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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 clade nov.. Show all posts

Wednesday, March 20, 2019

[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


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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.

[Paleontology • 2017] Habelia optata [Habeliida, ord. nov.] • Mandibulate Convergence in An Armoured Cambrian Stem Chelicerate ---ScRaBBlE


Habelia optata  Walcott, 1912

Aria & Caron, 2017.

Abstract
Background
Chelicerata represents a vast clade of mostly predatory arthropods united by a distinctive body plan throughout the Phanerozoic. Their origins, however, with respect to both their ancestral morphological features and their related ecologies, are still poorly understood. In particular, it remains unclear whether their major diagnostic characters were acquired early on, and their anatomical organization rapidly constrained, or if they emerged from a stem lineage encompassing an array of structural variations, based on a more labile “panchelicerate” body plan.

Results
In this study, we reinvestigated the problematic middle Cambrian arthropod Habelia optata Walcott from the Burgess Shale, and found that it was a close relative of Sanctacaris uncata Briggs and Collins (in Habeliida, ord. nov.), both retrieved in our Bayesian phylogeny as stem chelicerates. Habelia possesses an exoskeleton covered in numerous spines and a bipartite telson as long as the rest of the body. Segments are arranged into three tagmata. The prosoma includes a reduced appendage possibly precursor to the chelicera, raptorial endopods connected to five pairs of outstandingly large and overlapping gnathobasic basipods, antennule-like exopods seemingly dissociated from the main limb axis, and, posteriorly, a pair of appendages morphologically similar to thoracic ones. While the head configuration of habeliidans anchors a seven-segmented prosoma as the chelicerate ground pattern, the peculiar size and arrangement of gnathobases and the presence of sensory/tactile appendages also point to an early convergence with the masticatory head of mandibulates.

Conclusions
Although habeliidans illustrate the early appearance of some diagnostic chelicerate features in the evolution of euarthropods, the unique convergence of their cephalons with mandibulate anatomies suggests that these traits retained an unusual variability in these taxa. The common involvement of strong gnathal appendages across non-megacheirans Cambrian taxa also illustrates that the specialization of the head as the dedicated food-processing tagma was critical to the emergence of both lineages of extant euarthropods—Chelicerata and Mandibulata—and implies that this diversification was facilitated by the expansion of durophagous niches.

Keywords: Arthropoda, Chelicerata, Convergence, Macroevolution, Cambrian, Burgess Shale






Fig. 7 Convergences in head anatomy and morphology between Habelia (a) and selected mandibulates, in this case Ianiropsis sp. (Malacostraca: Isopoda; b; © Buz Wilson, Australian Museum) and Henicops washpoolensis (Myriapoda: Chilopoda; c; image provided by G. Edgecombe). Colours highlight the morpho-functional correspondence between sensory appendages (exopods in Habelia vs. antennae in mandibulates; green), masticatory appendages (gnathobases in Habelia vs. mandibles and maxillae in mandibulates; orange) and complimentary appendages aiding in food manipulation (seventh head appendage in Habelia vs. maxillipeds in mandibulates; blue). Note that masticatory appendages in Henicops are hidden by the large coxosternites of the maxillipeds

Systematic palaeontology

Superphylum Panarthropoda Nielsen, 1995.
Phylum Euarthropoda Lankester, 1904.

Clade Arachnomorpha Heider, 1913 (= Arachnata Lauterbach, 1973).

Diagnosis (emended from Størmer, 1944). Euarthropods with the following characters: Cephalic shield encompassing at least four pairs of appendages with well-developed endopods; originally, presence along body of at least one pair of appendages with basipod differentiated into a well-sclerotized gnathal sclerite bearing setae or teeth (“gnathobasic appendage”); third gnathobasic cephalic appendage also part of groundplan; post-cephalic endopods terminating in a trident of claws with various arrangements.

Order Habeliida, ord. nov. Aria and Caron

Type family. Habeliidae Simonetta and Delle Cave, 1975.
Other included taxa. Sanctacarididae Legg and Pates, 2016.

Diagnosis. Arachnomorph arthropods with the following characters: Cephalic shield with sub-triangular, sub-horizontal pleural expansions and with antero-lateral notches accommodating pair of lateral compound eyes with no peduncle; cephalic shield with large mesio-dorsal bulge accommodating stomach; five pairs of anterior, slender and segmented antennule-like exopods likely inserted below the eyes and dorsally to other head appendages; on ventral side of head, reduced pair of appendages inserted anteriormost (presumed in Sanctacarididae), followed by five pairs of appendages composed of gnathobasic basipods increasing in size posteriad and bearing seven-segmented spinose/setose enditic endopods projecting anteriad; trunk bearing paddle-like exopods fringed with thin lamellae.

Remarks. We maintain the family Sanctacarididae erected by Legg and Pates [33], since 10 trunk segments and a spatulate telson remain diagnostic of Sanctacaris uncata, Utahcaris orion [33] and Wisangocaris barbarahardyae [35]. The affinity of Messorocaris magna [34] is less clear, but the peculiar shape of its trunk pleurae may place it in its own family.

Habelia had previously been assigned to the orders Aglaspina by Walcott and Emeraldellia by Størmer [36]. Given the lack of cladistic support for these taxa, which would be para- or polyphyletically nested within Arachnomorpha, the lack of redescription for Molaria, and the fact that their diagnoses should be extensively revised in light of the new data gathered on aglaspidids and Emeraldella, we have not reused Aglaspina or Emeraldellia herein.

Family Habeliidae Simonetta and Delle Cave, 1975.
Type genus. Habelia Walcott, 1912.


Diagnosis. Habeliidan euarthropods with the following characters: Body elongate, 19-segmented, divided into three distinct tagmata: cephalon (or “prosoma”) of seven segments (or eight somites) and trunk (12 segments) composed of a five-segmented thorax (or “mesosoma”) and eight-segmented post-thorax (or “metasoma”); trunk tagmatization based on discrete limb differentiation between thorax and post-thorax; posteriormost cephalic appendage (7th) similar to thoracic appendages, all characterized by a cheiromorph morphology: large undifferentiated basipods, well-developed seven-segmented endopods without endites, and paddle-like exopods fringed with oblanceolate lamellae; telson elongate.

Remarks. We hereby establish a diagnosis for the family Habeliidae, as the original publication of the taxon was not associated with one [39]; we also formalize diagnoses and descriptions for Habelia optata hereafter. The genus Thelxiope was also included in Habeliidae by Simonetta and Delle Cave; however, the presence of eight post-cephalic tergites and a pygidium would rather seem to indicate a relationship with Mollisonia [54, 55]. Thelxiope is therefore removed from Habeliidae.

Genus Habelia Walcott, 1912.
Type species. Habelia optata Walcott, 1912.

Diagnosis. Habeliid arthropod with the following characters: Post-ocular lateral and postero-lateral cephalic margins as well as pleural margins of trunk segments adorned with triangular spines; cuticular surface of cephalon and posterior portion of trunk segments richly adorned with small blunt spines/tubercles; cephalic gnathobases with elongate proximal “arm”; gnathobasic teeth differentiated antero-posteriorly (slender and long to short and stout); cephalic endopods with setal brush on podomeres 5 and 6; five-segmented thorax bearing strong biramous appendages with robust, clawed endopods and long basipods; very long (subequal to slightly greater than head and trunk length) bipartite telson, with a long, dentate proximal portion adorned with lateral spines, and a short distal portion about 1/3rd as long as proximal portion.


  


Cédric Aria and Jean-Bernard Caron. 2017. Mandibulate Convergence in An Armoured Cambrian Stem Chelicerate. BMC Evolutionary Biology. 17:261.   DOI: 10.1186/s12862-017-1088-7

A 508-million-year-old sea predator with a 'jackknife' head  phy.so/433048787 @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.

[Paleontology • 2017] Troodontids (Theropoda) from the Dinosaur Park Formation, Alberta, with A Description of A Unique New Taxon, Latenivenatrix mcmasterae: Implications for Deinonychosaur Diversity in North America ---ScRaBBlE


Latenivenatrix mcmasterae
van der Reest & Currie, 2017 


ABSTRACT

Troodontids are known from Asia and North America, with the most complete specimens from the Jurassic of China and the Cretaceous of Mongolia. North American troodontids are poorly known, and specimens that have been described are isolated elements or partial skeletons with limited material. A new troodontid from the upper Dinosaur Park Formation (upper Campanian) is based on partial skulls, several vertebrae, ribs, gastralia, chevrons, a sacrum, partial pelvis, and partial fore and hind limbs. It is the largest troodontid known, with an estimated height of 180 cm and length of 350 cm. Like other troodontids, it possesses an elongated ambiens process and has a horizontal ventral margin of the postacetabular process. It differs from all other derived troodontids in that the slightly retroverted pubis has a shaft that curves anteroventrally. Some specimens from the Dinosaur Park Formation previously assigned to Troodon are reassigned to the new taxon, including multiple partial crania, an associated dentary and metatarsus, and a partial skeleton. Previously undescribed elements from the lower part of the Dinosaur Park Formation are assigned to the resurrected Stenonychosaurus inequalis. Distinct stratigraphic separation of Stenonychosaurus inequalis and the new taxon indicates a replacement in troodontid fauna, similar to the turnover of large ornithischians in the same formation. The new taxon is phylogenetically more closely related to Mongolian taxa, indicating the replacement of Stenonychosaurus may have been from an earlier Asian form immigrating into North America.


 Latenivenatrix mcmasterae
Life reconstruction by Julius Csotonyi. 

Systematic palaeontology
Theropoda Marsh, 1881
Maniraptora Gauthier, 1986
Troodontidae Gilmore, 1924 sensu Turner et al. 2012
Troodontinae, clade nov.

DEFINITION: The most inclusive clade containing Gobivenator mongoliensis and Zanabazar junior.
DIAGNOSIS: Troodontinae differs from all other more basal troodontids by possessing an elongated ambiens process that is present on the anterior margin of the iliopubic symphysis.


Latenivenatrix gen. nov. 

Latenivenatrix mcmasterae gen. et sp. nov.

ETYMOLOGY: The generic name derives from “latens” (Latin for latent and hiding) and “venatrix” (feminine form in Latin for hunter). “Latent” refers to the taxon having been in multiple collections for nearly 100 years but unrecognized until now. “Hiding” has a similar meaning to latent, but also refers to a predatory animal hiding in cover until a suitable time to attack its prey. “Hunter” refers to it being carnivorous. The specific epithet honours the late mother of the first author, Lynne (McMaster) van der Reest.


 Stenonychosaurus inequalis Sternberg, 1932


Aaron J. van der Reest and Philip J. Currie. 2017. Troodontids (Theropoda) from the Dinosaur Park Formation, Alberta, with A Description of A Unique New Taxon: Implications for Deinonychosaur Diversity in North America. Canadian Journal of Earth Sciences. 54; xx. DOI: 10.1139/cjes-2017-0031

 Introducing Latenivenatrix mcmasterae, new Troodontid from the DPF published in @CanJEarthSci this morning! Sorry Troodon formosus #invalid

Dino hips discovery unravels species riddle  bit.ly/2ulK0w6 via @ualberta @EurekAlert

Résumé: Les troodontidés connus proviennent d’Asie et d’Amérique du Nord, les spécimens les plus complets provenant du Jurassique de la Chine et du Crétacé de la Mongolie. Les troodontidés nord-américains sont peu connus et les spécimens décrits consistent en des éléments isolés ou des squelettes partiels représentés par une quantité limitée de matériau. Un nouveau troodontidé de la partie supérieure de la Formation de Dinosaur Park (Campanien supérieur) est basé sur des crânes partiels, plusieurs vertèbres, des côtes, une gastralia, des chevrons, un sacrum, un pelvis partiel et des membres antérieurs et postérieurs partiels. Il s’agit du plus grand troodontidé connu, dont la hauteur est estimée a` 180 cm et la longueur, a` 350 cm. À l’instar d’autres troodontidés, il présente un processus ambiens allongé et une marge ventrale horizontale du processus post-acétabulaire. Il se distingue de tous les autres troodontidés dérivés par son pubis légèrement rétroversé doté d’une diaphyse courbée antéroventralement. Certains spécimens de la Formation de Dinosaur Park auparavant attribués a` Troodon, incluant plusieurs crânes partiels, un os dentaire et un métatarse associés, ainsi qu’un squelette partiel, sont réaffectés au nouveau taxon. Des éléments non décrits auparavant de la partie inférieure de la Formation de Dinosaur Park sont affectés a` Stenonychosaurus inequalis. La séparation stratigraphique claire de Stenonychosaurus inequalis et du nouveau taxon indique un remplacement de la faune de troodontidés semblable au renouvellement des grands ornithischiens de la même formation. Le nouveau taxon est plus étroitement apparenté sur le plan phylogénétique aux taxons de Mongolie, ce qui indique que le remplacement de Stenonychosaurus pourrait être dû a` l’immigration en Amérique du Nord d’une forme asiatique plus ancienne.


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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.

[Paleontology • 2019] Iberodactylus andreui • A New Crested Pterodactyloid from the Early Cretaceous of the Iberian Peninsula and the Radiation of the Clade Anhangueria ---ScRaBBlE


Iberodactylus andreui 
 Holgado, Pêgas, Canudo, Fortuny, Rodrigues, Company & Kellner. 2019

[C: Hamipterus tianshanensis] twitter.com/pterosaurios
Illustration by Hugo Salais @metazoastudio 

Abstract
The pterosaur record from the Iberian Peninsula is mostly scarce and undefined, but in the last few years some new taxa have been described from different Lower Cretaceous sites of Spain. Here we describe a new genus and species of toothed pterodactyloid pterosaur from the Barremian of the Iberian Peninsula, Iberodactylus andreui gen. et sp. nov., that shows a close and rather unexpected relationship with Hamipterus tianshanensis from China. A review of the phylogenetic relationships of the Anhangueria reveals a new family of pterodactyloid pterosaurs, the Hamipteridae fam. nov. being recovered as sister-group of the Anhangueridae. This latter clade can be in turn divided into the new clades Anhanguerinae and Coloborhynchinae. The close relationships of Iberodactylus and Hamipterus shows an interesting palaeobiogeographical correlation between the Chinese and Iberian pterosaur faunas during the Barremian (Lower Cretaceous). The discovery of Iberodactylus strongly suggests that the clade Anhangueria has clear ancestral ties in eastern Laurasia.


a life reconstruction of a flock of Iberodactylus andreui gen. et sp. nov. 

by Hugo Salais @metazoastudio 

Figure 3 Comparison of the rostrum of Iberodactylus andreui gen. et sp. nov. (MPZ-2014/1) with a cast of a skull of Hamipterus tianshanensis (specimen stored at the Museu Nacional/Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil (MN), MN-7536-V). Pictures in right lateral (A,C) and palatal (B,D) views.

Systematic Palaeontology

Pterosauria Kaup, 1834.
Pterodactyloidea Plieninger, 1901.
Ornithocheiroidea Seeley, 1870 sensu Kellner (2003).
Pteranodontoidea Marsh, 1876 sensu Kellner (2003).

Lanceodontia Andres et al. (2014).
Ornithocheirae Seeley, 1870 sensu Andres et al. (2014).
Anhangueria Rodrigues & Kellner, 2013.

Hamipteridae fam. nov.

Branch-based definition: The most inclusive clade containing Hamipterus tianshanensis, but not Ludodactylus sibbickiColoborhynchus clavirostris, and Anhanguera blittersdorffi.

Diagnosis: Crested anhanguerian pterodactyloids with the following synapomorphies: well-defined parallel and forward curved striae and sulci on the anterior region of the premaxillary crest, and an anterior rounded expansion of the anterior margin of the premaxillary crest.

Included species: Hamipterus tianshanensis and Iberodactylus andreui gen. et sp. nov.


Iberodactylus andreui gen. et sp. nov.

Etymology: From the Iberian Peninsula and the Iberian System, where the specimen was recovered, and ‘dactylos’ (δάκτυλος), finger (ancient Greek), a common suffix in pterosaur names; in honour of Mr. Javier Andreu, a local collector who found the fossil.

Holotype: Museo de Ciencias Naturales de la Universidad de Zaragoza (MPZ, Zaragoza, Spain) MPZ-2014/1; an anterior portion of a rostrum, including premaxillae –with a premaxillary crest– and maxillae, both with alveoli and broken teeth.

Horizon and locality: Los Quiñones site, Morenillo limestones of the Blesa Formation, Barremian (Lower Cretaceous), Oliete sub-basin, Iberian Basin. Obón, Teruel Province, Aragón, northeast Spain.

Diagnosis: Hamipterid pterodactyloid with the following autapomorphies: relatively deep premaxillary tip, premaxillary crest with its anterior margin curvature at an angle of about 80°.

Figure 4 Skull characters of species from different lineages within Anhangueria. Each skull is based on the holotypes and paratypes (dark grey), and elements from other specimens (light grey) re-marked with broken lines. Hamipterus tianshanensis (IVPP V 18935.1), in righ lateral view (A) and palatal view (B) Ludodactylus sibbicki (specimen stored at the Staatliches Museum für Naturkunde Karlsruhe, Karlsruhe, Germany (SMNK), SMNK PAL 3828), in right lateral view (C) Caulkicephalus trimicrodon (specimen stored at the Isle of Wight County Museum Service, Sandown, Isle of Wight, England, United Kingdom (IWCMS), IWCMS 2002.189), in palatal view (D) Tropeognathus mesembrinus (specimen stored at the Bayerische Staatssammlung für Paläontologie und Geologie, Munich, Germany (BSP), BSP 1987 I 46), in right lateral view (E), and palatal view (F); Anhanguera blittersdorffi (MN 4805-V), in right lateral view (G), and palatal view (H) and Uktenadactylus wadleighi (specimen stored at the Southern Methodist University, Dallas, Texas, United States (SMU), SMU 73058), in right lateral view (I), and palatal view (J). Arrows show the character states in each skull. Scale bar 5 cm. See the Supplementary Information for details about number and state of characters.

Anhanguerinae clade nov.

Stem-based definition: The most inclusive clade containing Anhanguera blittersdorffi but not Coloborhynchus clavirostris.

Diagnosis: Anhanguerids with an enlarged fourth premaxillary tooth, larger than the fifth and sixth teeth and as large as or larger than the third tooth.

Content: AnhangueraCaulkicephalusCearadactylusGuidracoLiaoningopterusLudodactylus and Maaradactylus.


Coloborhynchinae clade nov.

Stem-based definition: The most inclusive clade containing Coloborhynchus clavirostris but not Anhanguera blittersdorffi or Ludodactylus sibbicki.

Diagnosis: Anhanguerids with a quadrangular expansion of the premaxillary tip and a flat anterior surface of the rostrum24.

Content: ColoborhynchusSiroccopteryx and Uktenadactylus.

Figure 5: Origin and radiation of the clade Anhangueria during the Early Cretaceous.
(A) Phylogenetic relationships of Iberodactylus andreui gen. et sp. nov. within Pterodactyloidea. Colours show their continental origin: Africa (brown), Asia (orange), Europe (red), North America (blue), and South America (green). Intermittent bars show uncertain temporal range.

(B) Barremian world map showing the distribution of the localities with Anhangueria remains: (1) Hastings Group (late Berriasian/Valanginian), England; (2) Hami, Tugulu Group (?Berriasian-Albian), Xinjiang, China; (3) Bol’shoi Kemchug, lower Ilek Formation (?Hauterivian-Barremian) Krasnoyarsk Krai, Russia; (4) Las Hoyas, La Huérgina Formation (Barremian), Cuenca, Spain; (5) Los Quiñones, Blesa Formation (Barremian), Teruel, Spain; (6) Isle of Wight, Wessex Formation (Barremian), England; 

(C) Albian world map showing the distribution of the localities with Anhangueria remains: (7) Mogoito, Murtoi Formation (Aptian), Buryatia, Russia; (8) Sekmenevka Formation (Aptian), Belgorod Oblast, Russia; (9) Jiufotang Formation (Aptian), Liaoning, China; (10) Elrhaz Formation (Aptian), Niger; (11) Krasnyi Yar, Khilok Formation (Aptian), Buryatia, Russia; (12) Pedra Furada, Recôncavo Basin, Marizal Formation? (Aptian), Bahia, Brazil; (13) Sierra de Perijá, Apón Formation (Aptian), Zulia, Venezuela; (13) Crato Formation (late Aptian), Ceará, Brazil; (15) Khuren–Dukh, Dzun–Bayin Formation (Aptian-Albian), Mongolia; (16) Sheskatovo, upper Ilek Formation (Aptian-Albian), Kemerovo Oblast, Russia; (17) Chenini Formation (early Albian), Tunisia; (18) Romualdo Formation (Albian), Ceará, Brazil; (19) Lightning Ridge, Griman Creek Formation (Albian), New South Wales, Australia; (20) Tarrant County, Paw Paw Formation (Albian), Texas, USA; (21) Boulia, Toolebuc Formation (Albian), Queensland, Australia; (22) Cortes de Arenoso, Utrillas Formation (Albian), Valencia, Spain; (23) Cambridge Greensand (Cenomanian, but fossils Albian in age), England; (24) Hughenden, Mackunda Formation (late Albian), Queensland, Australia. Rose indicates purported remains associated within the clade Anhangueria. Red indicates taxa (referenced each one in A) within the clade Anhangueria. Palaeogeographic world maps modified after PALEOMAP Project (www.scotese.com).

  
Borja Holgado, Rodrigo V. Pêgas, José Ignacio Canudo, Josep Fortuny, Taissa Rodrigues, Julio Company and Alexander W. A. Kellner. 2019. On A New Crested Pterodactyloid from the Early Cretaceous of the Iberian Peninsula and the Radiation of the Clade Anhangueria. Scientific Reports. volume 9, 4940. DOI: 10.1038/s41598-019-41280-4 

    

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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.

[Paleontology • 2018] Zhiwenia coronata • A Soft‐bodied Euarthropod from the early Cambrian Xiaoshiba Lagerstätte of China supports A New Clade, Protosutura nov., of Basal Artiopodans with Dorsal Ecdysial Sutures ---ScRaBBlE


 Zhiwenia coronata
Du, Ortega‐Hernández, Yang & Zhang, 2018

  DOI: 10.1111/cla.12344  

 Abstract
We describe the exceptionally well‐preserved non‐trilobite artiopodan Zhiwenia coronata gen. et sp. nov. from the Cambrian Stage 3 Xiaoshiba Lagerstätte in Yunnan, China. The exoskeleton consists of a cephalic shield with dorsal sutures expressed as lateral notches that accommodate stalked lateral eyes, an elongate trunk composed of 20 tergites—the first of which is reduced—and a short tailspine with marginal spines. Appendicular data include a pair of multi‐segmented antennae, and homonomous biramous trunk limbs consisting of an endopod with at least seven podomeres and a flattened exopod with lamellae. Although the presence of cephalic notches and a reduced first trunk tergite invites comparisons with the petalopleurans Xandarella, Luohiniella and Cindarella, the proportions and exoskeletal tagmosis of Zhiwenia do not closely resemble those of any major group within Trilobitomorpha. Parsimony and Bayesian phylogenetic analyses consistently support Zhiwenia as sister‐taxon to the Emu Bay Shale artiopodan Australimicola spriggi, and both of them as closely related to Acanthomeridion from the Chengjiang. This new monophyletic clade, Protosutura nov., occupies a basal phylogenetic position within Artiopoda as sister‐group to Trilobitomorpha and Vicissicaudata, illuminates the ancestral organization of these successful euarthropods, and leads to a re‐evaluation of the evolution of ecdysial dorsal sutures within the group.

Fig. 2. Completely articulated specimen of Zhiwenia coronata gen. et sp. nov. from the Cambrian Stage 3 Xiaoshiba Lagerst€atte. (a) YKLP 12370 Holotype, dorsal view of a complete individual. (b) Interpretative diagram.

Fig. 5. Morphological reconstruction of Zhiwenia coronata gen. et sp. nov. from the Xiaoshiba Lagerst€atte.

Euarthropoda Lankester, 1904 (see discussion in Ortega-Hernandez, 2016) 
Artiopoda Hou and Bergstrom, 1997 (see also Stein € and Selden, 2012). 

Protosutura nov. 

Diagnosis. Non-biomineralized artiopodan euarthropods characterized by a short semicircular cephalic shield with simple dorsal ecdysial sutures located on either side of the head (secondarily lost in some representatives). Trunk elongate and with homonomous construction, consisting exclusively of freely articulating tergites of subequal length that convey a subrectangular to suboval exoskeletal outline. Posterior trunk tergites strongly curved. Tailspine spinose and short—less than half the trunk length—occasionally bearing marginal spines of variable number and size. 

Etymology. Derived from the Greek prefix proto (first, primitive), and the Latin root sutura, referencing the presence of dorsal ecdysial sutures on the head shield. 

Included taxa. Acanthomeridion serratum Hou et al., 1989; Acanthomeridion anacanthus Hou et al., 2017; Australimicola spriggi Paterson et al., 2012; Zhiwenia coronata gen. et. sp. nov.


Zhiwenia coronata gen. et. sp. nov.

Type species, locality and stratigraphy. Zhiwenia coronata gen. et. sp. nov. from the Xiaoshiba section (Fig. 1), Kunming, Yunnan; Cambrian Stage 3 Hongjingshao Formation, YunnanocephalusChengjiangaspisHongshiyanaspis Biozone (Yang et al., 2013, 2014, 2015, 2016a, b, 2018).

Etymology. The new genus is named in memory of Professor Zhi-Wen Jiang for his contributions to microfossils and biostratigraphy of Yunnan Province; coron (Latin), crown, referring to the shape of the two-notch bearing cephalic shield. 

Fig. 6. Results of parsimony and Bayesian phylogenetic analyses. All trees depict a strict consensus. Asterisks indicate presence of dorsal ecdysial sutures on cephalic shield.
 (c) Implied weight parsimony, k = 5, 10 (1 MPT, CI = 0.41, RI = 0.73). 


Kun‐Sheng Du, Javier Ortega‐Hernández, Jie Yang and Xi‐Guang Zhang. 2018. A Soft‐bodied Euarthropod from the early Cambrian Xiaoshiba Lagerstätte of China supports A New Clade of Basal Artiopodans with Dorsal Ecdysial Sutures. Cladistics.  DOI: 10.1111/cla.12344  

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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.

[Paleontology • 2018] Ingentia prima • An Early Trend Towards Gigantism in Triassic Sauropodomorph Dinosaurs ---ScRaBBlE


Ingentia prima
 Apaldetti, Martínez, Cerda, Pol & Alcober, 2018

Illustration: Jorge A. Gonzalez   twitter.com/PolDiego

Abstract 
Dinosaurs dominated the terrestrial ecosystems for more than 140 Myr during the Mesozoic era, and among them were sauropodomorphs, the largest land animals recorded in the history of life. Early sauropodomorphs were small bipeds, and it was long believed that acquisition of giant body size in this clade (over 10 tonnes) occurred during the Jurassic and was linked to numerous skeletal modifications present in Eusauropoda. Although the origin of gigantism in sauropodomorphs was a pivotal stage in the history of dinosaurs, an incomplete fossil record obscures details of this crucial evolutionary change. Here, we describe a new sauropodomorph from the Late Triassic of Argentina nested within a clade of other non-eusauropods from southwest Pangaea. Members of this clade attained large body size while maintaining a plesiomorphic cyclical growth pattern, displaying many features of the body plan of basal sauropodomorphs and lacking most anatomical traits previously regarded as adaptations to gigantism. This novel strategy highlights a highly accelerated growth rate, an improved avian-style respiratory system, and modifications of the vertebral epaxial musculature and hindlimbs as critical to the evolution of gigantism. This reveals that the first pulse towards gigantism in dinosaurs occurred over 30 Myr before the appearance of the first eusauropods.





Fig. 1: Skeletal anatomy of Ingentia prima gen. et sp. nov. from the Quebrada del Barro Formation, northwestern Argentina.
a–k, Holotype (PVSJ 1086). l–s, Referred material (PVSJ 1087). a–d, Mid-posterior cervical vertebrae, C5–C10 articulated series (a), close up of the pneumatic fossa with internal subfossae on the centrodiapophyseal fossa (cdf)26 of C8 (b) and C9 (c), and a complex of subfossae on the prcdf26 of C10 (d). e, Right partial scapula. f–i, Right forelimb: humerus (f), and the radius and ulna in proximal (g) and anterior (h) view, and distal articulation (i). j, Right manus in plantar view. k,l, Metacarpal I in proximal (k) and dorsal (l) view. m,n, Radius and ulnae with respective proximal ulna: right radius-ulna (m) and left radius-ulna (n) in posterior view. o, Left proximal end of fibula. p–r, Right partial pes: distal tarsal III–IV in proximal view (p), metatarsal I and II in dorsal view (q) and isolated phalanges (r). s, Four anterior caudal vertebrae and a distal one (bottom left).

 cen, centrum; dp, diapophysis; dt, distal tubercles of radius-ulna; f-sf, fossa-subfossae complex; ft, fibular tubercle; nc, neural canal; ol, olecranum; pm, posteromedial margin of the ulna; prz, prezygapophysis; rf, radial fossa; rib, rib. Scale bars: 10 cm in a and i–s; 2 cm in b–d; 20 cm in e–h; 120 cm for the skeleton. Red, holotype; yellow, referred specimen; orange, holotype and referred specimen.

Systematic palaeontology
Dinosauria Owen, 1842 
Saurischia Seeley, 1888 
Sauropodomorpha von Huene, 1932 

Lessemsauridae clade nov. 

Etymology. Related to Lessemsaurus sauropoides Bonaparte, 1999. 

Definition. The clade Lessemsauridae is defined here as L. sauropoides Bonaparte, 1999 and Antetonitrus ingenipes Yates and Kitching, 2003, and all the descendants from their most common ancestor. 

Ingentia prima gen. et sp. nov. 

Etymology. Ingentia’, huge (fem., Latin); ‘prima’, first (fem. Latin), referring to the large body size acquired during the early evolution of Dinosauria.

....



Cecilia Apaldetti, Ricardo N. Martínez, Ignacio A. Cerda, Diego Pol and Oscar Alcober. 2018. An Early Trend Towards Gigantism in Triassic Sauropodomorph Dinosaurs. Nature Ecology & Evolution.  DOI: 10.1038/s41559-018-0599-y  
 twitter.com/PolDiego/status/1016383540387352578

Huge new gentle giant dinosaur the size of a double decker bus discovered  metro.co.uk/2018/07/09/huge-gentle-giant-dinosaur-size-double-decker-bus-discovered-argentina-7695748 via @MetroUK

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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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