts interfered with Pleistocene glacial cycles.

Figure 1.  Map of the region where field studies were carried out, with habitus of the taxa calderoni, zachi and nieva (m: male; f: female; f1 and f2: female morphs within the calderoni population). N1 and N2: sampling areas along the upper Río Nieva. Other localities where specimens were collected: AP: Abra Patricia; EF: El Afluente; OP: Oso Perdido; PM: Abra Pardo Miguel; V: Venceremos. Two specimens of nieva were also collected at Santa Cruz del Mirador (M), at ca. 20 km ESE from El Afluente. 

Conclusions
Simple relationships between Andean uplift and the diversification of various plant and animal groups, implying pre-Pleistocene driving processes, have been supposed by various authors. Doan (2003), for example, proposed the south-to-north speciation hypothesis, where the process of speciation should be related to the south-to-north progression of uplift throughout the Andes. Other authors emphasized the possible role of a rapid uplift that occurred during the Late Miocene and Early Pliocene, but often without establishing clear links between dated divergences and local geologic events (e.g. Casner & Pyrcz 2010; Mulch et al. 2010; Matos-Maraví et al. 2013; Lagomarsino et al. 2016). From a geological point of view, the concept of a progressive, general south-to-north uplift is an oversimplified view of a much more complex reality (Sempere et al. 2008). In the Central Andes, palaeo-elevation histories differ not only between the south and the north, but also between the western and the eastern cordilleras, notably in northern Peru (Picard et al. 2008; Eude et al. 2015; Margirier et al. 2015). The idea that the Northern Andes, as a whole, uplifted later than the Central Andes, as suggested by Doan (2003), and often admitted by other authors, is not supported by geological studies that also demonstrate that the timing of palaeo-elevation differed between the three Colombian Cordilleras (Restrepo- Moreno et al. 2009). Consistent with many other examples, notably the clearwing Oleriina butterflies (De-Silva et al. 2016), the M. sulkowskyi group illustrates the diversity of diversification histories throughout the Andes. It also demonstrates that Mio-Pliocene orogenic and Pleistocene climatic diversification drivers should not be opposed.



Romain Nattier, Claire Capdevielle-Dulac, Catherine Cassildé, Arnaud Couloux, Corinne Cruaud, Gilbert Lachaume, Gerardo Lamas, Jean-François Silvain and Patrick Blandin. 2017. Phylogeny and Diversification of the Cloud Forest Morpho sulkowskyi Group (Lepidoptera, Nymphalidae) in the Evolving Andes.  Zoologica Scripta.  DOI: 10.1111/zsc.12226

   

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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 • 2019] Amiga gen. n. • A Revision of the New Genus Amiga, described for Papilio arnaca Fabricius, 1776 (Lepidoptera, Nymphalidae, Satyrinae) ---ScRaBBlE


Amiga Nakahara, Willmott & Espeland

[upper] Amiga arnaca indianacristoi ssp. n. in nature, Altos de Pipe, Miranda, Venezuela

[lower] 
A. arnaca adela from Costa Rica, male; j A. arnaca adela from Costa Rica, female; 
A. arnaca adela from W Ecuador, holotype male; l A. arnaca adela from W Ecuador, female;

A. arnaca sericeella, male from Mexico; n A. arnaca sericeella from Mexico, female; 

o A. arnaca indianacristoi from NW Venezuela, paratype male; p A. arnaca indianacristoi from N Venezuela, paratype female.


in Nakahara, Lamas, Tyler, Marín, Huertas, et al., 2019. 

Abstract
We here propose a new, monotypic genusAmiga Nakahara, Willmott & Espeland, gen. n., to harbor a common Neotropical butterfly, described as Papilio arnaca Fabricius, 1776, and hitherto placed in the genus Chloreuptychia Forster, 1964. Recent and ongoing molecular phylogenetic research has shown Chloreuptychia to be polyphyletic, with C. arnaca proving to be unrelated to remaining species and not readily placed in any other described genus. Amiga arnaca gen. n. et comb. n. as treated here is a widely distributed and very common species ranging from southern Mexico to southern Brazil. A neotype is designated for the names Papilio arnaca and its junior synonym, Papilio ebusa Cramer, 1780, resulting in the treatment of the latter name as a junior objective synonym of the former. A lectotype is designated for Euptychia sericeella Bates, 1865, which is treated as a subspecies, Amiga arnaca sericeella (Bates, 1865), comb. n. et stat. n., based on molecular and morphological evidence. We also describe two new taxaAmiga arnaca adela Nakahara & Espeland, ssp. n. and Amiga arnaca indianacristoi Nakahara & Marín, ssp. n.new subspecies from the western Andes and eastern Central America, and northern Venezuela, respectively.

Keywords: DNA barcodes, Euptychiina, species delimitation, subspecies, systematics, taxonomy

Figure 2. Amiga arnaca spp. specimens spanning its range (dorsal on left, ventral on right):
a nominotypical subspecies from Suriname, neotype male (USNM) b nominotypical subspecies from Guyana, female (FLMNH-MGCL 263373) c nominotypical subspecies from E Ecuador, male (FLMNH-MGCL 257121) d nominotypical subspecies from Peru, female (FLMNH-MGCL 262953); e nominotypical subspecies from N Brazil, male (FLMNH-MGCL1036223) f Nominotypical subspecies from N Brazil, female (FLMNH-MGCL 207984) g Nominotypical subspecies from SE Brazil, male (FLMNH-MGCL 1036213); h nominotypical subspecies from SE Brazil, female (FLMNH-MGCL 1036218)

A. arnaca adela from Costa Rica, male (FLMNH-MGCL 207991) j A. arnaca adela from Costa Rica, female (FLMNH-MGCL 207992) k A. arnaca adela from W Ecuador, holotype male (FLMNH-MGCL 151127) l A. arnaca adela from W Ecuador, female (FLMNH-MGCL 257087) m A. arnaca sericeella, male from Mexico (FLMNH-MGCL 207900) n A. arnaca sericeella from Mexico, female (FLMNH-MGCL 207896) o A. arnaca indianacristoi from NW Venezuela, paratype male (FLMNH-MGCL 263107) p A. arnaca indianacristoi from N Venezuela, paratype female (FLMNH-MGCL 1036235).

Amiga Nakahara, Willmott & Espeland, gen. n.

Papilio arnaca Fabricius, 1776, 
by present designation

Systematic placement and diagnosis: 
Espeland et al. (2019) recovered Amiga arnaca comb. n. as sister to the “Pareuptychia clade”, whose composition partially corresponded to that found in Peña et al. (2010), with a high support (BS and PP > 0.95). The “Pareuptychia clade” itself was also well supported (BS and PP > 0.95), including Satyrotaygetis satyrina (Bates, 1865), Magneuptychia inani (Staudinger, [1886]), Euptychoides albofasciata (Hewitson, 1869), Neonympha areolatus (Smith, 1797), Erichthodes antonina (C. Felder & R. Felder, 1867), Pareuptychia ocirrhoe (Fabricius, 1776), Megeuptychia antonoe (Cramer, 1775), Splendeuptychia doxes (Godart, [1824]), Nhambikuara mima (Butler, 1867), and Euptychoides eugenia (C. Felder & R. Felder, 1867). Amiga gen. n. is distinguished from all members of the “Pareuptychia clade” by the presence of bluish-lilac coloration on the dorsal hindwing and by the purplish sheen in the tornal half of the VHW. Furthermore, the absence of cornuti and membranous lamella antevaginalis of Amiga gen. n. appear to be unusual character states among the clade. The type species of Chloreuptychia, Papilio chloris Cramer, 1780 (= Chloreuptychia chlorimene) was recovered as sister to a moderately supported (BS and PP > 0. 75 < 0. 95), clade including the “Pareuptychia clade”, “Taygetis clade”, “Splendeuptychia clade” and “Archeuptychia clade”.

Etymology: The new generic name is derived from the feminine Spanish noun “amiga”, meaning “a (female) friend”, alluding to the fact that this is a common, familiar butterfly. The generic name is regarded as feminine.

Distribution: This genus ranges from southern Mexico throughout virtually all of tropical Central and South America, where its southernmost distribution appears to be southern Brazil.


Taxonomy: 
Amiga gen. n. is regarded as monotypic, with total of four subspecies recognized, of which two are named and described herein.

Amiga Nakahara, Willmott & Espeland, gen. n.
(– denotes a subspecies, – – denotes a synonym)

Amiga arnaca (Fabricius, 1776) comb. n.
– –ebusa (Cramer, 1780)
– –priamis (D’Almeida, 1922)

Amiga arnaca adela Nakahara & Espeland, ssp. n.

Amiga arnaca sericeella (Bates, 1865) comb. n. et stat. n.

Amiga arnaca indianacristoi Nakahara & Marín, ssp. n.

Figure 7. Amiga arnaca indianacristoi ssp. n. in nature, Altos de Pipe, Miranda, Venezuela

(photographed by Indiana Cristóbal Ríos-Málaver,
 on 11 September 2011). 

Amiga arnaca indianacristoi Nakahara & Marín, subsp. n.

Etymology: This new species-group name is proposed in recognition of our friend and colleague, Indiana Cristóbal Ríos-Málaver, known as “Indiana Cristo”, who studied the butterflies of the area where this taxon occurs. Indiana Cristo has contributed to Neotropical lepidopterology in various ways, especially through social media, where he is bringing lepidopterology to the public. This species-group name is treated as a latinized masculine noun in the genitive case.

Distribution: This taxon occurs in the Venezuelan Cordillera de la Costa and northwestern Cordillera de Mérida, and possibly also into the Serranía de Perijá.


 Shinichi Nakahara, Gerardo Lamas, Stephanie Tyler, Mario Alejandro Marín, Blanca Huertas, Keith R. Willmott, Olaf H. H. Mielke and Marianne Espeland. 2019. A Revision of the New Genus Amiga Nakahara, Willmott & Espeland, gen. n., described for Papilio arnaca Fabricius, 1776 (Lepidoptera, Nymphalidae, Satyrinae). ZooKeys. 821: 85-152. DOI: 10.3897/zookeys.821.31782

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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 • 2018] Molecular Systematics of the Subfamily Limenitidinae (Lepidoptera: Nymphalidae) ---ScRaBBlE


  Subfamily Limenitidinae

 Examples of butterflies; 
Parthenos sylviaCymothoe caenisEuriphene tademaEuphaedra herbertiPseudacraea poggeiLebadea marthaNeptis idaLimenitis reducta and Adelpha californica

in Dhungel & Wahlberg,. 2018.

Abstract
 We studied the systematics of the subfamily Limenitidinae (Lepidoptera: Nymphalidae) using molecular methods to reconstruct a robust phylogenetic hypothesis. The molecular data matrix comprised 205 Limenitidinae species, four outgroups, and 11,327 aligned nucleotide sites using up to 18 genes per species of which seven genes (CycY, Exp1, Nex9, PolII, ProSup, PSb and UDPG6DH) have not previously been used in phylogenetic studies. We recovered the monophyly of the subfamily Limenitidinae and seven higher clades corresponding to four traditional tribes Parthenini, Adoliadini, Neptini, Limenitidini as well as three additional independent lineages. [CymothoiniPseudoneptini and Pseudacraeini] One contains the genera Harma Cymothoe and likely a third, Bhagadatta, and the other two independent lineages lead to Pseudoneptis and to Pseudacraea. These independent lineages are circumscribed as new tribes. Parthenini was recovered as sister to rest of Limenitidinae, but the relationships of the remaining six lineages were ambiguous. A number of genera were found to be non-monophyletic, with Pantoporia, Euthalia, Athyma, and Parasarpa being polyphyletic, whereas Limenitis, Neptis, Bebearia, Euryphura, and Adelpha were paraphyletic.

Figure 1: The Maximum Likelihood topology for Limenitidinae with associated bootstrap values. Major lineages that are considered tribes in this paper are coloured.
Examples of butterflies (voucher specimens for this work) from top: Parthenos sylviaCymothoe caenisEuriphene tademaEuphaedra herbertiPseudacraea poggeiLebadea marthaNeptis idaLimenitis reducta and Adelpha californica.

Conclusion: 
This study presents the most comprehensive phylogenetic analysis to date for the “trash-can” subfamily Limenitidinae. Based on fragments of up to 18 genes per species, 205 species and four outgroups, our results recovered Limenitidinae as a monophyletic clade and which comprises seven major lineages that deserve tribal status. Four tribes have been traditionally recognized: Parthenini, Neptini, Adoliadini, and Limenitidini, while three lineages are placed in new tribes here: Cymothoini, Pseudoneptini and Pseudacraeini. The new Cymothoini tribe includes two African genera Cymothoe and Harma, and quite likely an Asian genus Baghadatta. The latter two new tribes are monogeneric. At the genus level, we found several traditionally recognized genera to be either poly- or paraphyletic, i.e., Neptis, Euryphura, Pantoporia, Athyma, Parasarpa, Limenitis, and Adelpha. Further work increasing the taxon sampling is necessary to test the monophyly of these genera and revise their limits.


Bidur Dhungel and Niklas Wahlberg​. 2018. Molecular Systematics of the Subfamily Limenitidinae (Lepidoptera: Nymphalidae).    PeerJ. 6:e4311.  DOI: 10.7717/peerj.4311

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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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